Multiphoton photosensitization system

专利摘要:
A method of multiphoton photosensitizing a photoreactive composition includes irradiating the photoreactive composition with light sufficient to cause simultaneous absorption of two or more photons to cause one or more acid or radical initiated chemical reactions that expose the composition to light. . The composition comprises (a) at least two reactive species capable of carrying out the reaction; And (b) at least one multicomponent, multiphoton photoinitiator system.
公开号:KR20030011354A
申请号:KR1020027017095
申请日:2001-06-14
公开日:2003-02-07
发明作者:데보로버트제이
申请人:쓰리엠 이노베이티브 프로퍼티즈 캄파니；
IPC主号:

专利说明:

Multiphoton Dimming System {MULTIPHOTON PHOTOSENSITIZATION SYSTEM}
[2] The two-photon absorption of the molecule was foreseen in 1931 by Goppert-Mayer. According to the pulsed ruby laser invention of 1960, experimental observation of two-photon absorption was realized. Subsequently, two-photon excitation has been applied in biological and optical data storage as well as other fields.
[3] There are two important differences between two-photon-induced photoprocesses and single photon-induced processes. Single photon absorption changes linearly with the intensity of incident radiation, while two photon absorption changes with a quadratic function. Large absorbance changes with the associated large force of the incident intensity. As a result, the multi-photon process can be performed with 3-dimensional spatial decomposition. In addition, since the multiphoton process involves simultaneous absorption of two or more photons, each photon has insufficient energy to excite the chromophores individually, but many of the same photoexcited state energy and total energy of the multiphoton photoresist used are the same. Photons of excitation absorbing chromophores. Exciting light is not attenuated by single photon absorption in the curable matrix or material, so that by using a beam focused at its depth within the material, molecules can be selectively moved deeper into the material than would be possible through single photon excitation. Here you can These two phenomena also apply to excitation, for example in tissues or other biological substances.
[4] Significant advantages have been obtained by applying multiphoton absorption in the field of photocuring and microfabrication. For example, in multiphoton lithography or stereolithography, the ability to record characteristics in 3-dimensions, as well as the ability to record characteristics with non-linear correlations to the intensity of multiphoton absorption less than the dispersion limit of the light used. (Which also interests holography). However, this work has now been limited by the slow recording time and high laser power due to the low photosensitivity of multiphoton activated photoreactive compositions. Therefore, it has been recognized that there is a need for a method of enhancing the photosensitivity of the composition.
[1] The present invention relates to multiphoton methods of photo-induced chemical reactions.
[159] 1 is a plot (micrometers per second) of the threshold writing speed for the coated film of Example 7 (see below).
[5] Summary of the Invention
[6] The present invention provides a multiphoton photosensitive method of the photoreactive composition. The method includes irradiating the composition with light sufficient to cause simultaneous absorption of two or more photons (preferably pulsed irradiation), inducing a chemical reaction initiated with one or more acids or radicals to which the composition is exposed to light. do. The photoreactive composition may comprise (a) at least one reactive species capable of carrying out a chemical reaction initiated by an acid or radical (preferably a curable species, more preferably a curable species selected from the group consisting of monomers, oligomers and reactive polymers). ) And (b) at least one multiphoton photoinitiator system.
[7] Multiphoton photoinitiator system to absorb (1) two or more photons of light, and at the same time an effective amount of chemical cross-sectional area of fluorescein (generally, 50 x 10 ^-50 cm ⁴ sec / photon, and C.Xu WWWebb the J.Opt. Soc.Am.B, 13, 481 is (1996) or more with a large two-photon absorption cross-section than measured) according to the method described in photon photosensitizer, (2) Alternatively, the multiphoton photosensitizer and the electron donor is one or more different As the compound, an electron donor capable of donating electrons to an electron excited state of the photosensitive agent (preferably, an electron donor compound having an oxidation potential greater than 0 and less than or equal to the oxidation potential of p-dimethoxybenzene), and (3) Electron excitation of the photosensitive agent One or more photoinitiators (preferably iodonium salts, sulfonium salts, diazonium salts, azinium salts, chloromethylated triazines) that can be photosensitized by accepting electrons from the state and forming one or more free radicals and / or acids; Tria A photosensitive agent selected from the group consisting of imidazolyl dimers, provided that the photoreactive composition is capable of carrying out a chemical reaction initiated by an acid and comprises at least one reactive species that is a curable species or a non-curable reactive polymer. If so, the multiphoton photoinitiator system comprises one or more electron donor compounds.
[8] The method of the present invention provides a multiphoton photosensitive agent having a relatively large two-photon absorption cross-sectional area (compared to the absorption cross-sectional area of many commonly used pigments) to the electron donor to effectively form reaction initiating species (radicals, acids, etc.). By further combining with an improved photoinitiator (in photochemically effective amount) to provide improved multiphoton photosensitivity. The increased sensitivity of the method allows for rapid assembly of, for example, 3-dimigen structures and allows the use of low peak intensity lasers (e.g. strong industrial laser Nd: YAG lasers of nanoseconds and picoseconds) on exposure. This provides the utility.
[9] Another aspect of the invention is the ability to simultaneously absorb (a) at least one reactive species capable of carrying out a chemical reaction initiated by an acid or radical except for the curing reaction and (b) a photochemically effective amount of (1) at least two photons One or more multiphoton photosensitizers, (2) one or more electron donor compounds that are different from the multiphoton photosensitizer, different from reactive species and capable of donating electrons to the electron excitation state of the photosensitizer and (3) electrons from the electron excitation state of the photosensitizer A novel multiphoton activated photoreactive composition comprising at least one multiphoton photoinitiator system comprising at least one photoinitiator that can be photosensitized by receiving at least one free radical and / or acid, wherein the composition comprises It does not contain curable species.
[10] Term Definition
[11] As used herein, "multiphoton absorption" means the simultaneous absorption of two or more photons to reach a reactive electron excitation state that is actively inaccessible by absorption of a single photon of the same energy.
[12] "Simultaneous" means two or more events occurring over a period of 10 ^-14 seconds or less.
[13] An "electron excited state" means an electron state of a molecule that is higher in energy than the electron bottom state of the molecule, that is, a state accessible by absorption of electromagnetic waves and having a life time of 10 ^-13 seconds or more.
[14] "Cure" means to carry out polymerization and / or to carry out crosslinking.
[15] “Optical system” means a system for adjusting light, wherein the system includes one or more members selected from refractive optical members such as lenses, reflective optical members such as mirrors, and diffractive optical members such as gratings. Optical members may include diffusers, waveguides, and other members known in the art.
[16] "3-Dimensional light pattern" means an optical image in which the light energy distribution is present in multiple planes or in volumes rather than in a single plane.
[17] "Exposure system" means an optical system plus a light source.
[18] "Enough light" means light of sufficient intensity and adequate wavelength to enable multiphoton absorption.
[19] By "photosensitive agent" is meant a molecule that lowers the energy required to activate the photoinitiator by absorbing light of less energy than the photoinitiator requires for activation and interaction of the photoinitiator to generate the photoinitiating species.
[20] The "photochemically effective amount" (of the photoinitiator system component) is determined by the reactive species under selected exposure conditions (as evidenced, for example, by changing density, viscosity, color, pH, refractive index or other physical or chemical properties). It is meant an amount sufficient to allow at least a partial reaction to be carried out.
[21] Reactive species
[22] Reactive species suitable for use in the photoreactive composition include curable and non-curable species. Curable species typically include, for example, additive polymerizable monomers and oligomers and additional crosslinkable polymers (free radically polymerizable or crosslinkable ethylenically unsaturated species, such as, for example, acrylates, methacrylates and styrenes). Vinyl compounds), as well as cationic polymerizable monomers and oligomers and cationic crosslinkable polymers (these species are most commonly described as acids, including, for example, epoxides, vinylethers, cyanate esters, etc.) Mixtures and these are preferred.
[23] Suitable ethylenically unsaturated species are described, for example, in Palazzotto et al., US Pat. No. 5,545,676, column 1, line 65 to column 2, line 26 and include mono-, di-, poly-acrylates and methacrylates (eg, For example, methyl acrylate, methyl methacrylate, ethyl acrylate, isopropyl methacrylate, n-hexyl acrylate, stearyl acrylate, allyl acrylate, glycerol diacrylate, glycerol triacrylate, ethylene glycol di Acrylate, diethylene glycol diacrylate, triethylene glycol dimethacrylate, 1,3-propanediol diacrylate, 1,3-propanediol dimethacrylate, trimethylolpropane triacrylate, 1,2, 4-butanetriol trimethacrylate, 1,4-cyclohexanediol diacrylate, pentaerythritol triacrylate, pentaerythritol tetraa Relate, pentaerythritol tetramethacrylate, sorbitol hexaacrylate, bis [1- (2-acryloxy)]-p-ethoxyphenyldimethylmethane, bis [1- (3-acryloxy-2-hydroxy )]-p-propoxyphenyldimethylmethane, trihydroxyethyl-isocyanurate trimethacrylate, bis-acrylate and bis-methacrylate of polyethylene glycol having a molecular weight of about 200 to 500, US Pat. No. 4,652,274 Copolymerizable mixtures of acrylated monomers such as those disclosed herein, acrylate oligomers such as those disclosed in US Pat. No. 4,642,126); Unsaturated amides (eg methylene bis-acrylamide, methylene bis-methacrylamide, 1,6-hexamethylene bis-acrylamide, diethylene triamine tris-acrylamide and beta-methacrylaminoethyl methacrylate) ; Vinyl compounds (eg, styrene, diallyl phthalate, divinyl succinate, divinyl adipate and divinyl phthalate) and the like and mixtures thereof. Suitable reactive polymers include polymers having pendant (meth) acrylate groups, for example 1 to about 50 (meth) acrylate groups per polymer chain. Examples of such polymers include aromatic acid (meth) acrylate half ester resins such as Sarbox ^™ resins (eg, Sarbox ^™ 400, 401, 402, 404 and 405) available from Sartomer. Other useful reactive polymers that are curable by free radical chemistry include polymers having a hydrocarbyl backbone and having pendant peptide groups having free radical polymerizable functionality attached thereto, such as described in US Pat. No. 5,235,015 to Ali et al. ). Mixtures of two or more monomers, oligomers and / or reactive polymers may be used as needed. Preferred ethylenically unsaturated species include acrylates, aromatic acid (meth) acrylate half ester resins, and polymers having pendant peptide groups with free radical polymerizable functionality attached to the hydrocarbyl backbone.
[24] Suitable cationic reactive species are described, for example, in Oxman et al., US Pat. Nos. 5,998,495 and 6,025,406 and include epoxy resins. Such materials are broadly referred to as epoxides, which include monomeric epoxy compounds and epoxides in polymer form and may be aliphatic, cycloaliphatic, aromatic or heterocyclic. These materials usually have an average of at least one polymerizable epoxy group per molecule (preferably at least about 1.5, more preferably at least about 2). The polymerizable epoxide is a linear polymer having terminal epoxy groups (eg diglycidyl ether of polyoxyalkylene glycol), a polymer having an oxirane monomer skeleton (eg polybutadiene polyepoxide) and pendant epoxy groups. Having polymers (eg, glycidyl methacrylate polymers or copolymers). The epoxide may be a pure compound or may be a mixture of compounds containing one or more epoxy groups per molecule. These epoxy containing materials can vary greatly depending on the nature of their backbones and substituents. For example, the backbone may be in any form and the substituents thereon may be any group that does not substantially interfere with cationic cure at room temperature. Examples of acceptable substituents include halogens, ester groups, ethers, sulfonate groups, siloxane groups, nitro groups, phosphate groups and the like. The molecular weight of the epoxy containing material may vary from about 58 to about 100,000 or more.
[25] Useful epoxy containing materials include 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, 3,4-epoxy-2-methylcyclohexylmethyl-3,4-epoxy-2-methylcyclohexanecarbox And those containing cyclohexene oxide groups such as epoxycyclohexanecarboxylates exemplified by bixlate and bis (3,4-epoxy-6-methylcyclohexylmethyl) adipate. A more detailed list of useful epoxides of these properties is described in US Pat. No. 3,117,099.
[26] Other epoxy containing materials useful include glycidyl ether monomers of the formula:
[27]
[28] Wherein R 'is alkyl or aryl and n is an integer from 1 to 6. Examples include the reaction of polyhydric phenols with chlorohydrins such as excess epichlorohydrin (eg, diglycidyl ether of 2,2-bis- (2,3-epoxypropoxyphenol) -propane). The glycidyl ether of polyhydric phenol obtained by making is mentioned. Further examples of this type of epoxide are described in US Pat. No. 3,018,262 and in the Epoxy Resin Handbook , Lee and Nerville, McGraw-Hill Book Co., New York (1967).
[29] Various commercial epoxy resins can be used. Specifically, readily obtainable epoxides are octadecylene oxide, epichlorohydrin, styrene oxide, vinyl cyclohexene oxide, glycidol, glycidyl methacrylate, diglycidyl ether of bisphenol A ( For example, Epon ^TM 828, Epon ^TM 825, Epon ^TM 1004, Epon ^TM 1010 from Resolution Performance Products, formerly Shell Chemical Co., as well as DER ^TM -331, DER ^TM -332, from Dow Chemical Co., Commercially available under the trade name DER ^TM -334), vinylcyclohexene dioxide (e.g., ERL-4206 from Union Carbide Corp.), 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexene carboxylate ( For example, Union Carbide Corp.'s ERL-4221 or Cyracure ^™ UVR 6110 or UVR 6105), 3,4-epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methyl-cyclohexene carboxylate (E.g., ERL-4201 from Union Carbide Corp.), bis (3,4-epoxy-6-methylcyclohexylmethyl) adipate (e.g. Er, ERL-4289 from Union Carbide Corp., bis (2,3-epoxycyclopentyl) ether (e.g. ERL-0400 from Union Carbide Corp.), aliphatic epoxy modified from propylene glycol (e.g., ERL-4050 and ERL-4052 from Union Carbide Corp.), dipentene dioxide (e.g., ERL-4269 from Union Carbide Corp.), epoxidized polybutadiene (e.g. Oxiron ^TM 2001 from FMC Corp.) , Silicone resins containing epoxy functionality, flameproof epoxy resins (e.g., brominated bisphenol type epoxy resins available from Dow Chemical Co., DER ^TM -580), 1,4-butanediol diol of phenolformaldehyde novolac Glycidyl ethers (e.g., DEN ^TM -431 and DEN ^TM -438, available from Dow Chemical Co.,), resorcinol diglycidyl ether (e.g., Kopoxite ^{TM from} Koppers Company, Inc.) ), Bis (3,4-epoxycyclohexyl) adipate (e.g., ERL-4299 or UVR-6128 from Union Carbide Corp.,), 2- (3,4-epoxycyclo Sil-5,5-spiro-3,4-epoxy) cyclohexane-meth-dioxane (eg, ERL-4234 from Union Carbide Corp.), vinylcyclohexene monooxide 1,2-epoxyhexadecane (E.g., UVR-6216 from Union Carbide Corp.), alkyl C ₈ -C ₁₀ glycidyl ethers (e.g. Heloxy ^™ Modifier 7 from Resolution Performance Products), alkyl C ₁₂ -C ₁₄ glycidyl Ethers (e.g. Heloxy ^TM Modifier 8 from Resolution Performance Products), butyl glycidyl ethers (e.g. Heloxy ^TM Modifier 61 from Resolution Performance Products), cresyl glycidyl ethers (e.g. Resolution Performance Products Alkyl glycidyl ethers such as Heloxy ^TM Modifier 62), p-tert-butylphenyl glycidyl ether (e.g., Heloxy ^TM Modifier 65 from Resolution Performance Products), diglycidyl ether of 1,4-butanediol (for example, Heloxy Modifier 67 ^TM of Resolution Performance Products) polyfunctional glycidyl ethers, such as neopentyl Diglycidyl ether of a glycol (for example, Heloxy ^TM of Resolution Performance Products Modifier 68), cyclohexanedimethanol diglycidyl ether of di-methanol (for example, Heloxy ^TM Modifier 107 of Resolution Performance Products), trimethylol ethane Triglycidyl ether (e.g., Heloxy ^TM Modifier 44 from Resolution Performance Products), trimethylol propane triglycidyl ether (e.g. Heloxy ^™ Modifier 48 from Resolution Performance Products), polyglycidyl ether of aliphatic polyol ( For example, Heloxy ^™ Modifier 84 from Resolution Performance Products, polyglycol diepoxide (eg, Heloxy ^™ Modifier 32 from Resolution Performance Products) bisphenol F epoxide (eg, GY- from Ciba-Geigy Corp. 281 or Epon ^™ -1138) and 9,9-bis [4- (2,3-epoxypropoxy) -phenyl] florenone (eg, Epon ^™ 1079 from Resolution Performance Products).
[30] Other useful epoxy resins include copolymers of acrylic acid esters of glycidol (eg, glycidyl acrylate and glycidyl methacrylate) with one or more copolymerizable vinyl compounds. Examples of such copolymers include 1: 1 styrene-glycidyl methacrylate, 1: 1 methyl methacrylate-glycidyl acrylate and 62.5: 24: 13.5 methyl methacrylate-ethyl acrylate-glycidyl methacrylate. There is acrylate. Other useful epoxy resins are known and include epoxides such as epichlorohydrin, alkylene oxides (eg propylene oxide), styrene oxides, alkenyl oxides (eg butadiene oxide) and glycine Cylyl esters (eg ethyl glycidate).
[31] Useful epoxy functional polymers include epoxy functional silicones, such as those described in US Pat. No. 4,279,717 to Eckberg, which can be obtained from General Electric Company. These are polydimethylsiloxanes in which 1-20 mole% of silicon atoms are substituted with epoxyalkyl groups (preferably epoxy cyclohexylethyl as described in US Pat. No. 5,753,346 to Kessel).
[32] Mixtures of various epoxy containing materials can also be used. Such mixtures may include two or more weight average molecular weight distributions of the epoxy containing compound [(low molecular weight (200 or less), medium molecular weight (about 200 to 10,000) and high molecular weight (about 10,000 or more)). In addition, the epoxy resin may comprise a mixture of epoxy containing materials having different chemical properties (eg, aliphatic and aromatic), functional (eg, polar and nonpolar) Other cationic reactive polymers (eg, vinyl ether, etc.) ) May be additionally incorporated if necessary.
[33] Preferred epoxides include aromatic glycidyl epoxy (eg, Epon ^™ resin from Resolution Performance Products) and cycloaliphatic epoxy (eg, ERL-4221 and ERL-4299 from Union Carbide Corp.).
[34] Suitable cationic reactive species also include vinyl ether monomers, oligomers and reactive polymers [eg, methyl vinyl ether, ethyl vinyl ether, tert-butyl vinyl ether, isobutyl vinyl ether, triethylene glycol divinyl ether (Rapi- Cure ^TM DVE-3, available from International Specialty Products, Wayne, NJ), trimethylolpropane trivinyl ether (available from TMPTVE, BASF Corp., Mount Olive, NJ), Vectomer ^TM divinyl ether resin from Allied Signal (e.g. For example, Vectomer ^™ 2010, Vectomer ^™ 2020, Vectomer ^™ 4010 and Vectomer ^™ 4020 and their equivalents available from other manufacturers)] and mixtures thereof .. Mixtures of one or more vinyl ether resins and / or one or more epoxy resins (Any ratio) may also be used. Polyhydroxy functional materials (such as those described in US Pat. No. 5,856,373 (Kaisaki et al.)) May also be epoxy- and / or non- It can be used in combination with a neyl ether-functional material.
[35] Non-curable species include, for example, reactive polymers whose solubility can be increased with acid- or radical-derived reactions. Such reactive polymers include, for example, ester group-containing water-insoluble polymers that can be converted to water-soluble acid groups (eg, poly (4-tert-butoxycarbonyloxystyrene)) by photofabricated acids. Non-curable species are also described in chemically amplified photoresists (RDAllen, GM Wallraff, WDHinsberg and LLSimpson, "High Performance Acrylic Polymers for Chemically Amplified Photoresist Application" J.Vac.Sci.Technol.B. 9 , 3357 (1991)). ). The chemically amplified photoresist concept is now widely used for microchip fabrication, particularly for sub-0.5 micron (or sub 0.2 micron) properties. In such photoresist systems, catalytic species (typically hydrogen ions) can be produced by radiation, causing a cascade of chemical reactions. This cascade occurs when hydrogen ions initiate a reaction to produce more hydrogen ions or other acidic species, thereby amplifying the reaction rate. Examples of conventional acid catalyzed chemically amplified photoresist systems include deprotection (eg, TH-butoxycarbonyloxystyrene resists described in US Pat. No. 4,491,628, THP such as those described in US Pat. No. 3,779,778). Phenolic materials, tetrahydropyran (THP) methacrylate based materials, t-butyl methacrylate based materials such as those described in Proc. SPIE 2438 , 474 (1995) by RDAllen and the like); Depolymerization (eg, polyphthalaldehyde based materials); And rearrangements (eg, materials based on pinacol rearrangements).
[36] Useful non-curable species also include leuco dyes, which tend to be colorless until oxidized by the acid produced by the multiphoton photoinitiator system and exhibit a visible color once oxidized. (The oxidized pigments show color due to the absorption of light in the visible portion of the electromagnetic spectrum (about 400-700 nm).) The leuco dyes useful in the present invention can be oxidized or are reactive under intermediate oxidation conditions, Under conditions, they are not very reactive and do not oxidize. Many such chemical groups of leuco dyes are known to the ordinary chemist.
[37] Leuco dyes useful as the reactive species of the present invention include acrylated leucoazine, phenoxazine and phenothiazine, which may be represented in part by the formula:
[38]
[39] Wherein X is selected from O, S and -NR ¹¹ , S is preferred,
[40] R ¹ and R ² are independently selected from H and from 1 to about 4 alkyl groups, R ³ , R ⁴ , R ⁶ and R ⁷ are independently selected from H and from 1 to about 4 alkyl groups, Preferably methyl, R ⁵ is selected from 1 to about 16 carbon atoms of the carbon atom, 1 to about 16 alkoxy groups of carbon atoms and an aryl group of up to about 16 carbon atoms, and R ⁸ is -N (R ¹ ) Is selected from (R ² ), H, 1 to about 4 carbon atoms, wherein R ¹ and R ² are as described above and independently selected, and R ⁹ and R ¹⁰ are H and 1 to about carbon atoms. Independently selected from four alkyl groups, R ¹¹ is selected from from 1 to about 4 carbon atoms and aryl groups (preferably phenyl groups) of up to about 11 carbon atoms. The following compounds are examples of leuco dyes of these species.
[41]
[42]
[43] Kofichem II
[44]
[45] Other useful leuco dyes are Leuco Crystal Violet (4,4'4 "-methylidritris- (N, N-dimethylalanine)), Leuco Malachite Green (p, p'-benzylidenebis- (N, N-dimethyl) Aniline)), Leuco Atacryl Orange-LGM (Color Index Basic Orange 21, Comp.No.48035 (Fisher base compound)),
[46]
[47] Leuco Atacryl Brilliant Red-4G (Color Index Basic Red 14),
[48]
[49] Leuco Atacryl Yellow-R (Color Index Basic Yellow 11, Comp.No. 48055)
[50]
[51] Leuco Ethyl Violet (4,4 ', 4 "-methylidinetris- (N, N-diethylaniline), Leuco Victoria Blu-BGO (Color Index Basic Blue 728a, Comp.No. 44040; 4,4'-methyl Lidinbis- (N, N-dimethylaniline) -4- (N-ethyl-1-naphthalamine)), and LeucoAtlantic Fuchsine Crude (4,4 ', 4 "-methylidritris-aniline), It is not limited to this.
[52] The leuco dye (s) typically comprise at least about 0.01% by weight (preferably at least about 0.3% by weight, more preferably at least about 1% by weight, most preferably at least about 2 to 10% by weight) of the total weight of the photosensitive layer. May exist at the level. Other materials such as binders, plasticizers, stabilizers, surfactants, antistatic agents, coating aids, lubricants, fillers and the like may also be present in the photosensitive layer.
[53] If desired, mixtures of different types of reactive species may be used in the photoreactive composition. For example, mixtures of free radical reactive species and cationic reactive species, mixtures of curable species and non-curable species, and the like are also useful.
[54] Photoinitiator system
[55] (1) multiphoton photosensitizer
[56] Multiphoton photosensitizers suitable for use in multiphoton photoinitiator systems of photoreactive compositions are capable of simultaneously absorbing two or more photons when exposed to sufficient light and fluorescein (ie 3 ', 6'-dihydroxyspiro [isobenzo Furan-1 (3H), greater than 9 '-[9H] xanthene] 3-one). Typically, the cross-sectional area is described in the J.Opt.Soc.Am.B, 13, 481 (1996) ( See Marder and Perry et al., International Publication WO 98/21521, 85 side line 18-22) by C.Xu and WWWebb As measured by one method, it may be at least about 50 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[57] The method involves comparing the two-photon fluorescence intensity of the photosensitizer with the reference compound (under equivalent excitation intensity and photosensitizer concentration conditions). Reference compounds can be chosen to match the spectral ranges as closely as possible encompassed by photosensitizer absorption and fluorescence. In one possible experimental setting, the excitation beam can be divided into two arms, with 50% of the excitation intensity divided by the photosensitizer and 50% by the reference compound. The relative fluorescence intensity of the photosensitizer relative to the reference compound can then be measured using two photomultiplier tubes or other calibrated detectors. Finally, the fluorescence quantum efficiency of both compounds can be measured under one photon excitation.
[58] Methods of measuring fluorescence and phosphorescent quantum yields are known in the art. Typically, the area under the fluorescence (or phosphorescence) spectrum of the compound of interest is compared to the area under the fluorescence (or phosphorescence) spectrum of the standard luminescent compound having a known fluorescence (or phosphorescence) quantum yield and appropriate corrections are made (e.g. Optical intensity of the composition at the wavelength, the structure of the fluorescence detection device, the difference in the emission wavelength and the response of the detector to different wavelengths). Standard methods are described, for example, in IBBerlman, Handbook of Fluorescence Spectra of Aromatic Molecules , 2nd edition, p . 24-27, Academic Press, New York (1971); JNDemas and GACrosby, J. Phys. Chem. 75, 991-1024 (1971); JVMorris, MAMahoney and JRHuber, J. Phys. Chem. 80, are described in the 969-974 (1976).
[59] Assuming that the emission states are the same under one- and two-photon excitation (normal assumption), the two-photon absorption cross-sectional area of the photoresist, (δ _sam ), is equal to δ _ref K (I _sam / I _ref ) (φ _sam / φ _ref ) Where δ _ref is the two-photon absorption cross section of the reference compound, I _sam is the fluorescence intensity of the photosensitizer, I _ref is the fluorescence intensity of the reference compound, φ _sam is the fluorescence quantum efficiency of the photosensitizer, and φ _ref is the reference The fluorescence quantum efficiency of the compound, K is the correction factor that accounts for the two detector responses and the slight difference in the optical path. K can be determined by measuring the response with the same photosensitizer in both the sample and the reference arm. To assure valid measurements, one can confirm the apparent second-order dependence of the two-photon fluorescence intensity on the excitation power, and relatively low concentrations of both the sensitizer and the reference compound can be used (the effect of fluorescence resorption and sensitizer aggregation) To avoid).
[60] If the photosensitizer is not fluorescent, the yield of the electron excited state can be measured and compared with known standards. In addition to the above-described method for measuring fluorescence yield, various methods for measuring excited state yield are known (e.g., transient absorption, phosphorescence yield, photoproduct formation or disappearance of photoresist (from photoreaction), etc.).
[61] Preferably the two-photon absorption cross-sectional area of the photosensitizer is at least about 1.5 times greater than fluorescein (or alternatively, at least about 75 × 10 ⁻⁵⁰ cm ⁴ sec / photons, measured by the method described above), more preferably At least about 2 times (or alternatively, at least about 100 x 10 ^-50 cm ⁴ seconds / photons) fluorescein, and most preferably at least about 3 times, or at least about 150, fluorescein x ^10-50 cm ⁴ seconds / photon or more), optionally about 4 times or more (or alternatively, about 200 × ^10-50 cm ⁴ seconds / photon or more) of fluorescein.
[62] Preferably the photosensitizer is soluble in the reactive species (if the reactive species is a liquid), or is compatible with the reactive species and other conjugates included in the compositions (described below). Most preferably 2-methyl-4,6- under continuous irradiation (single photon absorption conditions) in a wavelength range superimposed on the single photon absorption spectrum of the photosensitive agent, using the test method described in US Pat. No. 3,729,313. Bis (trichloromethyl) -s-triazine can also be photosensitized. Using currently available materials, the test can be conducted as follows.
[63] Standard test solutions can be prepared having the following composition: 5.0 parts of a 5% (w / v) solution in methanol of polyvinyl butyral (Butvar ^™ B76, Monsanto) with a hydroxyl content of 45,000-55,000 molecular weight, 9.0-13.0%. ; Trimethylolpropane trimethacrylate and 0.3 parts of 2-methyl-4,6-bis (trichloromethyl) -s- triazine 0.03 parts (Bull.Chem.Soc.Japan, 42, 2924 - Reference (1969) 2930) . To this solution can be added 0.01 part of the compound to be tested as a photosensitizer. The resulting solution is then knife coated using a 0.05 mm knife orifice on a 0.05 mm transparent polyester film and the coating can be air dried for about 30 minutes. The 0.05 mm of transparent polyester cover film can be carefully placed so that the air content is minimal on a dry but soft sticky coating. The resulting sandwich structure can then be exposed for 3 minutes to incident light of 161,000 lux from a tungsten light source that provides light in the visible and ultraviolet range (FCH ^™ 650 Watt Quarters-Iodine Lamp, General Electric). The exposure may be through a stencil to provide exposed and unexposed areas in the structure. The cover film can be removed after exposure and the coating can be treated with finely divided colored powder (eg, color toner powder of the type commonly used in dry printing). If the compound tested is a photosensitizer, the trimethylolpropane trimethacrylate monomer is in the region exposed to light by the free radicals generated as light from 2-methyl-4,6-bis (trichloromethyl) -s-triazine. Will polymerize. Since the polymerized area will be substantially viscous, the colored powder is almost selectively attached only to the viscous, unexposed areas of the coating and provides a corresponding visual image in the stencil.
[64] Preferably, the photosensitizer may be selected in consideration of some storage stability. Thus, the choice of particular photosensitizer may vary to some extent depending on the particular reactive species used (as well as the choice of electron donor compound and / or photoinitiator).
[65] Particularly preferred multiphoton photosensitizers exhibit a large multiphoton absorption cross section, for example Rhodamine B (ie N- [9- (2-carboxyphenyl) -6- (diethylamino) -3H-xanthene-). 3-ylidene] -N-ethylethaneaminochloride or hexafluoroantimonate) and four groups of photosensitizers described in, eg, International Publications WO 98/21521 and WO 99/53242, such as, for example, Marder and Perry. The four groups can be described as follows: (a) a molecule linked to a π (pi) -electron bridge in which two donors are conjugated, (b) a conjugated π () in which two donors are substituted with one or more electron acceptors. pi)-a molecule linked to the electron bridge, (c) a π (pi) -linked molecule with two receptors conjugated and (d) a conjugated π (pi) with two receptors substituted with at least one electron donor group A molecule linked to an electron bridge, where "bridge" refers to a molecular fragment that connects two or more chemical groups, and a "donor" refers to an atom with a low ion potential that can be bound to a conjugated π (pi) -electron bridge or Atom group means "receptor" means an atom or group of atoms having a high electron affinity that can be bonded to the conjugated π (pi) -electron bridge.
[66] Representative examples of such preferred photosensitizers include:
[67]
[68]
[69]
[70]
[71]
[72] The aforementioned four groups of photosensitizers can be prepared under standard Wittig conditions or by reacting aldehydes with lides using a McMurray reaction (see International Patent Publication WO 98/21521).
[73] Other compounds have been described by Reinhardt et al. (Eg, US Pat. Nos. 6,100,405, 5,859,251 and 5,770,737) having large multiphoton absorption cross sections, but these cross sections were measured by methods other than those described above. Representative examples of such compounds include the following:
[74]
[75]
[76]
[77] (2) electron donor compound
[78] Electron donor compounds that can be used in the multiphoton photoinitiator system of the photoreactive composition are compounds (except for the photosensitizer itself) that can donate electrons to the electron excited state of the photosensitizer. Such compounds can optionally be used to increase the multiphoton photosensitivity of the photoinitiator system to reduce the exposure required to cause the photoreaction of the photoreactive composition to occur. The electron donor compound preferably has an oxidation potential of 0 or more and below an oxidation potential of p-dimethoxybenzene. It is preferable that the oxidation potential is about 0.3 to 1 volt with respect to the standard saturated magenta electrode ("S.C.E").
[79] The electron donor compound is also preferably soluble in the reactive species and is selected in part in view of storage stability (as described above). Suitable donors generally can increase the phase density or cure rate of the photoreactive composition upon exposure to light of the desired wavelength.
[80] Those skilled in the art will appreciate that when using cationic reactive species, the electron donor compound (if significantly basic) can adversely affect the cationic reaction (e.g., column 7 line 62 in column 6 of US Pat. No. 6,025,406 (Oxman et al.)). 8 see discussion on line 49].
[81] In general, electron donor compounds suitable for use with certain photosensitizers and photoinitiators can be selected by comparing the oxidation and reduction potentials of the three components (see, eg, US Pat. No. 4,859,572 (Farid et al.)). Such potentials can be measured experimentally (eg, by methods described in RJ Cox, Photographic Sensitivity , Chapter 15, Academic Press (1973)), or by NL Weinburg, Technique of Electroorganic Synthesis Part II Techniques of Chemistry , Vol. . V (1975) and by CK Mann and KK Barnes ( Electrochemical Reactions in Nonaqueous Systems (1970)). The potentials represent relative energy relationships and can be used in the following manner to assist in the electron donor compound selection.
[82] When the photosensitizer is in an electron excited state, the electrons in the most occupied molecular orbital (HOMO) of the photosensitizer are elevated to a higher energy level (ie, the lowest unoccupied molecular orbital (LUBO) of the photosensitizer) and the vacancy is the first occupied molecule. Is left on the orbital. Photoinitiators can accept electrons from higher energy orbitals and electron donor compounds can donate electrons to fill the voids of the initially occupied orbitals if certain relative energy relationships are satisfied.
[83] If the reduction potential of the photoinitiator is less negative (or a larger positive value) than the reduction potential of the photoresist, electrons in the higher energy orbital of the photoresist are easily transferred from the photoresist to the lowest unoccupied molecular orbital (LUMO) of the photoinitiator. Because it represents the process. Although this process is rather endothermic (ie, the reduction potential of the photosensitizer is a negative value up to 0.1 volts greater than the reduction potential of the photoinitiator) ambient thermal activation can easily overcome this small barrier.
[84] In a similar manner, electrons that move from the HOMO of the electron donor compound to the orbital vacancies of the photoconductor when the oxidation potential of the electron donor compound is less positive (or greater negative) than the oxidation potential of the photosensitizer It moves to a low potential, which also represents an exothermic process. Even if this process is a weak endothermic reaction (ie, the oxidation potential of the photosensitizer is a positive value up to 0.1 volts greater than the oxidation potential of the electron donor compound), ambient thermal activation can easily overcome this small barrier.
[85] Weak endothermic reactions where the reduction potential of the photosensitizer is a negative value up to 0.1 volts greater than the reduction potential of the photoinitiator, or the oxidation potential of the photosensitizer is a positive value up to 0.1 volts greater than the oxidation potential of the electron donor compound is a photoinitiator or electron donor compound This happens in all cases, regardless of whether they react first with the photosensitizer in this excited state. When the photoinitiator or electron donor compound reacts with the photosensitizer in an excited state, the reaction is preferably exothermic or only a weak endothermic reaction. If the photoinitiator or electron donor compound reacts with photosensitive ionic radicals, an exothermic reaction is still preferred, but in many cases more endothermic reactions can be expected to occur. Thus, the reduction potential of the photosensitizer may be a negative value up to 0.2 volts (or more) than the reduction potential of the second-to-react photoinitiator, or the oxidation potential of the photosensitizer may be second-to-react. It may be a positive value up to 0.2 volts (or more) than the oxidation potential of the reactant electron donor compound.
[86] Examples of suitable electron donor compounds are described in DF Eaton, Advances in Photochemistry , B. Voman et al., Volume 13, pp. 427-488, John Wiley and Sons, New York (1986); US Patent No. 6,025,406 to Oxman et al. (Columns 7 lines 42-61); And US Pat. No. 5,545,676 to Palazzotto et al. (Column 4 row 14 to column 5 row 18). Such electron donor compounds include amines such as triethanolamine, hydrazine, 1,4-diazabicyclo [2.2.2] octane, triphenylamine [and triphenylphosphine and triphenylarcin analogs thereof], aminoaldehydes and amino Silanes), amides (e.g. phosphoamides), ethers (e.g. thioethers), urea (e.g. thioureas), sulfinic acid and salts thereof, salts of ferrocyanide, ascorbic acid and salts thereof, dithiocarbamic acid And salts thereof, salts of xanthic acid, salts of ethylene diamine tetraacetic acid, (alkyl) _n (aryl) _m borate (n + m = 4) (preferably tetraalkylammonium salts), various organometallic compounds such as SnR ₄ compounds Wherein each R is independently selected from alkyl, aralkyl (especially benzyl), aryl and alkaryl groups (e.g., nC ₃ H ₇ Sn (CH ₃ ) ₃ , (allyl) Sn (CH ₃ ) ₃ and ( Benzyl) Sn (compounds such as nC ₃ H ₇ ) ₃ ), ferrocene and the like and mixtures thereof. The electron donor compound may be unsubstituted or substituted with one or more noninterfering substituents. Particularly preferred electron donor compounds include electron donor atoms (eg, nitrogen, oxygen, phosphorus or sulfur atoms) and removable hydrogen atoms bonded to carbon or silicon atoms at the alpha position of the electron donor atom.
[87] Preferred amine electron donor compounds include alkyl-, aryl-, alkaryl- and aralkyl-amines (e.g. methylamine, ethylamine, propylamine, butylamine, triethanolamine, amylamine, hexylamine, 2,4-dimethylaniline , 2,3-dimethylaniline, o-, m- and p-toluidine, benzylamine, aminopyridine, N, N'-dimethylethylenediamine, N, N'-diethylethylenediamine, N, N'-dibenzyl Ethylenediamine, N, N'-diethyl-1,3-propanediamine, N, N'-diethyl-2-butene-1,4-diamine, N, N'-dimethyl-1,6-hexanediamine, Piperazine, 4,4'-trimethylenedipiperidine, 4,4'-ethylenedipiperidine, pN, N-dimethyl-aminophenethanol and pN-dimethylaminobenzonitrile); Aminoaldehydes (eg, p-N, N-dimethylaminobenzaldehyde, p-N, N-diethylaminobenzaldehyde, 9-julolidine carboxaldehyde and 4-morpholinobenzaldehyde); And aminosilanes (eg trimethylsilylmorpholine, trimethylsilylpiperidine, bis (dimethylamino) diphenylsilane, tris (dimethylamino) methylsilane, N, N-diethylaminotrimethylsilane, tris (dimethylamino) phenyl Silane, tris (methylsilyl) amine, tris (dimethylsilyl) amine, bis (dimethylsilyl) amine, N, N-bis (dimethylsilyl) aniline, N-phenyl-N-dimethylsilylaniline and N, N-dimethyl- N-dimethylsilylamine); And mixtures thereof. Tertiary aromatic alkylamines, especially compounds having one or more electron withdrawing groups on aromatic rings, have been found to provide particularly good storage stability. Excellent storage stability was also obtained using amines that were solid at room temperature. The use of amines containing one or more zoloridinyl moieties resulted in good photography speeds.
[88] Preferred amide electron donor compounds include N, N-dimethylacetamide, N, N-diethylacetamide, N-methyl-N-phenylacetamide, hexamethylphosphoramide, hexaethylphosphoramide, hexapropylphosphor Amides, trimorpholinophosphine oxides, tripiperidinophosphine oxides and mixtures thereof.
[89] Preferred alkylaryl borate salts
[90]
[91] Where Ar is phenyl, naphthyl, substituted (preferably fluorine substituted) phenyl, substituted naphthyl, and a group having a greater number of fused aromatic rings), as well as tetramethylammonium n-butyl Triphenylborate and tetrabutylammonium n-hexyl-tris (3-fluorophenyl) borate (commercially available as CGI 437 and CGI 746 from Ciba Specialty Chemicals Corporation) and mixtures thereof.
[92] Suitable ether electron donor compounds include 4,4'-dimethoxybiphenyl, 1,2,4-trimethoxybenzene, 1,2,4,5-tetramethoxybenzene and mixtures thereof. Suitable urea electron donor compounds include N, N'-dimethylurea, N, N-dimethylurea, N, N'-diphenylurea, tetramethylthiourea, tetraethylthiourea, tetra-n-butylthiourea, N , N-di-n-butylthiourea, N, N'-di-n-butylthiourea, N, N-diphenylthiourea, N, N'-diphenyl-N, N'-diethylthiourea And mixtures thereof.
[93] Preferred electron donor compounds for free radical induction reactions include amines, alkylarylborate salts and salts of aromatic sulfinic acids comprising one or more zoloridinyl moieties. However, the electron donor compound may be excluded for this reaction as needed (eg to improve the storage stability of the photoreactive composition or to change the resolution, contrast and interrelationship). Preferred electron donor compounds for the acid induction reaction are 4-dimethylaminobenzoic acid, ethyl 4-dimethylaminobenzoate, 3-dimethylaminobenzoic acid, 4-dimethylaminobenzoin, 4-dimethylaminobenzaldehyde, 4-dimethylaminobenzonitrile, 4-dimethylaminophenethyl alcohol and 1,2,4-trimethoxybenzene.
[94] (3) photoinitiator
[95] Suitable photoinitiators (ie, electron acceptor compounds) of the reactive species of the photoreactive composition are those that can accept and photosensitize electrons from the electron excited state of the multiphoton photosensitive agent to form one or more free radicals and / or acids. Such photoinitiators include iodonium salts (eg, diaryliodonium salts), methylated triazines (eg 2-methyl-4,6-bis (trichloromethyl) -s-triazine, 2,4,6- Optionally with groups such as tris (trichloromethyl) -s-triazine and 2-aryl-4,6-bis (trichloromethyl) -s-triazine), diazonium salts (e.g. alkyl, alkoxy, halo or nitro) Substituted phenyldiazonium salts), sulfonium salts (e.g. triarylsulfonium salts optionally substituted with alkyl or alkoxy groups and optionally having a 2,2'oxy group bridge near the aryl moiety), azinium salts (e.g., N-alkoxypyridies Nium salts) and triarylimidazolyl dimers (preferably 2,4,5-triphenylimidazolyl dimers such as 2,2 ', 4,4', 5,5'-tetraphenyl-1,1'- Biimidazole, which may optionally be substituted by groups such as alkyl, alkoxy or halo) and the like and mixtures thereof.
[96] The photoinitiator is preferably soluble in the reactive species and is preferably storage stable (ie, does not spontaneously promote the reaction of the reactive species when dissolved in the presence of the photosensitizer and electron donor compound). Thus, the choice of particular photoinitiator may vary to some extent depending upon the particular reactive species, photosensitizer and electron donor compound selected as described above. Photoinitiators are onium salts (eg, iodonium, sulfonium or diazonium salts) if the reactive species can carry out an acid initiated chemical reaction.
[97] Suitable iodonium salts include those described in columns 2 28-46 of US Pat. No. 5,545,676 to Palazzotto et al. Suitable iodonium salts are also disclosed in US Pat. Nos. 3,729,313, 3,741,769, 3,808,006, 4,250,053, and 4,394,403. Iodonium salt is a simple salt (for ^{example, Cl -, Br -, I} - or C ₄ H ₅ SO ₃ ^- salt containing the same anion as) or a metal complex salt (for _{^{example, SbF 6 -, PF 6 -}} , BF 4 - It may be a salt containing a) ^-, tetrakis (perfluoro phenyl) borate, SbF ₅ OH ^- or AsF _6. If necessary, a mixture of iodonium salts can be used.
[98] Examples of useful aromatic iodonium complex salt photoinitiators include diphenyliodonium tetrafluoroborate; Di (4-methylphenyl) iodonium tetrafluoroborate; Phenyl-4-methylphenyliodonium tetrafluoroborate; Di (4-heptylphenyl) iodonium tetrafluoroborate; Di (3-nitrophenyl) iodonium hexafluorophosphate; Di (4-chlorophenyl) iodonium hexafluorophosphate; Di (naphthyl) iodonium tetrafluoroborate; Di (4-trifluoromethylphenyl) iodonium tetrafluoroborate; Diphenyliodonium hexafluorophosphate; Di (4-methylphenyl) iodonium hexafluorophosphate; Diphenyliodonium hexafluoroarsenate; Di (4-phenoxyphenyl) iodonium tetrafluoroborate; Phenyl-2-thienyliodonium hexafluorophosphate; 3,5-dimethylpyrazolyl-4-phenyliodonium hexafluorophosphate; Diphenyliodonium hexafluoroantimonate; 2,2'-diphenyliodonium tetrafluoroborate; Di (2,4-dichlorophenyl) iodonium hexafluorophosphate; Di (4-bromophenyl) iodonium hexafluorophosphate; Di (4-methoxyphenyl) iodonium hexafluorophosphate; Di (3-carboxyphenyl) iodonium hexafluorophosphate; Di (3-methoxycarbonylphenyl) iodonium hexafluorophosphate; Di (3-methoxysulfonylphenyl) iodonium hexafluorophosphate; Di (4-acetamidophenyl) iodonium hexafluorophosphate; Di (2-benzothienyl) iodonium hexafluorophosphate; And diphenyl iodonium hexafluoroantimonate and the like and mixtures thereof. Aromatic iodonium complex salts are described in Beringer et al ., J. Am. Chem. Soc. 81 , 342 (1959)] can be prepared by metathesis of the corresponding aromatic iodonium simple salts (eg, diphenyliodonium bisulfate, etc.).
[99] Preferred iodonium salts include diphenyl iodonium salts (e.g. diphenyl iodonium chloride, diphenyl iodonium hexafluorophosphate and diphenyl iodonium tetrafluoroborate), diaryl iodonium hexafluoro Antimonates (eg, SarCat ^™ SR 1012 available from Sartomer Caompany) and mixtures thereof.
[100] Useful methylated triazines include those described in US Pat. No. 3,779,778 (Smith et al.), Columns 8, lines 45-50, including 2,4-bis (trichloromethyl) -6-methyl-s- Triazines, 2,4,6-tris (trichloromethyl) -s-triazines, more preferred are chromophore substituted vinylhalomethyl-s disclosed in US Pat. Nos. 3,987,037 and 3,954,475 (Bonham et al.) -Triazine.
[101] Useful diazonium salts include those disclosed in US Pat. No. 4,394,433 (Gatzke), which refers to external diazonium groups (-N ⁺ = N) and anions bound thereto (e.g. chloride, tri-isopropyl naphthalene sulfonate And photosensitive aromatic moieties (eg, pyrrolidine, morpholine, aniline and diphenyl amine) with tetrafluoroborate and bis (perfluoroalkylsulfonyl) methide). Examples of useful diazonium cations include 1-diazo-4-anilinobenzene, N- (4-diazo-2,4-dimethoxy phenyl) pyrrolidine, 1-diazo-2,4-diethoxy- 4-morpholino benzene, 1-diazo-4-benzoyl amino-2,5-diethoxy benzene, 4-diazo-2,5-dibutoxy phenyl morpholino, 4-diazo-1-dimethyl aniline , 1-diazo-N, N-dimethylaniline, 1-diazo-4-N-methyl-N-hydroxyethyl aniline, and the like.
[102] Useful sulfonium salts include those that may be represented by the formula shown in column 1 line 66 to column 4 line 2 of US Pat. No. 4,250,053 to Smith.
[103]
[104] Wherein R ₁ , R ₂ and R ₃ are aromatic groups having from about 4 to about 20 carbon atoms (eg substituted or unsubstituted phenyl, naphthyl, thienyl and furanyl, wherein the substitution is alkoxy, alkylthio , Arylthio, halogen, and the like) and alkyl groups having 1 to about 20 carbon atoms. As used herein, "alkyl" includes substituted alkyl (eg, substituted with a group such as halogen, hydroxy, alkoxy or aryl). At least one of R ₁ , R ₂ and R ₃ is aromatic, preferably each independently aromatic. Z is a covalent bond, oxygen, sulfur, -S (= O)-, -C (= O)-,-(O =) S (= O)-and -N (R)-[R is aryl (carbon atom A number from about 6 to about 20, such as phenyl), acyl (from about 2 to about 20 carbon atoms, such as acetyl, benzoyl, etc.), a carbon-carbon bond, or-(R ₄ ) -C (- R ₅ )-[R ₄ and R ₅ are independently selected from the group consisting of hydrogen, alkyl groups having 1 to about 4 carbon atoms, alkenyl groups having about 2 to about 4 carbon atoms]. X ⁻ is an anion as described below.
[105] Anions X ⁻ suitable for sulfonium salts (and any other type of photoinitiator) include various anion types such as imides, metades, boron centers, phosphorus centers, antimony centers, arsenic centers and aluminum center anions.
[106] Non-limiting examples of suitable imide and metaide anions are
[107]
[108] There is this. Preferred anions of this type has the formula _{(R f SO 2) 3 C} - include compounds represented by _[f R is the alkyl radical being a perfluoroalkyl of 1 to about 4 carbon atoms.
[109] Non-limiting examples of suitable boron central anions include
[110]
[111] There is this. Preferred boron central anions generally comprise aromatic hydrocarbon radicals substituted with at least three halogens bonded to boron, with fluorine being the most preferred halogen. Non-limiting examples of the preferred anions include (3,5-bis _{(CF 3) C 6 H 3} ) 4 B -, (C 6 F 5) 4 B -, (C 6 F 5) 3 (nC 4 H 9) _{^{B -, (C 6 F 5}} ) 3 FB - and the like ^- and _{(C 6 F 5) 3 (} CH 3) B.
[112] Examples of suitable anions include other metal or metalloid center are (3,5-bis _{(CF 3) C 6 H 3} ) 4 Al -, (C 6 F 5) 4 Al -, (C 6 F 5) ^{_{2 F 4 P -, (C}} 6 F 5) F 5 P -, F 6 P -, (C 6 F 5) F 5 Sb -, F 6 Sb -, (HO) F 5 Sb - , and F ₆ As ^- There is. The above examples are only a partial description, and other useful anion containing other useful boron center nonnucleophilic salts and other metals or semimetals will be readily apparent to those skilled in the art from the above formula.
[113] Anion X ⁻ is combined with tetrafluoroborate, hexafluorophosphate, hexafluoroarsenate, hexafluoroantimonate and hydroxypentafluoroantimonate (e.g. cationic reactive species such as epoxy resins) It is preferable to select from).
[114] Examples of suitable sulfonium salt photoinitiators include
[115] Triphenylsulfonium tetrafluoroborate,
[116] Methyldiphenylsulfonium tetrafluoroborate,
[117] Dimethylphenylsulfonium hexafluorophosphate,
[118] Triphenylsulfonium hexafluorophosphate,
[119] Triphenylsulfonium hexafluoroantimonate,
[120] Diphenylnaphthylsulfonium hexafluoroarsenate,
[121] Tritolylsulfonium hexafluorophosphate,
[122] Anylsildiphenylsulfonium hexafluoroantimonate,
[123] 4-butoxyphenyldiphenylsulfonium tetrafluoroborate,
[124] 4-chlorophenyldiphenylsulfonium hexafluorophosphate,
[125] Tri (4-phenoxyphenyl) sulfonium hexafluorophosphate,
[126] Di (4-ethoxyphenyl) methylsulfonium hexafluoroarsenate,
[127] 4-acetonylphenyldiphenylsulfonium tetrafluoroborate,
[128] 4-thiomethoxyphenyldiphenylsulfonium hexafluorophosphate,
[129] Di (methoxysulfonylphenyl) methylsulfonium hexafluoroantimonate,
[130] Di (nitrophenyl) phenylsulfonium hexafluoroantimonate,
[131] Di (carbomethoxyphenyl) methylsulfonium hexafluorophosphate,
[132] 4-acetamidophenyldiphenylsulfonium tetrafluoroborate,
[133] Dimethylnaphthylsulfonium hexafluorophosphate,
[134] Trifluoromethyldiphenylsulfonium tetrafluoroborate,
[135] p- (phenylthiophenyl) diphenylsulfonium hexafluoroantimonate,
[136] 10-methylphenoxane hexafluorophosphate,
[137] 5-methylthianthrenium hexafluorophosphate,
[138] 10-phenyl-9,9-dimethylthioxanthium hexafluorophosphate,
[139] 10-phenyl-9-oxothioxanthium tetrafluoroborate,
[140] 5-methyl-10-oxotianthrenium tetrafluoroborate,
[141] 5-methyl-10,10-dioxothioanthrenium hexafluorophosphate is mentioned.
[142] Preferred sulfonium salts include triaryl substituted salts such as triarylsulfonium hexafluoroantimonate (e.g. SarCat ^TM SR1010 available from Sartomer Company), triarylsulfonium hexafluorophosphate (e.g. available from Sartomer Company) SarCat ^™ SR1011), and triarylsulfonium hexafluorophosphate (eg, SarCat ^™ KI85 available from Sartomer Company).
[143] Useful azinium salts include those described in column 8 51 to column 9 46 of US Pat. No. 4,859,572 (Farid et al.), Including azinium moieties such as pyridinium, diazinium, or triazinium moieties. Included. The azinium moiety may comprise one or more aromatic rings, typically carbocyclic aromatic rings (eg, quinolinium, isoquinolinium, benzodiazinium and naphthodiazonium moieties) fused with an azinium ring. The quaternized substituents of nitrogen atoms in the azinium ring can be dissociated as free radicals when electrons are transferred from the electron excited state of the photosensitizer to the azinium photoinitiator. In a preferable embodiment, the quaternized substituent is an oxy substituent. The oxy substituent -OT which quaternizes the ring nitrogen atom of an azinium part can be selected from the various oxy substituents which are easy to synthesize | combine. The T moiety can be, for example, an alkyl radical such as methyl, ethyl, butyl and the like. Alkyl radicals may be substituted. Aralkyl (eg benzyl and phenethyl) and sulfoalkyl (eg sulfomethyl) radicals may be useful. In another form T may be an acyl radical, such as an —OC (O) —T ¹ radical, where T ¹ may be any of the various alkyl and aralkyl radicals described above. In addition, T ¹ may be an aryl radical such as phenyl or naphthyl. Aryl radicals may also be substituted. For example T ¹ may be a tolyl or xylyl radical. T generally contains 1 to about 18 carbon atoms, preferably in each case the alkyl moiety is a lower alkyl moiety, in which case the aryl moiety contains about 6 to about 10 carbon atoms. The highest activity was realized when the oxy substituent -OT- contained 1 or 2 carbon atoms. The azinium nucleus need not contain substituents other than quaternized substituents. However, the presence of other substituents does not adversely affect the activity of these electron acceptor compounds.
[144] Useful triarylimidazolyl dimers include those described in columns 8, lines 18-28 of US Pat. No. 4,963,471 (Trout et al.). Examples of such dimers include 2- (o-chlorophenyl) -4,5-bis (m-methoxyphenyl) -1,1'-biimidazole; 2,2'-bis (o-chlorophenyl) -4,4 ', 5,5'-tetraphenyl-1,1'-biimidazole; And 2,5-bis (o-chlorophenyl) -4- [3,4-dimethoxyphenyl] -1,1'-biimidazole.
[145] Preferred photoinitiators include iodonium salts (more preferably aryliodonium salts), methylated triazines, triarylimidazolyl dimers (more preferably 2,4,5-triphenylimidazolyl dimers), sulfonium salts And diazonium salts. More preferred are aryliodonium salts, methylated triazines and 2,4,5-triphenylimidazolyl dimers, with aryliodonium salts and triazines being most preferred.
[146] Preparation of Photoreactive Compositions
[147] Reactive species, multiphoton photosensitizers, electron donor compounds and photoinitiators can be prepared by the methods described above or by other methods known in the art, many of which are commercially available. These four components are formulated under any "safe light" conditions (optionally stirring or shaking) using any combination order and manner, but it is often desirable to add photoinitiators last (in terms of shelf life and thermal stability). (And then optionally use any heating step to promote dissolution of other components). Solvents may be used as needed, provided that the solvents are selected so as not to react significantly with the components of the composition. Examples of suitable solvents include acetone, dichloromethane and acetonitrile. The reactive species itself may often act as a solvent for other components.
[148] The three components of the photoinitiator system are present in photochemically effective amounts (as described above). Generally, the composition comprises at least about 5% by weight (preferably at least about 10% by weight, more preferably at least about 1) of the at least one reactive species based on the total solids weight (ie, the total weight of the components other than the solvent). 20 wt% or more) about 99.79 wt% or less (preferably about 95 wt% or less, about 80 wt% or less; 0.01 wt% or more (preferably about 0.1 wt% or more, more preferably about 1 or more photosensitizers) 0.2 wt% or more) 10 wt% or less (preferably about 5 wt% or less, more preferably about 2 wt% or less); optionally about 10 wt% or less of the one or more electron donor compounds (preferably about About 5% by weight or less) (preferably about 0.1% by weight or more, more preferably about 0.1% to about 5% by weight) and about 0.1% to about 10% by weight (preferably one or more electron acceptor compounds) Is about 0.1 wt% to about 5 wt% or less) When the reactive species is a leuco dye, the composition typically contains from about 0.01% to about 10% by weight (preferably from about 0.3% to about 10% by weight, more preferably about 1% or more of reactive species) Weight percent to about 10 weight percent, most preferably about 2 weight percent to about 10 weight percent).
[149] Various adjuvants may be included in the photoreactive composition depending on the desired properties. Suitable auxiliaries include solvents, diluents, resins, binders, plasticizers, pigments, dyes, inorganic or organic reinforcing or extending fillers (preferred amounts of from about 10 to 90% by weight, based on the total weight of the composition), thixotropic agents, reaction indicators, inhibitors , Stabilizers, ultraviolet absorbers, pharmaceuticals (eg, porous fluorides), and the like. The amount of such adjuvants and the manner in which they are added to the composition and composition are well known to those skilled in the art.
[150] It is within the scope of the present invention to include non-reactive polymer binders in the composition, such as to control viscosity and provide film forming properties. Such polymeric binders may generally be selected to be compatible with the reactive species. For example, a polymeric binder may be used that is soluble in the same solvent as used for the reactive species and free of functional groups that may adversely affect the reaction process of the reactive species. The binder may have a molecular weight suitable for obtaining the desired film forming properties and solution flowability (eg, about 5,000 to 1,000,000 Daltons, preferably about 10,000 to 500,000 Daltons, more preferably about 15,000 to 250,000 Daltons). Examples of suitable polymeric binders include polystyrene, poly (methyl methacrylate), poly (styrene) -co- (acrylonitrile), cellulose acetate butyrate, and the like.
[151] Prior to exposure, the formed photoreactive composition can be coated onto the substrate, if desired, by any of a variety of coating methods known to those skilled in the art (eg, knife coating and spin coating). Substrates can be selected from a wide range of films, sheets and other surfaces depending on the particular application and the exposure method employed. It is preferable that the substrate is generally flat enough to produce a layer of photoreactive composition having a uniform thickness. For applications where the need for a coating is low, the photoreactive composition may be exposed alternately in bulk form.
[152] Exposure system and its use
[153] Useful exposure systems include one or more light sources (usually pulsed lasers) and one or more optical members. An example of a suitable light source is a titanium sapphire vibrator (eg, Coherent Mira Optima 900-F) in the vicinity of ^10-15 seconds infrared light, pumped by an argon ion laser (eg, coherent innova). The laser operates at 76 MHz, has a pulse width of less than 200 x 10 ^-15 seconds, can be tuned from 700 to 980 nm, and average power is less than 1.4 watts. In practice, however, any light source can be used that provides sufficient intensity at a suitable wavelength for the photoresist (used in the photoreactive composition) (to cause multiphoton absorption). (These wavelengths may generally range from about 300 to about 1500 nm, preferably from about 600 to about 1100 nm, more preferably from about 750 to about 850 nm. The peak intensity is generally about 10 ⁶ W / cm May be greater than or equal to ^2. The upper limit of pulse influence is generally determined by the flux threshold of the photoreactive composition). For example, Q-switched Nd: YAG lasers (e.g. Spectra-Physics Quanta-Ray PRO), visible wavelength dye lasers (e.g. Spectra-Physics Sirah pumped by Spectra-Physics Quanta-Ray PRO), and Q Switched diode pumped lasers (eg Spectra-Physics FCbar ^™ ) can also be used. Preferred light sources are near infrared pulse lasers having a pulse length of less than about 10 ⁻⁸ seconds (more preferably less than about 10 ⁻⁹ seconds, most preferably less than about 10 ⁻¹¹ seconds). Other pulse lengths may be used if the above detailed peak intensity and pulse impact criteria are met.
[154] Optical members useful for carrying out the method of the invention include reflective optical members (e.g. lenses and prisms), reflective optical members (e.g. retroreflectors or focus mirrors), diffractive optical members (e.g. diffraction gratings, image masks and holograms) , Polarizing optical members (eg, linear polarizers and wave plates), diffusers, Pockel cells, waveguides, wave plates, birefringent liquid crystals, and the like. Such optical members are useful for focusing, beam delivery, beam / mode shaping, pulse shaping and pulse timing. In general, combinations of optical members may be used, and other suitable combinations will be appreciated by those skilled in the art. It may often be desirable to use optical members with multiple effective apertures to provide high focus light. However, any optical member combination can be used that provides the desired intensity profile (and its spatial arrangement). For example, the exposure system may include a scanning confocal microscope (BioRad MRC600) equipped with a 0.75 NA objective (Zeiss 20X Fluar).
[155] In general, the exposure of the photoreactive composition can be performed using a light source (as described above) in conjunction with an optical system as a means for controlling the three-dimensional spatial distribution of light intensity in the composition. For example, light from the pulsed laser can pass through the focus lens such that the focus is in the volume of the composition. The focus can be scanned or deformed in a three-dimensional pattern corresponding to the desired shape to form a three-dimensional image of the desired shape. The exposed or illuminated volume of the composition can be scanned by moving the composition itself or by moving the light source (eg, by moving the laser beam using a galvanometer).
[156] If the light induces a reaction of the reactive species, for example producing a substance with different solubility properties from the reactive species, the resulting phase is exposed or unexposed through the use of a suitable solvent, such as through other means known in the art. It can be selectively developed by removing. Cured complex three-dimensional objects can be prepared in this manner.
[157] Exposure time is generally the type of exposure system used to induce phase formation (and additional variables such as the number of effective apertures, the shape of the light intensity spatial distribution, the peak light intensity during the laser pulse duration [larger intensity and shorter The pulse duration is largely consistent with the peak light intensity]) as well as the nature of the exposed composition (and the concentration of the photosensitizer, the photoinitiator concentration and the electron donor compound). In general, the higher the peak light intensity in the focal region, the shorter the exposure time and everything else is the same. Linear phase-forming or “writing” rates are about 10 ⁻⁸ to 10 ⁻¹⁵ seconds (preferably about 10 ⁻¹¹ to 10 ⁻¹⁴ seconds) and about 10 ² to 10 ⁹ pulses / second of laser pulse duration. (preferably about 10 ^{8 3-10} pulses / sec) when it can generally be from about 5-100000 microns / second using a.
[158] The features, aspects and advantages of the invention can be better understood with reference to the description, the claims and the drawings.
[160] The objects and advantages of the present invention will be explained in detail by the following examples, but the specific materials mentioned in the examples and their amounts as well as other conditions and details are not to be understood as unduly limiting the present invention.
[161] Glossary
[162] PSAN—available from Poly (styrene-co-acrylonitrile), Aldrich, Milwaukee, WI with a weight average molecular weight of about 165,000 and 25% by weight acrylonitrile.
[163] SR-9008-alkoxylated trifunctional acrylate ester, sold by Sartomer Co., Exton, PA.
[164] SR-368-tri (2-hydroxyethyl) isocyanate triacrylate, sold by Sartomer Co., Exton, PA.
[165] DPI PF ₆ -may be prepared using hexafluorophosphate as substantially described in column 4 of US Pat. No. 4,394,403 (Smith et al.).
[166] EDMAB-ethyl-4-dimethylaminobenzoate, available from Aldrich, Milwaukee, WI.
[167] TMSPMA-3- (trimethoxysilyl) propyl methacrylate, sold by Aldrich, Milwaukee, WI.
[168] DIDMA-commercially available from N- (2,6-diisopropyl) -N, N-dimethylaniline, Aldrich, Milwaukee, WI.
[169] CGI 7460-tetrabutyl ammonium n-hexyl-tris (3-fluorophenyl) borate, CIBA Specialty Chemicals Corp., Tarrytown, NY.
[170] H-Nu 470-5,7-diiodo-3-butoxy-6-fluoron, Spectra Group, Ltd., Maunee, OH commercially available.
[171] Rhodamine B-N- [9- (2-carboxyphenyl) -6- (diethylamino) -3H-xanthene-3-ylidene] -N-ethylethanealuminum chloride, sold by Aldrich, Milwaukee, WI.
[172] Epon ^TM SU-8-Bisphenol A novolac epoxy resin, known as Epicote ^TM 157, available from Resolution Performance Products, Houston, TX.
[173] CD-1012-4- (2-hydroxytetedecaneoxy) phenylphenyl iodonium hexafluoroantimonate, sold by Sartomer Co., Exton, PA.
[174] TMB-1,2,4-trimethoxybenzene, sold by Aldrich, Milwaukee, WI.
[175] DPI SbF ₆ -may be prepared using hexafluoroantimonate, substantially as described in column 4 of US Pat. No. 4,394,403 (Smith).
[176] PMMA-Poly (methylmethacrylate) of 120,000 molecular weight, available from Aldrich, Milwaukee, WI.
[177] Hydroxy cyan leuco dye-3 ', 5'-di-tert-butyl-4'-hydroxybenzoyl-3,7-di (N, N-diethylamino) oxazine, US Pat. No. 4,775,754 (Bogel et al. Can be prepared as described in Example 1.
[178] CAB-551-1-cellulose acetone butyrate, Eastman Chemicals, Kingsport, TN.
[179] Preparation of Multiphoton Photoresist I (MPS I)
[180] Reaction of 1,4-bis (bromomethyl) -2,5-dimethoxybenzene with triethyl phosphite:
[181] 1,4-bis (bromomethyl) 2,5-dimethoxybenzene was prepared substantially following the process described in the literature (Syper et al., Tetrahedron, 39 , 781-792, 1983). 1,4-bis (bromomethyl) -2,5-dimethoxybenzene (253 g, 0.78 mol) was placed in a 1000 mL round bottom flask. Triethyl phosphite (300 g, 2.10 mol) was added and the reaction was heated to vigorous reflux with stirring for 48 h under a nitrogen atmosphere. The reaction mixture was cooled down and excess triethyl phosphite was removed under vacuum using a Kugelrohr apparatus. Heating from 0.1 mmHg to 100 ° C. resulted in a clear oil. Cooling solidified the desired product, which was suitable for direct use in the next step. The H ¹ NMR spectrum of the product was consistent with the desired product. Recrystallization from toluene yielded a colorless needle.
[182] Synthesis of 1,4-bis- [4- (diphenylamino) styryl] -2,5- (dimethoxy) benzene (MPS I):
[183] The 1000 mL round bottom flask was fitted with a calibrated dropping funnel and magnetic stirrer. The flask was charged with the product (19.8 g, 45.2 mmol) prepared in the above reaction and with N, N-diphenylamino-p-benzaldehyde (25 g, 91.5 mmol, Fluka Chemical Corp., Milkwaukee, WI commercial). The flask was flushed with nitrogen and sealed with septa. Anhydrous tetrahydrofuran (750 mL) was cannulated into the flask and all solids dissolved. The dropping funnel was charged with potassium t-butoxide (1.0 M in THF, 125 mL). The solution in the flask was stirred and potassium t-butoxide solution was added into the contents of the flask for 30 minutes. The solution was then left to stir overnight at room temperature. Water (500 mL) was then added to stop the reaction. After about 30 minutes of continued stirring, a solid yellow solid was formed in the flask. The solid was separated by filtration, air dried and recrystallized from toluene (450 mL). The desired product (MPS I) was obtained in fluorescent needles (24.7, 81% yield). The ¹ H NMR spectrum of the product was consistent with the expected structure.
[184] Example 1-2
[185] The stock solution was prepared by adding 30 g PSAN to 120 g dioxane and mixed overnight on a roller. A second solution was prepared by adding 1 g of MPS I to 35 g of SR-9008, heating and stirring to partially dissolve the photosensitizer. The second solution was added to the stock solution and allowed to mix overnight on a roller. To this solution was added 35 g of SR-368 and the solution was allowed to mix overnight on a roller to provide Masterbatch A. In two separate vials, 11 g of Masterbatch A was prepared. 0.1 g of DPI PF6 was dissolved in 1 ml of acetonitrile and added to the first vial containing 11 g of Masterbatch A, and the resulting solution was mixed by shaking and used in Example 1. 0.1 g of DPI PF6 and 0.1 g of EDMAB were dissolved in 1 ml of acetonitrile and added to a second vial containing 11 g of Masterbatch A and the resulting solution was used in Example 2.
[186] 2 ml of each of the two solutions prepared above were filtered through a 0.45 μm syringe filter and coated on a silicon wafer (pretreated with TMSPMA) with a spin coater at 3000 RPM for 40 seconds and at 80 ° C. for 40 minutes. Firing removed the solvent.
[187] The resulting coated film was subjected to a Sptecra-Physics Ti-sapphire laser (100 fs pulse, 80 MHz, 800 nm) using a 10X, 0.25NA (Numeric Aperture) microscope objective (Sptecra-Physics, Mountain View, CA). Lasers, part of the "Hurricane" system, commercially available from the company, focus on the film and mount on a computer controlled, motorized XY stage (NEAT LM-600 stage, available from New England Affiliated Technologies, Lawrence, MA) It was shaped by moving the film. Based on Gaussian optics, the diameter of the focal point was about 8 μm. Average laser power was measured using an Ophire calibrated photodiode (commercially available from Ophire Optronics Inc., Danvers, MA). In order to measure the photosensitivity of the different formulations, the speed of the stage for each line was to cover the range of 77 to 27520 μm / sec. A line pattern was generated that was increased by the factor of. After imaging the pattern was developed by immersion in dimethylformamide for 1 minute, washed with isopropyl alcohol and air dried.
[188] Table 1 summarizes the threshold write rates for Examples 1 and 2. The threshold writing speed corresponds to the last line visible in the pattern when examined using an optical microscope.
[189] Threshold Recording Speeds of Two- and Three-Component Photoinitiator Systems in Acrylate Resin ExamplePhotopolymer formulationPhotoinitiator system (wt% of solid resin)Threshold recording speed (17 mW)Threshold recording speed (33 mW) OnePSAN, SR-9008, SR-368MPS I (1%), DPIPF6 (2%)1742 µm / sec3440 μm / sec 2PSAN, SR9008, SR368MPS I (1%), DPIPF6 (2%), EDMAB (2%)1742 µm / sec4960 µm / sec
[190] The results in Table 1 show high writing speeds, especially at high laser intensities when the electron donor compound, EDMAB, is used with photosensitizers and photoinitiators.
[191] Example 3-6 and Comparative Example CI
[192] The stock solution was prepared by adding 30 g PMMA to 120 g dioxane and mixed overnight on a roller. A second solution was prepared by adding 1 g of MPS I to 35 g of Sartomer ^™ SR9008, heating and stirring to partially dissolve the photosensitizer. The second solution was added to the stock solution and allowed to mix overnight on a roller. To this solution was added 35 g of Sartomer SR368 and the solution was allowed to mix on a roller overnight to give Masterbatch B. In five separate vials, 11 g of Masterbatch B was prepared. 1 ml of acetonitrile was added to the first vial containing 11 g of Masterbatch B and the solution was shaken and mixed (Comparative Example C1). 0.1 g of DPI PF6 was dissolved in 1 ml of acetonitrile and added to a second vial containing 11 g of Masterbatch B, followed by mixing by shaking the solution (Example 3). 0.1 g of DPI PF6 and 0.1 g of EDMAB were dissolved in acetonitrile and added to a third vial containing 11 g of masterbatch B and the resulting solution was mixed by shaking (Example 4). 0.1 g of DPI PF6 and 0.1 g of DIDMA were dissolved in acetonitrile and added to a third vial containing 11 g of Masterbatch B, and the resulting solution was mixed by shaking (Example 5). 0.1 g of DPI PF6 and 0.1 g of CGI7460 (alkyltriaryl borate salt) were dissolved in 1 ml of acetonitrile and added to a fourth vial containing 11 g of Masterbatch B, followed by mixing the resulting solution by shaking (Example 6). .
[193] 2 ml of each of the five solutions prepared above were filtered through a 0.45 μm syringe filter and coated on a silicon wafer (pretreated with TMSPMA) with a spin coater at 3000 RPM for 40 seconds and at 80 ° C. for 40 minutes. Firing removed the solvent.
[194] Using a 10x, 0.25NA microscope objective with a coated film, the output of the Sptecra-Physics Ti-sapphire laser (100 fs pulse, 80 MHz, 800 nm) was focused on the film, the NEAT LM-600 computer controlled and motor It was shaped by moving the film mounted on the attached XY stage. Based on Gaussian optics, the diameter of the focal point was about 8 μm. Average laser power was measured when the beam excited the object using an Ophire calibrated photodiode. In order to measure the photosensitivity of the different formulations, the speed of the stage for each line was to cover the range of 77 to 27520 μm / sec. A line pattern was generated that was increased by the factor of. After imaging the patterned film was developed by immersion in dimethylformamide for 1 minute, washed with isopropyl alcohol and air dried. The threshold writing speed corresponds to the last line visible in the pattern when examined using an optical microscope.
[195] Table 2 summarizes the threshold writing speeds for Example 3-6 and Comparative Example C1 with two different laser intensities. The threshold writing speed when the photosensitizer alone was used was 430 μm / sec at 75 mW average laser power.
[196] Threshold Recording Rates for One-, Two-, and Three-Component Systems in Acrylate Resin ExamplePhotopolymer formulationPhotoinitiator system (wt% of solid resin)Threshold recording speed (17 mW)Threshold recording speed (33 mW) C1PMMA, SR9008, SR368MPS I (1%)<< 77 μm / s55 μm / s 3PMMA, SR9008, SR368MPS I (1%), DPIPF6 (2%)1480 μm / s4960 μm / s 4PMMA, SR9008, SR368MPS I (1%), DPIPF6 (2%), EDMAB (2%)1720 μm / s4960 μm / s 5PMMA, SR9008, SR368MPS I (1%), DPIPF6 (2%), DIDMA (2%)1720 μm / s3440 μm / s 6PMMA, SR9008, SR368MPS I (1%), DPIPF6 (2%), CGI7460 (2%)3440 μm / s13760 µm / s
[197] The results in Table 2 indicate that high writing speeds are achieved when two- and three-substance photoresist systems are used, particularly at high laser intensities when the electron donor compound, EDMAB, is used with photoresists and photoinitiators. Indicates that
[198] Example 7
[199] The coated films were prepared and shaped substantially according to Example 6 at 4, 6, 11, 17 and 30 mW average laser speeds and the threshold writing speed was measured substantially as in Examples 3-6. The threshold writing speed changes from the average power to the second function (shown in FIG. 1), which is consistent with the two-photon induced photopolymerization.
[200] Comparative Example C9-C12 (Use of Fluorine Photosensitive Agent)
[201] The stock solution was prepared by adding 30 g PMMA to 120 g dioxane and mixed overnight on a roller. A second solution was prepared by adding 1 g of H-Nu 470 (photosensitive agent) to 35 g of Sartomer ^™ SR9008, heating and stirring to partially dissolve the photosensitive agent. The second solution was added to the stock solution and allowed to mix overnight on a roller. To this solution was added 35 g of Sartomer SR368 and the solution was allowed to mix overnight on a roller to provide Masterbatch B. Masterbatch B (1 g) was mixed with 10 g of the stock solution, then 0.025 g DPI PF6 and 0.025 g DIDMA were added and shaken to mix (Comparative Example C2). Three separate vials were placed with 11 g of Masterbatch B. 0.1 g of DIDMA was dissolved in 1 ml of acetonitrile and added to the first vial containing 11 g of masterbatch B with shaking and mixing (Comparative Example C3). 0.1 g of DPI PF6 was dissolved in 1 ml of acetonitrile and added to the second vial containing 11 g of masterbatch B with shaking and mixing (Comparative Example C4). 0.1 g of DPI PF6 and 0.1 g of DIDMA were dissolved in 1 ml of acetonitrile and added with shaking to a third vial containing 11 g of Masterbatch B (Comparative Example C5).
[202] 2 ml of each of the four solutions prepared above were filtered through a 0.45 μm syringe filter and coated on a silicon wafer (pretreated with TMSPMA) with a spin coater at 3000 RPM for 40 seconds and at 80 ° C. for 40 minutes. Firing removed the solvent.
[203] Using a 10x, 0.25NA microscope objective with a coated film, the output of the Sptecra-Physics Ti-sapphire laser (100 fs pulse, 80 MHz, 800 nm) was focused on the film, the NEAT LM-600 computer controlled and motor It was shaped by moving the film mounted on the attached XY stage. Based on Gaussian optics, the diameter of the focal point was about 8 μm. Average laser power was measured when the beam excited the object using an Ophire calibrated photodiode. In order to measure the photosensitivity of the different formulations, the speed of the stage for each line was to cover the range of 77 to 27520 μm / sec. A line pattern was generated that was increased by the factor of. After imaging the patterned film was developed by immersion in dimethylformamide for 1 minute, washed with isopropyl alcohol and air dried. The threshold writing speed corresponds to the last line visible in the pattern when examined using an optical microscope.
[204] Table 3 summarizes the threshold writing speed for Comparative Examples C2-C5 with two different laser intensities.
[205] Threshold Recording Rate of Compositions Containing Fluorine Photosensitive Agents Comparative examplePhotopolymer formulationPhotoinitiator system (wt% of solid resin)Threshold recording speed (250 mW)Threshold recording speed (331 mW) C2PMMA, SR9008, SR368H-Nu 470 (0.18%), DIDMA (1%), DPIPF6 (1%)0 μm / s0 μm / s C3PMMA, SR9008, SR368H-Nu 470 (1%), DIDMA (2%)0 μm / s215 μm / s C4PMMA, SR9008, SR368H-Nu 470 (1%), DPIPF6 (2%)0 μm / s77 μm / s C5PMMA, SR9008, SR368H-Nu 470 (1%), DIDMA (2%), DPIPF6 (2%)1240 μm / s3440 μm / s
[206] The results in Table 3 show that when H-Hu470 is used with an electron donor compound and / or a photoinitiator, the laser power is greater than that required for a composition using a photosensitive agent with a large two-photon absorption cross-sectional area.
[207] Example 8-11 (Epoxy Cationic Polymerization)
[208] Rhodamine B (4.2 g) was dissolved in 220 ml water and filtered through infusorial earth. To the filtrate was added 10.0 g of sodium hexafluoroantimonate with stirring and the mixture was allowed to stir for about 5 minutes. The resulting mixture with precipitate was filtered through frit and the solids were washed with water and dried in an oven at 80 ° C. overnight to yield 4.22 g of rhodamine B hexafluoroantimonate salt (Rh B SBF6). The structure was confirmed by photon and fluorine NMR.
[209] Epon ^™ SU-8 (60 g) was mixed with 60 g of methyl isobutyl ketone, warmed to 50-75 ° C. and shaken with magnetic stirring until dissolved to form a stock solution. To 25 g of the stock solution, 0.0625 g of Rh B SbF6, pre-dissolved in 0.2 ml acetonitrile, was added with shaking to form a masterbatch D. 5 g of Masterbatch D was added to each of the four vials. To the first vial, 0.025 g of SR-1012 was added with shaking (Example 8). To the second vial was added 0.025 g of SR-1012 and 0.0275 g of TMB with shaking (Example 9). 0.025 g of DPI SbF6 was added to the third vial with shaking (Example 10). To the fourth vial was added 0.025 g of DPI SbF6 and 0.0125 g of EDMAB with shaking and mixing (Example 11).
[210] 2 ml of each of the four resulting solutions prepared were filtered through a 0.45 μm syringe filter and coated on a silicon wafer (pretreated with TMSPMA) with a spin coater at 3000 RPM for 40 seconds and 40 minutes at 80 ° C. Firing to remove the solvent.
[211] Using a 10x, 0.25NA microscope objective with a coated film, the output of the Sptecra-Physics Ti-sapphire laser (100 fs pulse, 80 MHz, 800 nm) was focused on the film, the NEAT LM-600 computer controlled and motor It was shaped by moving the film mounted on the attached XY stage. Based on Gaussian optics, the diameter of the focal point was about 8 μm. The average laser power was measured when the beam excited the object using an Ophire calibrated photodiode. In order to measure the sensitization of different formulations, the speed of the stage for each line was to cover the range of 77 to 27520 μm / sec. A line pattern was generated that was increased by the factor of. After the pattern, each sample was baked after exposure at 130 ° C. for 5 minutes on a hotplate and the pattern was developed by immersing the patterned film in dimethylformamide for 1 minute, washed with isopropyl alcohol and air dried. The threshold writing speed corresponds to the last line visible in the pattern when examined using an optical microscope.
[212] Table 4 summarizes the threshold writing speed for Examples 8-11 with three different laser intensities.
[213] Threshold recording rate for cationic polymerization of epoxy resins including photosensitizers, electron donor compounds and / or photoinitiators ExamplePhotopolymer formulationPhotoinitiator system (wt% of solid resin)Threshold recording speed (144 mW)Threshold recording speed (337 mW) 8SU-8RhB SbF6 (0.5%), SR-1012 (1%)155 μm / sNR 9SU-8RhB SbF6 (0.5%), SR-1012 (1%), TMB (1.1%)155 μm / sNR 10SU-8RhB SbF6 (0.5%), DPISbF6 (1%)NR6880 μm / s 11SU-8RhB SbF6 (0.5%), DPISbF6 (1%), EDMAB (0.5%)NR1720 μm / s
[214] NR = not run
[215] The results in Table 4 show cationic polymerization occurring in the presence of an electron donor compound.
[216] Example 12
[217] Four solutions were prepared by excluding any ambient light from the solution and in the following amounts and compounds under “safety light”.
[218] Solution A:
[219] Hydroxy cyan leuco dye, 3mg
[220] SR-1012, 3mg
[221] Dichloromethane, 3g
[222] Solution B:
[223] Hydroxy cyan leuco dye, 5.5mg
[224] MPS I, 5.5 mg
[225] Dichloromethane, 5.5 g
[226] Solution C:
[227] SR-1012, 5mg
[228] MPS I, 5 mg
[229] Dichloromethane, 5 g
[230] Solution D:
[231] Hydroxy cyan leuco dye, 5mg
[232] SR-1012, 5mg
[233] MPS I, 5 mg
[234] Dichloromethane, 5 g
[235] Each solution A-D was dotted on a piece of hard filter paper. The solvent was evaporated. Each point on the filter paper was then fitted with a 10X, 0.25NA microscope objective to match the output of the Sptecra-Physics Ti-sapphire laser (100 fs pulse, 80 MHz, 800 nm) to the point on the filter paper, and the NEAT LM-600 computer control. And the filter paper mounted on the motor-attached XY stage was examined in the same manner as exposing a 1 mm x 1 mm square at the center of each point. The laser power was 75 mW. Only the spot of solution D was developed to change the color from light yellow to blue in the 1 mm x 1 mm area exposed to the laser. Thus, leuco dyes were developed through multiphoton absorption using a photoinitiator system consisting of a photosensitizer and photoinitiator.
[236] Example 13
[237] Small vials were filled with hydroxy cyan leuco dye (25 mg), SR-1012 (25 mg), MPS I (25 mg) and dichloromethane (4 g). To this vial was added 4 g of CAB-551-1 (20% solids in dichloropropane) without mixing light. The resulting solution was then spin coated onto a glass slide. After evaporation of dichloropropane, the resulting coating site of about 2 mm square was substantially exposed as in Example 12. This area and only this area were developed by color change from yellow to cyan.
[238] Example 14
[239] The coating solution can be prepared from acrylic monomers and oligomers (trimethylolpropane triacrylate, SR454 ^™ , sold by Sartomer Co., Inc., Exton, PA) and binders (e.g. poly (methylmethacrylate) in a suitable solvent (e.g. MEK). ), Sold by Aldrich Chemical Co., Milwaukee, WI) in a ratio of 60: 27.5: 12.5. Multiphoton photosensitizers (e.g. bis (diphenylamino) stilbene, Aldrich Chemical Co., commercially available), onium salts (e.g. diphenyliodonium hexafluoro) having a large cross-sectional area for multiphoton absorption in this solution A photoinitiator system was added that included an phosphate, US Pat. No. 5,545,676, Example 1) and an electron donor (Aldrich Chemical Co., commercially available) such as ethyl dimethylaminobenzoate. The amount of photoinitiator system compounds was chosen such that the concentration of each component as a percentage of solids was about 0.5% multiphoton photosensitizer, 1% onium salt, and 1% electron donor. The solution was coated (eg knife coated) onto a substrate (eg silicon wafer) and the solvent was evaporated to produce a coating with a dry thickness of about 0.125 mm. Exposure using a focused pulsed laser of about 700 nm (eg Ti-Sapphire laser) on the pattern polymerizes and insolubilizes the exposed coating by washing the coating with a solvent (such as MEK) and removes the unexposed coating. do.
[240] Example 15
[241] The coating solution can be prepared in an appropriate solvent (e.g. MEK) by epoxy-functional monomers (e.g. ERL 4221 ^™ , cycloaliphatic epoxy compounds, Union Carbide Co., Danbury, CT commercially available) and binders (e.g. poly (methyl) Methacrylate)) in a ratio of 60: 27.5: 12.5. This solution contains a multiphoton photosensitive agent (e.g., bis (diphenylamino) stilbene), an onium salt (e.g., diphenyliodonium hexafluoroantimonate and ethyl dimethylaminobenzo) having a large cross-sectional area for multiphoton absorption. A photoinitiator system was added that included an electron donor such as ate The amount of photoinitiator system compounds was chosen such that the concentration of each component as a percentage of solids was about 0.5% multiphoton photosensitizer, 1% onium salt, and 1% electron donor. The solution was coated (e.g. knife coated) on a substrate (e.g. a silicon wafer) and the solvent was evaporated to produce a coating with a dry thickness of about 0.125 mm The focus of the pattern about 700 nm (e.g. Ti-Sapphire laser) was Exposure using a tailored pulsed laser polymerizes and insolubilizes the exposed coating by cleaning the solvent (eg MEK) coating and removes the unexposed coating. The.
[242] Example 16
[243] MPS I (16.7 mg) and CPI PF ₆ (60 mg) were dissolved in 1 ml dioxane. The resulting solution was then added to 24.0 g of tetrahydropyranyl methacrylate (THP-MA) solution (14% solids in 1-methoxy-2-propanol) to form a bicomponent solution. The bicomponent solution film (-100 μm thick) was cast on a glass slide and fired at 90 ° C. for 15 minutes on a hotplate. The resulting sample was placed horizontally on the movable stage. Ti: Sapphire laser (Spectra-Physics, Inc .; part of the Hurricane ^™ system made by 800 nm, 100 fs pulse, 80 mHz) was used for the exposure of the film. The power used was 17 mW and the objective lens used was 10x (NA0.25). The laser beam was focused towards the film-glass slide interface. The stage moved over the range of speeds at which the film was exposed (starting at 28 μm / sec and ending at 5120 μm / sec). After baking (PEB) after exposure to 90 ° C. for 5 minutes on a hotplate, the film was developed for 5 minutes with 2% Na ₂ CO ₃ solution. Lines with recording speeds of 28, 40, 56 and 80 μm / sec were observed.
[244] Example 17
[245] 5.0 mg of trimethoxybenzene was added to 10 g of the bicomponent solution of Example 16 to provide a tricomponent solution. The film of the three component solution was cast, fired and exposed in the same manner as in Example 16. After developing for 5 minutes in a 2% Na ₂ CO ₃ solution, lines with recording speeds of 28, 40, 56 and 80 μm / sec were observed.
[246] The entire disclosures of patents, patent documents and publications cited herein are incorporated by reference as if individually cited. Various modifications and alterations of this invention will be apparent to those skilled in the art without departing from the original meaning and scope of this invention. The present invention should not be unreasonably limited by the specific aspects and embodiments described herein and it should be understood that these embodiments and aspects exist as examples within the scope of the invention, which are limited only by the claims which follow. do.

权利要求:
Claims (38)
[1" claim-type="Currently amended] (a) one or more reactive species capable of carrying out an acid or radical initiated chemical reaction and (2) (i) one having a two-photon absorption cross-sectional area that can simultaneously absorb two or more photons and is greater than fluorosane The above multiphoton photosensitive agent; (ii) optionally, at least one electron donor compound that is different from the multiphoton photosensitizer and capable of donating electrons to the electron excited state of the photosensitizer; And (iii) one or more multiphoton photoinitiator systems comprising in photochemically effective amounts one or more photoinitiators that are photosensitized by accepting electrons from the electron excited state of the photosensitizer to form one or more free radicals and / or acids. Preparing the composition, and
(b) irradiating the composition with light sufficient to cause simultaneous absorption of two or more photons to induce at least one acid or radical initiated chemical reaction to which the composition is exposed to the light
A multiphoton photoinitiator system comprising: a multiphoton photoinitiator system, provided that said photoreactive composition is capable of carrying out an acid initiated chemical reaction and comprises at least one reactive species, a reactive polymer, which is a curable species or a non-curable species The multiphoton photosensitive method of this containing one or more electron donor compound.
[2" claim-type="Currently amended] The method of claim 1, wherein the reactive species is a curable species.
[3" claim-type="Currently amended] The method of claim 2, wherein the curable species is selected from the group consisting of monomers, oligomers, reactive polymers, and mixtures thereof.
[4" claim-type="Currently amended] The method of claim 3, wherein the curable species is selected from the group consisting of addition-polymerizable monomers and oligomers, addition-crosslinkable polymers, cationic polymerizable monomers and oligomers, cationic-crosslinkable polymers and mixtures thereof. How to be.
[5" claim-type="Currently amended] The method of claim 1, wherein the reactive species is a non-curable species.
[6" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 50 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[7" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross-sectional area that is about 1.5 times greater than fluorescein.
[8" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 75 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[9" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross-sectional area that is about twice as large as fluorescein.
[10" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 100 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[11" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section that is about three times greater than fluorescein.
[12" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 150 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[13" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross-sectional area that is about four times greater than fluorescein.
[14" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 200 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[15" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer is rhodamine B.
[16" claim-type="Currently amended] The method of claim 1, wherein the multiphoton photosensitizer is selected from the following compounds:








[17" claim-type="Currently amended] The method of claim 1, wherein the oxidation potential of the electron donor compound is greater than zero and less than or equal to the oxidation potential of p-dimethoxybenzene.
[18" claim-type="Currently amended] The method of claim 1, wherein the oxidation potential of the electron donor compound is about 0.3 to 1 volts relative to a standard saturated magenta electrode.
[19" claim-type="Currently amended] The method of claim 1, wherein the electron donor compound is an amine, amide, ether, urea, sulfinic acid and salts thereof, salts of ferrocyanide, ascorbic acid and salts thereof, dithiocarbamic acid and salts thereof, xanthate salts. Salts of ethylene diamine tetraacetic acid, salts of (alkyl) _n (aryl) _m borate (n + m = 4), SnR ₄ compounds, wherein each R is independent from the group consisting of alkyl, aralkyl, aryl and alkaryl groups Selected from the group consisting of ferrocene and mixtures thereof.
[20" claim-type="Currently amended] The method of claim 19, wherein the electron donor compound is an amine containing at least one zoloridinyl moiety, alkylarylborate salt, salt of aromatic sulfinic acid, 4-dimethylaminobenzoic acid, ethyl 4-dimethylaminobenzoate, 3-dimethylamino Benzoic acid, 4-dimethylaminobenzoic acid, 4-dimethylaminobenzaldehyde, 4-dimethylaminobenzonitrile, 4-dimethylaminophenethyl alcohol, 1,2,4-trimethoxybenzene and mixtures thereof Way.
[21" claim-type="Currently amended] The method of claim 1, wherein the photoreactive composition does not comprise an electron donor compound.
[22" claim-type="Currently amended] The method of claim 1, wherein the photoinitiator is selected from the group consisting of iodonium salts, sulfonium salts, diazonium salts, azinium salts, chloromethylated triazines, triarylimidazolyl dimers, and mixtures thereof. Way.
[23" claim-type="Currently amended] The method of claim 22, wherein the photoinitiator is selected from the group consisting of iodonium salts, methylated triazines, triarylimidazolyl dimers, sulfonium salts, diazonium salts, and mixtures thereof.
[24" claim-type="Currently amended] 24. The method of claim 23, wherein said photoinitiator is selected from the group consisting of an aryl iodonium salt, methylated triazine, 2,4,5-triphenylimidazolyl dimer, and mixtures thereof.
[25" claim-type="Currently amended] The photoreactive composition of claim 1, wherein the photoreactive composition comprises from about 5 wt% to about 99.79 wt% of the at least one reactive species, from about 0.01 wt% to about 10 wt% of the at least one multiphoton photosensitizer, based on the total mass of the solid; At least about 10% by weight of at least one electron donor compound, and from about 0.1% to about 10% by weight of at least one photoinitiator.
[26" claim-type="Currently amended] The photoreactive composition of claim 1, wherein the photoreactive composition consists of a solvent, diluent, resin, binder, plasticizer, pigment, dye, inorganic or organic reinforcing or extending filler, thixotropic agent, indicator, inhibitor, stabilizer, ultraviolet absorber and medicament. And at least one adjuvant selected from the group.
[27" claim-type="Currently amended] The method of claim 1, wherein said radiation is pulsed radiation.
[28" claim-type="Currently amended] The method of claim 27, wherein said pulse irradiation is performed using a near imfrared pulsed laser having a pulse of about 10 ⁻⁸ seconds or less.
[29" claim-type="Currently amended] The method of claim 1, wherein the method provides a linear imaging speed of about 5 to about 100,000 microns / second using laser pulse durations of about 10 ⁻⁸ to 10 ⁻¹⁵ seconds and pulses of 10 ² to 10 ⁹ per ^second . Way.
[30" claim-type="Currently amended] (a) (1) at least one curable species capable of carrying out a radical-initiated chemical reaction; And (2) (i) rhodamine B; (ii) optionally, at least one alkylarylborate salt; And (iii) at least one multiphoton photoinitiator system comprising at least one iodonium salt in a photochemically effective amount; And
(b) irradiating the composition with light sufficient to cause simultaneous absorption of two or more photons to induce one or more radical-initiated chemical reactions in which the composition is exposed to light
Multiphoton photosensitive method comprising a.
[31" claim-type="Currently amended] A multiphoton photocuring method comprising curing a multiphoton-curable composition exposed to light by pulsed irradiating the multiphoton-curable composition with light sufficient to cause simultaneous absorption of two or more photons, wherein the multiphoton-curable The composition is
At least one curable species selected from the group consisting of monomers, oligomers and reactive polymers;
At least one multiphoton photosensitizer capable of simultaneously absorbing two or more photons and having a two photon absorption cross section greater than 50 × 10 ⁻⁵⁰ cm ⁴ seconds / photon; And a photochemically effective amount of at least one electron donor compound that is different from the multiphoton photosensitizer and whose oxidation potential of the electron donor is greater than zero and less than or equal to the oxidation potential of p-dimethoxybenzene; And
At least one photoinitiator selected from the group consisting of aryliodonium salts, methylated triazines and 2,4,5-triphenylimidazolyl dimers
It is to include a multiphoton photosensitive method.
[32" claim-type="Currently amended] 32. The compound of claim 31 wherein the multiphoton photosensitive agent is exposed in the wavelength range of the single photon absorption spectrum of the photosensitive agent under conditions where no measurable multiphoton absorption occurs. How triazine can be photosensitized.
[33" claim-type="Currently amended] The method of claim 31, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 100 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[34" claim-type="Currently amended] The method of claim 31, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 150 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[35" claim-type="Currently amended] The method of claim 31, wherein the multiphoton photosensitizer has a two photon absorption cross section greater than about 200 × 10 ⁻⁵⁰ cm ⁴ seconds / photon.
[36" claim-type="Currently amended] (a) one or more reactive species capable of carrying out acid or radical initiated chemical reactions other than the curing reaction; And
(b) one or more multiphoton photosensitizers capable of simultaneously absorbing two or more photons, (2) different from the multiphoton photosensitizer, different from the reactive species, and donating electrons to the electron excited state of the photosensitizer At least one electron donor compound, and (3) at least one photoinitiator that is photosensitized by accepting electrons from the electron excited state of the photosensitizer to form at least one free radical and / or acid. Multiphoton Photoinitiator System
A multiphoton activated photoreactive composition comprising: wherein the composition does not comprise a curable species.
[37" claim-type="Currently amended] 37. The composition of claim 36, wherein said reactive species is selected from the group consisting of leuco dyes, chemically amplified photoresists and reactive polymers whose solubility can be increased upon reactions initiated with acids or radicals.
[38" claim-type="Currently amended] 37. The photoinitiator of claim 36, wherein the multiphoton photosensitive agent has a two photon absorption cross-sectional area greater than fluorescein, the oxidation potential of the electron donor compound is greater than zero and less than or equal to the oxidation potential of p-dimethoxybenzene. The composition selected from the group consisting of nium salts, sulfonium salts, diazonium salts, azinium salts, methylated triazines, triarylimidazolyl dimers and mixtures thereof.

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同族专利:

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公开号 | 公开日

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EP1297021B1|2009-03-18|

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EP1297021A2|2003-04-02|

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WO2001096409A2|2001-12-20|

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KR100813320B1|2008-03-12|

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KR20070118164A|2007-12-13|

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JP5059273B2|2012-10-24|

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DE60138021D1|2009-04-30|

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AT425993T|2009-04-15|

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WO2001096409A3|2002-04-04|

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JP2004503616A|2004-02-05|

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AU6844301A|2001-12-24|

引用文献:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

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法律状态:
2000-06-15|Priority to US21170300P

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2000-06-15|Priority to US60/211,703

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2001-06-14|Application filed by 쓰리엠 이노베이티브 프로퍼티즈 캄파니

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2001-06-14|Priority to PCT/US2001/019164

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2003-02-07|Publication of KR20030011354A

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2008-03-12|Application granted

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2008-03-12|Publication of KR100813320B1

优先权:

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申请号 | 申请日 | 专利标题

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US21170300P| true| 2000-06-15|2000-06-15|

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US60/211,703|2000-06-15|

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PCT/US2001/019164|WO2001096409A2|2000-06-15|2001-06-14|Multiphoton photosensitization system|