CA1306998C - Propiophenone derivatives as photoinitiators for photopolymerisation - Google Patents

Propiophenone derivatives as photoinitiators for photopolymerisation

Info

Publication number
CA1306998C
CA1306998C CA000437979A CA437979A CA1306998C CA 1306998 C CA1306998 C CA 1306998C CA 000437979 A CA000437979 A CA 000437979A CA 437979 A CA437979 A CA 437979A CA 1306998 C CA1306998 C CA 1306998C
Authority
CA
Canada
Prior art keywords
hydrogen
phenyl
alkyl
same time
radical
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA000437979A
Other languages
French (fr)
Inventor
Rinaldo Husler
Kurt Dietliker
Werner Rutsch
Rudolf Kirchmayr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Schweiz AG
Original Assignee
Ciba Geigy AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Application granted granted Critical
Publication of CA1306998C publication Critical patent/CA1306998C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/26—Radicals substituted by doubly bound oxygen or sulfur atoms or by two such atoms singly bound to the same carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
    • C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
    • C07C49/83—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups polycyclic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
    • C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/46—Polymerisation initiated by wave energy or particle radiation
    • C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
    • C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/031—Organic compounds not covered by group G03F7/029
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S522/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S522/901—Dark storage stabilizer

Abstract

3-14117/+
Propiophenone derivatives as photoinitiators for photopolymerisation Abstract:
Propiophenones of the formula I

Description

~ ~3~39B

3-14117/+

Propiophenone derivatives as photoinitiators for ~otopoLymerisation The invention relates to the use of selected aromatic-aliphatic ketones as initiators for the photopolymerisation of ethylenically unsaturated compounds or the photochemical crosslinking of polyolefines, and to the photopolymerisable or crosslinkable systems containing in;tiators of this type.
Photochemical polymerisation processes have acquired considerable importance in industry, particularly in cases where thin films have to be cured with;n a short time, ~or example when curing lacquer coatings or ~hen drying printing inks. Compared with conventional curing processes, UV
irradiation in the presence of photo;nit;ators has a number of advantages, of which perhaps the most important is the high rate of photo-curing. The rate depends greatly on the photoinitiator used, and there has been no lack of attempts to replace the conventional initiators by increasingly better and more effective compounds.
Amongst the most important photoinitiators are deriv-atives of aromatic-aliphatic ketones, particularly propio-phenone derivatives such as are described, for example, in U.S. Patent Specification 4,318,791, in U.S~ Patent Specifi-cation 4,07Z,694 and ;n 6erman Offenlegungssch~if~ 2,357,866.
However~ the properties of compounds of this type are still not optimal, particularly in respect of stability on storage, reactivity and tendency to yellowing.
There is, therefore, a need in industry for photo-init;ators which are readily soluble in the substrate and - :~3~

initiate photopolymerisation more rapidly, while having good stability when stored in the dark, and which produce an even higher polymer yield per time unit than ~he known photoinitiators. The use of such improved photoinitiators would enable the expensive industrial UV irradiation equip~
ment to be utilised better.
It has been found that certain aromatic-aliphatic propiophenones possess excellent properties as photo-initiators and thereby improve the photopolymerisation of ethylenically unsaturated compounds.
The invention ~elates to photopolymerisable compositions comprising at least one ethylenically unsaturated photo-polymerisable compound and an effective quanti-ty o~ a propiophenone derivative of the formula I
ORl oR2 (I) R R
in which R1 is hydrogen or C1-C4-alkyl, -Si(CH3)3, allyl or benzyl, R2 is hydrogen, C1-C8-alkyl, C1-C4-alkyl which is substituted by C1-C4-alkoxy or -OH, (CH2-CH2-o)n-R5 where n is 2 to 20 anc` R5 is H or C1-C4-alkyl, -Si(CH3)3, benzyl, C3-C6-alkenyl, C3-C4-alkynyl, 2-tetrahydropyranyl or 2-tetrahydrofuranyl, or R1 and R2 together are a C1-C6 alkylidene radical or a C2-C6-alkylidene radical which is sub stituted by hydroxyl, C1-C4-alkoxy or phenyl, a linear or branched C2-C6-alkanediyl radical, a benzylidene, cyclo-pentylidene or cyclohexylidene radical or a 2,2,2-trichloro-ethylidene, 2-furylmethylidene or dimethylsilylidene radical, R3 is phenyl which is unsubstituted or substituted, for example by one or more -Cl, C1-C4-alkyl, C1-C4-alkoxy or C1-C4-alkylthio ra~icals, and is also benzoylphenyl, phen-oxyphenyl or phenylthiophenyl, R4 is C1-C~-alkyl or phenyl which is unsubstituted or substituted by one or more -Cl, C1-C4-alkyl or C1-C4-alkoxy rad;cals, and R5 is hydrogen or C1-C4-alkyl, or R4 and R5 together are a trimethylene or tetramethylene radical, and R6 is hydrogen, C1-C4-:

.
~, ' ~3()~

alkyl, -CCl3 or phenyl, subject to the condition that, if R2, R5 and R6 at the same time are hydrogen and if R3 and R4 are at the same time phenylr R1 must not be hydrogen or c1-C4-alkyl, and also, if R3 and R4 at the same time are phenyl and R5 and R6 are at the same time hydrogen, R1 and R2 together must not be alkylidene or benzylidene, and also, if R3 and R4 at the same time are p-methoxyphenyl and R2, RS and R6 are at the same time hydrogen, R1 must not be hydrogen, and, finally, if R2 and R6 at the same time are hydrogen and R3, R4 and R5 are at the same time phenyl, R must not be hydrogen. These compounds ~re initi~tors Eor the photopoly~erisation of ethylenically unsaturated com-pounds and for thephotochemical crosslinkingof polyolefines.
C1-C4-Alkyl radicals R1, R2, R4, R5 and R6 are, for example, linear or branched alkyl groups, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl and tert.-butyl, but especially methyl.
C1-C4-Alkyl subst;tuents in phenyl as R3 and R4 are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl or tert.-butyl substituents.
C1-C4-Alkoxy or C1-C4-alkylthio substituents in phenyl as R3 are, for example, methoxy, ethoxy, propoxy or tert.-butoxy groups or methylthio, ethylthio~ propylthio or tert.-butylthio substituents, respectively~
A C1-C6-alkyl;dene radical formed by R1 and R2 together is, for example, methylene, ethylidene, propylidene or especially isopropylidene, while a linear or branched C2-C6-alkadiyl radical formed by R1 and R2 together is, for example, ethanediyl or methylethanediyl.
A C2-C6-alkylidene radical substituted by hydroxyl which is formed by R1 and R2 together is, preferably, 1-hydroxy-2-propylidene, a C2-Cb-alkylidene radical sub-stituted by C1-C4~alkoxy which is formed by R1 and R2 together is, preferably, 1-methoxy-2-propylidene, while a C2-C6-alkylidene radical substituted by phenyl which is formed by R1 and R2 to~ether is, in particular, 1-phenyl-1-ethylidene~

~3~

C1-C4-Alkoxy substituents in phenyl as R4 are, for example, me~hoxy, ethoxy, propoxy or tert.-butoxy groups.
A C3-C6-alkenyl radical R2 is, for example, prop-2-enyl, n-but-2-enyl, 2-methylprop-2-enyl, n-pent-2-enyl or n-hex-2-enyl, while a C3-C4-alkinyl radical R2 is, for example, prop-1-inyl or 3-buten-1-inyl.
C1-C8-Alkyl substituents ;n R2 are, for example, l;near or branched subst;tuents, for example methyl, ethyl~
n-propyl, ;sopropyl, n-butyl, sec.-butyl, tert~-butyl, pentyl, hexyl, heptyl or octyl.
All the pos;tion isomers are possible in the case of a C1-C4-alkyl radical R2 which is substituted by C1-C4-alkoxy or ~OHn n is preferably 2 to 10 and R5 is preferably methyl or ethyl in an R2 radical which is substituted by -(CH2-CH2-O) -R5 Preferred compounds of the formula I are those in which R1 and R2 are hydrogen, -Si(CH3)3 or C1-C4-alkyl, especially methyl, R3 is phenyl, R4 is C1-C4-alkyl and R5 is hydrogen, or in which R1 and R2 together are iso-propylidene or benzylidene, or R4 and R5 together are a tri-methylene or tetramethylene radical and R6 is hydrogen. Pre-ferred compounds of the formula I are also those in which R1 and R2 together are a dimethylsilylidene radical.
Compounds of the formula I which are particularly preferred are those in wh;ch R1, R5 and R6 are hydrogen, R2 and R4 are methyl and R3 is phenyl, or, if R1 is hydro-gen, R2 is methyl, R3 is phenyl, R~ and R5 together are tetramethylene and R6 is hydrogen, or in which R1 and R2 together are isopropylidene.
Compounds of the formula I which are particularly preferred are those in which R1 is hydrogen, R2 is hydro~en, methyl or -Si(CH3)3~ or R1 and R2 together are isopropyl-idene, benzylidene or dimethylsilylidene, R3 is phenyl, R4 is methyl or phenyl, R is hydrogen, or R and R together are a tetramethylene radical and R is hydrogen or phenyl, subject to the condition that R , R and R at the same ~3~69~B

time may not be hydrogen or R may not be phenyl, and if R is phenyl and R and R at the same time are hydrogen, R and R to~ether ~ay not be isopropylidene or benzyli-dene, and finally, R may not be hydrogen or R and R
at the same time may not be phenyl.
The ~ollowing are examples o~ individual compounds of the ~ormula I: 2-hydroxy-3-methoxy-2-methyi-1-phenylprop-an-1-one, 3-benzyloxy-2-hydroxy-2-methyl-1-phenylpropan-1-one, 1,3-diphenyl-2-hydroxy-3-methoxy-Z-methylpropan-1-one, Z-hydroxy-3-methoxy-2-methyl-1-phenyl-3-trichloromethylpro-pan-1-one, 1,2-diphenyl-2-hydroxy-3-methoxypropan-1-one, 3-allyloxy-1,2-diphenyl-2-hydroxypropan 1-one, 1,2-diphenyl-2-hydroxy-3-trimethylsiloxypropan-1-one, 1,2-d;phenyl-2-hydroxy-3-(2-tetrahydropyranyloxy)-propan-1~one, 2,3-di~
hydroxy-2-methyl-1-phenyl-3-trichloromethylpropan-1-one, 1-benzoyl-1-hydroxy-2-trimethylsilyloxycyclohexane, 1-benzoyl-1-hydroxy-2-methoxycyclohexane, 1-benzoyl-1,2-dihydroxycyclo-hexane, 4-benzoyl-5-trichloromethyl-2,2,4-trimethyl-1,3-dioxo-lane, 2,3-(dimethylsilylenedioxy)-1,2-diphenylpropan-1-one, 2,3-~dimethylsilylenedioxy)-2-methyl-1-phenylpropan-1-one, 2,3-(dimethylsilylenedioxy)-2-methyl-1-(4-methoxyphenyl)-propan-1-one, 4-benzoyl-4-methyl-2-phenyl-1,3-dioxolane, 4-benzoyl-2,2,4-trimethyl-1,3-dioxolane, 4-(4-chlorobenzoyl)-4-(4-chLorophenyl)-2-phenyl-1,3-dioxolane, 4-benzoyl-4,5-dimethyl-2-phenyl-1,3-dioxolane, 4-benzoyl-4-methyl-1,3-dioxolane, 4-benzoyL-4-methyl-2,2-pentamethylene-1,3-dioxo-lane, 4-benzoyl-2,2-pentamethylene-4-phenyl-1,3-dioxolane, 4-ethyl-4-benzoyl-2,2-tetramethylene-1,3-dioxolane, 4-ethyl-4-~4-methoxybenzoyl)-2-propyl-1,3-dioxolane, 4-benzoyl-2,4-dimethyl-2-ethyl-5-phenyl-1,3-dioxolane, 4-ethyl-4-benzoyl-2-isopropyl-5-phenyl-1,3-dioxolane, 2-benzoyl-2-methyl-3-phenyl-1,4-dioxolane, 2-benzoyl-5-methyl-2-phenyl-1,4-dioxo-lane, 1,2-(dimethylsilylenedioxy)-1-benzoylcyclohexane, 1-benzoyl-8,8-dimethyl-7,9-dioxabicycloC4.3.0]nonane, 1-benzoyl-8,8-pentamethylene-7,9-dioxabicyclo[4.3aO~nonane, 2-hydroxy-3-isopropoxy-2-methyl~1~phenyl~1-propan-1-one, 2-ethyl-3-~` ~L3~69g~

(2-ethylhexyl)oxy-2-hydroxy~1~(3~tolyl)~propan-1-one, 2-hydroxy-3-(2-methoxyethyl)oxy~2~methyl~1~(4-methylthiophenyl)-3-phenylpropan-1-one, 2-ethyloxymethyl 2-hydroxy-1-(4-pr oxyphenyl) -hexan-1-one, 1-(4-benzoylphenyl)-2-hydroxy-2-methyl-3-(2-tetrahydrofuranyloxy)-propan-1-one~ 1,2-diphenyl-2-hydroxy-4~7~lo-trioxaundecan-1-one~ 2~hydroxy-1-(4-methoxy-3-methylphenyl)-2-methyl-4,7,10-trioxadodecan-1-one, 1~2-di-phenyl-2-hydroxy-4,7,10,13,16,19,22,25,28,31-decaoxatritri-acontan-1-one, 1-(2-chloro-4-phenylthiophenyl)-2-ethyl-2-hydroxy-3-(2-propinyl)oxypropan-1-one, 1-(3,4-dimethylphenyl)-3-butoxy-2-hydroxy-2-methyl-3-phenylpropan-1-one, 2,3-di-meth-yl-2-hydroxy-3-methoxy-1-phenylbutan~1-one, 3-(2-butenyl)oxy-2-hydroxy-2-methyl-1-(2,4,6-trimethylphenyl)-propan-1-one, 1-(3,4-dimethoxyphenyl)-2-hydroxy-2-methoxymethylbutan-1-one, 1,2-diphenyl-2,3-bis(trimethylsiloxy)-propan-1-one, 1,2-bis-(4-methoxyphenyl)-2,3-bis(allyloxy)-propan-1-one, 2,3-di-benzyloxy-Z-methyl-1-(4-propylthiophenyl)-propan-1-one, 1-(4-tert.-butylphenyl)-2-ethyl-2,3-dimethoxy-3-phenylpropan-1-one, 3-hydroxy-1,2-bis(4-methoxyphenyl)-2-trimethylsiloxy-propan-1-one~ 3-hydroxy-2-isopropyloxy~1,2,3-triphenylpropan-1-one, 2-allyloxy-1,2-diphenyl-3-hydroxypropan-1-one, 2-butyl-2-hydroxy-3~methoxy-4-methyl-1~t4-phenylthiophenyl)-pentan-1-one, 2-hydroxy-2-methyl-1-(4-phenoxyphenyl)-3-tri-methylsiloxypropan-1-one and 1-14-chlorophenyl)-2~hydroxy-3-t2-hydroxypropyl)oxy-2-methylpropan-1-one.
The compounds of the formula I are novel and are therefore also a subject of the present invent;on. Their preparation is effected analogously to that of the known com-pounds, for example in accordance with the relevant processes indicated in U.S. Patent Specifications 4,318,791 and 4,072,694.
The following route of synthes;s is particularly advantageous:

'' '' ' :
.

, ~ ~L31~

~ R3-co-c~lcl-R4 ~
R -Co-CH2-R4 R5-C-R R -CO-C - C-R6 (II) ~` ~ o-R6 ~ R4 R5 ~3-co-C=c-R6 (~ (V) (IV) -CO-R8 ~ ~ ~ R -0~1 / Dloxolane formation (VI (VI) oRl oR2Alkylation, H OR
CO-C - C Rsi lylation or 3 1 1 6 dioxolane formation R -CO-C - C - R

Starting from a propiophenone derivative of the formula II, the compound of the formula V is prepared either by means of Cl2 via the chlorinated compound of the formula III or via the compound of the formula IV, and, after being reacted with an appropriate alcohol of the formula VI or with H20, is converted into the compound~ according to the inven-tion, of the formula I and, after further alkylation, silyl-ation or dioxolane formation, is converted into the compound, according to the invention, of the formula I. Compounds of the formula I can also be formed direct from compounds of the formula V by dioxolane formation using a ketone or alde-hyde of the formula VII. In this case, R7 is hydrogenO
C1-C5-alkyl or phenyl, R8 is hydrogen or C1-C2-alkyl and R7 and R8 together are a tetramethylene or pentamethyl-ene radical. In the formulae I, IIr III" IV" V and VI, the radicals R1 to R6 are as defined above.
The numbers in circles indicate the literature ---` 13~)65~

references in which analogous processes of this type are des-cribed: ~ J. Chem. Soc., 79, 928 (1901), ~ J. Org. Chem., 28, 250, (1963~ or Org. Syntheses, 55, 52 (1976), ~ J. Am.
Chem. Soc., 75, 2042 (1953), ~ J. Chem. Soc., 73, 3293 (1958) or Houben-Weyl, Methoden der organischen Chemie (Methods of Organic Chemistry), volume VI/3, 40-44, 456-457, (1965), ~ T.W. Greene, Protective Groups in Organic Synthesis, pages 40-~2, (1981) or Houben-~leyl, Methoden der organischen Chemie (Methods of Organic Chemistry), volume VI/3, 229-232 (1963), ~ J. Am. Chem. Soc. 92, 5394 (1970), ~ Khim. Geterotsikl. Soedin 1975, 907.
Examples o-f such compounds are unsaturated monomers, such as esters of acrylic or methacrylic acid, for example methyl, ethyl, n-butyl, tert.-butyl, isooctyl or hydroxyethyl acrylate, methyl or ethyl methacrylate~ ethylene diacrylate, neopentyl diacrylate, trimethylolpropane trisacrylate~ penta-erythritol tetraacrylate or pentaerythritol trisacrylate;
acrylonitrile, methacrylonitrile, acrylamide, methacrylamide or N-substituted (meth)acrylamides, vinyl esters, for ex-ample v;nyl acetate, propionate, acrylate or succinate, other vinyl compounds, such as vinyl ethers, styrene, alkylstyrenes, halogenostyrenes, divinylbenzene, vinylnaphthalene, N vinyl-pyrrolidone, vinyl chloride or vinylidene chloride; allyl compounds, such as diallyl phthalate, diallyl maleate, tri-allyl isocyanurate, triallyl phosphate or ethylene glycol diallyl ether, and mixtures of such unsaturated monomers~
Ot~er photopolymerisable compounds are unsaturated oligomers or polymers and mixtures thereof with unsaturated monomers. These compounds include thermoplastic resins con~
ta;ning unsaturated groups, such as fumaric acid esters, allyl groups or acrylate or methacrylate groups. In most cases these unsaturated ~roups are linked to the main chain of these linear polymers via funct;onal groups. Mixtures of oligomers with monounsaturated and polyunsaturated monomers are of great ;mportance. Examples of such ol;gomers are unsaturated polyesters~ unsaturated acrylic resins and iso-cyanate-mod;fied or epoxide-modified acrylate ollgomers and ~V6~B

g also polyether acrylate oligorners. Examples of polyunsatur-ated compounds are especially the acrylates of diols and polyols, -for example hexamethylene diacrylate or pentaerythri-tol tetraacrylate. Acrylates, -for example butyl acrylate, phenyl acrylate, benzyl acrylate, 2-ethylhexyl acrylate or Z-hydroxypropyl acrylate, are also preferred as mono-unsaturated monomers. 8y selecting the three components from the various representatives it is possible to vary the consistency of the unpolymerised mixture and aLso the plasti-city of the polymerised resin.
As well as these three-component mixtures, two-component mixtures, in particular, play an important part in polyester resins. Tnese mixtures consist in most cases of an unsaturated polyester and a vinyl compound. The unsatur-ated polyesters are oligomeric esterif;cation products of at least one unsaturated dicarboxylic acid, for example maleic, fumaric or citraconic acid, and, ;n most cases, at least one saturated d;carboxylic ac;d, for example phthalic ac;d, succ;n;c acid, sebacic ac;d or ;sophthalic ac;d, w;th glycols, for example ethylene glycol~ 1,2-propaned;ol, diethylene glycol, tr;ethylene glycol or tetramethylene glycol, mono-carboxylic acids and monoalcohols also be;ng used concomit-antly for mod;f;cation in most cases. These unsaturated polyesters are usually dissolved in a v;nyl or allyl com-pound, styrene being preferably used for th;s purpose.
Preferred ethylenically unsaturated photopolymer;s-able compounds are monofunct;onal~ b;funct;onal or poly-funct;onal acryl;c esters and/or methacryl;c esters or m;x-tures thereof.
Many of the compounds employed in the practice of this invention are also suitable for use as initiators in aqueous photopolymerisable and curable systems. Examples of aqueous dispersions are described in the following publications: EP 12339, EP 21078, EP all25, DE-OS 2936039 and DE-OS 3 005 036.
: Photopolymerisable systems such as are used for various purposes iD most cases contain a number of other 13~G9~3~

additives besides the photopolymerisable compounds and the photoinitiator. Thus it is often customary to add thermal inhibitors which are intended to pro-tect the systems from premature polymerisation, especially while the systems are being prepared by mixing the components. ExampLes of com-pounds used for this purpose are hydroqu;none, hydroquinone derivatives, p-methoxyphenol, ~-naphthylamine or ~-naphthols.
It is also poss;ble to add small quant;t;es of UV absorbers, for example those of the benzotriazole or benzophenone type.
Stability to storage in the dark can be increased by adding copper compounds, such as copper naphthenate, stearate or octoate, phosphorus compounds, such as tr;phenyl-phosphine, tr;butylphosph;ne, tr;ethyl phosphite, triphenyl phosphite or tribenzyl phosphite, quaternary ammonium compounds, such as tetramethylammonium chloride or trimethyl-benzylammonium chloride or hydroxylamine derivat;ves, for example N-diethylhydroxylamine. The photopolymer;sable systems can also conta;n cha;n transfer agents, for example N-methyldiethanolam;ne, tr;ethanolam;ne or cyclohexene.
In order to exclude the inhib;ting act;on of the oxygen of the air, paraffin or similar waxlike substances are frequently added to photocurable systems. These float to the top at the start of polymerisation owing to inade-quate solubil;ty in the polymer, and form a transparent surface layer wh;ch prevents the access of air~ It is also possible to deactivate the oxygen of the air by introducing autooxidisable groups, for example allyl groups, into the resin to be cured.
The photoinitiators can also be used in combination with free radical ;nitiators, for example peroxides, hydro-peroxides, ketone peroxides or percarboxylic acid esters.
Depending on their end use, photopolymerisable sys-tems also cor,tain fillers, such as sil;ca, talc or gypsum, p;gments, dyes, fibres, thixotropic agents or flow control auxiliaries.
It is also possible to use combinations conta;ning known photoinit;ators, such as benzoin ethers, dialkoxyaceto-phenones or benzil ketals.

~3~69~8 Combinations of the photoinitiators according to the invention with amines and/or aromatic ketones can be used, in particular, for the photopolymerisation of thin layers and printing inks. Examples of am;nes are triethylamine, N-methyldiethanolamine, N-dimethylethanolamine or p-dimethyl-aminobenzoic acid esters Examples of ketones are benzo-phenone, substituted benzophenone derivatives, Michler's ketone, anthraquinone and anthraquinone derivatives~ coumarin derivatives and thioxanthone and derivatives thereof.
The photocuring of printing inks is of great ;mport-ance, s;nce the drying t;me of the binder ;s a dec;sive factor for the rate of product;on of graph;c products and should have an order of magnitude of fractions of a second.
The in;t;ators according to the ;nvent;on are also very su;t-able for photocurable systems for the production of pr;n-ting plates. Mixtures of soluble linear polyamides with photo-polymerisable monomers, for example acrylamides, and a photo-initiator are, for example, used in this case. Films and plates belonging to these systems are exposed v;a the negat-ive (or positive) of the print original, and the uncured portions are then eluted by means of a solvent.
A further field of use for UV curing is metal coat-ing, for example in the lacquering of metal sheets for tubes, cans or bottle closures, and also the UV curing of plastic coatings, for example floor coverings or wall coverings based on PVC.
Examples of the UV curing of paper coat;ngs are the colourless lacquering of labels, gramophone record sleeves or book covers.
The compounds of the formula I can also be used in accordance with the ;nvention as ;nitiators for the photo-chemical crosslinking of polyolefines. Examples of poly-olefines suitable for this purpose are polypropylene, poly-butylene, polyisobutylene and copolymers, for example ethy-lene/propylene copolymers, but preferably low-density, medium-density or h;gh-density polyethylene.
For the fields of use mentioned~ it is advantageous . ~"

~3~

to use the photoinitiators in amounts of 0.1 to 2U ~ by weight, preferably about 0.5 to 5 % by weight, based on the photopolymerisable or crosslinkable composition. Composi-tion is to be understood in this context as meaning the mix-ture of the photopolymerisable or crosslinkable compound, the photoin;tiator and the other fillers and additives, as used in the particular application.
The addition of the photoinitiators to the photo-polymerisable compositions is generally effected merely by stirring in, since most of these compositions are liquid or readily soluble. In most cases a solut;on of the initiators according to the invention is used, which ensures uniform distribution of the latter and also transparency of the polymers.
The polymerisation is effected in accordance with known methods of photopolymerisation by irradiation with light rich in short-wave radiation. Examples of suitable light sources are medium-pressure, hi~h-pressure and low-pressure mercury vapour lamps, and also superactinic fluor-escent tubes having emission maxima in the range between 250 and 400 nm.
The propiophenones of the formula I according to the invention possess an improved reactivity and stability on storage and also an increased resistance to yellowing.
The preparation and use of the photoinitiators according to the invention is described in greater detail in the examples which follow. In these examples, parts and percentages are by weight.
Example 1: Pre~ration of 3-methoxy-2-hydroxy-2-methyl-1-phenylpropan--1-one 20 parts (0~12 mol) of the educt, 2-benzoyl-2-methyl-oxirane of the formula r~ ~~CO~C/--\CH

~ 3 [prepared from ~-chloropropiophenone and paraformaldehyde by means of K0C(CH3)3/HOCtCH3)3 analogously to the l;terature reference J. Am. Chem. Soc. 75, 2042 (1953)], are taken up in 50 ml of methanol, and a catalyt;c amount tapprox. 5-10 mol %) of an acid, such as p-toluenesulfonic acid, is added carefully. The mixture is then stirred at room temperature until the educt is no longer present. The reaction solution thus obtained is then diluted with 2~0 ml of ether, washed twice with water, dried over sodium sulfate and finally concentrated on a rotary evaporator at ~0C. The crude reaction product obta;ned ;s purified by column chroma-tography tcarrier: sil;ca gel; mobile phase: hexane ~ 20 %
by volume o~ ethyl acetate). This gives 12 parts of a pure, colourless, oily product of the formula OH

Analytical data:
Combustion analysis for C11H1~03:
Calculated C % 68.03 H % 7 27 Found C ~ 68 04 H ~ 7.42 NMR spectrum ~CDCl3, ~ (in ppm)]:
1.43 (S,3H); 3.22 (S,3H); 3.38 and 3.84 tAB system~ J = 9Hz, 2H); 4.18 (S,lH); 7.1-7.~ (M,3H); 7.8-3.05 (M,2H).
S is singlet and M is multiplet.
Further compounds of the formula I were prepared analogously to the above example. They are listed in Table 1 below.

, . "

;L3~

Table 1:
Example Structure of the compounds Melting po1nt (oC)7 _ of the formula I _ 2 ~ C- \i U2 - 84 3O OH /OCH3 8~ - ~7 ¦ 4\ / I H2 H2 \ / ¦ (oiL~
5\ / C C - C -OCU3 '-.

-` 13~i9~3 Table 1: (continuation) Example ¦Structure of the compounds Melting point ~oC~¦
¦ of the formula I
r * prepared by silylating the correspond;ng alcohols by means of cl-si(cH3)3 and NtC2Hs)3, 2 2 Ex_mple 8: Preparation of 4-benzoYl-2 2,4-trimethYl-1 r3-di-oxolane 16.2 9 (0.1 mol) of 2-benzoyl-2-methylox;rane (see Example 1) are dissolved in 35 9 (0.6 mol) of acetone, and a solution of 1.42 9 (0.01 mol) of boron trifluoride-ether-ate in 35 g (0.6 mol) of acetone is then added dropwise while the mixture is cooled by means of an ice bath. The mixture is then stirred for 2 hours at room temperature and is then heated under reflux for 5 hours. The reaction solu-tion is cooled, rendered alkaline, with cooling, by means of 50 ml of saturated methanolic sodium hydroxide solution, and diluted with 200 ml of water. The product is extracted with ether. The ether solution is dried with potassium car-bonate and concentrated. The residue is distilled in vacuo at 95~C and 0.5 mbar. The distillate is purified by medium-pressure chromatography, a colourless oil being obtained.

;

9E~

Analyt;cal data:
Combustion analysis for C13H1603 Calcula-ted: C % 70.89 H % 7.33 Found: C % 70 76 H % 7.31 1H-NMR spectrum ~CDCl3, ~ (in ppm)]:
8 25-7 95 (~, 2H); 7.45-7.2 (M, 3H); 4.64 and 3.70 (AB system, J = 16 Hz, 2H); 1.57 (S,3H); 1.43 tS,3H); 1~10 (S,3H), S being singlet and M being rnultiplet.
Example 9: Preparation of 4-benzoyl-4-methyl-2-phenyl-1,3-dioxolane 4-Ben~oyl-~-methyl-2-phenyl-1,3 dioxolane was also prepared us;ng benzaldehyde analogously to the above Example 8 (an oil having a bo;l;ng po;nt of 145C at 0.07 mbar).
Analyt;cal data:
Combust;on analys;s for C17H16o3 Calculated: C % 76.10 H % 6.01 Found: C % 76.11 H % 6.02 1H-NMR spectrum ~CDCl3, ~ (ppm)]:
8 25-7.85 (M, 2 aromat;c H); ~.5-6.9 (M, 8 aromat;c H);
5.95 (S, O.S H,H-C(2)); 5.62 (S, 0.5 H,H-C(2)); 4.85 and 3.69 ~1.0 H, signals of an AB system, J = 8 Hz~ 2H-C(S)); 4~55 and 3.85 (1.0 H, s;gnals of an Aa system, J = 8 Hz, 2H C(5));
1.63 (S, CH3-C(4)); 1.60 (S, CH3-C(4)). The presence of a m;xture of c;s-trans-;somers (44 % and 56 ~) of 4-benzoyl-4-methyl-2-phenyl-1,3-d;oxolane is deduced from the 1H-NMR
spectrum and the gas chromatogram.
Use Examples:
Example 10: A res;n m;xture composed of 20 parts of Plex~
6616 (an acryl;c res;n made by Rohm, Darmstadt), 5 parts of tr;methylolpropane tr;sacrylate and 0.5 part of 3-methoxy-2-hydroxy-2-methyl-1-phenylpropan~1-one ;s appl;ed to a sheet of glass ;n a th;ckness of 40 ,um dry layer th;ckness by means of a f;lm appl;cator. Th;s f;lm ;s exposed to the a;r for approx. 20 seconds and ;s then ;rradiated w;th a UV appar-atus (PPG-QC-processor model). The sample ;s then passed under the UV lamp on a conveyor belt at a speed of 17 m/
m;nute. The film is resistant to w;p;ng after 3 passes~
. .

:~3~65~

The pendulum hardness (DIN 53,158) of the film cured in this way is 176 seconds.
Example~ A resin mixture composed of ~0 parts of PLe 6616 (acrylic resin made by Rohm, Darmstadt), Z0 parts of trimethylolpropane trisacrylate and 2 parts of pho-toinitiator is applied to sheets of glass in a thickness of 40 ~m dry layer thickness by means of a film applicator. These films are exposed to the air for approx. 20 seconds and are then irradiated with a medium-pressure Hg lamp (Hanovia-Gerat, model 45,080). The samples are then passed under the UV
lamp on a conveyor belt at a speed such that an effective exposure time of 0.16 second per pass results.
The number of passes (P) required to give tack-free films (resistant to wiping) is given in the second column of Table 2 below.
The third column gives the hardness of the films after the number of passes stated, measured with the Konig pendulum apparatus. Discolouration (yellowing) is assessed by determining the yellowness index as specified in ASTM D
1925-70.
Table 2:
. _ . _ Photoinitiator¦Passes Konig pendulum Yellowness according to required hardness when index Example (P) resistant to wiping (seconds:

___ Example 12 A resin mixture composed of 80 parts of Ebecryl~
593 (acrylic resin made by UCB, Erussels), 20 parts of DQM-~672 (acrylic monomer made by Rohm and Haas, Philadelphia~ llSA) and 2 parts of photoinitiator is applied to sheets of glass l~ tB

in a thickness of 40 ,um dry layer thickness by means of a film applicator. These films are exposed to the air for approx~ 20 seconds and then irradiated with a medium-pressure Hg lamp ~Hanovia~Gerat, model 45,080). This is effected by passing the samples under the UV lamp on a conveyor belt at a speed such that an effective exposure time of 0.16 second per pass results.
The number of passes (P) required to produce tack-free films (resistant to wiping) is given in the second column of Table 3 below.
The third coLumn gives the hardness of the f;lms after the number of passes stated, measured with the K~n;g pendulum apparatus. Discolouration (yellowing) is assessed by determining the yellowness index as specified in ASTM D

Table 3:
_ ~
Photoinitiator Passes Konig pendulum Yellowness according to required hardness when index Example (P) resistant to wiping (seconds ) _ - ~ 4 129 _ _ 3 1l3 ~ 3 Example 13: A resin mixture composed of 0 parts of Acty a ~J20 (acrylic resin made by SNPE, Paris Cedex), 15 parts of DQ~ 672 (acrylic monomer made by Rohm and Haas, Philadelphia~
USA), 15 parts each of trismethylolpropane triacrylate and hexanediol diacrylate (polyfunctional monomers made by Degussa, Frankfurt), 10 parts of N-vinylpyrrolidone (reactive thinner made by GAF, New York, USA) and 2 parts of photo;nitiator is applied to sheets of glass in a thickness of 40 ~m dry layer th;ckness by means of a film applicator. These films are exposed to the air for approx. 20 seconds and are then ir-radiated with a high-pressure Hg lamp (UV-processor model ,.0 ~.

~3~ B

1202 AN made by PPG Radiation Polymer Company, USA)~ This is effected by passing the samples under the UV lamp on a conveyor belt at a belt speed such that an effective exposu,-e time of 1.05 seconds per pass results.
The number of passes (P) required to give tack-free films (resistant to wiping) is given in the second column of Table 4.below.
The third column gives the hardness oF the films after the number of passes stated, measured by the Konig pendulum apparatus.
The discolouration (yellowing) is assessed by deter-mining the yellowness index as specified in ASTM D 1925-70.
Table 4:
~ , Photo;nitiator Passes Konig pendulum Yellowness according to required hardness when index Example (P) resistant to wiping (seconds) 1 8 151 _

Claims (11)

1. A photopolymerisable composition comprising at least one ethylenically unsaturated photopolymerisable compound and a compound of the formula I

(I) in which R1 is hydrogen or C1-C4-alkyl, -Si(CH3)3, allyl or benzyl, R2 is hydrogen, C1-C8-alkyl, C1-C4-alkyl which is substituted by C1-C4-alkoxy or -OH, -(CH2-CH2-O)n-R5 where n is 2 to 20 and R5 is H or C1-C4-alkyl, -Si(CH3)3, benzyl, C3-C6-alkenyl, C3-C4-alkynyl, 2-tetrahydropyranyl or 2-tetrahydrofuranyl, or R1 and R2 together are a C1-C6-alkylidene radical or a C2-C6-alkylidene radical which is substituted by hydroxyl, C1-C4-alkoxy or phenyl, a linear or branched C2-C6-alkanediyl radi-cal, a benzylidene, cyclopentylidene or cyclohexylidene radi-cal or a 2,2,2-trichloroethylidene, 2-furylmethylidene or dimethylsilylidene radical, R3 is phenyl which is unsub-stituted or substituted by one or more -Cl, C1-C4-alkyl, C1-C4-alkoxy or C1-C4-alkylthio radicals, and is also benzoylphenyl, phenoxyphenyl or phenylthiophenyl, R4 is C1-C4-alkyl, or phenyl which is unsubstituted or substituted by one or more -Cl, C1-C4-alkyl or C1-C4-alkoxy radicals, and R5 is hydrogen or C1-C4-alkyl, or R4 and R5 together are a trimethylene or tetramethylene radical, and R6 is hydrogen, C1-C4-alkyl, -CCl3 or phenyl, subject to the condition that, if R2, R5 and R6 at the same time are hydrogen and R3 and R4 are at the same time phenyl, R1 must not be hydrogen or C1-C4-alkyl, also, if R3 and R4 at the same time are phenyl and R5 and R6 are at the same time hydrogen, R1 and R2 together must not be alkylidene or benzylidene, and also, if R3 and R4 at the same time are p-methoxyphenyl and R2, R5 and R6 are at the same time hydrogen, R1 must not be hydrogen, and, finally, if R2 and R6 at the same time are hydrogen and R3, R4 and R5 are at the same time phenyl, R1 must not be hydrogen.
2. A composition according to claim 1 comprising compounds of the for-mula 1 in which R2 is hydrogen or C1-C4-alkyl, R3 is phenyl, R4 is C1-C4-alkyl and R5 is hydrogen, and R4 and R5 together are a trimethylene or tetramethylene radical and R6 is hydrogen.
3. A composition according to claim 1 comprising compounds of the for-mula l in which R2 is methyl.
4. A compositon according to claim 1 comprising compounds of the formula 1 in which R1, R5 and R6 are hydrogen, R2 and R4 are methyl and R3 is phenyl.
5. A composition according to claim 1 comprising compounds of the formula 1 in which R1 and R6 are hydrogen, R2 is methyl, R3 is phenyl and R4 and R5 together are tetramethylene.
6. A composition according to claim 1, comprising, as the ethylenically unsaturated photopolymerisable compound, a monofunctional, bifunctional or polyfunctional acrylic acid ester or methacrylic acid ester or mix-tures thereof.
7. A printing ink comprising at least one ethylenically unsaturated photo-polymerisable compound and pigments and/or dyes and a compound of the formula 1 according to claim 1.
8. Metal, plastics and paper coatings comprising at least one ethyleni-cally unsaturated photopolymerisable compound and a compound of the for-mula 1 according to claim 1.
9. A compound of the formula 1 - 21a - 21489-6364 (I) in which R1 is hydrogen or C1-C4-alkyl, -Si(CH3)3, allyl or benzyl, R2 is hydrogen, C1-C8-alkyl, C1-C4-alkyl which is substituted by C1-C4-alkoxy or -OH, -(CH2-CH2-O)n-R5 where n is 2 to 20 and R5 is H or C1-C4-alkyl, -Si(CH3)3, benzyl, C3-C6-alkenyl, C3-C6-alkynyl, 2-tetrahydro-pyranyl or 2-tetrahydrofuranyl, or R1 and R2 together are a C1-C6-alkylidene radical or a C2-C6-alkylidene radi-cal which is substituted by hydroxyl, C1-C4-alkoxy or phenyl, a linear or branched C2-C6-alkanediyl radical, a benzylidene, cyclopentylidene or cyclohexylidene radical or a 2,2,2-tri-chloroethylidene, 2-furylmethylidene or dimethylsilylidene radical, R3 is phenyl which is unsubstituted or substituted by one or more -Cl, C1-C4-alkyl, C1-C4-alkoxy or C1-C4-alkylthio radicals, and is also benzoylphenyl, phenoxyphenyl or phenylthiophenyl, R4 is C1-C4-alkyl, or phenyl which is unsubstituted or substituted by one or more -Cl, C1-C4-alkyl or C1-C4-alkoxy radicals, and R5 is hydrogen or C1-C4-alkyl, or R4 and R5 together are a trimethylene or tetramethylene radical, and R6 is hydrogen, C1-C4-alkyl, -CCl3 or phenyl, subject to the condition that, if R2, R5 and R6 at the same time are hydrogen and R3 and R4 are at the same time phenyl, R1 must not be hydrogen or C1-C4-alkyl, also, if R3 and R4 at the same time are phenyl and R5 and R6 are at the same time hydrogen, R1 and R2 together must not be alkylidene or benzylidene, and also, if R3 and R4 at the same time are p-methoxyphenyl and R2, R5 and R6 are at the same time hydrogen, R1 must not be hydrogen, and, finally, if R2 and R5 at the same time are hydrogen and R3, R4 and R6 are at the same time phenyl, R1 must not be hydrogen.
10. A compound of the formula I, according to claim 9, in which R1 is hydrogen, R2 is hydrogen, methyl or -Si(CH3)3, or R1 and R2 together are isopropylidene, benzylidene or dimethylsilylidene, R3 is phenyl, R4 is methyl or phenyl, R5 is hydrogen or R4 and R5 together are a tetramethylene radical and R6 is hydrogen or phenyl, subject to the condition that R2, R5 and R6 at the same time may not be hydrogen or R4 may not be phenyl, and if R4 is phenyl and R5 and R6 at the same time are hydrogen, R1 and R2 together may not be isopropylidene or benzylidene, and finally, R2 may not be hydrogen or R4 and R6 at the same time may not be phenyl.
11. A compound of the formula I, according to claim 9, selected from the group comprising: 3-methoxy-2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-benzoyl-1,2-dihydroxycyclo-hexane, 1,3-diphenyl-2-hydroxy-3-methoxy-2-methylpropan-1-one, 1,2-diphenyl-2-hydroxy-3-trimethylsiloxypropan-1-one, 4-benzoyl-4-methyl-2-phenyl-1,3-dioxolane, 4-benzoyl-2,2,4-trimethyl-1,3-dioxolane and 2,3-(dimethylsilylene-dioxy)-1,2-diphenylpropan-1-one.
CA000437979A 1982-10-01 1983-09-29 Propiophenone derivatives as photoinitiators for photopolymerisation Expired - Lifetime CA1306998C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH580782 1982-10-01
CH5807/82-2 1982-10-01

Publications (1)

Publication Number Publication Date
CA1306998C true CA1306998C (en) 1992-09-01

Family

ID=4299636

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000437979A Expired - Lifetime CA1306998C (en) 1982-10-01 1983-09-29 Propiophenone derivatives as photoinitiators for photopolymerisation

Country Status (5)

Country Link
US (2) US4795766A (en)
EP (1) EP0108037B1 (en)
JP (1) JPS5993024A (en)
CA (1) CA1306998C (en)
DE (1) DE3380028D1 (en)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5288917A (en) * 1986-04-15 1994-02-22 Ciba-Geigy Corporation Liquid photoinitiator mixtures
GB8715435D0 (en) * 1987-07-01 1987-08-05 Ciba Geigy Ag Forming images
DE4105355A1 (en) * 1991-02-21 1992-08-27 Basf Ag COMPOUNDS CONTAINING CARBONATE AND CARBONYL GROUPS, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE
US5721287A (en) 1993-08-05 1998-02-24 Kimberly-Clark Worldwide, Inc. Method of mutating a colorant by irradiation
US5865471A (en) 1993-08-05 1999-02-02 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms
US5733693A (en) 1993-08-05 1998-03-31 Kimberly-Clark Worldwide, Inc. Method for improving the readability of data processing forms
US5773182A (en) 1993-08-05 1998-06-30 Kimberly-Clark Worldwide, Inc. Method of light stabilizing a colorant
US6017661A (en) 1994-11-09 2000-01-25 Kimberly-Clark Corporation Temporary marking using photoerasable colorants
US6017471A (en) 1993-08-05 2000-01-25 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US5700850A (en) 1993-08-05 1997-12-23 Kimberly-Clark Worldwide Colorant compositions and colorant stabilizers
US6211383B1 (en) 1993-08-05 2001-04-03 Kimberly-Clark Worldwide, Inc. Nohr-McDonald elimination reaction
US5681380A (en) 1995-06-05 1997-10-28 Kimberly-Clark Worldwide, Inc. Ink for ink jet printers
US5643356A (en) 1993-08-05 1997-07-01 Kimberly-Clark Corporation Ink for ink jet printers
US5645964A (en) 1993-08-05 1997-07-08 Kimberly-Clark Corporation Digital information recording media and method of using same
CA2120838A1 (en) 1993-08-05 1995-02-06 Ronald Sinclair Nohr Solid colored composition mutable by ultraviolet radiation
US6242057B1 (en) 1994-06-30 2001-06-05 Kimberly-Clark Worldwide, Inc. Photoreactor composition and applications therefor
US5739175A (en) 1995-06-05 1998-04-14 Kimberly-Clark Worldwide, Inc. Photoreactor composition containing an arylketoalkene wavelength-specific sensitizer
US5685754A (en) 1994-06-30 1997-11-11 Kimberly-Clark Corporation Method of generating a reactive species and polymer coating applications therefor
US6071979A (en) 1994-06-30 2000-06-06 Kimberly-Clark Worldwide, Inc. Photoreactor composition method of generating a reactive species and applications therefor
DE4435487A1 (en) * 1994-10-04 1996-04-11 Hoechst Ag Silicon-compatible photoinitiators and light-sensitive mixtures containing them
US6008268A (en) 1994-10-21 1999-12-28 Kimberly-Clark Worldwide, Inc. Photoreactor composition, method of generating a reactive species, and applications therefor
US5849411A (en) 1995-06-05 1998-12-15 Kimberly-Clark Worldwide, Inc. Polymer film, nonwoven web and fibers containing a photoreactor composition
US5798015A (en) 1995-06-05 1998-08-25 Kimberly-Clark Worldwide, Inc. Method of laminating a structure with adhesive containing a photoreactor composition
CA2219450A1 (en) 1995-06-05 1996-12-12 Ronald Sinclair Nohr Novel pre-dyes
US5811199A (en) 1995-06-05 1998-09-22 Kimberly-Clark Worldwide, Inc. Adhesive compositions containing a photoreactor composition
US5786132A (en) 1995-06-05 1998-07-28 Kimberly-Clark Corporation Pre-dyes, mutable dye compositions, and methods of developing a color
US5747550A (en) 1995-06-05 1998-05-05 Kimberly-Clark Worldwide, Inc. Method of generating a reactive species and polymerizing an unsaturated polymerizable material
ES2161357T3 (en) 1995-06-28 2001-12-01 Kimberly Clark Co STABILIZING COLORING COMPOSITION.
US6099628A (en) 1996-03-29 2000-08-08 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5782963A (en) 1996-03-29 1998-07-21 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5855655A (en) 1996-03-29 1999-01-05 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
SK102397A3 (en) 1995-11-28 1998-02-04 Kimberly Clark Co Colorant stabilizers
US5891229A (en) 1996-03-29 1999-04-06 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
FR2750429B1 (en) * 1996-06-27 1998-08-07 Essilor Int CROSS-LINKED SILICONE-BASED MATERIAL COMPRISING A FIXED PHOTO-INITIATOR, METHOD FOR PREPARING IT, HYDROPHILIC POLYMERIC PRODUCT OBTAINED FROM THIS MATERIAL AND METHOD FOR PREPARING IT, AND NEW PHOTO-INITIATORS
US6524379B2 (en) 1997-08-15 2003-02-25 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
SK1542000A3 (en) 1998-06-03 2001-11-06 Kimberly Clark Co Neonanoplasts produced by microemulsion technology and inks for ink jet printing
KR20010022593A (en) 1998-06-03 2001-03-26 로날드 디. 맥크레이 Novel Photoinitiators and Applications Therefor
US6228157B1 (en) 1998-07-20 2001-05-08 Ronald S. Nohr Ink jet ink compositions
JP2003533548A (en) 1998-09-28 2003-11-11 キンバリー クラーク ワールドワイド インコーポレイテッド Chelates containing quinoid groups as photopolymerization initiators
DE60002294T2 (en) 1999-01-19 2003-10-30 Kimberly Clark Co DYES, COLOR STABILIZERS, INK COMPOSITIONS AND METHOD FOR THE PRODUCTION THEREOF
US6331056B1 (en) 1999-02-25 2001-12-18 Kimberly-Clark Worldwide, Inc. Printing apparatus and applications therefor
US6294698B1 (en) 1999-04-16 2001-09-25 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6368395B1 (en) 1999-05-24 2002-04-09 Kimberly-Clark Worldwide, Inc. Subphthalocyanine colorants, ink compositions, and method of making the same
WO2002000735A1 (en) 2000-06-19 2002-01-03 Kimberly-Clark Worldwide, Inc. Novel photoinitiators and applications therefor
GB0019251D0 (en) * 2000-08-04 2000-09-27 Lintfield Limited Photoinitiated reactions
US7081291B2 (en) * 2002-01-11 2006-07-25 Domco Tarkett Inc. Selectively embossed surface coverings and processes of manufacture
WO2008060844A1 (en) * 2006-11-09 2008-05-22 Albemarle Corporation Polymerization inhibitor compositions, their preparation, and their use
GB2476976A (en) 2010-01-18 2011-07-20 Lintfield Ltd Protected aryl ketones and their use as photoinitiators

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3344148A (en) * 1965-10-29 1967-09-26 Olin Mathieson 4, 4-substituted-1, 3-dioxolanes and preparing them
DE1769854C3 (en) * 1968-07-26 1982-08-19 Bayer Ag, 5090 Leverkusen Photoinitiators and processes for photopolymerization
US3636026A (en) * 1968-11-06 1972-01-18 Bayer Ag Benzoin-silyl-esters
US3657088A (en) * 1969-12-17 1972-04-18 Bayer Ag Moulding and coating masses hardenable by uv irradiation
US3689565A (en) * 1970-05-04 1972-09-05 Horst Hoffmann {60 -methylolbenzoin ethers
US3801329A (en) * 1971-12-17 1974-04-02 Union Carbide Corp Radiation curable coating compositions
DE2232497C2 (en) * 1972-07-01 1982-06-03 Basf Ag, 6700 Ludwigshafen Benzoin compounds containing acetal groups, processes for their preparation and their use as photoinitiators
DE2357866A1 (en) * 1972-12-06 1974-06-12 Sun Chemical Corp COMPOSITIONS HARDABLE UNDER RADIATION
US3944509A (en) * 1973-06-11 1976-03-16 Sun Chemical Corporation Keto dioxolanes
US4072694A (en) * 1975-09-15 1978-02-07 Lee Pharmaceuticals Dioxolane derivatives and use as photoinitiators
DE2600318C3 (en) * 1976-01-07 1982-04-08 Bayer Ag, 5090 Leverkusen Process for the production of copolymers
DE2616408A1 (en) * 1976-04-14 1977-11-03 Basf Ag MIXTURES POLYMERIZABLE BY UV RADIATION
US4144156A (en) * 1976-04-14 1979-03-13 Basf Aktiengesellschaft Manufacture of unsymmetric monoacetals of aromatic 1,2-diketones employable as photoiniatiators
EP0003002B1 (en) * 1977-12-22 1984-06-13 Ciba-Geigy Ag Use of aromatic-aliphatic ketones as photoinitiators, photopolymerisable systems containing such ketones and aromatic-aliphatic ketones

Also Published As

Publication number Publication date
JPS5993024A (en) 1984-05-29
EP0108037A3 (en) 1984-09-05
JPH0460121B2 (en) 1992-09-25
EP0108037A2 (en) 1984-05-09
DE3380028D1 (en) 1989-07-13
US4795766A (en) 1989-01-03
EP0108037B1 (en) 1989-06-07
US5147901A (en) 1992-09-15

Similar Documents

Publication Publication Date Title
CA1306998C (en) Propiophenone derivatives as photoinitiators for photopolymerisation
US4190602A (en) Monoacetals or aromatic 1,2-diketones
CA1234242A (en) Sensitizers for photopolymerisation
KR950008287B1 (en) Titanocenes and their use
US4672079A (en) Polymeric or polymerizable aromatic-aliphatic ketones suitable for use as polymerization photoinitiators
EP1499645B1 (en) Incorporable photoinitiator
JP3834738B2 (en) Alkoxyphenyl substituted bisacylphosphine oxide
EP1072326B1 (en) Surface active photoinitiator
KR101327711B1 (en) Photopolymerisable systems containing low-extractable and low-volatile coinitiators
US4987159A (en) Carbonyl derivatives of 1-phenylindan suitable for use as polymerization photoinitiators, their preparation and use
DE60128105T2 (en) PROCESS FOR PREPARING COATINGS USING PHOTOINITIATORS COLLECTING ON THE SURFACE
US5192642A (en) Oxygen-containing titanocenes, and the use thereof
KR19990022661A (en) Method for optical generation of amines from a-aminoacetophenones
AU2003283441A1 (en) Improvement in the storage stability of photoinitiators
US9353207B2 (en) Alkylphenyl derivatives and application thereof as photoinitiator
JPS63150303A (en) Liquid photoinitiator mixture
KR910000199B1 (en) Liquid blend of photoinitiator
US4279721A (en) Mercaptophenyl ketones as initiators for the photopolymerization of ethylenically unsaturated compounds
US4950795A (en) Oligomeric benzil ketals and their use as photoinitiators
US5021512A (en) Thiol/ene compositions
JP4222945B2 (en) Surfactant siloxane photoinitiator
US6287749B1 (en) Biradical photoinitiators and photopolymerizable compositions
US4088554A (en) Initiators for photopolymerization
US5095044A (en) Oligomeric benzil ketals and their use as photoinitiators
US5288917A (en) Liquid photoinitiator mixtures

Legal Events

Date Code Title Description
MKLA Lapsed