Process for production of positive images using sulfonic acid precursors

Claim 2

A process for the production of an image comprising (i) forming a composition which comprises (A) a film-forming organic material consisting essentially of an aqueous base-soluble material having a phenolic hydroxyl group or a carboxylic, sulfonic, phosphonic or phosphoric acid group, and (B) a substance which releases a sulfonic acid on exposure to actinic radiation, thereby effecting a reduction of the dissolution rate of said film-forming material in aqueous base, and (ii) exposing said composition to actinic radiation in a predetermined pattern, thereby nullifying said dissolution rate reduction to render the composition more soluble in an aqueous base developer in exposed areas than in unexposed areas, and (iii) removing the composition in the exposed areas by treatment with the aqueous base developer.

Claim 3

A process according to claim 1, in which the substance (B) is a sulfonate ester of an aromatic alcohol containing a carbonyl group or an aromatic N-sulfonyloxyimide.

Claim 4

A process according to claim 2, in which the sulfonate is of formula ##STR5## where n is 1 or 2, R 1 is phenyl or naphthyl which is unsubstituted, or substituted by 1,2 or 3 of --Cl, --Br, --CN, NO 2 , C 1 -C 12 alkyl, C 1 -C 4 --alkoxy phenyloxy, tolyloxy, phenylthio, tolylthio, C 1 -C 8 --alkylthio, --SCH 2 CH 2 OH, C 1 -C 4 --alkylsulfonyl, phenylsulfonyl, C 2 -C 4 --alkoxycarbonyl, C 1 -C 4 --alkylamino, C 2 -C 4 --dialkylamino, phenyl--CONH-- or C 1 -C 4 --alkyl--CONH--, or by benzoyl, or R 1 is anthryl, phenanthryl, thienyl, pyridyl, furyl, indolyl or tetrahydronaphthyl, and R 2 and R 3 independently of one another are each hydrogen, or C 1 -C 8 alkyl which is unsubstituted or substituted by --OH, --Cl, C 1 -C 4 --alkoxy, --CN, C 2 -C 5 --alkoxycarbonyl, phenyl, chlorophenyl, C 7 -C 10 alkylphenyl or C 7 -C 10 --alkoxyphenyl, or they are benzoyl, in addition R 3 is phenyl which is unsubstituted or substituted by --Cl, C 1 -C 4 alkyl, C 1 -C 4 --alkoxy or C 1 -C 4 --alkylthio, or it is C 2 -C 8 --alkoxycarbonyl, --CN, C 1 -C 4 --alkyl--NH--CO--, phenyl--NH--CO-- or --CONH 2 , or R 2 and R 3 together with the carbon atom to which they are bound form a C 4 -C 6 --cycloalkyl ring, R 4 is, when n=1, C 1 -C 18 --alkyl, phenyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl, C 1 -C 4 alkoxy, C 1 -C 4 --alkyl-- CONH--, phenyl--CONH--, --NO 2 or benzoyl, or it is naphthyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl or C 1 -C 4 --alkoxy, or it is C 5 -C 6 --cycloalkyl, C 7 -C 9 --aralkyl, campheryl, --CF 3 , --CCl 3 , --F, or --NH 2 , and R 4 is, when n=2, a --(CH 2 ) m group, wherein m is 2 to 8, or phenylene or naphthylene each unsubstituted or substituted by C 1 -C 15 --alkyl, R 9 represents a hydrogen atom or one, two or three --Cl, --Br, --NO 2 , C 1 -C 12 alkyl, C 1 -C 4 alkoxy, phenoxy, phenylthio, C 1 -C 8 alkylthio, or --SCH 2 CH 2 OH substituents, X represents --O--, --S--, --SO 2 --, --CH 2 --, --C(CH 3 ) 2 -- or >NCOR 10 , where R 10 is C 1 -C 4 alkyl or phenyl, Y represents a direct bond or --CH 2 --, and R 11 represents a hydrogen atom; C 1 -C 8 alkyl, C 1 -C 8 alkyl substituted by --OH, --Cl, C 1 -C 4 alkoxy, CN, C 2 -C 5 alkoxycarbonyl, phenyl, chlorophenyl, C 7 -C 10 alkylphenyl, or C 7 -C 10 alkoxyphenyl; phenyl, phenyl substituted by --Cl, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or C 1 -C 4 alkylthio; C 2 -C 8 alkoxycarbonyl; or CN.

Claim 5

A process according to claim 2, in which the sulfonate is of formula ##STR6## where n is 1 or 2, R 4 is, when n=1, C 1 -C 18 --alkyl, phenyl which is unsubstituted or substituted by halogen. C 1 -C 12 --alkyl, C 1 -C 4 alkoxy, C 1 -C 4 --alkyl-- CONH--, phenyl--CONH--, --NO 2 or benzoyl, or it is naphthyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl or C 1 -C 4 --alkoxy, or it is C 5 -C 6 --cycloalkyl, C 7 -C 9 --aralkyl, campheryl, --CF 3 , --CCl 3 , --F, or --NH 2 , and R 4 is, when n=2, a --(CH 2 ) m group, wherein m is 2 to 8, or phenylene or naphthylene each unsubstituted or substituted by C 1 -C 15 --alkyl, R 5 is phenyl or naphthyl which are each unsubstituted or substituted by 1,2 or 3 of --Cl, --Br, C 1 -C 12 --alkyl, phenyl, C 1 -C 8 --alkoxy, phenyloxy, benzyloxy, C 1 -C 8 --alkylthio, phenylthio, --SCH 2 CH 2 OH, C 1 -C 4 --alkyl--CONH--, benzoylamino or dimethylamino, or by benzoyl, or R 5 is anthryl or phenanthryl, R 6 is hydrogen, --OH, C 1 -C 4 --alkoxy, --OSi(CH 3 ) 3 , --OCOCH 3 , or C 1 -C 8 --alkyl which is unsubstituted or substituted by phenyl, R 7 is hydrogen, or C 1 -C 8 --alkyl which is unsubstituted or substituted by phenyl, or R 7 is --CN, benzoyl, C 1 -C 4 --alkylcarbonyl, C 2 -C 5 --alkoxycarbonyl or phenyl, R 8 is hydrogen, C 1 -C 8 --alkyl which is unsubstituted or substituted by --OH, --Cl or phenyl, or it is phenyl which is unsubstituted or substituted by --OH, --Cl, C 1 -C 4 --alkyl or C 1 -C 4 --alkoxy, or R 8 is C 2 -C 6 --alkenyl, C 8 -C 9 --phenylalkenyl, furyl, thienyl or --CCl 3 , or saturated or unsaturated C 5 -C 6 --cycloalkyl, and moreover R 5 with R 7 or R 6 with R 7 , together with the carbon structure to which they are bound, form a 5- or 6-membered ring which contains 1 to 5 --CH 2 --, --CH(CH 3 )--, --(CH 3 ) 2 --, --O--, --S--, --SO--, --SO 2 --, --CO--, --N(CO--C 1 -C 4 --alkyl)-- or N(COC 6 H 5 )-- groups.

Claim 6

A process according to claim 2, in which the sulfonyloxyimide is of formula ##STR7## where n is 1 or 2, R 16 represents arylene, substituted arylene, alkylene, substituted alkylene, alkenylene, or substituted alkenylene, C 2 -C 6 straight, branched, or cyclic alkylene, unsubstituted or substituted by phenyl, naphthyl, or C 1 -C 4 alkyl; C 2 -C 4 alkenylene or C 2 -C 4 alkenylene substituted by phenyl or C 1 -C 2 alkyl; and R 17 represents, where n=1, C 1 -C 18 straight or branched alkyl, unsubstituted or substituted by halogen or C 1 -C 4 alkoxy; C 6 -C 12 aryl, C 6 -C 12 aryl substituted by C 1 -C 15 alkyl, C 1 -C 4 alkylCONH, phenylCONH, or NO 2 ; C 5 -C 6 cycloalkyl, campheryl; CF 3 ; CCl 3 ; CH 2 Cl; F; or NH 2 , or R 17 represents, where n=2, C 2 -C 6 alkylene, phenylene, or naphthylene, with the proviso that at least one of R 16 and R 17 is, or contains, an aromatic group.

Claim 7

A process according to claim 2, in which (B) is a sulfonate ester of benzoin or alpha-methylolbenzoin, or a N-sulfonyloxy derivative of 1,8-naphthalimide.

Claim 8

A process according to claim 1, in which the film-forming organic material (A) contains a phenolic hydroxyl group or a carboxylic, sulfonic, phosphonic or phosphoric acid group.

Claim 9

A process according to claim 7, in which the film-forming organic material (A) is a novolak resin or a homopolymer or copolymer of an ethylenically unsaturated carboxylic acid or carboxylic acid anhydride.

Claim 10

A process according to claim 1, in which the composition contains from 0.05 to 0.8 part by weight of the sulfonic acid-releasing substance (B) per part by weight of the film-forming organic material (A).

Claim 11

A substrate bearing an image produced by a process according to claim 1.

Claim 12

A photosensitive composition, suitable for carrying out the process of claim 1, which comprises (A) a film-forming organic material consisting essentially of an aqueous base-soluble material having a phenolic hydroxyl group or a carboxylic, sulfonic, phosphonic or phosphoric acid group, and (B) a substance which releases a sulfonic acid on exposure to actinic radiation, the composition being substantially free from ethylenically unsaturated material which is polymerized by means of free radicals and from material which is polymerized by sulfonic acids.

Claim 13

A composition according to claim 11, in which the substance (B) is a sulfonate ester of an aromatic alcohol containing a carbonyl group or an aromatic N-sulphonyloxyimide.

Claim 14

A composition according to claim 12, in which the sulfonate is of formula ##STR8## where n is 1 or 2, R 1 is phenyl or naphthyl which is unsubstituted, or substituted by 1,2 or 3 of --Cl, --Br, --CN, NO 2 , C 1 -C 12 alkyl, C 1 -C 4 --alkoxy phenyloxy, tolyloxy, phenylthio, tolylthio, C 1 -C 8 --alkylthio, --SCH 2 CH 2 OH, C 1 -C 4 --alkylsulfonyl, phenylsulfonyl, C 2 -C 4 --alkoxycarbonyl, C 1 -C 4 --alkylamino, C 2 -C 4 --dialkylamino, phenyl--CONH-- or C 1 -C 4 --alkyl--CONH--, or by benzoyl, or R 1 is anthryl, phenanthryl, thienyl, pyridyl, furyl, indolyl or tetrahydronaphthyl, and R 2 and R 3 independently of one another are each hydrogen, or C 1 -C 8 alkyl which is unsubstituted or substituted by --OH, --Cl, C 1 -C 4 -alkoxy, --CN, C 2 -C 5 --alkoxycarbonyl, phenyl, chlorophenyl, C 7 -C 10 alkylphenyl or C 7 -C 10 --alkoxyphenyl, or they are benzoyl, in addition R 3 is phenyl which is unsubstituted or substituted by --Cl, C 1 -C 4 alkyl, C 1 -C 4 --alkoxy or C 1 -C 4 --alkylthio, or it is C 2 -C 8 --alkoxycarbonyl, --CN, C 1 -C 4 --alkyl--NH--CO--, phenyl--NH--CO-- or --CONH 2 , or R 2 and R 3 together with the carbon atom to which they are bound form a C 4 -C 6 --cycloalkyl ring, R 4 is, when n=1, C 1 -C 18 --alkyl, phenyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl, C 1 -C 4 alkoxy, C 1 -C 4 --alkyl----CONH--, phenyl--CONH--, --NO 2 or benzoyl, or it is naphthyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl or C 1 -C 4 --alkoxy, or it is C 5 -C 6 --cycloalkyl, C 7 -C 9 --aralkyl, campheryl, --CF 3 , --CCl 3 , --F, or --NH 2 , and R 4 is, when n=2, a --(CH 2 ) m group, wherein m is 2 to 8, or phenylene or naphthylene each unsubstituted or substituted by C 1 -C 15 --alkyl, R 9 represents a hydrogen atom or one, two or three --Cl, --Br, --NO 2 , C 1 -C 12 alkyl, C 1 -C 4 alkoxy, phenoxy, phenylthio, C 1 -C 8 alkylthio, or --SCH 2 CH 2 OH substituents, X represents --O--, --S--, --SO 2 --, --CH 2 --, --C(CH 3 ) 2 -- or >NCOR 10 , where R 10 is C 1 -C 4 alkyl or phenyl, Y represents a direct bond or --CH 2 --, and R 11 represents a hydrogen atom; C 1 -C 8 alkyl, C 1 -C 8 alkyl substituted by --OH, --Cl, C 1 -C 4 alkoxy, CN, C 2 -C 5 alkoxycarbonyl, phenyl, chlorophenyl, C 7 -C 10 alkylphenyl, or C 7 -C 10 alkoxyphenyl; phenyl, phenyl substituted by --Cl, C 1 -C 4 alkyl. C 1 -C 4 alkoxy or C 1 -C 4 alkylthio; C 2 -C 8 alkoxycarbonyl: or CN.

Claim 15

A composition according to claim 12, in which the sulfonate is of formula ##STR9## where n is 1 or 2, R 4 is, when n=1, C 1 -C 18 --alkyl, phenyl which is unsubstituted or substituted by halogen. C 1 -C 12 --alkyl, C 1 -C 4 alkoxy. C 1 -C 4 --alkyl-- CONH--, phenyl--CONH--, --NO 2 or benzoyl or it is naphthyl which is unsubstituted or substituted by halogen, C 1 -C 12 --alkyl or C 1 -C 4 --alkoxy, or it is C 5 -C 6 --cycloalkyl, C 7 -C 9 --aralkyl, campheryl, --CF 3 , --CCl 3 , --F, or --NH 2 , and R 4 is, when n=2, a --(CH 2 ) m group, wherein m is 2 to 8, or phenylene or naphthylene each unsubstituted or substituted by C 1 -C 15 --alkyl, R 5 is phenyl or naphthyl which are each unsubstituted or substituted by 1,2 or 3 of --Cl, --Br, C 1 -C 12 --alkyl, phenyl, C 1 -C 8 --alkoxy, phenyloxy, benzyloxy, C 1 -C 8 --alkylthio, phenylthio, --SCH 2 CH 2 OH, C 1 -C 4 --alkyl--CONH--, benzoylamino or dimethylamino, or by benzoyl, or R 5 is anthryl or phenanthryl, R 6 is hydrogen, --OH, C 1 -C 4 --alkoxy, --OSi(CH 3 ) 3 , --OCOCH 3 , or C 1 -C 8 --alkyl which is unsubstituted or substituted by phenyl, R 7 is hydrogen, or C 1 -C 8 --alkyl which is unsubstituted or substituted by phenyl, or R 7 is --CN, benzoyl, C 1 -C 4 --alkylcarbonyl, C 2 -C 5 --alkoxycarbonyl or phenyl, R 8 is hydrogen, C 1 -C 8 --alkyl which is unsubstituted or substituted by --OH, --Cl or phenyl, or it is phenyl which is unsubstituted or substituted by --OH, --Cl, C 1 -C 4 --alkyl or C 1 -C 4 --alkoxy, or R 8 is C 2 -C 6 --alkenyl, C 8 -C 9 --phenylalkenyl, furyl, thienyl or --CCl 3 , or saturated or unsaturated C 5 -C 6 --cycloalkyl, and moreover R 5 with R 7 or R 6 with R 7 , together with the carbon structure to which they are bound, form a 5- or 6-membered ring which contains 1 to 5 --CH 2 --, --CH(CH 3 )--, --CH(CH 3 ) 2 --, --O--, --S--, --SO--, --SO 2 --, --CO--, --N(CO--C 1 -C 4 --alkyl)-- or N(COC 6 H 5 )--groups.

Claim 16

A composition according to claim 12, in which (B) is a sulfonate ester of benzoin or alpha-methylolbenzoin.

Claim 17

A composition according to claim 12, in which the sulfonyloxyimide is of formula ##STR10## where n is 1 or 2, R 16 represents arylene, substituted arylene, alkylene, substituted alkylene, alkenylene, or substituted alkenylene, C 2 -C 6 straight, branched, or cyclic alkylene, unsubstituted or substituted by phenyl, naphthyl, or C 1 -C 4 alkyl; C 2 -C 4 alkenylene or C 2 -C 4 alkenylene substituted by phenyl or C 1 -C 2 alkyl; and R 17 represents, where n=1, C 1-C 18 straight or branched alkyl, unsubstituted or substituted by halogen or C 1 -C 4 alkoxy; C 6 -C 12 aryl, C 6 -C 12 aryl substituted by C 1 -C 15 alkyl, C 1 -C 4 alkylCONH, phenylCONH, or NO 2 ; C 5 -C 6 cycloalkyl, campheryl; CF 3 ; CCl 3 ; CH 2 Cl; F; or NH 2 , or R 17 represents, where n=2, C 2 -C 6 alkylene, phenylene, or naphthylene, with the proviso that at least one of R 16 and R 17 is, or contains, an aromatic group.

Claim 18

A composition according to claim 16, in which (B) is a N-sulfonyloxy derivative of 1,8-naphthalimide.

Claim 19

A composition according to claim 11, in which the film-forming organic material (A) contains a phenolic hydroxyl group or a carboxylic, sulfonic, phosphonic or phorphoric acid group.

Claim 20

A composition according to claim 18, in which the film-forming organic material (A) is a novolak resin or a homopolymer or copolymer of an ethylenically unsaturated carboxylic acid or carboxylic acid anhydride.

Claim 21

A composition according to claim 11, which contains from 0.05 to 0.8 part by weight of the sulfonic acid-releasing substance (B) per part by weight of the film-forming organic material (A).