Polymer for heat-sensitive lithographic printing plate precursor
A polymer for a heat-sensitive lithographic printing plate precursor is disclosed wherein the polymer comprises a phenolic monomeric unit wherein the phenyl group of the phenolic monomeric unit is substituted by a group having the structure —S-(L) k -Q wherein S is covalently bound to a carbon atom of the phenyl group, L is a linking group, k is 0 or 1 and Q comprises a heterocyclic group and wherein the substitution of the polymer increases the chemical resistance of the coating of the printing plate precursor.
1 . a polymer comprising a phenolic monomeric unit wherein the phenyl group of the phenolic monomeric unit is substituted by a group having the structure —S-(L) k -Q wherein S is covalently bound to a carbon atom of the phenyl group, wherein L is a linking group, k is 0 or 1 and q comprises a heterocyclic group.
2 . A polymer according to claim 1 wherein said heterocyclic group is aromatic.
3 . A polymer according to claim 1 wherein said heterocyclic group contains at least one nitrogen atom in the ring of the heterocyclic group.
4 . A polymer according to claim 1 wherein said heterocyclic group has a 5- or 6- membered ring structure, and is optionally annelated with another ring system.
5 . A polymer according to claim 1 wherein the heterocyclic group is selected from an optionally substituted tetrazole, triazole, thiadiazole, oxadiazole, imidazole, benzimidazole, thiazole, benzthiazole, oxazole, benzoxazole, pyrazole, pyrrole, pyrimidine, pyrasine, pyridasine, triazine or pyridine group.
6 . A polymer according to claim 1 wherein —S-(L) k -Q comprises the following formula
wherein Z represents the necessary atoms to form a 5- or 6- membered heterocyclic aromatic group, and is optionally annelated with another ring system.
7 . A polymer according to claim 6 wherein the —S-(L) k -Q comprises the following formula
wherein R 1 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group.
8 . A polymer according to claim 6 wherein —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2, 3, 4 or 5, wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NH—R,—NH—SO 2 —R,—CO—NR—R,—NR—CO—R, —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R 3 , —O—CO—NR 2 —R 3 , —O—CO—R 5 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 5 , —SO 2 —R 2 , —SO—R 5 , —P(═O)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 , —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, where in R 2 to R 4 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 5 is an optionally substituted alkyl, alkenyl, alknyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 and R 5 together represent the necessary atoms to form a cyclic structure.
9 . A polymer according to claim 6 wherein —S-(L) k -Q comprises the following formula
wherein X is 0, S or NR 3 , wherein R is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or -L 1 —R 2 , where in L 1 is a linking group, wherein R 2 is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or —CN, wherein R 3 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from R 1 , R 2 and R 3 represent the necessary atoms to form a cyclic structure.
10 . A polymer according to claim 6 wherein —S-(L) k -Q comprises the following formula
wherein X is 0, S or NR 4 , wherein R 1 and R 2 are independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or -L1—R3 wherein L 1 is a linking group, wherein R 3 is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or —CN, wherein R 4 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from R 1 , R 2 , R 3 and R 4 together represent the necessary atoms to form a cyclic structure.
11 . A polymer according to claim 6 wherein the —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2, 3 or 4, wherein X is 0, S or NR 5 , wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NH—R 2 , —NH—SO 2 —R 6 , —CO—NR 2 —R 3 , —NR 2 —CO—R 6 , —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R 3 , —O—CO—NR 2 —R 3 , —O—CO—R 6 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 6 , —SO 2 —R 2 , —SO—R 6 , —P(═o)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 , —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, wherein R 2 to R 5 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 6 is an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 , R 5 and R 6 represent the necessary atoms to form a cyclic structure.
12 . A polymer according to claim 6 wherein the —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2 or 3, wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NR—R 2 , —NR—SO 2 —R 5 , —CO—NR 2 —R 3 , —NR 2 —CO—R 5 , —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R 3 , —O—CO—NR 2 —R 3 , —O—CO—R 5 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 5 , —SO 2 —R 2 , —SO—R 5 , —P(═O)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 , —CN, —NO 2 or -M-R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, wherein R 2 to R 4 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 5 is an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 and R 5 together represent the necessary atoms to form a cyclic structure.
13 . A polymer according to claim 6 wherein the —S-(L) k -Q comprises one of the following formula:
14 . A polymer according to claim 1 , wherein said polymer comprising a phenolic monomeric unit is a novolac, resol or polyvinylphenol.
15 . A heat-sensitive lithographic printing plate precursor comprising a support having a hydrophilic surface and an oleophilic coating provided on the hydrophilic surface, said coating comprising an infrared light absorbing agent and a polymer comprising a phenolic monomeric unit wherein the phenyl group of the phenolic monomeric unit is substituted by a group having the structure —S-(L) k -Q wherein S is covalently bound to a carbon atom of the phenyl group, wherein L is a linking group k is 0 or 1 and Q comprises a heterocyclic group.
16 . A heat-sensitive lithographic printing plate precursor according to claim 15 , wherein said coating further comprises a dissolution inhibitor and wherein said precursor is a positive working lithographic printing plate precursor.
17 . A heat-sensitive lithographic printing plate precursor according to claim 16 , wherein said dissolution inhibitor is selected from the group consisting of
an organic compound which comprises at least one aromatic group and a hydrogen bonding site,
a polymer or surfactant comprising siloxane orperfluoroalkyl units and mixtures thereof.
18 . (canceled)
19 . A heat-sensitive lithographic printing plate precursor according to claim 15 , wherein said coating further comprising a latent Brönsted acid and an acid-crosslinkable compound and wherein said precursor is a negative working lithographic printing plate precursor.
20 . (canceled)
21 . A polymer according to claim 2 wherein said heterocyclic group contains at least one nitrogen atom in the ring of the heterocyclic group.
22 . A polymer according to claim 2 wherein said heterocyclic group has a 5- or 6-membered ring structure, and is optionally annelated with another ring system.
23 . A polymer according to claim 3 wherein said heterocyclic group has a 5- or 6-membered ring structure, and is optionally annelated with another ring system.
24 . A polymer according to claim 3 wherein said heterocyclic group has a 5- or 6-membered ring structure, and is annelated with another ring system.
25 . A polymer according to claim 24 wherein the heterocyclic group is selected from an optionally substituted tetrazole, triazole, thiadiazole, oxadiazole, imidazole, benzimidazole, thiazole, benzthiazole, oxazole, benzoxazole, pyrazole, pyrrole, pyrimidine, pyrasine, pyridasine, triazine or pyridine group.
26 . A polymer according to claim 5 , wherein said polymer comprising a phenolic monomeric unit is a novolac, resol or polyvinylphenol.
27 . A polymer according to claim 15 wherein the heterocyclic group is selected from an optionally substituted tetrazole, triazole, thiadiazole, oxadiazole, imidazole, benzimidazole, thiazole, benzthiazole, oxazole, benzoxazole, pyrazole, pyrrole, pyrimidine, pyrasine, pyridasine, triazine or pyridine group.
28 . A heat-sensitive lithographic printing plate precursor according to claim 15 wherein —S-(L) k -Q comprises the following formula
wherein Z represents the necessary atoms to form a 5- or 6-membered heterocyclic aromatic group, and is optionally annelated with another ring system.
29 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein the —S-(L) k -Q comprises the following formula
wherein R 1 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group.
30 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2, 3, 4 or 5, wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NH—R,—NH—SO 2 —R,—CO—NR—R,—NR—CO—R, —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R 3 , —O—CO—NR 2 —R 3 , —O—CO—R 5 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 5 , —SO 2 —R 2 , —SO—R 5 , —P(═O)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 , —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, where in R 2 to R 4 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 5 is an optionally substituted alkyl, alkenyl, alknyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 and R 5 together represent the necessary atoms to form a cyclic structure.
31 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein —S-(L) k -Q comprises the following formula
wherein X is 0, S or NR 3 , wherein R is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or -L 1 -R 2 , where in L 1 is a linking group, wherein R 2 is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or —CN, wherein R 3 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from R 1 , R 2 and R 3 represent the necessary atoms to form a cyclic structure.
32 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein —S-(L) k -Q comprises the following formula
wherein X is 0, S or NR 4 , wherein R 1 and R 2 are independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or -L1—R3 wherein L 1 is a linking group, wherein R 3 is selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen or —CN, wherein R 4 is selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from R 1 , R 2 , R 3 and R 4 together represent the necessary atoms to form a cyclic structure.
33 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2, 3 or 4, wherein X is 0, S or NR 5 , wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NH—R 2 , —NH—SO 2 —R 6 , —CO—NR 2 —R 3 , —NR 2 —CO—R 6 , —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R 3 , —O—CO—NR 2 —R 3 , —O—CO—R 6 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 6 , —SO 2 —R 2 , —SO—R 6 , —P(═o)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, wherein R 2 to R 5 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 6 is an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 , R 5 and R 6 represent the necessary atoms to form a cyclic structure.
34 . A heat-sensitive lithographic printing plate precursor according to. claim 28 wherein —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2 or 3, wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NR—R 2 , —NR—SO 2 —R 5 , —CO—NR 2 —R 3 , —NR 2 —CO—R 5 , —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R3, —O—CO—NR 2 —R 3 , —O—CO—R 5 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 5 , —SO 2 —R 2 , —SO—R 5 , —P(═O)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 —R 3 , —O—R 2 , —S—R 2 , —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, wherein R 2 to R 4 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 5 is an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 and R 5 together represent the necessary atoms to form a cyclic structure.
35 . A heat-sensitive lithographic printing plate precursor according to claim 28 wherein —S-(L) k -Q comprises the following formula
wherein n is 0, 1, 2 or 3, wherein each R 1 is independently selected from hydrogen, an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, halogen, —SO 2 —NR—R 2 , —NR—SO 2 —R 5 , —CO—NR 2 —R 3 , —NR 2—CO—R 5 , —NR 2 —CO—NR 3 —R 4 , —NR 2 —CS—NR 3 —R 4 , —NR 2 —CO—O—R3, —O—CO—NR 2 —R 3 , —O—CO—R 5 , —CO—O—R 2 , —CO—R 2 , —SO 3 —R 2 , —O—SO 2 —R 5 , —SO 2 —R 2 , —SO—R 5 , —P(═O)(—O—R 2 )(—O—R 3 ), —O—P(═O)(—O—R 2 )(—O—R 3 ), —NR 2 R 3 , —O—R 3 , —S—R 2 , —CN, —NO 2 or -M—R 2 , wherein M represents a divalent linking group containing 1 to 8 carbon atoms, wherein R 2 to R 4 are independently selected from hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, wherein R 5 is an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic, aryl, heteroaryl, aralkyl or heteroaralkyl group, or wherein at least two groups selected from each R 1 , R 2 , R 3 , R 4 and R 5 together represent the necessary atoms to form a cyclic structure.
36 . A heat-sensitive lithographic printing plate precursor according to claim 16 wherein the heterocyclic group is selected from an optionally substituted tetrazole, triazole, thiadiazole, oxadiazole, imidazole, benzimidazole, thiazole, benzthiazole, oxazole, benzoxazole, pyrazole, pyrrole, pyrimidine, pyrasine, pyridasine, triazine or pyridine group.
37 . A heat-sensitive lithographic printing plate precursor according to claim 19 wherein the heterocyclic group is selected from an optionally substituted tetrazole, triazole, thiadiazole, oxadiazole, imidazole, benzimidazole, thiazole, benzthiazole, oxazole, benzoxazole, pyrazole, pyrrole, pyrimidine, pyrasine, pyridasine, triazine or pyridine group.