Photoinitators
AssigneeColoplast A/S
InventorsCharlotte Juel Fristrup, Petr Sehnal, Bahar Bingol
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Abstract
A photoinitiator is provided which incorporates a camphorquinone photoinitiator moiety.
Claims22
-15. (canceled)
A photoinitiator of the formula (I)
- in which R3, R4, R5 and R6 are selected from H or C1-C6 alkyl;
- wherein one of R1, R2, R7 or R8 has a structure of formula (Ia):
- in which:
- Z1 is a linker comprising one or more linker units selected from a single bond, —O—, —S—, optionally-substituted —(C1-C12 alkylene)-, optionally-substituted —(C1-C12 alkenylene)-, —SO2—, —CO—, —NR′—, —Si(R′)2—, optionally-substituted heterocyclyl and optionally-substituted aryl in which R′ is H or C1-C6 alkyl;
- wherein linker —Z1-, optionally in combination with —Z2-, comprises at least one sulfonamide, a sulfonic ester, a carboxamide or a carboxylate ester moiety;
- Z2 is a trivalent nitrogen atom or Z2 is C(R″), in which R″ is H or C1-C6 alkyl;
- provided that—when Z2 is a nitrogen atom—the linker unit in Z1 adjacent to Z2 is —SO2— or —CO—;
- each of X1 and X2 are independently selected from a single bond, or a linker comprising one or more linker units selected from —O—, —S—, optionally-substituted —(C1-C12 alkylene)-, optionally-substituted —(C1-C12 alkenylene)-, —SO2—, —CO—, —NR′—, optionally-substituted heterocyclyl and optionally-substituted aryl in which R′ is H or C1-C6 alkyl;
- and wherein X1 and X2 may be linked to one another or to Z1 to form one or more ring structures;
- and
- wherein the remaining R1, R2, R7 and R8 are selected from H or C1-C6 alkyl.
The photoinitiator according to claim 1, wherein R1 and R2 are both methyl.
The photoinitiator according to claim 1, wherein at least one linker unit in Z1 is selected from —SO2—, —O— or —CO—.
The photoinitiator according to claim 1, wherein —Z1-Z2- has a structure selected from —SO2—N—;
- —CO—N—;
- —CO—O—CR″—;
- —O—CO—CR″—;
- alkylene)-SO2—N—;
- —(C1-C12 alkylene)-CO—N—;
- —(C1-C12 alkylene)-CO—O—CR″—;
- alkylene)-O—CO—CR″—, alkylene)-SO2—O—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-SO2—NR′—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-O—SO2—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-NR′—SO2—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-CO—O—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-O—CO—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-CO—NR′—(C1-C12 alkylene)-Z2-;
- or —(C1-C12 alkylene)-NR′—CO—(C1-C12 alkylene)-Z2.
The photoinitiator according to claim 1, wherein —Z1-Z2- has a structure selected from —SO2—N—;
- —CO—N—;
- —CO—O—CR″—;
- —O—CO—CR″;
- —(C1-C12 alkylene)-SO2—N—;
- —(C1-C12 alkylene)-CO—N—;
- —(C1-C12 alkylene)-CO—O—CR″—;
- alkylene)-O—CO—CR″—;
- —(C1-C12 alkylene)-SO2—O—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-SO2—NR′—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-CO—O—(C1-C12 alkylene)-Z2-;
- —(C1-C12 alkylene)-CO—NR′—(C1-C12 alkylene)-Z2-.
The photoinitiator according to claim 1, wherein —Z1-Z2- has a structure selected from —SO2—N—;
- —CO—N—;
- —(C1-C12 alkylene)-SO2—N—;
- —(C1-C12 alkylene)-CO—N—;
- —(C1-C12 alkylene)-SO2—O—(C1-C12 alkylene)-Z2-;
- or —(C1-C12 alkylene)-CO—O—(C1-C12 alkylene)-Z2-.
The photoinitiator according to claim 1, wherein Z2 is N.
The photoinitiator according to claim 1, wherein Z2 is C(R″), wherein R″ is H, methyl, ethyl or propyl.
The photoinitiator according to claim 1, wherein the —(C1-C12 alkylene)- linker unit in Z1 is a —(C1-C6 alkylene)-.
The photoinitiator according to claim 1, wherein X1 and X2 are each independently selected from —O—, —S—, optionally-substituted —(C1-C12 alkylene)-, —SO2—, —CO—, and —NR′— in which R′ is H or C1-C6 alkyl.
The photoinitiator according to claim 1, wherein the —(C1-C12 alkylene)- linker unit in X1 and X2 is a —(C1-C6 alkylene)-.
The photoinitiator according to claim 1, wherein X1 and X2 are the same.
The photoinitiator according to claim 1, wherein one of R1, R2, R3, R4, R5, R6, R7 or R8 is selected from:
The photoinitiator according to claim 1, comprising:
Dependencies are inferred from the claim text.