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 Use of aromatic-aliphatic ketones as photo sensitizers

Details
Inventors: Felder, Louis; Kirchmayr, Rudolf;
Assignee: Ciba-Geigy Corporation (Ardsley, NY)
Primary Examiner: Bleutge; John C.
Assistant Examiner: Koeckert; A. H.
Attorney, Agent or Firm: Wenderoth, Lind & Ponack

Aromatic-aliphatic ketones of the formulae I, II, III or IV ##STR1## wherein n is 1 or 2, Ar is an aryl radical, R.sup.1 and R.sup.2 are monovalent aliphatic, cycloaliphatic or araliphatic radicals, R.sup.3 is a direct bond or a divalent organic radical, X is a hydroxyl or amino group or the monovalent etherification or silylation products thereof, and X' is a divalent amino, ether or silyloxy group, Y is a direct bond or CH.sub.2 and Z is O, S, SO.sub.2, CH.sub.2 or C(CH.sub.3).sub.2, are suitable sensitizers for the photopolymerization of unsaturated compounds and for the photochemical crosslinking of polyolefins. Some of these compounds are novel and can be obtained by methods analogous to those for obtaining the known compounds of this type.

DETAILED DESCRIPTION What is claimed is: 1.
In a method for the photopolymerisation of unsaturated compounds employing a sensitizer, the improvement according to which the sensitizer is a compound of the formula ##STR58## wherein n is 1 or 2, Ar, if n is 1, represents aryl of 6 to 14 carbon atoms, phenyl which is substituted by CN, OH, alk, --Oalk, --Salk, --SO.
sub.
2 alk, --SO.
sub.
2 phenyl, --COOalk, --SO.
sub.
2 NH.
sub.
2, --SO.
sub.
2 Nalk.
sub.
2, --NHalk, --Nalk.
sub.
2, --Ophenyl, NHCOalk, --SO.
sub.
2 NHalk or --CO.
sub.
2 N(alk).
sub.
2, or represents thienyl, pyridyl or furyl, wherein alk represents a lower alkyl radical of 1 to 4 carbon atoms, and, if n is 2, represents arylene of 6 to 12 carbon atoms or a phenylene-T-phenylene group, X represents one of the groups --NR.
sup.
4 R.
sup.
5, --OR.
sup.
6, --O--Si(R.
sup.
7)(R.
sup.
8).
sub.
2, hydroxymethoxy, (C.
sub.
1 -C.
sub.
4 alkoxy)methoxy, (C.
sub.
2 -C.
sub.
8 acyloxy)methoxy or together with R.
sup.
1 represents --OCH(C.
sub.
1 -C.
sub.
8 alkyl)--O(CH.
sub.
2).
sub.
1-2 --, --OCH(C.
sub.
6 -C.
sub.
14 aryl)--O--(CH.
sub.
2 ).
sub.
1-2 --, --OCH(C.
sub.
1 -C.
sub.
8 alkyl)-- or --OCH(C.
sub.
6 -C.
sub.
14 aryl), T represents --O--, --S--, --SO.
sub.
2 --, --CH.
sub.
2 -- or --CH.
dbd.
CH--, R.
sup.
1, if n is 1 and X is --OR.
sup.
6, represents C.
sub.
1 -C.
sub.
8 alkyl which can be substituted by C.
sub.
2 -C.
sub.
8 acyloxy, --COO--(C.
sub.
1 -C.
sub.
4) alkyl or --CN, or represents C.
sub.
5 -C.
sub.
6 cycloalkyl or C.
sub.
7 -C.
sub.
9 phenylalkyl, and, in all other cases, represents alkyl of 1 to 8 carbon atoms which can be substituted by OH, C.
sub.
1 -C.
sub.
4 alkoxy, C.
sub.
2 -C.
sub.
8 acyloxy, --COO--(C.
sub.
1 -C.
sub.
4)alkyl or --CN, or represents cycloalkyl of 5 to 6 carbon atoms or phenylalkyl of 7 to 9 carbon atoms, R.
sup.
2 has one of the meanings assigned to R.
sup.
1 or represents allyl, methallyl, 2-carbamoylethyl, 2-(N-C.
sub.
1 -C.
sub.
4 alkylcarbamoyl)ethyl, 2-(N,N-di-C.
sub.
1 -C.
sub.
4 alkylcarbamoyl)ethyl, 2-(2-pyridyl)ethyl, 2-(2-oxo-1-pyrrolidinyl)ethyl or 2-(di-O-C.
sub.
1 -C.
sub.
4 alkylphosphono)ethyl, or R



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