Ethylenically unsaturated oligomers

Patent metadata

Field	Value
Publication number	US-9394244-B2
Application number	US-201314430934-A
Country	US
Kind code	B2
Filing date	Oct 22, 2013
Priority date	Oct 23, 2012
Publication date	Jul 19, 2016
Grant date	Jul 19, 2016

Abstract

Disclosed are functional polyallophanate oligomers comprising ethylenically unsaturated groups and polymer stabilizer groups selected from hindered amine light stabilizers, ultraviolet light absorbers, antioxidants and dihydrocarbylhydroxylamines. The ethylenically unsaturated groups and the polymer stabilizer groups are bound to the polyallophanate oligomers through allophanate and/or carbamate groups. The polyallophanate oligomers are useful in curable coatings, inks and varnishes. The present polyallophanate oligomers are derived from a) organic polyisocyanates, b) compounds containing at least one isocyanate reactive group and at least one ethylenically unsaturated group and c) polymer stabilizers containing at least one isocyanate reactive group.

First claim

The invention claimed is:

1. An oligomer containing one or more ethylenically unsaturated groups bound through allophanate groups and/or carbamate groups and containing at least one polymer stabilizer group covalently bound through allophanate groups and/or carbamate groups, wherein the oligomer is derived from a) one or more organic polyisocyanates, b) one or more compounds containing at least one isocyanate reactive group and at least one ethylenically unsaturated group and c) one or more compounds, containing at least one isocyanate reactive group and the at least one polymer stabilizer group, selected from the group consisting of H1-H11, UV1-UV7, AO1-AO3,

N,N-dibenzylhydroxylamine, N,N-diethylhydroxylamine, N,N-dihexylhydroxylamine, N,N-dioctylhydroxylamine, N,N-dilaurylhydroxylamine, N,N-didodecylhydroxylamine, N,N-ditetradecylhydroxylamine, N,N-dihexadecylhydroxylamine, N,N-dioctadecylhydroxylamine, N-hexadecyl-N-tetradecylhydroxylamine, N-hexadecyl-N-heptadecylhydroxylamine, N-hexadecyl-N-octadecylhydroxylamine, N-heptadecyl-N-octadecylhydroxylamine, N-methyl-N-octadecylhydroxylamine and N,N-di(C 16 -C 18 alkyl)hydroxylamine.

2. An oligomer according to claim 1 derived from

and one or more compounds, containing at least one isocyanate reactive group and at least one polymer stabilizer group, selected from the group consisting of H1-H11, UV1-UV7, AO1-AO3,

N,N-dibenzylhydroxylamine, N,N-diethylhydroxylamine, N,N-dihexylhydroxylamine, N,N-dioctylhydroxylamine, N,N-dilaurylhydroxylamine, N,N-didodecylhydroxylamine, N,N-ditetradecylhydroxylamine, N,N-dihexadecylhydroxylamine, N,N-dioctadecylhydroxylamine, N-hexadecyl-N-tetradecylhydroxylamine, N-hexadecyl-N-heptadecylhydroxylamine, N-hexadecyl-N-octadecylhydroxylamine, N-heptadecyl-N-octadecylhydroxylamine, N-methyl-N-octadecylhydroxylamine and N,N-di(C 16 -C 18 alkyl)hydroxylamine.

3. An oligomer according to claim 1 where the number average molecular weight is from about 900 to about 3000 g/mol.

4. A curable coating, ink or varnish composition comprising an oligomer according to claim 1 .

5. A curable composition according to claim 4 further comprising a photoinitiator.

6. A process for the preparation of an oligomer according to claim 1 , which process comprises reacting a) one or more organic polyisocyanates, b) one or more compounds containing at least one isocyanate reactive group and at least one ethylenically unsaturated group and c) one or more compounds, containing at least one isocyanate reactive group and at least one polymer stabilizer group, selected from the group consisting of H1-H11, UV1-UV7, AO1-AO3,

N,N-dibenzylhydroxylamine, N,N-diethylhydroxylamine, N,N-dihexylhydroxylamine, N,N-dioctylhydroxylamine, N,N-dilaurylhydroxylamine, N,N-didodecylhydroxylamine, N,N-ditetradecylhydroxylamine, N,N-dihexadecylhydroxylamine, N,N-dioctadecylhydroxylamine, N-hexadecyl-N-tetradecylhydroxylamine, N-hexadecyl-N-heptadecylhydroxylamine, N-hexadecyl-N-octadecylhydroxylamine, N-heptadecyl-N-octadecylhydroxylamine, N-methyl-N-octadecylhydroxylamine and N,N-di(C 16 -C 18 alkyl)hydroxylamine, neat or in the presence of a suitable solvent, in the presence of a suitable catalyst and at a suitable temperature.

7. A process according to claim 6 where
a) and b) are reacted to form an intermediate with allophanate bound ethylenically unsaturated groups and unreacted isocyanate groups, followed by reacting the intermediate with c) or
a) and c) are reacted to form an intermediate with allophanate bound polymer stabilizer groups and unreacted isocyanate groups, followed by reacting the intermediate with b) or
a), b) and c) are reacted in a 1 step process.

8. An oligomer according to claim 1 where the number average molecular weight is from about 1000 to about 2500 g/mol.

9. An oligomer according to claim 1 where the number average molecular weight is from about 1000 to about 2000 g/mol.

Assignees

• Basf Se

Inventors

• Sitzmann Eugene Valentine
• Trumbo David
• Wood Mervin

Classifications

• C07C275/60 Primary

  Y being an oxygen atom, e.g. allophanic acids · CPC title

• C07D211/94

  Oxygen atom, e.g. piperidine N-oxide · CPC title

• C07D401/14 Primary

  containing three or more hetero rings · CPC title

• C07D251/24

  to three ring carbon atoms · CPC title

• C09D135/02

  Homopolymers or copolymers of esters (C09D135/06, C09D135/08 take precedence) · CPC title