Addition-fragmentation oligomers having high refractive index groups
Addition-fragmentation oligomers of the general formula Z—B y -A-(B-A) x -B-A-B y —Z, where the A monomers units are derived from a diester or diacid, the B monomer units are derived from a difunctional monomer having functional groups co-reactive with the acid or ester groups of the A monomer, x+y is zero to 60, Z comprises an ethylenically unsaturated, polymerizable group, A monomers comprise a 1-methylene-3,3-dimethylpropyl group, and at least one B monomer unit comprises a high refractive index group.
1. An addition-fragmentation oligomer of the formula
wherein
R A is
R B a (hetero)hydrocarbyl group, wherein at least 50% of the R B units are substituted with a high refractive index group,
X 1 is —O— or NR 5 —, where R 5 is H or C 1 -C 4 alkyl;
Z comprises an ethylenically unsaturated polymerizable group;
y is 0 or 1;
x is 0 or 1.
2. The addition-fragmentation oligomer of claim 1 , wherein at least 75% of the R B units are substituted by a high refractive index group.
3. The addition-fragmentation oligomer of claim 1 , wherein the high refractive index group is selected from benzyl, 2-, 3-, and 4-biphenyl, 1-, 2, 3-, 4-, and 9-fluorenyl, 4-(1-methyl-1-phenethyl)phenoxyethyl; phenylthio; 1-, 2-, 3- and 4-napthyl, 1- and 2-naphthylthio; 2,4,6-tribromophenoxy; 2,4-dibromophenoxy; 2-bromophenoxy; 1-, and 2-naphthyloxy; 3-phenoxy-; 2-, 3- and 4-phenylphenoxy; 2,4-dibromo-6-sec-butylphenyl; 2,4-dibromo-6-isopropylphenyl; 2,4-dibromophenyl; pentabromobenzyl and pentabromophenyl.
4. The addition-fragmentation oligomer of claim 1 derived from A compounds of the formula:
R 1 —O—CO—R A —CO—O—R 1 , wherein R A is a 1-methylene-3,3-dimethylpropyl group and R 1 is H, alkyl, aryl or R FG , where R FG is an aryl or an alkyl further substituted with a nucleophilic or electrophilic functional group.
5. The addition-fragmentation oligomer of claim 4 derived from B compounds of the formula:
X 2 —R B —X 2 , wherein R B is a (hetero)hydrocarbyl group and X 2 is functional group reactive with the functional groups of the A compound.
6. The addition-fragmentation oligomer of claim 5 wherein the compound of the formula X 2 —R B —X 2 is selected from difunctional epoxides, diols, aziridines, isocyanates and diamines.
7. The addition-fragmentation oligomer of claim 1 where x+y is 0 to 2.
8. The addition-fragmentation oligomer of claim 1 where x+y is 1 to 2.
9. A polymerizable composition comprising the addition-fragmentation oligomer of claim 1 , at least one free-radically polymerizable monomer, and an initiator.
10. The polymerizable composition of claim 9 comprising:
a) 85 to 100 parts by weight of an (meth)acrylic acid ester;
b) 0 to 15 parts by weight of an acid functional ethylenically unsaturated monomer;
c) 0 to 10 parts by weight of a non-acid functional, ethylenically unsaturated polar monomer;
d) 0 to 5 parts vinyl monomer; and
e) 0 to 100 parts of a multifunctional (meth)acrylate;
based on 100 parts by weight total monomer a) to d), and
f) 0.1 to 12 parts by weight of the addition-fragmentation oligomer, based on 100 parts by weight of a) to e), and
g) an initiator.
11. The polymerizable composition of claim 10 further comprising 0.01 to 100 parts of a multifunctional (meth)acrylate based on 100 parts by weight total monomer a) to d).
12. The polymerizable composition of claim 9 further comprising an inorganic filler.
13. An article comprising the cured polymerizable composition of claim 9 on a substrate.
14. A method of bonding two substrates together comprising the steps of coating the polymerizable composition of claim 9 to a surface of one or both substrates, contacting the coated surfaces, optionally with pressure, and curing the polymerizable compositions.
15. A hardcoat composition comprising one or more multifunctional (meth)acrylate monomers or (meth)acrylate oligomers, and the addition-fragmentation oligomer of claim 1 .
16. The hardcoat composition of claim 15 comprising:
a) 0.1-10 wt. % of the addition fragmentation oligomer;
b) 20-80 wt. % of multifunctional (meth)acrylate monomers and/or multifunctional (meth)acrylate oligomers,
c) 0 to 25 wt. % range of (meth)acrylate diluent, (0-25 wt. %); and
d) 20 to 75 wt. % of silica.
17. A curable dental composition comprising:
a) at least one dental resin comprising at least two ethylenically unsaturated group;
b) an addition-fragmentation oligomer of claim 1 ; and
c) optionally an inorganic oxide filler.
18. The dental composition of claim 17 wherein the inorganic oxide filler comprises nanoparticles.