IP Library Granted Patent US 9,730,864
Granted Patent B2
US 9,730,864 · App. 15/112,220 · Granted Aug 15, 2017

Addition-fragmentation oligomers having high refractive index groups

Inventors: Ann R. Fornof (Austin, TX); William H. Moser (Edina, MN); Guy D. Joly (Shoreview, MN)
Assignee: 3M Innovative Properties Company
A61K6/0835A61K6/0005B32B37/10B32B37/12C09D4/00C09J4/00C09J4/06B32B2255/26B32B2305/72
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,730,864
App. No.
15/112,220
Granted
Aug 15, 2017
Kind
B2
Abstract

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.

Claims (42)

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.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2016
From: FORNOF, ANN R.; MOSER, WILLIAM H.; JOLY, GUY D.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 039176/0276 →
Continuity (2)
Provisional Application 61940937 · Feb 18, 2014
Related Publication 20160346170A1 · Dec 1, 2016