IP Library Granted Patent US 10,370,322
Granted Patent B2
US 10,370,322 · App. 15/410,919 · Granted Aug 6, 2019

Addition-fragmentation agents

Inventors: Guy D. Joly (Shoreview, MN); Larry R. Krepski (White Bear Lake, MN); Ann R. Fornof (Austin, TX); Serkan Yurt (St. Paul, MN); Babu N. Gaddam (Woodbury, MN); Ahmed S. Abuelyaman (Woodbury, MN)
Assignee: 3M Innovative Properties Company
C07C67/26C07C67/14C07C69/593C07C269/02C07C271/16C08F220/68C08K3/22C08K3/36C08K5/11C08K5/12C08K5/205C09D133/08C09J5/00C09J133/08C08L33/10C09J2433/00
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Quick Facts
Patent No.
US 10,370,322
App. No.
15/410,919
Granted
Aug 6, 2019
Kind
B2
Abstract

Addition-fragmentation agents of the formula are disclosed: wherein R 1 , R 2 and R 3 are each independently Z-Q-, a (hetero)alkyl group or a (hetero)aryl group with the proviso that at least one of R 1 , R 2 and R 3 is Z m -Q-, Q is a linking group have a valence of m+1; Z is an ethylenically unsaturated polymerizable group, m is 1 to 6; each X 1 is independently —O— or —NR 4 —, where R 4 is H or C 1 -C 4 alkyl, and n is 0 or 1.

Claims (35)

1. A non-aqueous polymerizable composition comprising at least one free-radically polymerizable monomer, an initiator and an addition-fragmentation agent of the formula:

wherein

R 1 , R 2 and R 3 are each independently Z m -Q-, a (hetero)alkyl group or a (hetero)aryl group with the proviso that at least two of R 1 , R 2 and R 3 is Z m -Q-,

Q is a linking group having a valence of m+1;

Z is an ethylenically unsaturated polymerizable group,

m is 1 to 6;

each X 1 is independently —O— or —NR 4 —, where R 4 is H or C 1 -C 4 alkyl, and

n is 0 or 1.

2. The polymerizable composition of claim 1 where Z comprises a vinyl, vinyloxy, (meth)acryloxy, (meth)acrylamido, styrenic and acetylenic functional groups.

3. The polymerizable composition of claim 1 where Z is selected from:

wherein R 4 is H or C 1 -C 4 alkyl.

4. The polymerizable composition of claim 1 wherein Q is selected from

from —O—, —S—, —NR 4 —, —SO 2 —, —PO 2 —, —CO—, —OCO—, —R 6 —, —NR 4 —CO—NR 4 —, —NR 4 —CO—O—, —NR 4 —CO—NR 4 —, —CO—O—R 6 —, —CO—NR 4 —R 6 —, —R 6 —CO—O—R 6 —, —O—R 6 —, —S—R 6 —, —NR 4 —R 6 —, —SO 2 —R 6 —, —PO 2 —R 6 —, —CO—R 6 —, —OCO—R 6 —, —NR 4 —CO—R 6 —, and NR 4 —R 6 —CO—O—, wherein each R 4 is hydrogen, a C 1 to C 4 alkyl group, or aryl group, each R 6 is an alkylene group having 1 to 6 carbon atoms, a 5- or 6-membered cycloalkylene group having 5 to 10 carbon atoms, or a divalent arylene group having 6 to 16 carbon atoms, with the proviso that Q-Z does not contain peroxidic linkages.

5. The polymerizable composition of claim 1 where Q is an alkylene.

6. The polymerizable composition of claim 5 wherein Q is an alkylene of the formula —C r H 2r —, where r is 1 to 10.

7. The polymerizable composition of claim 1 where Q is a hydroxyl-substituted alkylene.

8. The polymerizable composition of claim 1 where Q is —CH 2 —CH(OH)—CH 2 —.

9. The polymerizable composition of claim 1 where Q is an aryloxy-substituted alkylene.

10. The polymerizable composition of claim 1 where R 5 is an alkoxy-substituted alkylene.

11. The polymerizable composition of claim 1 wherein R 1 —X 1 — groups and R 3 —X 1 — groups are selected from H 2 C═C(CH 3 )C(O)—O—CH 2 —CH(OH)—CH 2 —O—, H 2 C═C(CH 3 )C(O)—O—CH 2 —CH(O—(O)C(CH 3 )═CH 2 )—CH 2 —O—, H 2 C═C(CH 3 )C(O)—O—CH(CH 2 OPh)-CH 2 —O—, H 2 C═C(CH 3 )C(O)—O—CH 2 CH 2 —N(H)—C(O)—O—CH(CH 2 OPh)-CH 2 —O—, H 2 C═C(CH 3 )C(O)—O—CH 2 —CH(O—(O)C—N(H)—CH 2 CH 2 —O—(O)C(CH 3 )C═CH 2 )—CH 2 —O—, H 2 C═C(H)C(O)—O—(CH 2 ) 4 —O—CH 2 —CH(OH)—CH 2 —O—, H 2 C═C(CH 3 )C(O)—O—CH 2 —CH(O—(O)C—N(H)—CH 2 CH 2 —O—(O)C(CH 3 )C═CH 2 )—CH 2 —O—, CH 3 —(CH 2 ) 7 —CH(O—(O)C—N(H)—CH 2 CH 2 —O—(O)C(CH 3 )C═CH 2 )—CH 2 —O—, H 2 C═C(H)C(O)—O—(CH 2 ) 4 —O—CH 2 —CH(—O—(O)C(H)═CH 2 )—CH 2 —O— and H 2 C═C(H)C(O)—O—CH 2 —CH(OH)—CH 2 —O—.

12. The polymerizable composition of claim 1 comprising:

a) 85 to 100 parts by weight of an (meth)acrylic acid ester of non-tertiary alcohol;

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 5 parts of a multifunctional (meth)acrylate;

based on 100 parts by weight total monomer, and

f) 0.1 to 10 parts by weight of the addition-fragmentation agent, based on 100 parts by weight of a) to e).

13. The polymerizable composition of claim 12 further comprising 0.01 to 5 parts of a multifunctional (meth)acrylate.

14. The polymerizable composition of claim 1 further comprising an organic solvent.

15. The polymerizable composition of claim 1 having less than 0.1 wt. % water.

16. An article comprising a layer of the polymerizable composition of claim 1 on a substrate.

17. An article comprising the cured polymerizable composition of claim 1 on a substrate.

18. A method of bonding two substrates together comprising the steps of coating the polymerizable composition of claim 1 to a surface of one or both substrates, contacting the coated surfaces, optionally with pressure, and curing the polymerizable composition.

19. A method of bonding two substrates together comprising the steps of coating the polymerizable composition of claim 1 to a surface of one or both substrates, wherein the coating of polymerizable composition is at least partially cured, contacting the coated surfaces optionally with pressure, and further curing the polymerizable compositions if necessary.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066445/0328 →
Continuity (3)
Continuation In Part 13169306 · Jun 27, 2011
Provisional Application 61442980 · Feb 15, 2011
Related Publication 20170210693A1 · Jul 27, 2017