Olefin-acrylate copolymers with pendant hydroxyl functionality and use thereof

1. A copolymer prepared by the reaction of:

(A) 10-89 mol % of an unactivated olefin;

(B) 10-89 mol % of an activated olefin; and

(C) 1-50 mol % of a hydroxyl functional unactivated olefin selected from the group consisting of allyl alcohol, 3-buten-1-ol, 4-penten-1-ol, 5-hexen-1-ol, 9-decen-1-ol, 10-undecen-1-ol, and mixtures thereof;

wherein the total mol % is 100 mol %;

wherein the copolymer comprises a plurality of pendant hydroxyl groups; and

wherein the weight average molecular weight (Mw) is from about 84,000 to about 2,000,000.

2. The copolymer of claim 1 , wherein the unactivated olefin is selected from the group consisting of an unsubstituted alkene, monosubstituted alkene, disubstituted alkene, and trisubstituted alkene.

3. The copolymer of claim 1 , wherein the unactivated olefin is selected from the group consisting of ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 2-methyl-pentene, 3-methyl-1-butene, diisobutylene, diisobutylene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, dimethylpentene, vinylcyclohexane, cyclopropene, cyclobutene, cyclopentene, cyclohexane, norbornene, limonene, α-pinene, β-pinene, camphene, cis-cyclooctene and trans-cyclooctene.

4. The copolymer of claim 3 , wherein the unactivated olefin is 2-methylpentene, isobutylene or 1-octene.

5. The copolymer of claim 1 , wherein the activated olefin is selected from the group consisting of (meth)acrylate ester, acrylonitrile, (meth)acrylamide, maleimide, itaconimide, citroconimide, maleic anhydride, (meth)acrylate ester, maleate ester, fumarate ester, crotonates and cinnamates.

6. The copolymer of claim 5 , wherein the (meth)acrylate is methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, isobutyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, isooctyl(meth)acrylate, glycidyl(meth)acrylate, cyclohexyl(meth)acrylate, isobornyl(meth)acrylate, benzyl(meth)acrylate, 2-hydroxy(meth)acrylate, trimethoxybutyl(meth)acrylate, ethylcarbitol(meth)acrylate, phenoxyethyl(meth)acrylate, 2-hydroxy ethyl(meth)acrylate, trimethylolpropanetri(meth)acrylate, tetramethylolmethane tetra(meth)acrylate, pentaerythritol hexa(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol monohydroxy penta(meth)acrylate, dipentaerythritol hexa(meth)acrylate, 1,4-butyleneglycol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, polyethyleneglycol di(meth)acrylate and oligoester(meth)acrylate.

7. The copolymer of claim 6 , wherein the (meth)acrylate is methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, isobutyl(meth)acrylate, 2-ethylhexyl(meth) acrylate, isooctyl(meth)acrylate, glycidyl(meth)acrylate or cyclohexyl(meth)acrylate.

8. An adhesive comprising the copolymer of claim 1 .

9. The adhesive of claim 8 further comprising a tackifier, plasticizer, filler, antioxidant, adhesion promoters, desiccants, UV stabilizers, preservatives, emollients, excipients, opacifiers or mixtures thereof.

10. A method of forming a copolymer having a backbone of olefin-acrylate with pendant hydroxyl functionality comprising the steps of:

(1) pre-complexing a first amount of an activated olefin and a Lewis acid to form a pre-complex;

(2) adding the pre-complex to a solution of (i) an unactivated olefin, (ii) a second amount of the activated olefin, and (iii) a hydroxyl functional unactivated olefin in (iv) a solvent to form a mixture; and

(3) polymerizing the mixture in a temperature range of −78° C. to 100° C.;

wherein the first amount of the activated olefin is an equimolar amount of the activated olefin with the Lewis acid, and the second amount of the activated olefin is the rest of the molar amount of the activated olefin;

wherein the amount of Lewis acid ranges from about 1 to about 99 mol % of the activated olefin;

wherein the copolymer is the reaction product of:

(A) 10-89 mol % of an unactivated olefin;

(B) 10-89 mol % of an activated olefin; and

(C) 1-50 mol % of a hydroxyl functional unactivated olefin selected from the group consisting of allyl alcohol, 3-buten-1-ol, 4-penten-1-ol, 5-hexen-1-ol, 9-decen-1-ol, 10-undecen-1-ol, and mixtures thereof;

wherein the total mol % is 100 mol %;

wherein the copolymer comprises a plurality of pendant hydroxyl groups; and

wherein the weight average molecular weight (Mw) is from about 84,000 to about 2,000,000.

11. The method of claim 10 , wherein a coordinating solvent is added to the solution, wherein the coordinating solvent that has a heteroatom in the structure.

12. The method of claim 10 , wherein a radical initiator is added after step (2) (iii) and before step (3).

13. The method of claim 10 , wherein the unactivated olefin is selected from the group consisting of an unsubstituted alkene, monosubstituted alkene, disubstituted alkene, and trisubstituted alkene.

14. The method of claim 10 , wherein the activated olefin is selected from the group consisting of (meth)acrylate, acrylonitrile, (meth)acrylamide, maleimide, itaconimide, citroconimide, maleic anhydride, cyanoacrylate, maleate, and fumarate.

15. A pressure sensitive hot melt adhesive comprising:

(i) a copolymer prepared by the reaction of:

(A) 10-89 mol % of an unactivated olefin;

(B) 10-89 mol % of an activated olefin; and

(C) 1-50 mol % of a hydroxyl functional unactivated olefin selected from the group consisting of allyl alcohol, 3-buten-1-ol, 4-penten-1-ol, 5-hexen-1-ol, 9-decen-1-ol, 10-undecen-1-ol, and mixtures thereof;

wherein the total mol % is 100 mol %;

wherein the copolymer comprises a plurality of pendant hydroxyl groups; and

wherein the weight average molecular weight (Mw) is from about 84,000 to about 2,000,000; and

(ii) optionally, tackifier, plasticizer, antioxidant, inorganic fillers, desiccants, and/or adhesion promoters;

wherein the pressure sensitive hot melt adhesive is optically clear.

16. An article comprising the pressure sensitive hot melt adhesive of claim 15 .