BRANCHED POLYOLEFIN POLYMER TETHERED WITH POLYMERIZABLE METHACRYLOYL GROUPS AND PROCESS FOR PREPARING SAME

• US 20090253878A1
• Filed: 02/27/2009
• Published: 10/08/2009
• Est. Priority Date: 02/29/2008
• Status: Abandoned Application

• Current Assignee: Jianli Wang, Kejian Zhang, Zhibin Ye
• Original Assignee: Jianli Wang, Kejian Zhang, Zhibin Ye
• Inventors: Ye, Zhibin, Wang, Jianli, Zhang, Kejian
• Application Number:
  US12/394,540
• Publication Number:
  US 20090253878A1
• Time in Patent Office: Days
• US Class Current: 526/171
• CPC Class Codes: C08F 110/02 Ethene
• CPC Class Codes: C08F 210/02 Ethene
• CPC Class Codes: C08F 220/26 Esters containing oxygen in addition to the carboxy oxygen
• CPC Class Codes: C08F 2500/09 Long chain branches
• CPC Class Codes: C08F 4/80 selected from iron group metals or platinum group metals

Abstract

A polyolefin polymer comprising one or more terminal polymerizable methacryloyl groups (i.e. tethered to the main body of the polymer) and a novel process for preparing same are herein disclosed. A hyperbranched polyethylene polymer and a process for preparing same are also disclosed. The polymer is prepared by a novel one-pot copolymerization reaction of an olefin, such as ethylene, and a heterobifunctional comonomer comprising a methacryloyl group, catalyzed by a late transition metal α-diimine catalyst which is selectively non-reactive towards methacryloyl groups. The process allows for preparation of polymers with various chain topologies, including linear, branched, and hyperbranched topologies. The terminal methacryloyl groups within the polymer are reactive in further polymerization reactions. Thus, the polymer may be used in materials and applications which require cross-linking or further polymerization, for example, UV/thermal/radical curable crosslinkers for use in thermoset applications.

Claims

1. A polyolefin polymer comprising one or more terminal methacryloyl groups, wherein said polymer is a reaction product of an olefin and a bifunctional comonomer, wherein said bifunctional comonomer is of formula (I):

wherein L¹ is selected from the group consisting of

n is an integer selected from 1 to 15; and

R¹ and R² are same or different, and each of R¹ and R² are independently selected from the group consisting of;

hydrogen, halide, alcohol (—

OH),

C₁-C₆ alkyl optionally substituted with one or more functionalities selected from the group consisting of halide, alcohol (—

OH), ester, aldehyde and ketone,

and C₆-C₁₂ aryl optionally substituted with one or more functionalities selected from the group consisting of alkyl, halide, alcohol (—

OH), ester, aldehyde and ketone.

2. The polymer of claim 1, wherein a terminus of said polymer is of formula (II):

wherein L² is

n is an integer selected from 1 to 15;

R¹ and R² are same or different, and each of R¹ and R² are independently selected from the group consisting of;

hydrogen,

C₁-C₆ alkyl optionally substituted with one or more functionalities selected from the group consisting of halide, alcohol (—

OH), ester, aldehyde and ketone,

and C₆-C₁₂ aryl optionally substituted with one or more functionalities selected from the group consisting of alkyl, halide, alcohol (—

OH), ester, aldehyde and ketone.

3. The polymer of claim 1 wherein a terminus of said polymer is of formula (III):

4. The polymer of claim 1, wherein a terminus of said polymer is of formula (IV):

5. The polymer of claim 1, wherein said polymer is a reaction product of an olefin and two or more different bifunctional comonomers, wherein each of said bifunctional comonomers is independently selected and is as defined in formula (I).

6. The polymer of claim 1, wherein said olefin is selected from the group consisting of ethylene, propylene, 1-butene and styrene.

7. The polymer of claim 1, wherein said polymer is linear, branched or hyperbranched.

23. The use according to claim 20 to prepare the polymer of claim 1.

8. A process for preparing a polyolefin polymer comprising one or more terminal methacryloyl group(s), comprising:

(a) charging a reaction vessel with (i) optionally, an organic solvent, (ii) an olefin, and (iii) at least one bifunctional comonomer, wherein said bifunctional comonomer is of formula (I);

wherein L¹ is

n is an integer selected from 1 to 15;

R¹ and R² are same or different, and each of R¹ and R² are independently selected from the group consisting of;

hydrogen, halide, alcohol (—

OH),

C₁-C₆ alkyl optionally substituted with one or more functionalities selected from the group consisting of halide, alcohol (—

OH), ester, aldehyde and ketone,

and C₆-C₁₂ aryl optionally substituted with one or more functionalities selected from the group consisting of alkyl, halide, alcohol (—

OH), ester, aldehyde and ketone; and

(b) catalyzing a copolymerization reaction with a palladium(II) α

-diimine catalyst or a nickel(II) α

-diimine catalyst to form said polymer.

9. The process of claim 8, wherein said olefin is selected from the group consisting of ethylene, propylene, 1-butene and styrene.

10. The process of claim 9, wherein pressure is maintained at 1 atm during copolymerization.

11. The process of claim 8, wherein said polymer is linear, branched or hyperbranched.

12. The process of claim 8 wherein the catalyst is

[(ArN═

C(Me)-(Me)C═

NAr)Pd^II(CH₃)(N≡

CMe)]⁺SbF₆⁻

wherein Ar is 2,6-(iPr)₂C₆H₃.

13. The process of claim 8 wherein two or more different bifunctional commoners are charged into said reaction vessel, and wherein each of said bifunctional commoners is independently selected and is as defined in formula (I).

14. The process of claim 8 wherein the at least one bifunctional comonomer is selected from the group consisting of acryloyloxyethyl methacrylate (AEM) and 2,2-dimethyl-4-pentenyl methacrylate (DMPM).

15. The process of claim 8 wherein said organic solvent is non-polar.

16. The process of claim 15, wherein said organic solvent is selected from the group consisting of alkanes, benzene, chlorobenzene, toluene, chloroform, carbon tetrachloride and dichloromethane.

17. The process of claim 8 wherein the copolymerization reaction is carried out at ambient temperature or higher.

18. The process of claim 8 wherein the copolymerization reaction is allowed to progress for around 24 hours.

19. The polymer as prepared by the process of claim 8.

20. Use of a palladium(II) α

-diimine catalyst or a nickel(II) α

-diimine catalyst to prepare a polyolefin polymer comprising one or more terminal methacryloyl groups.

21. The use according to claim 20, wherein a constituent olefin of said polyolefin polymer is selected from the group consisting of ethylene, propylene, 1-butene and styrene.

22. The use according to claim 20 wherein said polymer is linear, branched or hyperbranched.

24. The use according to claim 20, wherein said palladium(II) α

-diimine catalyst is [(ArN═

C(Me)-(Me)C═

NAr) Pd^II(CH₃)(N≡

CMe)]⁺SbF₆⁻

, wherein Ar is 2,6-(iPr)₂C₆H₃.