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Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by ?-Diimine Palladium Catalysts.

ABSTRACT: In this work, we studied propylene polymerization using some ?-diimine palladium catalysts with systematically varied ligand sterics. In propylene polymerization, the ligand steric effect exhibits significant variations on the catalytic activity, polymer molecular weight, and branching density. However, the regio control for the polymer microstructure is poor. Furthermore, copolymerization of 1-octene with the highly challenging and biorenewable comonomer acrylic acid was investigated. High copolymer molecular weights and high comonomer incorporation ratios could be achieved in this system. This study provides a novel access for the direct synthesis of branched carboxylic acid functionalized polyolefins.

SUBMITTER: Guo L 

PROVIDER: S-EPMC6432235 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts.

Guo Lihua L   Zou Chen C   Dai Shengyu S   Chen Changle C  

Polymers 20170327 4

In this work, we studied propylene polymerization using some α-diimine palladium catalysts with systematically varied ligand sterics. In propylene polymerization, the ligand steric effect exhibits significant variations on the catalytic activity, polymer molecular weight, and branching density. However, the regio control for the polymer microstructure is poor. Furthermore, copolymerization of 1-octene with the highly challenging and biorenewable comonomer acrylic acid was investigated. High copo  ...[more]

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