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

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. Howe...

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Detalles Bibliográficos
Autores principales: Guo, Lihua, Zou, Chen, Dai, Shengyu, Chen, Changle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432235/
https://www.ncbi.nlm.nih.gov/pubmed/30970801
http://dx.doi.org/10.3390/polym9040122
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author Guo, Lihua
Zou, Chen
Dai, Shengyu
Chen, Changle
author_facet Guo, Lihua
Zou, Chen
Dai, Shengyu
Chen, Changle
author_sort Guo, Lihua
collection PubMed
description 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 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.
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spelling pubmed-64322352019-04-02 Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts Guo, Lihua Zou, Chen Dai, Shengyu Chen, Changle Polymers (Basel) Article 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 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. MDPI 2017-03-27 /pmc/articles/PMC6432235/ /pubmed/30970801 http://dx.doi.org/10.3390/polym9040122 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guo, Lihua
Zou, Chen
Dai, Shengyu
Chen, Changle
Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title_full Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title_fullStr Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title_full_unstemmed Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title_short Direct Synthesis of Branched Carboxylic Acid Functionalized Poly(1-octene) by α-Diimine Palladium Catalysts
title_sort direct synthesis of branched carboxylic acid functionalized poly(1-octene) by α-diimine palladium catalysts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432235/
https://www.ncbi.nlm.nih.gov/pubmed/30970801
http://dx.doi.org/10.3390/polym9040122
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