Synthesis of Hydroxy‐Functionalized Polyethylene via Radical Copolymerization of Ethylene with Alkenyl Boronate and Post‐Polymerization Oxidation

T Tomoaki Kanazawa (Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University Kyoto‐Daigaku Katsura, Nishikyo‐ku Kyoto 615‐8510 Japan) T Tommaso Posenato (Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France) S Sébastien Norsic (Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France) T Tsuyoshi Nishikawa (Department of Polymer Chemistry, Graduate School of Engineering) M Makoto Ouchi (Department of Polymer Chemistry, Graduate School of Engineering) J Jean Raynaud (Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France) F Franck D'Agosto (Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France)

Abstract

Abstract Radical copolymerization of ethylene was performed with alkenyl boronate, and post‐polymerization oxidation was conducted to synthesize hydroxy‐functionalized polyethylene (PE). The copolymerization behavior was dependent on the molecular structure of the boron monomer: the copolymerization with α‐methyl substituted monomer carrying boronic acid pinacol ester [isopropenylboronic acid pinacol ester (IPBpin)] afforded copolymers with higher molar masses than the vinyl‐type monomer [i.e., vinylboronic acid pinacol ester (VBpin)]. The content of the boron‐pendant units was up to 7 mol%, and kinetic studies suggested the incorporation of boron‐pendant units in a discrete manner. The post‐polymerization oxidation of the boron pendants on the copolymer proceeded quantitatively, affording a hydroxy‐containing polyethylene. The introduction of a hydroxy group had a significant impact on the crystallization behaviors.

Article Details

Volume / Issue Vol. 64, Issue 45
Published November 03, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

T

Tomoaki Kanazawa

Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University Kyoto‐Daigaku Katsura, Nishikyo‐ku Kyoto 615‐8510 Japan

T

Tommaso Posenato

Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France

S

Sébastien Norsic

Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France

T

Tsuyoshi Nishikawa

Department of Polymer Chemistry, Graduate School of Engineering

M

Makoto Ouchi

Department of Polymer Chemistry, Graduate School of Engineering

J

Jean Raynaud

Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France

F

Franck D'Agosto

Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M) 43 Bd du 11 novembre 1918 69616 Villeurbanne France