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DALIAN UNIVERSITY OF TECHNOLOGY Login 中文
Liu Ye

Researcher
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates


Gender:Male
Alma Mater:大连理工大学
Degree:Doctoral Degree
School/Department:化工学院
Discipline:Applied Chemistry. Fine Chemicals. Polymer Chemistry and Physics
Business Address:Dalian University of Technology
F-207 West Campus, No.2 Linggong Road, High-Tech Zone, Dalian 116024, China

Contact Information:liuye@dlut.edu.cn
E-Mail:liuye@dlut.edu.cn
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Current position: Home >> Scientific Research >> Paper Publications

Highly Active, Bifunctional Co(III)-Salen Catalyst for Alternating Copolymerization of CO2 with Cyclohexene Oxide and Terpolymerization with Aliphatic Epoxides

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Indexed by:期刊论文

Date of Publication:2010-02-09

Journal:MACROMOLECULES

Included Journals:SCIE、EI

Volume:43

Issue:3

Page Number:1396-1402

ISSN No.:0024-9297

Abstract:The cobalt(III) complex of a salen ligand bearing one quaternary ammonium salt on the three-position of one aromatic ring is a highly active catalyst for the alternating copolymerization of cyclohexene oxide (CHO) and CO2 to afford the corresponding poly(cyclohexene carbonate) (PCHC) at various temperatures. The cobalt-based catalyst exhibited excellent activity and selectivity for polymer formation at high temperatures up to 120 degrees C and even under low CO2 pressures of 0.1 MPa. Also, the cobalt(III)-salen complex could operate very efficiently for the terpolymerization of CHO and aliphatic epoxides with CO2 to provide selectively polycarbonates with a narrow polydispersity at high temperatures. The polycarbonates resulting from the terpolymerization of equimolar CHO and propylene oxide (PO) with CO2 have a close content for both cyclohexene carbonate and propylene carbonate units. This is ascribed to the presence of CHO significantly inhibiting the reactivity of PO and thereby causing a matched reactivity for both epoxides during the terpolymerization. The competition coordination of CHO and PO to the electrophilic cobalt(III) ion has no effect on regioselective ring-opening of PO in the terpolymerization.