Kinetic and mechanistic investigation for the copolymerization of CO2 and cyclohexene oxide catalyzed by trizinc complexes. Issue 23 (2nd June 2017)

• Record Type: Journal Article
• Authors: Xu, Yonghang; Lin, Limiao; He, Chun-Ting; Qin, Jiaxiang; Li, Zhong; Wang, Shuanjin; Xiao, Min; Meng, Yuezhong
• Is Part Of: Polymer chemistry. Volume 8:Issue 23(2017)
• Page Start: 3632
• Page End: 3640
• Publication Date: 2017-06-02
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c7py00403f
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : The mechanism of CO2 /epoxide copolymerization catalyzed by Schiff base trizinc complexes. Abstract : The trizinc complexes Zn3 (OAc)4 (Ln)2, 1a and1b, which were coordinated with Schiff-base ligands via a simple and economical method, have been examined and found to be highly effective and efficient toward the copolymerization of CO2 and cyclohexene oxide (CHO). In this work, the kinetics for the copolymerization of CO2 and CHO using1b as the catalyst was monitored via in situ ATR-FTIR spectroscopy. The reaction orders' dependencies on catalyst concentration, initial CHO concentration and CO2 pressure, as well as activation energies ( E a ) of polycarbonate and cyclic carbonate formation, were investigated in detail. The practical amount of active zinc sites in the copolymerization was calculated using the parameters obtained from 1 H NMR and GPC measurements. The initiating reaction details were simulated using density functional theory, and the potential energy surfaces were obtained. Based on the results of all characterizations and kinetic investigations, a unique initiating reaction and copolymerizing mechanism were proposed when using Zn3 (OAc)4 (Ln)2 as the catalyst.