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Small molecule activation and biomimetic catalysis
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基于被包围状态和马尔可夫模型的显著性检测
Release time:2019-03-09 Hits:
Indexed by: Journal Papers
First Author: Ren, Wei-Min
Correspondence Author: Ren, WM (reprint author), Dalian Univ Technol, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China.
Co-author: Liu, Ye,Xin, An-Xiang,Fu, Song,Lu, Xiao-Bing
Date of Publication: 2015-12-08
Journal: MACROMOLECULES
Included Journals: SCIE、EI、Scopus
Document Type: J
Volume: 48
Issue: 23
Page Number: 8445-8450
ISSN No.: 0024-9297
Abstract: Unprecedented activity (TOP > 270 000 h(-1)), high polymer selectivity (>99%), and excellent durability (TON > 600 000) were observed in the copolymerization of carbonyl sulfide (COS) and epoxides mediated by the single-site bifunctional chromium catalyst containing a Lewis acidic metal center and a sterically hindered organic base in a molecule, selectively producing the corresponding poly(thiocarbonate)s with completely alternating structure, high molecular weight, and narrow monodispersity. No oxygen sulfur exchange reaction occurred even at an elevated temperature of 80 degrees C. Nevertheless, this catalyst was not efficient for CO2/epoxides copolymerization. The presence of CO2 completely inhibits the reactivity of COS. Contrarily, the corresponding Co(III) complex with the same ligand showed very low activity for COS/epoxides copolymerization but excellent activity (TOP > 13 000 h(-1)) for CO2/epoxides copolymerization at both ambient and high temperatures, affording the polycarbonates with >99% carbonate linkages and high molecular weight up to 467.0 kg/mol.
Translation or Not: no