Alternating copolymerization of carbonyl sulfide and Cyclohexene Oxide catalyzed by zinc-cobalt double metal cyanide complex

被引:42
作者
Luo, Ming [1 ]
Zhang, Xing-Hong [1 ]
Du, Bin-Yang [1 ]
Wang, Qi [1 ]
Fan, Zhi-Qiang [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
Carbonyl sulfide; Cyclohexene oxide; Copolymerization; PROPYLENE-OXIDE; STEREOCHEMISTRY CONTROL; GLOBAL SOURCES; STYRENE OXIDE; CO2; DISULFIDE; DIOXIDE; EPOXIDES; OCS; CS2;
D O I
10.1016/j.polymer.2014.05.065
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This paper describes the first example of alternating copolymerization of carbonyl sulfide (COS) with cyclohexene oxide (CHO) via heterogenous catalysis of a nano-lamellar zinc-cobalt(III) double metal cyanide complex (Zn-Co(III) DMCC), providing an efficient method for converting COS to poly(-cyclohexene monothiocarbonate) (PCHMTC) with an alternating degree up to 93%. The number-average molecular weight (M-n) of PCHMTC was 6.5-25.0 kg/mol with polydispersities (PDIs) of 1.6-2.1. The productivity of the catalyst was up to 970 g polymer/g catalyst (5.0 h). The oxygen-sulfur exchange reaction (O/S ER) caused by Zn-Co(III) DMCC was largely suppressed when the reaction was performed at 100-110 degrees C in the presence of THF or CH2Cl2, and thus the selectivity of the monothiocarbonate over carbonate linkages was up to 98%. The mechanisms of the copolymerization and O/S ER were proposed based on the ESI-MS, GC-MS and FT-IR spectra. The obtained PCHMTC is highly transparent and exhibits good solubility in various organic solvents, high T-g of 112 degrees C, initial decomposition temperature of 214 degrees C and high refractive index of 1.705. Crown Copyright (C) 2014 Published by Elsevier Ltd. All rights reserved.
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页码:3688 / 3695
页数:8
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