Alternating copolymerization of carbon dioxide and cyclohexene oxide catalyzed by silicon dioxide/Zn-CoIII double metal cyanide complex hybrid catalysts with a nanolamellar structure

被引:62
作者
Sun, Xue-Ke [1 ]
Zhang, Xing-Hong [1 ]
Liu, Fei [1 ]
Chen, Shang [2 ]
Du, Bin-Yang [1 ]
Wang, Qi [1 ]
Fan, Zhi-Qiang [1 ]
Qi, Guo-Rong [1 ]
机构
[1] Zhejiang Univ, Minist Educ, Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Hangzhou 310027, Peoples R China
[2] Jishou Univ, Coll Chem & Chem Engn, Jishou 416000, Peoples R China
关键词
catalysts; carbon dioxide; copolymerization; double metal cyanide complex; polycarbonates;
D O I
10.1002/pola.22666
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Air-stable hybrid catalysts of silicon dioxide/double metal cyanide complexes (Si-DMCCs) based on Zn-3[Co(CN)(6)](2) (ZHCC) were prepared by an in situ Sol-gel method. The Si-DMCCs showed low crystallinity and a nanolamellar structure with a thickness of similar to 40-60 nm. In particular, a lamellar structure of regular hexagonal shape was observed for Si-DMCCs with low SiO2 content. These catalysts had very high catalytic activity for alternating copolymerization of cyclohexene oxide (CHO) and carbon dioxide. A turnover number of 11,444, turnover frequency of 3815 h(-1), and apparent efficiency of 7.5 kg polymer/g ZHCC (similar to 24.0 kg polymer/g Zn) were achieved at 3.8 MPa and 100 degrees C. The poly(cyclohexenylene carbonate) (PCHC) polymers obtained were completely atactic with a molecular weight (Mn) of similar to 10 kg/mol and polydispersity of 2.0-3.0. The PCHCs had a structure of nearly alternating CHO and CO2 units, with a molar fraction of carbonate units of 0.44-0.47. Preliminary investigations of the mechanism suggest that nucleophilic attack by neighboring oxygen atoms is involved in copolymerization initiation with Zn-Co-III DMCCs. (C) 2008 Wiley Periodicals, Inc.
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页码:3128 / 3139
页数:12
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