Trinuclear salphen-chromium(III)chloride complexes as catalysts for the alternating copolymerization of epoxides and cyclic anhydrides

被引:27
作者
Cui, Lei [1 ]
Ren, Bai-Hao [1 ]
Lu, Xiao-Bing [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
copolymerization; polyester; synergistic effect; trinuclear chromium complex; RING-OPENING COPOLYMERIZATION; CARBON-DIOXIDE; MESO-EPOXIDES; PHTHALIC-ANHYDRIDE; CYCLOHEXENE OXIDE; ASYMMETRIC COPOLYMERIZATION; LACTIDE POLYMERIZATION; VERSATILE CATALYSTS; CO2;
D O I
10.1002/pol.20210334
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Although the alternating copolymerization of epoxides and cyclic anhydrides is a promising route to aliphatic polyesters, improved catalysts are required to realize commercialization of this process. Herein, trinuclear chromium complexes of salicylaldimine, in conjunction with a nucleophilic cocatalyst, are demonstrated as excellent catalysts for epoxide/cyclic anhydride copolymerization, selectively affording perfectly alternating polyesters. The effect of the distance between the chromium species is investigated by varying the bridging skeleton in a series of trinuclear salphen-Cr(III)Cl complexes for obtaining different Cr-Cr distances. Trinuclear salphenCr(III)-complexes with Cr-Cr distances of approximately 7.3 angstrom are found to be efficient copolymerization catalysts, even at high temperatures and extremely low catalyst loadings. In particular, a high activity of 10,620 h(-1) is obtained for the copolymerization of cyclohexene oxide (CHO) and phthalic anhydride (PA) under a low catalyst loading (<0.01 mol%) at 100 degrees C. In situ infrared spectroscopy studies suggest that the activation energy of the trinuclear Cr(III)-salphen catalyst for CHO/PA copolymerization is 15 kJ mol(-1) lower than that of the corresponding mononuclear catalyst owing to an intramolecular synergistic effect among the metal atoms.
引用
收藏
页码:1821 / 1828
页数:8
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