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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.
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页码:1821 / 1828
页数:8
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