Chromium complexes with tridentate NN′O Schiff base ligands as catalysts for the coupling of CO2 and epoxides

被引:28
|
作者
Iksi, Siham [1 ]
Aghmiz, Ali [1 ]
Rivas, Raquel [1 ]
Dolores Gonzalez, M. [1 ]
Cuesta-Aluja, Laia [1 ]
Castilla, Javier [1 ]
Orejon, Arantxa [1 ]
El Guemmout, Farid [2 ]
Masdeu-Bulto, Anna M. [1 ]
机构
[1] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, E-43007 Tarragona, Spain
[2] Univ Abdelmalek Essaadi, Fac Sci, Tetouan 93030, Morocco
关键词
Carbonates; Carbon dioxide; Catalysis; Chromium; Tridentate Schiff bases; RING-OPENING POLYMERIZATION; DIIMINATE ZINC CATALYSTS; CARBON-DIOXIDE; ALTERNATING COPOLYMERIZATION; SALEN COMPLEXES; CYCLOHEXENE OXIDE; MECHANISTIC ASPECTS; CYCLIC CARBONATES; CRYSTAL-STRUCTURE; METAL-COMPLEXES;
D O I
10.1016/j.molcata.2013.11.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
New Cr(III) hexacoordinated complexes with tridentate NN'O-donor Schiff base ligands, M(NN'O)(2)Cl, have been prepared. They form active catalytic systems for the coupling of epoxides and carbon dioxide in the presence of co-catalysts. Best results were obtained with the complex with N-(2-pyridylmethyl)-3,5-ditert-butyl-salicylaldimine (1) ligand and a co-catalyst. Cyclohexene oxide reacts with carbon dioxide in the presence of these catalysts to form mixtures of polycarbonate (PC) (productivity up to ca. 900 g PC/g Cr) and cyclic carbonate depending on the co-catalyst and conditions employed. Cyclopentene, styrene and propylene oxides form selectively the cyclic carbonates at the conditions studied (epoxide conversion up to 97%). Although some of the co-catalysts are also active for the cycloaddition, the presence of both complex and co-catalyst has proved to be beneficial. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 152
页数:10
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