Covalent immobilization of the Jacobsen catalyst on mesoporous phenolic polymer: A highly enantioselective and stable asymmetric epoxidation catalyst

被引:16
|
作者
De Decker, Jeroen [1 ]
Bogaerts, Thomas [1 ,2 ]
Muylaert, Ilke [1 ]
Delahaye, Sander [3 ]
Lynen, Frederic [3 ]
Van Speybroeck, Veronique [2 ]
Verberckmoes, An [4 ]
Van der Voort, Pascal [1 ]
机构
[1] Univ Ghent, Ctr Ordered Mat Organometall & Catalysis, Dept Inorgan & Phys Chem, B-9000 Ghent, Belgium
[2] Univ Ghent, Ctr Mol Modeling, B-9052 Zwijnaarde, Belgium
[3] Univ Ghent, Dept Organ Chem, B-9000 Ghent, Belgium
[4] Univ Coll Ghent, Dept Appl Engn Sci, B-9000 Ghent, Belgium
基金
欧洲研究理事会;
关键词
Polymers; Microporous materials; Chemical synthesis; Fourier Transform Infrared Spectroscopy (FTIR); Chemisorption; Oxidation; ALKENE EPOXIDATION; HETEROGENEOUS CATALYST; SALEN COMPLEXES; METAL-COMPLEXES; OXIDATION; MN(III); OLEFINS; SPECTROSCOPY; CHEMISTRY; EPOXIDES;
D O I
10.1016/j.matchemphys.2013.06.035
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The Jacobsen catalyst, N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese (III) chloride is covalently immobilized on mesoporous phenolic resin through a direct and simple procedure. The immobilization is evident from nitrogen sorption and quantitative XRF measurements. A complex loading of 0.09 mmol g(-1) is obtained, corresponding to well dispersed Mn-complexes on the surface of the mesoporous phenolic resin. This novel catalytic system shows good catalytic activity and excellent enantioselectivity in the asymmetric epoxidation of 1,2-dialin. The heterogenized Jacobsen catalyst is demonstrated to be a re-usable and non-leaching catalytic system. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:967 / 972
页数:6
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