Molybdenum complex tethered to the surface of activated carbon as a new recoverable catalyst for the epoxidation of olefins

被引:27
|
作者
Masteri-Farahani, M. [1 ]
Abednatanzi, S. [1 ]
机构
[1] Kharazmi Univ, Fac Chem, Tehran, Iran
关键词
Molybdenum; Activated carbon; Tethering; Heterogeneous catalysis; Epoxidation; SCHIFF-BASE COMPLEXES; MANGANESE(III) SALEN COMPLEXES; HETEROGENEOUS CATALYSTS; EFFICIENT CATALYSTS; COVALENT ATTACHMENT; MESOPOROUS MCM-41; IMMOBILIZATION; DIOXOMOLYBDENUM(VI); STRATEGIES; OXIDATION;
D O I
10.1016/j.apcata.2014.04.008
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
A new recoverable catalyst for the epoxidation of olefins was developed by covalent attachment of aminopropyl groups on the surface of oxidized activated carbon (AC) and next reaction with bis(acetylacetonato)dioxomolybdenum(VI). Characterization of the prepared catalyst was performed with different physicochemical methods such as Fourier transform infrared and atomic absorption spectroscopies, scanning electron microscopy, energy-dispersive X-ray and nitrogen sorption analyses. Nitrogen adsorption-desorption analysis revealed that the textural characteristics of the support were changed during the grafting experiments but the channels remained relatively accessible despite sequential reduction in surface area, pore volume and pore size. Elemental analysis showed the presence of 0.06 mmol g(-1) molybdenum in the catalyst. The prepared catalyst catalyzed the epoxidation of olefins and allyl alcohols with tert-butyl hydroperoxide (TBHP) and cumene hydroperoxide (CHP) quantitatively with excellent selectivity toward the corresponding epoxides under mild reaction conditions. The results indicated that the hydrophobicity of the AC support promoted the catalytic efficiency of the catalyst in the epoxidation of olefins. (C) 2014 Elsevier B.V. All rights reserved.
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页码:211 / 218
页数:8
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