Structural and catalytic studies of a trimethyltin vanadate coordination polymer

被引:6
作者
Abrantes, Marta
Balula, Maria Salete
Valente, Anabela A.
Paz, Filipe A. Almeida
Pillinger, Martyn
Romao, Carlos C.
Rocha, Joao
Goncalves, Isabel S.
机构
[1] Univ Aveiro, Dept Chem, CICECO, P-3810193 Aveiro, Portugal
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Estacao Agron Nacl, P-2780157 Oeiras, Portugal
关键词
vanadium(V); metavanadate; trimethyltin(IV); coordination polymer; olefin epoxidation;
D O I
10.1007/s10904-006-9080-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The organotin vanadate [Me3SnVO3] (1) has been prepared and characterised in the solid state by powder X-ray diffraction (XRD), thermogravimetric analysis, multinuclear magic-angle spinning (MAS) NMR, IR and Raman spectroscopy. The phase purity and structure of microcrystalline 1 were confirmed by carrying out a full Rietveld structural refinement at ambient temperature and from conventional powder XRD. V-51 and Sn-119 MAS NMR data for compound 1 were in agreement with the predicted structure, showing two equally-abundant, nonequivalent Me3Sn groups and two equally-abundant, nonequivalent vanadium atoms. The compound was applied as a catalyst for the liquid-phase epoxidation of olefins at 55 degrees C using tert-butyl hydroperoxide (tBuOOH) as the oxidant. The reaction rate for the different substrates followed the order cis-cyclooctene > (R)-(+)-limonene congruent to trans-2-octene > cyclododecene > styrene > 1-octene; the corresponding epoxides were the only observed products. Leaching tests indicated that the catalytic epoxidation of cyclooctene was mainly heterogeneous in nature.
引用
收藏
页码:215 / 222
页数:8
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