Selective dihydroxylation over titanium silicate molecular sieves

被引:50
作者
Bhaumik, A [1 ]
Tatsumi, T [1 ]
机构
[1] Univ Tokyo, Sch Engn, Engn Res Inst, Tokyo 113, Japan
基金
日本学术振兴会;
关键词
D O I
10.1006/jcat.1998.2055
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
Titanium silicate molecular sieve, TS-1, has been found to be a highly efficient and selective catalyst in dihydroxylation of olefins under triphase reaction conditions in the presence of dilute hydrogen peroxide. Among the substrates unsaturated alcohols (greater than or equal to C-4) give selectively corresponding triol in a very high yield with very high H2O2 efficiency. Unsaturated halides give the corresponding diols even at a faster reaction rate. Whereas under the conventional biphase system (in the presence of a cosolvent to homogenize the liquid layers) epoxide is obtained as the major final product in high yield. The substrate nature, i.e., steric hindrance at the active site and hydrophobicity/hydrophilicity of both substrate and epoxide intermediate, is considered to account for the product distribution. Acidity generated in situ over TS-1 in the presence of water (used as the dispersion medium) is responsible for the bifunctional (oxidation and acidic) behavior of the titanium silicate. (C) 1998 Academic Press.
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页码:305 / 309
页数:5
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