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Selective dihydroxylation over titanium silicate molecular sieves

机译:硅酸钛分子筛上的选择性二羟基化

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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. [References: 23]
机译:已经发现,在稀的过氧化氢的存在下,在三相反应条件下,硅酸钛分子筛TS-1是烯烃二羟基化中的高效选择性催化剂。在底物中,不饱和醇(大于或等于C-4)以很高的产率和很高的H2O2效率选择性地产生相应的三醇。不饱和卤化物即使以更快的反应速率也能给出相应的二醇。而在常规的双相体系下(在助溶剂均质以使液体层均质的情况下),环氧化物以高收率获得了主要的最终产物。底物的性质,即活性位点的位阻以及底物和环氧化物中间体的疏水性/亲水性被认为是产物分布的原因。在水存在下(用作分散介质)在TS-1上原位产生的酸度负责硅酸钛的双功能(氧化和酸性)行为。 (C)1998年学术出版社。 [参考:23]

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