Catalytic activity of anchored vanadyl complexes

Q4 Chemical Engineering 分子催化 Pub Date : 1994-09-27 DOI:10.1016/0304-5102(94)00086-7
Rajinder Kaur Bhatia , G.N. Rao
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引用次数: 10

Abstract

Vanadyl complexes anchored to polymers are effective as catalysts in the oxidation of sulfoxide to sulfone by tert-butyl hydroperoxide. To study the effect of ligand bound to vanadium in such catalytic reactions, vanadyl complexes of salicylaldoxime (a), 3-2(thenoyl-1,1,1-trifluoroacetone) (b) and (o-phenylene-bis-salicylimine) (c) were anchored to polymers and the effectiveness of the catalysts in the oxidation of dimethylsulfoxide and diphenylsulfoxide by tert.-butylhydroperoxide was investigated. The order of catalytic activity was a ≈ b > c in both cases. In the homogeneous systems using the same complexes, the order of catalytic activity was found to be b > c > a. The polymeric beads isolated at the end of oxidation reaction were used for successive runs and the catalytic activity was similar in the first three cycles. The results are discussed on the basis of structural features of the ligands and the reactants.

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锚定钒基配合物的催化活性
锚定在聚合物上的钒基配合物是过氧化叔丁基将亚砜氧化为砜的有效催化剂。为了研究与钒结合的配体在这种催化反应中的作用,将水杨醛肟(a)、3-2(壬基-1,1,1-三氟丙酮)(b)和(邻苯基-双水杨胺)(c)的钒基配合物固定在聚合物上,并研究了催化剂在叔特氧化二甲亚砜和二苯基亚砜中的效果。对-丁基过氧化氢进行了研究。催化活性的顺序为a≈b >两种情况都是C。在使用相同配合物的均相体系中,发现催化活性的顺序为b >c比;a.氧化反应结束时分离的聚合物珠连续运行,前三个循环的催化活性相似。根据配体和反应物的结构特征对结果进行了讨论。
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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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