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首页> 外文期刊>Macromolecular symposia >Efficient epoxidation of terminal and internal alkenes using t-butylhydroperoxide catalysed by polybenzimidazole-supported Mo(VI)center dot(PBI center dot Mo)
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Efficient epoxidation of terminal and internal alkenes using t-butylhydroperoxide catalysed by polybenzimidazole-supported Mo(VI)center dot(PBI center dot Mo)

机译:聚苯并咪唑负载的Mo(VI)中心点(PBI中心点Mo)催化叔丁基过氧化氢对末端和内部烯烃的有效环氧化

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摘要

A polybenzimidazole-supported Mo complex (PBI.Mo) has been prepared by a method already reported. Extensive investigation of digestion procedures has shown a dry-ashing method using NaNO3/HNO3 (conc.) at 560 degrees C to be an optimal method for preparing samples for Mo analysis by atomic absorption spectrophotometric methodology. Mo loadings in the range 1.32-0.62 mmol Mo g(-1) polymer were demonstrated. PBI.Mo has been used as a heterogeneous catalyst in the epoxidation of cyclohexene, methylene-cyclohexane, 4-vinyl cyclohexene, styrene, 1,3-pentadiene and allyl chloride, bromide and alcohol using t-butylhydroperoxide as the oxidant. The catalyst is very effective for the first four substrates, somewhat less active than soluble MoO(2)acac(2), but providing final yields and purity of products generally better than using MoO(2)acac(2). The 1,3-pentadiene displays an overall conversion of similar to 35% with a distribution of the four possible monoepoxide isomers similar to that obtained with MoO(2)acac(2) as catalyst. The allylic substrates showed poor conversion probably as a result of secondary (oligomerisation) reactions involving the epoxide products. Running the epoxidations for extended periods in air allows in situ generation of alkyl hydroperoxides in the case of cyclohexene and 4-vinylcyclohexene and these are then effective internal oxidants for further Mo catalysed epoxidation of these alkenes. When run under anaerobic conditions the reactions are very clean with no evidence of any free radical processes contributing. In all cases Mo leaching is minimal. Good activity is seen in the recycling of PBI.Mo in the case of styrene and 1,3- [GRAPHICS] pentadiene, although with cyclohexene and 4-vinylcyclohexene steady deactivation is seen, probably as a result of catalyst fouling. Thermogravimetric analyses suggest that it might be possible to burn off the foulant without destroying the catalyst. [References: 18]
机译:聚苯并咪唑负载的Mo络合物(PBI.Mo)已通过已报道的方法制备。大量的消化过程研究表明,使用NaNO3 / HNO3(浓)在560摄氏度下进行干灰化方法是制备用于原子吸收分光光度法进行Mo分析的样品的最佳方法。证明了Mo负载量为1.32-0.62 mmol Mo g(-1)聚合物。 PBI.Mo在使用叔丁基过氧化氢作为氧化剂的环己烯,亚甲基-环己烷,4-乙烯基环己烯,苯乙烯,1,3-戊二烯和烯丙基氯,溴化物和醇的环氧化中已用作多相催化剂。该催化剂对于前四种底物非常有效,活性略低于可溶性MoO(2)acac(2),但提供的最终收率和产品纯度通常优于使用MoO(2)acac(2)。 1,3-戊二烯的总转化率接近35%,四种可能的单环氧化物异构体的分布与MoO(2)acac(2)作为催化剂获得的分布相似。烯丙基底物显示出不良的转化,这可能是由于涉及环氧化物产物的二次(低聚)反应的结果。在环己烯和4-乙烯基环己烯的情况下,在空气中长时间进行环氧化可以原位生成烷基氢过氧化物,然后它们是有效的内部氧化剂,用于进一步Mo催化这些烯烃的环氧化。在厌氧条件下运行时,反应非常干净,没有任何自由基过程参与的证据。在所有情况下,钼的浸出都是最小的。在苯乙烯和1,3- [GRAPHICS]戊二烯的情况下,在PBI.Mo的再循环中看到了良好的活性,尽管在环己烯和4-乙烯基环己烯中也观察到稳定的失活,这可能是由于催化剂结垢的结果。热重分析表明,有可能在不破坏催化剂的情况下燃烧掉污垢。 [参考:18]

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