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通过串联烷烃脱氢-烯烃复分解实现催化烷烃复分解反应

Catalytic alkane metathesis by tandem alkane dehydrogenation-olefin metathesis.

作者信息

Goldman Alan S, Roy Amy H, Huang Zheng, Ahuja Ritu, Schinski William, Brookhart Maurice

机构信息

Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ 08854, USA.

出版信息

Science. 2006 Apr 14;312(5771):257-61. doi: 10.1126/science.1123787.

Abstract

With petroleum supplies dwindling, there is increasing interest in selective methods for transforming other carbon feedstocks into hydrocarbons suitable for transportation fuel. We report the development of highly productive, well-defined, tandem catalytic systems for the metathesis of n-alkanes. Each system comprises one molecular catalyst (a "pincer"-ligated iridium complex) that effects alkane dehydrogenation and olefin hydrogenation, plus a second catalyst (molecular or solid-phase) for olefin metathesis. The systems all show complete selectivity for linear (n-alkane) product. We report one example that achieves selectivity with respect to the distribution of product molecular weights, in which n-decane is the predominant high-molecular-weight product of the metathesis of two moles of n-hexane.

摘要

随着石油供应的减少,人们对将其他碳原料转化为适用于运输燃料的碳氢化合物的选择性方法越来越感兴趣。我们报道了用于正构烷烃复分解反应的高产率、明确的串联催化体系的开发。每个体系都包含一种分子催化剂(一种“钳形”配体铱配合物),它能实现烷烃脱氢和烯烃加氢,外加第二种用于烯烃复分解反应的催化剂(分子或固相)。这些体系均对线性(正构烷烃)产物表现出完全的选择性。我们报道了一个在产物分子量分布方面实现选择性的例子,其中正癸烷是两摩尔正己烷复分解反应的主要高分子量产物。

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