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Mass Spectrometry Special Feature: Gas-phase activation of methane by ligated transition-metal cations

机译:质谱特征:连接的过渡金属阳离子气相活化甲烷

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摘要

Motivated by the search for ways of a more efficient usage of the large, unexploited resources of methane, recent progress in the gas-phase activation of methane by ligated transition-metal ions is discussed. Mass spectrometric experiments demonstrate that the ligands can crucially influence both reactivity and selectivity of transition-metal cations in bond-activation processes, and the most reactive species derive from combinations of transition metals with the electronegative elements fluorine, oxygen, and chlorine. Furthermore, the collected knowledge about intramolecular kinetic isotope effects associated with the activation of C–H(D) bonds of methane can be used to distinguish the nature of the bond activation as a mere hydrogen-abstraction, a metal-assisted mechanism or more complex reactions such as formation of insertion intermediates or σ-bond metathesis.
机译:通过寻找更有效地利用大量未开发的甲烷资源的方法的动机,讨论了通过连接的过渡金属离子气相活化甲烷的最新进展。质谱实验表明,配体可以在键活化过程中同时影响过渡金属阳离子的反应性和选择性,并且反应性最高的物种来自过渡金属与负电性元素氟,氧和氯的组合。此外,所收集的与甲烷的C–H(D)键活化有关的分子内动力学同位素效应的知识可用于区分键活化的性质是单纯的吸氢,金属辅助机理或更复杂反应,例如插入中间体的形成或σ键易位。

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