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硼化钒团簇阳离子VB(n = 3 - 6)对甲烷的热活化作用

Thermal activation of methane by vanadium boride cluster cations VB (n = 3-6).

作者信息

Chen Qiang, Zhao Yan-Xia, Jiang Li-Xue, Li Hai-Fang, Chen Jiao-Jiao, Zhang Ting, Liu Qing-Yu, He Sheng-Gui

机构信息

State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Phys Chem Chem Phys. 2018 Feb 14;20(7):4641-4645. doi: 10.1039/c8cp00071a.

Abstract

Investigation on the reactivity of atomic clusters represents an important approach to discover new species to activate and transform methane, the most stable alkane molecule. While a few types of transition metal species have been found to be capable of cleaving the C-H bond of methane, methane activation by the transition metal boride species has not been explored yet. This study reports that vanadium boride cluster cations VB (n = 3-6) can dehydrogenate methane under thermal collision conditions. The mechanistic details of the efficient reactions have been elucidated by quantum chemistry calculations on the VB reaction system. Compared to the non-polar bare B cluster, the B moiety in VB can be polarized by the V cation and thus its reactivity toward methane can be much enhanced. This study provides new insights into the rational design of boron-based catalysts for methane activation.

摘要

对原子团簇反应活性的研究是发现新物种以活化和转化甲烷(最稳定的烷烃分子)的重要途径。虽然已发现少数几种过渡金属物种能够裂解甲烷的C-H键,但过渡金属硼化物物种对甲烷的活化作用尚未得到探索。本研究报告称,硼化钒团簇阳离子VB(n = 3 - 6)在热碰撞条件下可使甲烷脱氢。通过对VB反应体系的量子化学计算阐明了高效反应的机理细节。与非极性裸B团簇相比,VB中的B部分可被V阳离子极化,因此其对甲烷的反应活性可大大增强。本研究为合理设计用于甲烷活化的硼基催化剂提供了新的见解。

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