Chen Qiang, Zhao Yan-Xia, Jiang Li-Xue, Li Hai-Fang, Chen Jiao-Jiao, Zhang Ting, Liu Qing-Yu, He Sheng-Gui
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Phys Chem Chem Phys. 2018 Feb 14;20(7):4641-4645. doi: 10.1039/c8cp00071a.
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.
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。