Tachikawa Hiroto
Division of Materials Chemistry, Graduate School of Engineering, Hokkaido University, Kita-ku, Sapporo 060-8628, Japan.
J Chem Phys. 2015 Feb 14;142(6):064301. doi: 10.1063/1.4906944.
Metal catalyzed carbon-carbon (C-C) bond formation is one of the important reactions in pharmacy and in organic chemistry. In the present study, the electron and hole capture dynamics of a lithium-benzene sandwich complex, expressed by Li(Bz)2, have been investigated by means of direct ab-initio molecular dynamics method. Following the electron capture of Li(Bz)2, the structure of Li(Bz)2 was drastically changed: Bz-Bz parallel form was rapidly fluctuated as a function of time, and a new C-C single bond was formed in the C1-C1' position of Bz-Bz interaction system. In the hole capture, the intermolecular vibration between Bz-Bz rings was only enhanced. The mechanism of C-C bond formation in the electron capture was discussed on the basis of theoretical results.
金属催化的碳-碳(C-C)键形成反应是药学和有机化学中的重要反应之一。在本研究中,通过直接从头算分子动力学方法研究了锂-苯夹心配合物Li(Bz)₂的电子和空穴俘获动力学。在Li(Bz)₂发生电子俘获后,[Li(Bz)₂]⁻的结构发生了剧烈变化:Bz-Bz平行形式随时间迅速波动,并且在Bz-Bz相互作用体系的C1-C1'位置形成了一个新的C-C单键。在空穴俘获过程中,Bz-Bz环之间的分子间振动仅增强。基于理论结果讨论了电子俘获中C-C键形成的机理。