化学
立体化学
机制(生物学)
结晶学
药物化学
认识论
哲学
作者
Wei Xu,Peili Li,Yin Huang
出处
期刊:Organometallics
[American Chemical Society]
日期:2025-03-27
卷期号:44 (7): 840-846
标识
DOI:10.1021/acs.organomet.4c00489
摘要
MClx-catalyzed (MClx = CuCl2/FeCl3) arene sp2 C–H chlorination was calculated at the DKH//B3LYP-D3//DKH-def2-TZVP level in solvent. The mechanism consists of two competing paths: (i) the arene insertion path into the M–Cl bond and (ii) the M–Cl addition-like path onto the arene ring. The latter path has fewer steps and lower activation energies. In both paths, one M–Cl bond breaks at the first step and then the valence state stays at Cu(I)/Fe(II) for the main part of the following steps. Cu exhibits better catalytic performance due to its lesser bonding capability. Weak M–H interactions were observed in the insertion mechanism.
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