化学
亲核细胞
债券
药物化学
有机化学
催化作用
财务
经济
作者
Stefan Andrew Harry,Nathaniel G. Garrison,Andrea Zhu,Michael Richard Xiang,Maxime A. Siegler,Thomas Lectka
标识
DOI:10.1021/acs.joc.2c01788
摘要
In this note, we present a series of rigid molecules that show close enforced interactions between Ar–F moieties and −CH2X groups in a "tetrel bond" configuration similar to a nascent SN2 attack. We explore the spectroscopic, crystallographic, and chemical reactivity consequences of these unusual interactions, including significant through-space spin–spin couplings, short C–F···CH2X distances, and differential SN1 and SN2 reaction pathways. We also reveal experimental evidence of carbon-based tetrel bonds influencing chemical reactivity in solution. Finally, density functional theory (DFT) calculations are employed throughout this study to confirm and illuminate our experimental data.
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