氢键
共价键
化学物理
化学键
红外光谱学
渡线
化学
飞秒
分子
物理
计算机科学
有机化学
量子力学
人工智能
激光器
作者
Bogdan Dereka,Qi Yu,Nicholas H. C. Lewis,William Benjamin Carpenter,Joel M. Bowman,Andrei Tokmakoff
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-01-07
卷期号:371 (6525): 160-164
被引量:222
标识
DOI:10.1126/science.abe1951
摘要
Hydrogen bonds (H-bonds) can be interpreted as a classical electrostatic interaction or as a covalent chemical bond if the interaction is strong enough. As a result, short strong H-bonds exist at an intersection between qualitatively different bonding descriptions, with few experimental methods to understand this dichotomy. The [F-H-F]- ion represents a bare short H-bond, whose distinctive vibrational potential in water is revealed with femtosecond two-dimensional infrared spectroscopy. It shows the superharmonic behavior of the proton motion, which is strongly coupled to the donor-acceptor stretching and disappears on H-bond bending. In combination with high-level quantum-chemical calculations, we demonstrate a distinct crossover in spectroscopic properties from conventional to short strong H-bonds, which identify where hydrogen bonding ends and chemical bonding begins.
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