covalent chemical bond
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Science ◽  
2021 ◽  
Vol 371 (6525) ◽  
pp. 160-164 ◽  
Author(s):  
Bogdan Dereka ◽  
Qi Yu ◽  
Nicholas H. C. Lewis ◽  
William B. Carpenter ◽  
Joel M. Bowman ◽  
...  

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.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Daniel S. Levine ◽  
Martin Head-Gordon

Abstract Lowering of the electron kinetic energy (KE) upon initial encounter of radical fragments has long been cited as the primary origin of the covalent chemical bond based on Ruedenberg’s pioneering analysis of H$${}_{2}^{+}$$ 2 + and H2 and presumed generalization to other bonds. This work reports KE changes during the initial encounter corresponding to bond formation for a range of different bonds; the results demand a re-evaluation of the role of the KE. Bonds between heavier elements, such as H3C–CH3, F–F, H3C–OH, H3C–SiH3, and F–SiF3 behave in the opposite way to H$${}_{2}^{+}$$ 2 + and H2, with KE often increasing on bringing radical fragments together (though the total energy change is substantially stabilizing). The origin of this difference is Pauli repulsion between the electrons forming the bond and core electrons. These results highlight the fundamental role of constructive quantum interference (or resonance) as the origin of chemical bonding. Differences between the interfering states distinguish one type of bond from another.


2007 ◽  
Vol 119 (9) ◽  
pp. 1491-1494 ◽  
Author(s):  
Björn O. Roos ◽  
Antonio C. Borin ◽  
Laura Gagliardi

2007 ◽  
Vol 46 (9) ◽  
pp. 1469-1472 ◽  
Author(s):  
Björn O. Roos ◽  
Antonio C. Borin ◽  
Laura Gagliardi

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