When Is a Bond Broken? The Polarizability Perspective.

被引:12
|
作者
Hait, Diptarka [1 ,2 ,3 ,4 ]
Head-Gordon, Martin [1 ,2 ]
机构
[1] Univ Calif Berkeley, Kenneth S Pitzer Ctr Theoret Chem, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Chem Sci Div, Berkeley, CA 94720 USA
[3] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[4] Stanford Univ, PULSE Inst, Stanford, CA 94305 USA
关键词
chemical bonding; static polarizability; bond dissociation; electron localization; reaction paths; ELECTRON LOCALIZATION; HYDROGEN; VALENCE; DISSOCIATION; PRINCIPLES; HARDNESS;
D O I
10.1002/anie.202312078
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The question of when a chemical bond can be said to be broken is of fundamental chemical interest but has not been widely studied. Herein we propose that the maxima of static polarizability along bond dissociation coordinates naturally define cutoff points for bond rupture, as they represent the onset of localization of shared electron density into constituent fragments. Examples of computed polarizability maxima over the course of bond cleavage in main-group and transition metal compounds are provided, across covalent, dative and charge-shift bonds. The behavior along reaction paths is also considered. Overall, the static polarizability is found to be a sensitive reporter of electronic structure reorganization associated with bond stretching, and thus can serve as a metric for describing bond cleavage (or diagnose the absence of a chemical bond). Static polarizability maxima along bond dissociation coordinates represent the onset of electron density localization and thus can used to be define when is a chemical bond broken.image
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页数:7
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