Whence the Energy Term of the Rate Constant?

被引:5
作者
Zavitsas, Andreas A. [1 ]
机构
[1] Long Isl Univ, Dept Chem & Biochem, Brooklyn, NY 11201 USA
关键词
HYDROGEN ABSTRACTION REACTIONS; DIRECT DYNAMICS CALCULATIONS; COUPLED ELECTRON-TRANSFER; TRANSITION-STATE THEORY; H-2 REVERSIBLE CH4+H; ACTIVATION-ENERGY; RADICALS; BOND; EXCHANGE; ATOM;
D O I
10.1021/jp101183w
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Insights into the causes of energy barriers to reactions are obtained from our E* model for hydrogen abstractions. Results of the model are in good agreement with all eight experimentally studied symmetrical reactions of the type X-H + (center dot)X -> X(center dot) + H-X. The E* energy is broken down into three components: energy needed to overcome triplet repulsion between the terminal Xs, energy needed to bring the H-X bonds to their transition state distances, and energy gain by the resonance stabilization of delocalization of the odd electron over three atoms. The strength of the X-H bond is a minor factor. The conclusion that triplet repulsion is a major factor is supported by the London equation and by results of recent high level theoretical calculations. The E* model requires inputs of bond dissociation energies, bond lengths, and infrared stretching frequencies of X-H and X-X. Some reported failures of E* are shown to have been caused by use of input values subsequently found to be incorrect.
引用
收藏
页码:5113 / 5118
页数:6
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