Shortcomings of Basing Radical Stabilization Energies on Bond Dissociation Energies of Alkyl Groups to Hydrogen

被引:16
作者
Zavitsas, Andreas A. [1 ]
Rogers, Donald W. [1 ]
Matsunaga, Nikita [1 ]
机构
[1] Long Isl Univ, Dept Chem & Biochem, Brooklyn, NY 11201 USA
关键词
PARADIGM SHIFTING IMPLICATIONS; ENTHALPIES;
D O I
10.1021/jo101127m
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Stabilization energies (SEH) of carbon radicals (R-center dot) are traditionally defined as the difference between the bond dissociation energy (BDE) of CH3-H, as a reference point, and of R-H. The term "stabilization energy" implies that it is an intrinsic property of the radical and a quantitative measure of stability. Applicable only to carbon-centered radicals, SEH stabilization energies are not transferable and cannot be used to estimate carbon-carbon BDE[R-R'], symmetrical BDE[R-R], or any other BDE[R-X]. SEH values by themselves are neither an intrinsic property nor a quantitative measure of stability. There is available an alternative that is not limited only to carbon-carbon and carbon-hydrogen bonds, does not depend on any one particular molecule or BDE as a reference point, and is accurate with several hundred different types of bonds.
引用
收藏
页码:5697 / 5700
页数:4
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