An assessment of theoretical procedures for the calculation of reliable radical stabilization energies †‡

Abstract

The performance of a variety of theoretical methods in computing stabilization energies of the substituted methyl and vinyl radicals ˙CH₂F, ˙CH₂CN, ˙CH₂CH[double bond, length half m-dash]CH₂, ˙CH₂CH[double bond, length half m-dash]O, CH₂[double bond, length half m-dash]C˙F and CH₂[double bond, length half m-dash]C˙CN is examined. The influence of electron correlation (UHF, UMP2, PMP2, RMP2, UB3-LYP, UQCISD, UQCISD(T), UCCSD(T), URCCSD(T) and RRCCSD(T)) and basis set size (from 6-31G(d) to 6-311++G(3df,3pd)) on stabilization energies is evaluated, as well as the performance of compound methods such as G2, G3, CBS-Q and CBS-APNO and their variants. The results indicate that generally reliable radical stabilization energies can be obtained at modest cost using RMP2/6-311+G(2df,p)//RMP2/6-31G(d) energies. A slightly less accurate but more economical procedure is RMP2/6-311+G(d)//B3-LYP/6-31G(d). UMP2 and PMP2 are unsuitable for obtaining radical stabilization energies for spin-contaminated radicals, while UB3-LYP appears generally to overestimate stabilization energies.

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