Effect of substituents on the stabilities of multiply-substituted carbon-centered radicals

A.S. Menon; D.J. Henry; T. Bally; L. Radom

doi:10.1039/c1ob05196b

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Effect of substituents on the stabilities of multiply-substituted carbon-centered radicals

Journal article

Open access

Peer reviewed

Effect of substituents on the stabilities of multiply-substituted carbon-centered radicals

A.S. Menon, D.J. Henry, T. Bally and L. Radom

Organic & Biomolecular Chemistry, Vol.9(10), pp.3636-3657

2011

DOI: https://doi.org/10.1039/c1ob05196b

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Abstract

The bond dissociation energies (BDEs) and radical stabilization energies (RSEs) which result from 166 reactions that lead to carbon-centered radicals of the type center dot CH2X, center dot CHXY and center dot CXYZ, where X, Y and Z are any of the fourteen substituents H, F, Cl, NH2, OH, SH, CH=CH2, C equivalent to CH, BH2, CHO, COOH, CN, CH3, and CF3, were calculated using spin-restricted and -unrestricted variants of the double-hybrid B2-PLYP method with the 6-311+G(3df, 2p) basis set. The interactions of substituents X, Y, and Z in both the radicals (center dot CXYZ) and in the precursor closed-shell molecules (CHXYZ), as well as the extent of additivity of such interactions, were investigated by calculating radical interaction energies (RIEs), molecule interaction energies (MIEs), and deviations from additivity of RSEs (DARSEs) for a set of 152 reactions that lead to di-(center dot CHXY) and tri-(center dot CXYZ) substituted carbon-centered radicals. The pairwise quantities describing the effects of pairs of substituents in trisubstituted systems, namely pairwise MIEs (PMIEs), pairwise RIEs (PRIEs) and deviations from pairwise additivity of RSEs (DPARSEs), were also calculated for the set of 61 reactions that lead to trisubstituted radicals (center dot CXYZ). Both ROB2-PLYP and UB2-PLYP were found to perform quite well in predicting the quantities related to the stabilities of carbon-centered radicals when compared with available experimental data and with the results obtained from the high-level composite method G3X(MP2)-RAD. Particular selections of substituents or combinations of substituents from the current test set were found to lead to specially stable radicals, increasing the RSEs to a maximum of +68.2 kJ mol(-1) for monosubstituted radicals center dot CH2X (X = CH=CH2), +131.7 kJ mol(-1) for disubstituted radicals center dot CHXY (X = NH2, Y = CHO), and +177.1 kJ mol(-1) for trisubstituted radicals center dot CXYZ (X = NH2, Y = Z = CHO).

Details

Title: Effect of substituents on the stabilities of multiply-substituted carbon-centered radicals
Authors/Creators: A.S. Menon (Author/Creator)
D.J. Henry (Author/Creator)
T. Bally (Author/Creator)
L. Radom (Author/Creator)
Publication Details: Organic & Biomolecular Chemistry, Vol.9(10), pp.3636-3657
Publisher: Royal Society of Chemistry
Identifiers: 991005540270707891
Murdoch Affiliation: School of Chemical and Mathematical Science
Language: English
Resource Type: Journal article

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 2 Chemistry; 2.15 Physical Chemistry; 2.15.3 Quantum Chemistry
Web Of Science research areas: Chemistry, Organic
ESI research areas: Chemistry