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Comparison of G3 and G4 Theories for Radical Addition and Abstraction Reactions
Author(s) -
Ching Yeh Lin,
Jennifer L. Hodgson,
Mansoor Namazian,
Michelle L. Coote
Publication year - 2009
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/jp900649j
Subject(s) - chemistry , hydrogen atom abstraction , abstraction , oniom , computational chemistry , benchmark (surveying) , systematic error , absolute deviation , set (abstract data type) , radical , term (time) , molecule , organic chemistry , statistics , computer science , quantum mechanics , mathematics , physics , philosophy , epistemology , geodesy , geography , programming language
A test set of 21 radical addition and 28 hydrogen abstraction reactions has been studied at the W1, G4, G3X, G3X(MP2), and G3X(MP2)-RAD levels of theory with a view to establishing whether the recently introduced G4 theory offers improved performance over the G3 methods. All methods tested approximated the benchmark W1 values to within a mean absolute deviation (MAD) of 4 kJ mol(-1) or less, although maximum absolute deviations for problematic reactions (such as radical addition to thiocarbonyl compounds) can be as much as 10 kJ mol(-1) for the G3 methods. The new noncanceling higher-level correction (HLC) term in G4 was found to be capable of mitigating these errors in radical addition, but it introduced a systematic error to the reaction energies of the abstraction reactions, and its format may therefore require re-examination. G3 methods were shown to offer "chemical accuracy" even for these problematic cases, provided they were corrected to the W1 level of theory via an ONIOM-based approach.

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