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Combined ab initio and density functional study of ring chain tautomerism in benzofurazan‐1‐oxide
Author(s) -
Rauhut Guntram
Publication year - 1996
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/(sici)1096-987x(199612)17:16<1848::aid-jcc5>3.0.co;2-n
Subject(s) - tautomer , ab initio , density functional theory , computational chemistry , ring (chemistry) , transition state , chemistry , chain (unit) , hybrid functional , thermodynamics , physics , quantum mechanics , stereochemistry , catalysis , organic chemistry
Abstract The ring chain tautomerism of benzofurazan‐1‐oxide (benzofuroxan) has been reinvestigated using ab initio as well as nonlocal density functional theory. The failure in predicting energies and geometries of this reaction by wave functions at the Hartree‐Fock or even at the MP2 level could be overcome by using the nonlocal three‐parameter hybrid exchange correlation functional of Becke and Lee, Young, and Parr (B3‐LYP). Two possible reaction paths via ortho ‐dinitrosobenzene have been studied, considering both ground and transition states. At the B3‐LYP level of theory, both mechanisms show very similar activation energies which are in excellent agreement with experimental results. Solvent effects, simulated by a self‐consistent reaction field (SCRF) model, cause alternations in the preferred mechanism as well as in the most stable intermediates. © 1996 by John Wiley & Sons, Inc.

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