Premium
Theoretical calculation of bond dissociation energies and heats of formation for nitromethane and polynitromethanes with density functional theory
Author(s) -
Su Xinfang,
Cheng Xinlu,
Liu Yonggang,
Li Qinghuan
Publication year - 2006
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.21155
Subject(s) - density functional theory , nitromethane , chemistry , hybrid functional , dissociation (chemistry) , bond dissociation energy , yield (engineering) , computational chemistry , standard enthalpy of formation , thermodynamics , physics , organic chemistry
The CNO 2 bond dissociation energies (BDEs) and the heats of formation (HOFs) of nitromethane and polynitromethanes (dinitromethane, trinitromethane, and tetranitromethane) system in gas phase at 298.15 K were calculated theoretically. Density functional theory (DFT) B3LYP, B3P86, B3PW91, and PBE0 methods in combination with different basis sets were employed. It was found that the CNO 2 bond BDEs can be improved from B3LYP to B3PW91 to B3P86 or PBE0 functional. Levels of theory employing B3P86 and PBE0 functionals were found to be sufficiently reliable without the presence of diffusion functions. As the number of NO 2 groups on the same C atom increases, the PBE0 functional performs better than the B3P86 functional. Regarding the calculated HOFs, all four functionals can yield satisfactory results with deviations of <2 kcal mol −1 from experimental ones for CH 2 (NO 2 ) 2 and CH(NO 2 ) 3 , when the diffusion functions are not augmented. For the C(NO 2 ) 4 molecule, the large basis sets augmented with polarization functions and diffusion functions are required to yield a good result. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007