V. Petrov, N. Giricheva, G. Girichev
Mar 31, 2011
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Journal
Journal of Structural Chemistry
Abstract
A combined gas electron diffraction and quantum chemical (B3LYP/6-311+G**, B3LYP/cc-pVTZ) study of the molecular structure of 2-nitrobenzenesulfonic acid (2-NBSA) is performed. Quantum chemical calculations show that the 2-NBSA molecule has five conformers, and the Gibbs energy of one of them is lower by more than 4.5 kcal/mol than the energy of the other conformers. It is found experimentally that the saturated vapor of 2-NBSA at T = 394(5) K contains only the low-energy conformer that has an intramolecular hydrogen bond between the H atom of the hydroxyl group and one of the O atoms of the NO2 group. The C-C-S-O(H) torsion angle determining the position of the S-O(H) bond is −72(7)°, while the NO2 group is substantially turned relative to the benzene ring plane (C1-C2-N-O = 40(5)°). The following experimental values of the internuclear distances are obtained for this conformer (Å): rh1(C-H)av = 1.07(2), rh1(C-C)av = 1.401(4), rh1(C-S) = 1.767(6), rh1(S=O)av = 1.412(4), rh1(S-O) = 1.560(6), rh1(N-O)av = 1.217(5), rh1(C-N) = 1.461(8), rh1(O-H) = 0.99(3).