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Richard, R.M., Lao, K.U. and Herbert, J.M. (2013) Achieving the CCSD (T) Basis-Set Limit in Sizable molecular Clusters: Counterpoises Corrections for the Many-Bady Expansion. The Journal of Physical Chemistry, 4, 2674-2680.

has been cited by the following article:

• TITLE: Quantum Chemical Characterization of Hydrogen Bonding Sites in Three 4-(4-Halo-Phenyl)-6-(Furan-2-yl) Pyrimidin-2-Amine Derivatives

  AUTHORS: Yafigui Traore, Kafoumba Bamba, Nahossé Ziao, Sopi Thomas Affi, Mamadou Guy-Richard Kone

  KEYWORDS: Analgesic, Hydrogen Bonding, Pyrimidine Derivatives, Quantum Chemistry

  JOURNAL NAME: Computational Chemistry, Vol.5 No.3, July 5, 2017

  ABSTRACT: Hydrogen bonding (HB) sites in three pyrimidine compounds derivatives (DP), namely 4-(4-fluorophenyl)-6-(furan-2-yl) pyrimidin-2-amine (DP-1), 4-(4-chlorophenyl)-6-(furan-2-yl) pyrimidin-2-amine (DP-2) and 4-(4-bromophenyl)-6-(furan-2-yl) pyrimidin-2-amine (DP-3), have been investigated by quantum chemistry methods, especially at HF/6-311+G(d,p) and B3PW91/6-311+G(d,p) levels. Hydrogenfluori deserved as probe for hydrogen bonding complexes. Molecular electrostatic potential maps, geometricparameters of HB complexes, as well as energetic parameters of the complexation reactions have been computed. Finally, one out of two nitrogen atoms of pyrimidine nucleus has been identified as the major hydrogen bonding site in the three pyrimidine derivatives, with respective percentages of around 83.0% and 93.2% at HF/6-311+G(d,p) and B3PW91/6-311+G(d,p) levels.