Noncovalent Interactions and Structural Investigation Via SC-XRD and
Quantum Chemical Studies of Newly Synthesized O-Benzenesulfonylated
Pyrimidines
Abstract
In the current research chor, we are reporting the synthesis of
2-amino-6-methylpyrimidin-4-yl benzenesulfonate (AMPBS) and
2,6-diaminopyrimidin-4-yl benzenesulfonate (DAPBS) via
O-benzenesulfonylation of 2-amino-6-methylpyrimidin-4-ol 1 and
2,6-diaminopyrimidin-4-ol 2 respectively. The structures of the
synthesized compounds were characterized unambiguously by single crystal
analysis (SC-XRD).Hirshfeld surface study showed that C-H…O,
C-H…N and especially C-H…C hydrogen bond interactions are
the key contributors to the intermolecular stabilisation in the crystal.
The quantum chemical understanding about optimized geometry, natural
bond orbitals (NBOs), frontier molecular orbitals (FMOs) and nonlinear
optical (NLO) analysis for AMPBS and DAPBS were obtained by applying
density functional theory (DFT) at B3LYP level and 6-311G(d,p) basis
set. Time dependent density functional theory (TD-DFT)/ B3LYP/
6-311G(d,p) level were employed to determine the photo physical
properties of compounds. As a whole, the simulated results were found to
have an excellent concurrence to the experimental results. The charge
transfer phenomenon entitled compounds was determined by FMOs. Global
reactivity parameters were obtained by using HOMO–LUMO energies of
compounds. Overall, the computational results of AMPBS and DAPBS have
outstanding agreement to experimental data. The computational study also
showed that the title compounds have remarkable NLO properties.