Crystallographic and first-principles density functional theory study on the structure,noncovalent interactions,and chemical reactivity of 1,5-benzodiazepin-2-ones derivatives |
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Authors: | Melek Hajji Hasan Mtiraoui Nesrine Amiri Moncef Msaddek Taha Guerfel |
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Institution: | 1. Research Unit: Electrochemistry, Materials and Environment, University of Kairouan, Kairouan, Tunisia;2. Laboratory of Heterocyclic Chemistry, Natural Products and Reactivity CHPNR, Faculty of Science of Monastir, University of Monastir, Monastir, Tunisia;3. Laboratory of Physical Chemistry of Materials, Avenue of the Environment, University of Monastir, Monastir, Tunisia |
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Abstract: | The present work arose out of a desire to fundamentally understand the molecular geometry, weak interactions, electron density delocalization, and chemical reactivity features of 1,5-benzodiazepines-containing family. Herein, a complete X-ray crystallographic study, supported by trustworthy sets of computational approaches, has been reported for two organic crystals. Quantifying intramolecular and intermolecular interactions by Hirshfeld-Becke surfaces analysis conjointly with noncovalent interaction-reduced density gradient topological study revealed that supramolecular assemblies are stabilized by N-H … O (inter) and O-H … N (intra) hydrogen bonds, Cg … Cg (π … π) and C-H(O) … π intercontacts, as well as Van der Waals interactions and steric effects. The long-range-corrected functional wB97XD, which uses Grimme's D2 dispersion model, seems to be just right for our systems. The quantum theory of atoms in molecules analysis confirms that both significant O1-H1…N1 and N2-H2A…O2 H-bonds are weak and electrostatic in nature. Furthermore, global reactivity indices computed via the conceptual density functional theory framework allows these molecules to be classified as moderate electrophiles and marginal nucleophiles. The active sites favorable for nucleophilic/electrophilic attacks were also predicted based on local Parr functions. Finally, a comparative evaluation on the aromaticity character and π-π stacking ability has been done for different (pseudo) rings. |
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Keywords: | 1 5-benzodiazepines aromaticity conceptual DFT reactivity indices NCI-QTAIM topological analyses noncovalent interactions |
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