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Ajani, O.O., Iyaye, K.T., Audu, O.Y., Olorunshola, S.J., Kuye, A.O. and Olanrewaju, I.O. (2018) Microwave Assisted Synthesis and Antimicrobial Potential of Quinoline-Based 4-Hydrazide-Hydrazone Derivatives. Journal of Heterocyclic Chemistry, 55, 302-312.

has been cited by the following article:

• TITLE: Theoretical Investigation on the Stability and Reactivity of Imidazo [1,2-a] Pyridine N-Acylhydrazone Derivatives Using Density Functional Theory

  AUTHORS: Camara Tchambaga Etienne, Sangare Kassoum, Dosso Ouehi, Ablo Evrard, Sekou Diomande, Souleymane Coulibaly, Siomenan Coulibali

  KEYWORDS: N-Acylhydrazones, Imidazo [1, 2-a] Pyridine, DFT, Molecular Electrostatic Potential, Reactivity, Stability

  JOURNAL NAME: Computational Chemistry, Vol.12 No.1, January 31, 2024

  ABSTRACT: The reactivity and stability of seventeen (17) imidazo [1,2-a]pyridine N-acylhydrazone derivatives were investigated using density functional theory at the B3LYP/6-31+ G (d, p) level. Analysis of the molecular electrostatic potential (MEP) and determination of the dual descriptor revealed that in most cases, the nitrogen atoms of the 6-πelectron conjugation, the oxygen, and the sulfur atom are nucleophilic site. Chemical reactivity of the compounds was assessed through analysis of frontier molecular orbitals (HOMO and LUMO), energy gap ( Δℰ ), chemical hardness (η), and the softness (S). Consequently, the compound 9e exhibited the lowest reactivity, least electron donating, and the highest stability. This comprehensive study offers valuable insights into the chemical behavior of these derivatives, crucial for further exploration and potential applications.