Journal of Molecular Structure p. 80 - 89 (2017)
Update date:2022-08-30
Topics:
Arshad, Muhammad
Jadoon, Mehwish
Iqbal, Zafar
Fatima, Mehwish
Ali, Muhammad
Ayub, Khurshid
Qureshi, Ashfaq Mahmood
Ashraf, Muhammad
Arshad, Muhammad Nadeem
Asiri, Abdullah M.
Waseem, Amir
Mahmood, Tariq
Two new isatin derivatives (E)-N′-(1-allyl-2-oxoindolin-3-ylidene)-4-methylbenzenesulfono-hydrazide (5) and (E)-N′-(1-allyl-2-oxoindolin-3-ylidene)-4-chlorobenzenesulfono-hydrazide (6) were synthesized in good yields by adopting two component synthetic methodology. The structure elucidation was accomplished with the help of UV–vis., FT-IR and NMR (1H and 13C) spectroscopic techniques. Suitable crystals were grown by slow evaporation method and structures were confirmed unequivocally with the help of single crystal X-ray diffraction analysis. Both isatin derivatives 5 and 6 exist in triclinic crystal packing having space group P-1. Crystal structures of both compounds showed that the geometries are stabilized by several intermolecular hydrogen bonds. Quantum mechanical calculations performed at density functional theory (DFT) level confirmed the experimental spectroscopic (UV–vis., FT-IR and 1H NMR) as well as X-ray diffraction results. Kinetic stability, reactivity, electrophilicity and nucleophilic behavior of both the derivatives was elaborated using frontier molecular orbitals (FMOs) and molecular electrostatic potential (MEP) analyses. Enzyme inhibition potential of both compounds was tested in vitro against Bacillus pasteurii urease and both compounds retarded the enzymatic activity with IC50 values of 39.46 ± 0.12 μM and 148.35 ± 0.16 μM respectively.
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