Literature DB >> 24747930

Synthesis, characterization, crystal structure and theoretical study of a compound with benzodiazole ring: antimicrobial activity and DNA binding.

P Latha1, P Kodisundaram1, M L Sundararajan1, T Jeyakumar2.   

Abstract

2-(Thiophen-2-yl)-1-((thiophen-2-yl)methyl)-1H-1,3-benzodiazole (HL) is synthesized and characterized by elemental analysis, UV-Vis, FT-IR, (1)H, (13)C NMR, mass spectra, scanning electron microscope (SEM) and single crystal X-ray diffraction. The crystal structure is stabilized by intermolecular CH⋯N and CH⋯π interactions. The molecular structure is also optimized at the B3LYP/6-31G level using density functional theory (DFT). The structural parameters from the theory are nearer to those of crystal, the calculated total energy of coordination is -1522.814a.u. The energy of HOMO-LUMO and the energy gap are -0.20718, -0.04314, 0.16404a.u, respectively. All data obtained from the spectral studies support the structural properties of the compound HL. The benzimidazole ring is essentially planar. The in vitro biological screening effects of the synthesized compound is tested against four bacterial and four fungal strains by well diffusion method. Antioxidant property and DNA binding behaviour of the compound has been investigated using spectrophotometric method.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  1,2-Phenylenediamine; 2-Thiophenecarboxaldehyde; DFT; DNA binding; X-ray crystallography

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Year:  2014        PMID: 24747930     DOI: 10.1016/j.saa.2014.03.067

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  1 in total

1.  Evaluation of DNA Binding, Radicals Scavenging and Antimicrobial Studies of Newly Synthesized N-Substituted Naphthalimides: Spectroscopic and Molecular Docking Investigations.

Authors:  Pattan Sirajuddin Nayab; Madhusudana Pulaganti; Suresh Kumar Chitta; Mohammad Abid; Rahis Uddin
Journal:  J Fluoresc       Date:  2015-10-13       Impact factor: 2.217

  1 in total

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