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	<dc:title xml:lang="en-US">Synthesis, physicochemical characterisation and DNA binding study of a novel azo Schiff base Ni(II) complex</dc:title>
	<dc:creator>Singha, Uttam Kumar</dc:creator>
	<dc:creator>Pradhan, Sudarshan</dc:creator>
	<dc:creator>Mishra, Dipu Kumar</dc:creator>
	<dc:creator>Gurung, Pritika</dc:creator>
	<dc:creator>Chettri, Anmol</dc:creator>
	<dc:creator>Sinha, Biswajit</dc:creator>
	<dc:subject xml:lang="en-US">CT-DNA</dc:subject>
	<dc:subject xml:lang="en-US">Ni(II) complex</dc:subject>
	<dc:subject xml:lang="en-US">Azo Schiff base</dc:subject>
	<dc:subject xml:lang="en-US">DNA binding study</dc:subject>
	<dc:subject xml:lang="en-US">Molecular docking</dc:subject>
	<dc:subject xml:lang="en-US">DNA cleavage study</dc:subject>
	<dc:description xml:lang="en-US">The azo Schiff base ligand was synthesised, along with its Ni(II) complex, by diazotisation of salicylaldehyde with 4-nitroaniline in accordance with the accepted literature approach. Using a variety of spectroscopic techniques, the resulting complex is analysed both quantitatively and qualitatively (Elemental analysis, FT-IR spectroscopy, UV-VIS spectroscopy, 1H NMR, etc.). Spectral measurements of the complex revealed a mole ratio of 1:1. The non-electrolytic nature of the complex is confirmed by molar conductance investigation. The unique azo compound had a tetrahedral shape as a result of the tetra coordination of two phenolic oxygen and two imine nitrogen. The ability of the metal complexes to bind DNA was examined using absorption spectroscopy, fluorescence spectroscopy, viscosity tests, and thermal denaturation methods. Experimental research suggests that complexes bind to DNA through intercalation.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2023-06-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/2375</dc:identifier>
	<dc:identifier>10.5155/eurjchem.14.2.280-286.2375</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 14 No. 2 (2023): June 2023; 280-286</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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	<dc:rights xml:lang="en-US">Copyright (c) 2023 Authors</dc:rights>
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