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Synthesis, structural and spectral properties of Au complexes: luminescence properties and their non-covalent DNA binding studies

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dc.contributor.author Huerta-Aguilar, C.
dc.contributor.author Gómez, J. M. T.
dc.contributor.author Thangarasu, P.
dc.contributor.author Camacho-Arroyo, I.
dc.contributor.author González-Arenas, A.
dc.contributor.author Narayanan, J.
dc.contributor.author Srivastava, R.
dc.date.accessioned 2021-10-26T18:51:27Z
dc.date.available 2021-10-26T18:51:27Z
dc.date.issued 2021-10-27
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/3144
dc.description.abstract Gold complexes of 1,3- bis-pyridylimidazolium chloride (L1 ), 1,3-bis-[2,6-diisopropylphenyl]imidazolium chloride (L2 ) and 1,3-bis-[benzyl]benzimidazolium chloride (L3 ) were synthesized and characterized by analytical methods. For the complexes, electronic spectral results show that there is a marked difference in the band feature observed in the spectra, ascribed to the greater relativistic effect of gold. In fluorescence studies, the complexes develop emission bands in the visible region (400–600 nm) after excitation at around 350 nm. Au complex–DNA binding was studied, and it was observed that genomic DNA isolated from the U373-GB cell line was fragmented and in some cases degraded by the Au complexes. Furthermore, the intensity of the DNA band increased when concentration of the metal complex was augmented. This study shows that the DNA cleavage is mediated by the Au complex. Copyright en_US
dc.language.iso en_US en_US
dc.subject gold complexes en_US
dc.subject DNA binding en_US
dc.subject DFT en_US
dc.title Synthesis, structural and spectral properties of Au complexes: luminescence properties and their non-covalent DNA binding studies en_US
dc.type Article en_US


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