Title:
N-(naphthyl)-N′-(methoxy carbonyl)thiocarbamide and its Cu(I) complex: Synthesis, spectroscopic, X-ray, DFT and in vitro cytotoxicity study

dc.contributor.authorDurga P. Singh
dc.contributor.authorSeema Pratap
dc.contributor.authorSunil K. Pandey
dc.contributor.authorRay J. Butcher
dc.contributor.authorGaetano Marverti
dc.date.accessioned2026-02-07T06:12:23Z
dc.date.issued2015
dc.description.abstractThe structural characterization of two new compounds N-naphthyl-N′-methoxycarbonyl thiocarbamide (NMCT) (1) and its Cu(I) complex, bis(N-naphthyl-N′-methoxycarbonyl thiocarbamide) copper(I) chloride [(NMCT)2CuCl] (1a) have been done by spectroscopic techniques (FT-IR, 1H NMR, 13C NMR and electronic spectroscopy) and X-ray crystallography. To get a deeper insight of vibrational frequencies and electronic transitions, DFT and TD-DFT studies have also been performed. X-ray study revealed trigonal planar geometry around copper(I). The ligand coordinates through thione sulfur only. The cytotoxicity of 1 and 1a has been assayed in five human carcinoma cell lines, 2008, C13∗ (cervical carcinoma), A2780, A2780/CP and IGROV-1 (ovarian carcinoma). Both the compounds exhibited cytotoxicity. The inhibitory activity of copper complex was better than ligand against all the cell lines. © 2014 Taylor & Francis.
dc.identifier.doi10.1080/00958972.2014.979165
dc.identifier.issn958972
dc.identifier.urihttps://doi.org/10.1080/00958972.2014.979165
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/28095
dc.publisherTaylor and Francis Ltd.
dc.subjectCytotoxicity
dc.subjectDFT study
dc.subjectN-Naphthyl-N′-methoxycarbonyl thiocarbamide
dc.subjectSpectral techniques
dc.subjectTrigonal planar geometry
dc.subjectX-ray crystallography
dc.titleN-(naphthyl)-N′-(methoxy carbonyl)thiocarbamide and its Cu(I) complex: Synthesis, spectroscopic, X-ray, DFT and in vitro cytotoxicity study
dc.typePublication
dspace.entity.typeArticle

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