Synthesis, characterization, cytotoxicity and antimicrobial studies on Bi(III) dithiocarbamate complexes containing furfuryl group and their use for the preparation of Bi₂O₃ nanoparticles

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• 作者：Sundaramoorthy Tamilvanan^a ; Govindasamy Gurumoorthy^b ; Subbiah Thirumaran^b ; ^{sthirumaran@yahoo.com} ; Samuele Ciattini^c
• 关键词：Bismuth(III) dithiocarbamates ; Antimicrobial ; Cytotoxicity ; Bismuth oxide nanoparticles ; Photodegradation
• 刊名：Polyhedron
• 出版年：2017
• 出版时间：10 January 2017
• 年：2017
• 卷：121
• 期：Complete
• 页码：70-79
• 全文大小：2977 K
• 卷排序：121

文摘

Bismuth(III) dithiocarbamate complexes, tris(N-furfuryl-N-propyldithiocarbamato-S,S′)bismuth(III) (1), tris(N-furfuryl-N-butyldithiocarbamato-S,S′)bismuth(III) (2) and tris(N-furfuryl-N-benzyldithiocarbamato-S,S′)bismuth(III) (3), have been prepared and characterized by microanalysis, and spectroscopy (IR and NMR). Structure of 3 has been obtained by single crystal X-ray diffraction. This complex contains distorted pentagonal pyramidal Bi(III) centres which attain an overall distorted pentagonal bipyramidal coordination via long range intermolecular Bi⋯S interactions. DFT quantum mechanical studies of 3 were carried out, supporting the partial double bond character of C–N (thioureide) and C–S bonds in dithiocarbamate ligands. All the compounds have been screened against a panel of microbes viz. Vibrio cholerae, Bacillus subtilis, Klebsiella pneumoniae, Escherichia coli, Staphylococcus aureus, Aspergillus niger and Candida albicans. Complexes 1 and 3 were found to have better activity against K. pneumoniae, V. cholerae, A. niger and C. albicans than the complex 2. Complexes 1–3 have been evaluated for their in vitro cytotoxic activity against KB cells. Complexes 1 and 3 showed higher activity than 2. Bi2O3 obtained from thermal decomposition of 3 has been characterized by PXRD, HRTEM, EDAX, UV–Vis and Fluorescence spectroscopy. PXRD study showed that the sample is composed of monoclinic phase of α-Bi2O3. Photocatalytic activity of as-prepared α-Bi2O3 was determined by decolourization of rhodamine-B in aqueous solution under ultra violet irradiation.