Synthesis, spectroscopic, DFT and in vitro biological studies of vanadium(III) complexes of aryldithiocarbonates

被引:17
作者
Andotra, Savit [1 ]
Kumar, Sandeep [1 ]
Kour, Mandeep [1 ]
Vikas [2 ,3 ]
Chayawan [2 ,3 ]
Sharma, Vishal [4 ,5 ]
Jaglan, Sundeep [4 ,5 ]
Pandey, Sushil. K. [1 ]
机构
[1] Univ Jammu, Dept Chem, Baba Sahib Ambedkar Rd, Jammu 180006, J&K, India
[2] Punjab Univ, Dept Chem, Quantum Chem Grp, Chandigarh 160014, India
[3] Punjab Univ, Ctr Adv Studies Chem, Chandigarh 160014, India
[4] Indian Inst Integrat Med, CSIR, Qual Control & Qual Assurance Div, Canal Rd, Jammu 180001, India
[5] Indian Inst Integrat Med, CSIR, Acad Sci & Innovat Res AcSIR, Canal Rd, Jammu 180001, India
关键词
Dithiocarbonates; Antimicrobial; TGA; Antioxidant; DFT method; NBO ANALYSIS; HOMO-LUMO; COPPER; XANTHATES; SEPARATION;
D O I
10.1016/j.saa.2017.03.003
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Vanadium(III) tris(dithiocarbonates), [(ROCS2)(3)V] (R = o-, m-, p-CH3C6H4 and 4-Cl-3-CH3C6H3) and donor stabilized addition complexes [(ROCS2)(2)V(Cl)center dot V(Cl) center dot L] = NC5H5 or P(C6H5)(3)] were synthesized and characterized by elemental analyses, IR, mass, TGA/DTA, SEM magnetic susceptibility and heteronuclear NMR (H-1, C-13 and P-31) spectroscopic studies. The cytotoxicity of the complexes was measured in vitro using the cultivated human cell lines. In addition, the antioxidant activities of the ligands and its vanadium complexes were also investigated through their scavenging effect on DPPH radicals. The antimicrobial activity of ligands and some complexes has been conducted against three bacterial strains and fungus. The density functional theory (OFF) calculations of ligands and vanadium complexes were performed by the DFT/B3LYP/LANL2DZ method to obtain the optimized molecular geometry, vibrational frequencies, the highest occupied molecular orbital (HOMO), the lowest unoccupied molecular orbital (LUMO), thermodynamic properties and various other quantum-mechanical parameters. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 137
页数:11
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