Datta Amitabha, Das Kuheli, Sen Chandana, Karan Nirmal Kumar, Huang Jui-Hsien, Lin Chia-Her, Garribba Eugenio, Sinha Chittaranjan, Askun Tulin, Celikboyun Pinar, Mane Sandeep B
Department of Physics, Faculty of Sciences and Arts, University of Balikesir, Cagis Campus, 10145 Balikesir, Turkey.
Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata 700032, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Sep 5;148:427-34. doi: 10.1016/j.saa.2015.04.014. Epub 2015 Apr 15.
Doubly end-on azido-bridged mixed-valence trinuclear cobalt complex, [Co3(L)2(N3)6(CH3OH)2] (1) is afforded by employing a potential monoanionic tetradentate-N2O2 Schiff base precursor (2-[{[2-(dimethylamino)ethyl]imino}methyl]-6-methoxyphenol; HL). Single crystal X-ray structure reveals that in 1, the adjacent Co(II) and Co(III) ions are linked by double end-on azido bridges and thus the full molecule is generated by the site symmetry of a crystallographic twofold rotation axis. Complex 1 is subjected on different spectral analysis such as IR, UV-vis, emission and EPR spectroscopy. On variable temperature magnetic study, we observe that during cooling, the χMT values decrease smoothly until 15K and then reaches to the value 1.56 cm(3) K mol(-1) at 2 K. Complex 1 inhibits the cell growth on human lung carcinoma (A549 cells), human colorectal (COLO 205 and HT-29 cells), and human heptacellular (PLC5 cells) carcinoma cells. Complex 1 exhibits anti-mycobacterial activity and considerable efficacy on Mycobacterium tuberculosis H37Rv ATCC 27294 and H37Ra ATCC 25177 strains.
通过使用一种潜在的单阴离子四齿 - N₂O₂席夫碱前体(2 - [{[2 - (二甲氨基)乙基]亚氨基}甲基] - 6 - 甲氧基苯酚;HL),得到了双端基叠氮桥连的混合价态三核钴配合物[Co₃(L)₂(N₃)₆(CH₃OH)₂] (1)。单晶X射线结构表明,在1中,相邻的Co(II)和Co(III)离子通过双端基叠氮桥相连,因此整个分子由晶体学二重旋转轴的点对称性生成。对配合物1进行了不同的光谱分析,如红外光谱、紫外可见光谱、发射光谱和电子顺磁共振光谱。在变温磁性研究中,我们观察到在冷却过程中,χMT值平稳下降,直到15K,然后在2K时达到1.56 cm³K mol⁻¹的值。配合物1抑制人肺癌(A549细胞)、人结肠直肠癌(COLO 205和HT - 29细胞)以及人肝癌(PLC5细胞)癌细胞的生长。配合物1对结核分枝杆菌H37Rv ATCC 27294和H37Ra ATCC 25177菌株表现出抗分枝杆菌活性和显著疗效。