Stannoxane capping derived from chiral tridentate NN donor ligand for nickel and copper macrocycles: Comparative binding studies of stannoxane moiety and its modulated copper complex with CTDNA

被引:35
作者
Chauhan, Mala [1 ]
Arjmand, Farukh [1 ]
机构
[1] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
关键词
stannoxane capping; binding studies; CT-DNA; 5'GMP; UV-Vis; fluorescence; cyclic voltammetry;
D O I
10.1016/j.jorganchem.2007.07.044
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Novel stannoxane type dinuclear tin complex C16H13N4O2Sn2Cl7 (1) and its modulated macrocyclic complexes [C24H36N10O3Sn2CUCl7] ClO4 (2) and [C24H34N10O2Sn2NiCl7) ClO4 (3) were synthesized and characterized by elemental analysis and various spectroscopic techniques (1R, H-1, C-13, Sn-119 NMR, ESI-MS, EPR and UV-Vis). Sn-119 NMR shows the presence of two tin metal centers in different environment. The proposed pseudo-octahedral geometry of copper in complex 2 and square pyramidal geometry of nickel in complex 3 were established by the analysis of spectroscopic data. Absorption and fluorescence spectral studies and viscosity measurements have been carried out to assess the comparative binding of dinuclear stannoxane complex 1 and its modulated copper complex 2 with calf thymus DNA. The intrinsic binding constants K-b of the complex 1 and 2 were determined as 4.4 x 10(4) M-1 and 7.5 x 10(4) M-1, respectively. Cyclic voltammetric studies have also been employed to ascertain the binding of complex 2 with CTDNA. The results suggest that the complex 2 binds to CTDNA twice in the order of magnitude compared to complex 1. Interaction studies of complex 2 with guanosine 5'-monophosphate further confirm the binding via N-7 position of guanine and phosphate moiety. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:5156 / 5164
页数:9
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