Chemical Laboratory, Central Leather Research Institute (Council of Scientific and Industrial Research), Adyar, Chennai, 600 020, India.
Dalton Trans. 2010 Feb 28;39(8):2087-97. doi: 10.1039/b913464f. Epub 2010 Jan 8.
Two new mixed ligand complexes of cobalt(iii) containing ancillary biimidazole ligands, Co(phen)(2)H(2)biim(3).0.5(H(7)O(3))(ClO(4)) (1) and Co(bpy)(2)H(2)biim(3).3H(2)O (2) have been synthesized and characterized by various spectroscopic and electrochemical techniques. Both complexes and , have been characterized by the single crystal X-ray diffraction method. While cobalt complex was found to crystallize in the triclinic system with the P1[combining macron] space group, complex was found to crystallize in the orthorhombic system with the Pbca space group. The unit cell packing of complex shows the presence of a water cluster, which is buttressed by oxygen atoms present in the perchlorate anions and water with an average OO bond distance of 2.41-2.86 A. Interaction of these complexes with calf thymus DNA (CT-DNA) was investigated by electronic spectral titrations. The results suggest that complexes and bind to DNA through the groove via hydrogen bonding. This is due to the presence of -NH in the ancillary ligand biimidazole, which favors hydrogen bonding with DNA base pairs. The intrinsic DNA binding constant values for complexes and were found to be (5.18 +/-0.23) x 10(4) M(-1) and (1.26 +/- 0.13) x 10(4) M(-1) respectively. Groove binding of these complexes with DNA is further supported by viscosity measurements, thermal denaturation and circular dichroism studies. Among the two cobalt complexes, complex possesses greater DNA binding strength due to the presence of the conjugated aromatic structure of the phen ligand which increases the hydrophobic interactions with DNA. DNA cleavage experiments using plasmid DNA pUC 18 show that these complexes exhibit efficient photonuclease activity in the presence of molecular oxygen.
两种新的钴(III)配合物,包含辅助双咪唑配体,Co(phen)(2)H(2)biim(3).0.5(H(7)O(3))(ClO(4))(1)和Co(bpy)(2)H(2)biim(3).3H(2)O(2),已经通过各种光谱和电化学技术合成并表征。这两种配合物和,都已经通过单晶 X 射线衍射方法进行了表征。钴配合物被发现结晶于三斜晶系,空间群为 P1[combining macron],而配合物则被发现结晶于正交晶系,空间群为 Pbca。配合物的单元晶胞堆积显示存在一个水分子簇,该水分子簇由过氯酸阴离子和水中的氧原子支撑,平均 OO 键距离为 2.41-2.86Å。通过电子光谱滴定法研究了这些配合物与小牛胸腺 DNA(CT-DNA)的相互作用。结果表明,配合物和通过氢键与 DNA 沟槽结合。这是由于辅助配体双咪唑中的-NH 存在,有利于与 DNA 碱基对形成氢键。配合物和的固有 DNA 结合常数分别为(5.18 +/-0.23) x 10(4) M(-1)和(1.26 +/- 0.13) x 10(4) M(-1)。这些配合物与 DNA 的沟槽结合进一步得到了粘度测量、热变性和圆二色性研究的支持。在这两种钴配合物中,由于 phen 配体的共轭芳香结构的存在,增加了与 DNA 的疏水相互作用,因此配合物具有更强的 DNA 结合能力。使用质粒 DNA pUC 18 的 DNA 切割实验表明,这些配合物在分子氧存在下具有有效的光解酶活性。