Senthilkumar Kabali, Gopalakrishnan Mohan, Palanisami Nallasamy
Materials Chemistry Division, School of Advanced Sciences, VIT University, Vellore 632014, Tamilnadu, India.
Materials Chemistry Division, School of Advanced Sciences, VIT University, Vellore 632014, Tamilnadu, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Sep 5;148:156-62. doi: 10.1016/j.saa.2015.03.133. Epub 2015 Apr 4.
A mixed Cd(II) complex {[Cd(FcCOO)2(dpyam)(H2O)][Cd(dpyam)2 (H2O)2]·(ClO4)2·CH3OH} (1) (where FcCOO=ferrocenecarboxylic acid and dpyam=2,2'-dipyridylamine), has been synthesized and characterized by FT-IR, (1)H &(13)C NMR, UV-Vis spectroscopy and elemental analysis. The molecular structure of compound 1 has been determined by the single crystal X-ray diffraction technique, which consists of mixed two different cadmium(II) complexes and two uncoordinated perchlorate ions. The crystal packing shows that the compound 1 self-assembled by intermolecular hydrogen bonding via pyridyl N-H⋯O and coordinated water O⋯H-O-H⋯O, to afford the molecule 2D supramolecular network. Compound 1 exhibits high-energy intraligand (π-π(∗)) fluorescence emission. In electrochemical studies of compound 1 shows negative potential compared with ferrocenecarboxylic acid due to formation of coordination complex with Cd ions. The antibacterial study against the distinct bacterial strains show compound 1 has significant activity.
一种混合镉(II)配合物{[Cd(FcCOO)₂(dpyam)(H₂O)][Cd(dpyam)₂ (H₂O)₂]·(ClO₄)₂·CH₃OH}(1)(其中FcCOO = 二茂铁羧酸,dpyam = 2,2'-联吡啶胺)已通过傅里叶变换红外光谱、¹H和¹³C核磁共振、紫外可见光谱和元素分析进行了合成与表征。化合物1的分子结构已通过单晶X射线衍射技术确定,它由两种不同的镉(II)配合物和两个未配位的高氯酸根离子组成。晶体堆积表明,化合物1通过吡啶基N - H⋯O和配位水O⋯H - O - H⋯O的分子间氢键自组装,形成二维超分子网络。化合物1表现出高能的配体内(π - π*)荧光发射。在化合物1的电化学研究中,由于与镉离子形成配位络合物,与二茂铁羧酸相比显示出负电位。对不同细菌菌株的抗菌研究表明化合物1具有显著活性。