Université Joseph Fourier Grenoble I, Département de Chimie Moléculaire, UMR CNRS-5250, Institut de Chimie Moléculaire de Grenoble, FR CNRS-2607, BP 53, 38041, Grenoble Cedex 9, France.
Inorg Chem. 2010 Mar 15;49(6):2592-9. doi: 10.1021/ic901832q.
Soluble homo- and heterometallic coordination polymers containing transition metal cations (Cu(2+), Fe(2+), Co(2+), and Ni(2+) ions) were prepared in a two-step procedure using a polytopic bis(terpyridine)dioxocyclam ligand 1H(2) (dioxocyclam = 1,4,8,11-tetraazacyclotetradecane-5,7-dione). These supramolecular systems incorporate two different metal complexes, the metal cations being located both between two terpyridine units and in the macrocyclic framework. The characterization of these soluble architectures was investigated by cyclic voltammetry, mass spectrometry, viscosimetry, and UV-vis absorption and electron paramagnetic resonance (EPR) spectroscopies. Our results clearly indicate the formation of well-organized heterometallic polymers in which two different metal ions alternate in the self-assembled structure. These investigations furthermore brought to light an original acid-controlled disassembling process of the homometallic copper(II) polymer into dinuclear complexes.
采用多齿双(三吡啶基)二氧环戊二烯配体 1H(2)(dioxocyclam = 1,4,8,11-四氮杂环十四烷-5,7-二酮)通过两步法制备了含有过渡金属阳离子(Cu(2+)、Fe(2+)、Co(2+)和 Ni(2+)离子)的均相和杂相配位聚合物。这些超分子体系包含两个不同的金属配合物,金属阳离子位于两个三吡啶单元之间和大环骨架中。通过循环伏安法、质谱法、粘度法、紫外可见吸收光谱和电子顺磁共振(EPR)光谱研究了这些可溶性结构的特性。我们的结果清楚地表明,在自组装结构中形成了组织良好的杂金属聚合物,其中两个不同的金属离子交替存在。这些研究还揭示了一种新颖的酸控制的同核铜(II)聚合物解组装过程,形成双核配合物。