Departments of †Polymer Science and ‡Chemistry, The University of Akron , 170 University Cr., Akron, Ohio 44325, United States.
J Am Chem Soc. 2014 Dec 31;136(52):18149-55. doi: 10.1021/ja511341z. Epub 2014 Dec 19.
A terpyridine-based, concentration-dependent, facile self-assembly process is reported, resulting in two three-dimensional metallosupramolecular architectures, a bis-rhombus and a tetrahedron, which are formed using a two-dimensional, planar, tris-terpyridine ligand. The interconversion between these two structures is concentration-dependent: at a concentration higher than 12 mg mL(-1), only a bis-rhombus, composed of eight ligands and 12 Cd(2+) ions, is formed; whereas a self-assembled tetrahedron, composed of four ligands and six Cd(2+) ions, appears upon sufficient dilution of the tris-terpyridine-metal solution. At concentrations less than 0.5 mg mL(-1), only the tetrahedron possessing an S4 symmetry axis is detected; upon attempted isolation, it quantitatively reverts to the bis-rhombus. This observation opens an unexpected door to unusual chemical pathways under high dilution conditions.
报道了一种基于三吡啶的、浓度依赖的、简便的自组装过程,得到了两种三维金属超分子结构,一种是双菱形,另一种是四面体,它们是由二维、平面的三吡啶配体形成的。这两种结构之间的相互转化是浓度依赖的:在浓度高于 12 mg mL(-1)时,只形成由八个配体和 12 个 Cd(2+)离子组成的双菱形;而当三吡啶-金属溶液充分稀释时,会出现由四个配体和六个 Cd(2+)离子组成的自组装四面体。在浓度小于 0.5 mg mL(-1)时,只检测到具有 S4 对称轴的四面体;当试图分离时,它定量地返回到双菱形。这一观察结果为在高稀释条件下的异常化学途径开辟了一扇意想不到的大门。