Department of Physics, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China.
J Am Chem Soc. 2010 Aug 11;132(31):10756-61. doi: 10.1021/ja1018578.
Surface-supported supramolecular self-assembly has been used to generate multicomponent two-dimensional metal-organic coordination networks on a Au(111) surface. The networks consist of linker ligands of 4',4''''-(1,4-phenylene)bis(2,2':6',2''-terpyridine) and nodal ligands of 5,10,15,20-tetra(4-pyridyl)porphyrin that are connected by pyridine-Fe-terpyridine motifs. Scanning tunneling microscopy revealed the coexistence of two polymorphic types of network structures (rhombus and Kagome). Through control of the dosage of the constituent ligands, homogeneous structural phases were obtained selectively. In particular, the rhombus structure could be converted into the more complex and more open Kagome structure by inclusion of guest molecules. Finally, coordination networks providing structural and chemical homogeneity were realized by judiciously choosing the dosages of the constituent ligands and the chemical substitution of the porphyrin ligands.
表面支撑的超分子自组装已被用于在 Au(111)表面上生成多组分二维金属-有机配位网络。这些网络由连接配体 4',4''''-(1,4-亚苯基)双(2,2':6',2''-三联吡啶)和节点配体 5,10,15,20-四(4-吡啶基)卟啉组成,通过吡啶-Fe-三联吡啶基序连接。扫描隧道显微镜揭示了两种晶型的网络结构(菱形和 Kagome 型)共存。通过控制组成配体的用量,可以有选择性地获得均匀的结构相。特别是,通过包含客体分子,菱形结构可以转化为更复杂和更开放的 Kagome 结构。最后,通过巧妙地选择组成配体的用量和卟啉配体的化学取代,实现了具有结构和化学均一性的配位网络。