π-Conjugated bis(terpyridine) metal complex molecular wires

被引:124
|
作者
Sakamoto, Ryota [1 ]
Wu, Kuo-Hui [1 ]
Matsuoka, Ryota [1 ]
Maeda, Hiroaki [1 ]
Nishihara, Hiroshi [1 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
关键词
SELF-ASSEMBLED MONOLAYERS; RANGE ELECTRON-TRANSFER; BY-LAYER GROWTH; REDOX CONDUCTION; OLIGOMER WIRES; CARBON NANOTUBES; THIN-FILMS; ZINC TETRAPYRIDYLPORPHYRIN; ELECTROCHEMICAL-BEHAVIOR; PHOTOCURRENT GENERATION;
D O I
10.1039/c5cs00081e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bottom-up approaches have gained significant attention recently for the creation of nano-sized, ordered functional structures and materials. Stepwise coordination techniques, in which ligand molecules and metal sources are reacted alternatively, offer several advantages. Coordination bonds are stable, reversible, and self-assembling, and the resultant metal complex motifs may contain functionalities unique to their own characteristics. This review focuses on metal complex wire systems, specifically the bottom-up fabrication of linear and branched bis(terpyridine) metal complex wires on electrode surfaces. This system possesses distinct and characteristic electronic functionalities, intra-wire redox conduction and excellent long-range electron transport ability. This series of comprehensive studies exploited the customizability of bis(terpyridine) metal complex wires, including examining the influence of building blocks. In addition, simple yet effective electron transfer models were established for redox conduction and long-range electron transport. A fabrication technique for an ultra-long bis(terpyridine) metal complex wire is also described, along with its properties and functionalities.
引用
收藏
页码:7698 / 7714
页数:17
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