期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 16, 页码 6150-6153出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja2010434
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资金
- Hong Kong RGC [602008, 602409]
- NSFC [20902020]
- Shanghai Pujiang Talent Program [09PJI403500]
We investigated the thermodynamic processes of two-dimensional (2D) metallo-supramolecular self-assembly at molecular resolution using scanning tunneling microscopy and variable-temperature low-energy electron diffraction. On a Au-(111) substrate, tripyridyl ligands coordinated with Cu in a twofold Cu-pyridyl binding mode or with Fe in a threefold Fe-pyridyl binding mode, forming a 2D open network structure in each case. The network structures exhibited remarkable thermal stability (600 K for the Cu-coordinated network and 680 K for the Fe-coordinated network). The Fe-pyridyl binding was selected thermodynamically as well as kinetically in self-assembly involving both modes. The selectivity can be effectively suppressed in a specifically designed self-assembly route.
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