From Amphiphilic Organic Ligands to Metal-Coordinated Complexes: Structural Difference in Their Self-Organizations Studied by STM
From Amphiphilic Organic Ligands to Metal-Coordinated Complexes: Structural Difference in Their Self-Organizations Studied by STM
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DOI:
10.1021/jp0670790
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发表时间:
2007-03
影响因子:
3.7
通讯作者:
Shan-shan Li;Zhi-Yong Yang;Cunji Yan;Hui-Juan Yan;L. Wan;P. Guo;Minghua Liu
中科院分区:
文献类型:
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作者:
Shan-shan Li;Zhi-Yong Yang;Cunji Yan;Hui-Juan Yan;L. Wan;P. Guo;Minghua Liu
Amphiphilic organic ligands, 5-octadecyloxy-2-(2-pyridylazo)phenol (PARC18) and 1,10-bis[3‘-hydroxy-4‘-(2‘ ‘-pyridylazo)phenoloxy]decane (PAR)2C10, are coordinated with Cu(II) ions, resulting in two complexes. Scanning tunneling microscopy (STM) images provide direct structural evidence for the coordination from organic ligands to resulted complexes. The appearance and conformation differences in ligands and corresponding complexes can be clearly seen in STM images recorded from their self-organizations on highly oriented pyrolytic graphite (HOPG). The adlayer structures of PARC18−Cu and (PAR)2C10−Cu complexes are significantly different from those of their corresponding ligands. A phase separation is found in the adlayer formed with the PARC18 ligand and its complex. The results demonstrate that STM is a powerful tool in coordination chemistry in analyzing ligand and coordinated complex. The coordination from ligands to complexes with metal ions would be a facile approach to surface modification and func...