Self-Assembly of Metallo-Supramolecules with Dissymmetrical Ligands and Characterization by Scanning Tunneling Microscopy

被引:37
|
作者
Shi, Junjuan [1 ,2 ]
Li, Yiming [2 ,3 ]
Jiang, Xin [1 ]
Yu, Hao [1 ]
Li, Jiaqi [1 ]
Zhang, Houyu [1 ]
Trainer, Daniel J. [4 ]
Hla, Saw Wai [4 ]
Wang, Heng [2 ]
Wang, Ming [1 ]
Li, Xiaopeng [2 ,5 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China
[2] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518055, Guangdong, Peoples R China
[3] Univ S Florida, Dept Chem, Tampa, FL 33620 USA
[4] Argonne Natl Lab, Nanosci & Technol Div, Lemont, IL 60439 USA
[5] Shenzhen Univ, Gen Hosp, Clin Med Acad, Shenzhen 518055, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
RING-IN-RING; GUEST-BINDING; TRANSITION-METAL; COORDINATION CHEMISTRY; MOLECULAR TRIANGLES; DRIVEN; CAGES; CONSTRUCTION; TETRANUCLEAR; COMPLEX;
D O I
10.1021/jacs.0c12508
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Asymmetrical and dissymmetrical structures are widespread and play a critical role in nature and life systems. In the field of metallo-supramolecular assemblies, it is still in its infancy for constructing artificial architectures using dissymmetrical building blocks. Herein, we report the self-assembly of supramolecular systems based on two dissymmetrical double-layered ligands. With the aid of ultra-high-vacuum, low-temperature scanning tunneling microscopy (UHV-LT-STM), we were able to investigate four isomeric structures corresponding to four types of binding modes of ligand LA with two major conformations complexes A. The distribution of isomers measured by STM and total binding energy of each isomer obtained by density functional theory (DFT) calculations suggested that the most abundant isomer could be the most stable one with highest total binding energy. Finally, through shortening the linker between inner and outer layers and the length of arms, the arrangement of dissymmetrical ligand LB could be controlled within one binding mode corresponding to the single conformation for complexes B.
引用
收藏
页码:1224 / 1234
页数:11
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