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Fluorescent Cross-Linked Supramolecular Polymer Constructed by Orthogonal Self-Assembly of Metal-Ligand Coordination and Host-Guest Interaction
被引:22
|作者:
Qian, Xiaomin
[1
]
Gong, Weitao
[1
]
Li, Xiaopeng
[2
]
Fang, Le
[1
]
Kuang, Xiaojun
[1
]
Ning, Guiling
[1
]
机构:
[1] Dalian Univ Technol, Sch Chem Engn, Sate Key Lab Fine Chem, 2 Linggong Rd, Dalian, Peoples R China
[2] Texas State Univ, Dept Chem & Biochem, San Marcos, TX 78666 USA
基金:
中国国家自然科学基金;
关键词:
fluorescence;
host-guest systems;
morphology;
self-assembly;
supramolecular chemistry;
PI-PI;
MOLECULAR RECOGNITION;
SHAPE-PERSISTENT;
FACILE SYNTHESIS;
COMPLEXES;
TERPYRIDINE;
CHAIN;
BINDING;
DRIVEN;
GELS;
D O I:
10.1002/chem.201600561
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A new host molecule consists of four terpyridine groups as the binding sites with zinc(II) ion and a copillar[5]arene incorporated in the center as a spacer to interact with guest molecule was designed and synthesized. Due to the 120 degrees angle of the rigid aromatic segment, a cross-linked dimeric hexagonal supramolecular polymer was therefore generated as the result of the orthogonal self-assembly of metal-ligand coordination and host-guest interaction. UV/Vis spectroscopy, (HNMR)-H-1 spectroscopy, viscosity and dynamic light-scattering techniques were employed to characterize and understand the cross-linking process with the introduction of zinc(II) ion and guest molecule. More importantly, well-defined morphology of the self-assembled supramolecular structure can be tuned by altering the adding sequence of the two components, that is, the zinc(II) ion and the guest molecule. In addition, introduction of a competitive ligand suggested the dynamic nature of the supramolecular structure.
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页码:6881 / 6890
页数:10
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