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.
引用
收藏
页码:6881 / 6890
页数:10
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