超分子化学
发光
氢键
分子间力
配体(生物化学)
单体
自组装
铕
酰胺
配位复合体
材料科学
化学
结晶学
分子
纳米技术
聚合物
晶体结构
金属
有机化学
生物化学
光电子学
受体
作者
Yan Chen,Huimin Li,Yakun Zhang,Zhiqiang Li,Daqing Yang
出处
期刊:Small
[Wiley]
日期:2024-01-14
卷期号:20 (25): e2309542-e2309542
被引量:14
标识
DOI:10.1002/smll.202309542
摘要
Smart luminescent materials that have the ability to reversibly adapt to external environmental stimuli and possess a wide range of responses are continually emerging, which place higher demands on the means of regulation and response sites. Here, europium ions (Eu3+)-directed supramolecular metallogels are constructed by orthogonal self-assembly of Eu3+ based coordination interactions and hydrogen bonding. A new organic ligand (L) is synthesized, consisting of crown ethers and two flexible amide bonds-linked 1,10-phenanthroline moieties to coordinate with Eu3+. Synergistic intermolecular hydrogen bonding in L and Eu3+-L coordination bonding enable Eu3+ and L to self-assemble into shape-persistent 3D coordination metallogels in MeOH solution. The key to success is the utilization of crown ethers, playing dual roles of acting both as building blocks to build L with C2-symmetrical structure, and as the ideal monomer for increasing the energy transfer from L to Eu3+'s excited state, thus maintaining the excellent luminescence of metallogels. Interestingly, such assemblies show K+, pH, F-, and mechano-induced reversible gel-sol transitions and tunable luminescence properties. Above findings are useful in the studies of molecular switches, dynamic assemblies, and smart luminescent materials.
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