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
受体
光电子学
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)
被引量:3
标识
DOI:10.1002/smll.202309542
摘要
Abstract 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 (Eu 3+ )‐directed supramolecular metallogels are constructed by orthogonal self‐assembly of Eu 3+ 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 Eu 3+ . Synergistic intermolecular hydrogen bonding in L and Eu 3+ ‐ L coordination bonding enable Eu 3+ 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 C 2 ‐symmetrical structure, and as the ideal monomer for increasing the energy transfer from L to Eu 3+ ’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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