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镧系超分子水凝胶的协同组装及其发光多刺激响应。

Coordination-Assembly of Lanthanide Supramolecular Hydrogels with Luminescent Multi-stimulus Response.

机构信息

College of Chemistry and Materials Science, Fujian Normal University, 32 Shangsan Road, Fuzhou 350007, China.

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, PR China.

出版信息

Inorg Chem. 2021 Dec 6;60(23):18192-18198. doi: 10.1021/acs.inorgchem.1c02827. Epub 2021 Nov 8.

Abstract

Luminescent supramolecular hydrogels have shown extensive potential for a variety of applications due to their unique optical properties and biocompatibility. Coordination self-assembly provides a promising strategy for the preparation of supramolecular hydrogels. In this contribution, a series of luminescent lanthanide (Ln) supramolecular hydrogels HG-LnL are synthesized by coordination self-assembly of Ln ions and V shaped bis-tetradentate ligands (HL and HL) with different bent angles (∠). Two rigid conjugated ligands HL and HL with bent angles (∠ ≈ 150°) featuring a 2,6-pyridine bitetrazolate chelating moiety were designed and synthesized, which generated hydrogels via the deprotonation self-assembly with lanthanide ions. Characteristic Eu and Yb emissions were realized in the corresponding hydrogels, with intriguing multi-stimulus response behaviors. The luminescence of the HG-EuL hydrogel can be enhanced or quenched when stimulated by diverse metal ions, attributed to the replacement of the coordinated lanthanide ions and changes in the intersystem crossing efficiency of the ligand. Furthermore, pH-responsive emission of the HG-EuL hydrogel has also been observed. Our work provides potential strategies for the design of next-generation smart responsive hydrogel materials with variable structures.

摘要

由于独特的光学性质和生物相容性,发光超分子水凝胶在各种应用中显示出了广泛的潜力。配位自组装为制备超分子水凝胶提供了一种很有前途的策略。在本研究中,通过镧系离子(Ln 离子)与 V 型双四齿配体(HL 和 HL)的配位自组装,合成了一系列发光镧系(Ln)超分子水凝胶 HG-LnL。HL 和 HL 是两种刚性共轭配体,具有约 150°的弯曲角(∠),并带有 2,6-吡啶双四唑螯合部分。通过与镧系离子的去质子化自组装,生成了水凝胶。相应的水凝胶实现了特征性的 Eu 和 Yb 发射,并表现出有趣的多刺激响应行为。HG-EuL 水凝胶的发光可以通过不同金属离子的刺激增强或猝灭,这归因于配位镧系离子的取代和配体的系间窜越效率的变化。此外,还观察到 HG-EuL 水凝胶的 pH 响应发射。我们的工作为设计具有可变结构的下一代智能响应水凝胶材料提供了潜在的策略。

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