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三芳基硼中心的 N-杂环卡宾笼的可控光物理性质的合成。

Synthesis of triarylborane-centered N-heterocyclic carbene cages with tunable photophysical properties.

机构信息

Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, Xi'an Key Laboratory of Functional Supramolecular Structure and Materials, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, P. R. China.

出版信息

Chem Commun (Camb). 2023 Feb 21;59(16):2291-2294. doi: 10.1039/d2cc06584c.

Abstract

Triarylborane-based discrete metal-carbene supramolecular cages M(1) (M = Ag, Au) were synthesized and characterized. The new hexacarbene assemblies show a significant solvatochromic effect in solvents of different polarity. Furthermore, the reversible fluoride binding property of Au(1) was investigated by UV-vis absorption and fluorescence titrations. This work holds promise for future developments in the area of highly emissive and stimulus-responsive NHC-metal assemblies.

摘要

基于三芳基硼的离散金属卡宾超分子笼 M(1)(M = Ag,Au)被合成并进行了表征。这些新型六卡宾组装体在不同极性溶剂中表现出显著的溶剂化变色效应。此外,通过紫外-可见吸收和荧光滴定研究了 Au(1) 对氟离子的可逆结合性能。这项工作为开发具有高发光性和刺激响应性的 NHC-金属组装体提供了可能。

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