Low‐entropy‐penalty synthesis of giant macrocycles for good self‐assembly and emission enhancement

Aggregate Pub Date : 2024-08-13 DOI:10.1002/agt2.607
Xiao‐Na Sun, Ao Liu, Kaidi Xu, Zhe Zheng, Kai Xu, Ming Dong, Bo Ding, Jian Li, Zhi‐Yuan Zhang, Chunju Li
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Abstract

Macrocycles are key tools for molecular recognition and self‐assembly. However, traditionally prevalent macrocyclic compounds exhibit specific cavities with diameters usually less than 1 nm, limiting their range of applications in supramolecular chemistry. The efficient synthesis of giant macrocycles remains a significant challenge because an increase in the monomer number results in cyclization‐entropy loss. In this study, we developed a low‐entropy‐penalty synthesis strategy for producing giant macrocycles in high yields. In this process, long and rigid monomers possessing two reaction modules were condensed with paraformaldehyde via Friedel–Crafts reaction. A series of giant macrocycles with cavities of sizes ranging from 2.0 to 4.7 nm were successfully synthesized with cyclization yields of up to 72%. Experimental results and theoretical calculations revealed that extending the monomer length rather than increasing the monomer numbers could notably reduce the cyclization‐entropy penalty and avoid configuration twists, thereby favoring the formation of giant macrocycles with large cavities. Significantly, the excellent self‐assembly capacity of these giant macrocycles promoted their assembly into organogels. The xerogels exhibited enhanced photoluminescence quantum efficiencies of up to 83.1%. Mechanism investigation revealed the excellent assembly capacity originated from the abundant π–π interactions sites of the giant macrocycles. The outstanding emission enhancement resulted from the restricted nonradiative decay processes of rotation/vibration and improved radiative decay process of fluorescence. This study provides an effective and general method for achieving giant macrocycles, thereby expanding the supramolecular toolbox for host–guest chemistry and assembly applications. Moreover, the intriguing assembly and photophysical properties demonstrate the feasibility of developing novel and unique properties by expanding the macrocycle size.

Abstract Image

低熵熵合成巨型大环,实现良好的自组装和发射增强功能
大环是分子识别和自组装的关键工具。然而,传统上流行的大环化合物表现出直径通常小于 1 纳米的特定空腔,限制了它们在超分子化学中的应用范围。由于单体数量的增加会导致环化熵损失,因此高效合成巨型大环仍然是一项重大挑战。在这项研究中,我们开发了一种低熵熵合成策略,可以高产率合成巨型大环。在这一过程中,具有两个反应模块的刚性长单体通过弗里德尔-卡夫反应与多聚甲醛缩合。成功合成了一系列具有 2.0 至 4.7 nm 大小空腔的巨型大环,环化产率高达 72%。实验结果和理论计算显示,延长单体长度而不是增加单体数量可以显著降低环化熵罚,避免构型扭曲,从而有利于形成具有大空腔的巨型大环。值得注意的是,这些巨型大环的出色自组装能力促进了它们组装成有机凝胶。这些异构凝胶的光致发光量子效率最高可达 83.1%。机理研究表明,巨型大环的优异组装能力源于其丰富的π-π相互作用位点。由于旋转/振动的非辐射衰变过程受到限制,而荧光的辐射衰变过程得到改善,因此发射增强效果显著。这项研究为实现巨型大环提供了一种有效而通用的方法,从而扩大了超分子工具箱在主宾化学和组装方面的应用。此外,引人入胜的组装和光物理特性证明了通过扩大大环尺寸来开发新的独特特性的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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