Multi-dimensional Hydrogen Bonds Regulated Emissions of Single Molecule Enabling Hydrophobicity/Hydrophilicity Mapping

Hao Gu, Rui Li, Qiuying Li, Sheng Lu, Yahui Chen, Xiaoning Yang, Huili Ma, Zhijun Xu, Xiaoqiang Chen
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Abstract

Constructing multi-dimensional hydrogen bond (H-bond) regulated single-molecule systems with multi-emission remains a challenge. Herein, we report an excited-excited intramolecular transfer (ESIPT) featured chromophore (HBT-DPI) that shows flexible emission tunability via the multi-dimensional regulation of intra- and intermolecular H-bonds. The feature of switchable intramolecular H-bonds is induced via incorporating two hydrogen bond acceptors into a single-molecule system, HBT-DPI, allowing the “turn on/off” of ESIPT process by forming isomers with distinct intramolecular H-bonds. In response to different solvent environments, the obtained four types of crystal/cocrystals vary in the contents of isomers and the molecular packing modes, which are mainly guided by the intermolecular H-bonds, exhibiting non-emissive features or emissions ranging from green to orange. Moreover, we demonstrate the practical utility of this fluorescent material for visualizing hydrophobic/hydrophilic areas on large-scale heterogeneous surfaces of modified PVDF membranes and quantitatively estimate the surface hydrophobicity, providing a new approach for hydrophobicity/hydrophilicity monitoring and measurement.
多维氢键调节单分子的发射,实现疏/亲水性作图
构建多维氢键调控的多发射单分子体系仍然是一个挑战。在此,我们报道了一种具有激发态-激发态分子内转移(ESIPT)特征的发色团(HBT-DPI),它通过分子内和分子间氢键的多维调节显示出灵活的发射可调性。通过将两个氢键受体结合到单分子体系hpt - dpi中,诱导了分子内氢键可切换的特征,通过形成具有不同分子内氢键的异构体,允许ESIPT过程的“开启/关闭”。在不同的溶剂环境下,得到的四种晶体/共晶在异构体的含量和分子填充模式上有所不同,主要由分子间氢键引导,表现出非发射特征或从绿色到橙色的发射。此外,我们还展示了该荧光材料在改性PVDF膜的大规模非均相表面上的疏水/亲水区域可视化和定量估计表面疏水性的实用性,为疏水/亲水性监测和测量提供了一种新的方法。
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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