Multi-Stimuli Responsive Luminescent β-Diketones and Difluoroboron Complexes with Heterocyclic Substituents

被引:7
|
作者
Wang, Fang [1 ]
Song, Daniel [1 ]
Dickie, Diane A. [1 ]
Fraser, Cassandra L. [1 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
基金
美国国家科学基金会;
关键词
beta-Diketone; Difluoroboron complex; Heterocycles; Multi-stimuli responsive luminescence; Six-membered ring; AGGREGATION-INDUCED EMISSION; MECHANOCHROMIC LUMINESCENCE; QUANTUM YIELDS; FLUORESCENCE; VISCOSITY; SOLVENTS; PROBES;
D O I
10.1007/s10895-020-02626-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Emissive beta-diketones (bdks) and difluoroboron complexes (BF(2)bdks) exhibit multi-stimuli responsive luminescence, including solvatochromism, viscochromism, aggregation induced emission, thermal and mechanochromic luminescence, halochromism and pH sensing. In this study, a series of six-membered heterocycle-substituted (piperidine, morpholine, 1-methyl piperazine) bdk ligands and boron complexes were synthesized, and their luminescent properties were investigated. All the compounds exhibited red-shifted emission in more polar solvents due to intramolecular charge transfer as well as higher emission intensity in more viscous environments. In response to solubility changes in water/tetrahydrofuran mixtures, while the piperazine bdk ligand showed aggregation caused quenching, the piperidine and morpholine bdks displayed enhanced emission upon aggregation. In the solid state, all ligands exhibited mechanochromism. More dramatic halochromism was observed for the piperidine boron dye spin cast film. In solution, for the boron dyes under varying pH values (1-13), different protonated and deprotonated forms were analyzed according to the measured emission spectra.
引用
收藏
页码:39 / 49
页数:11
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