Self- assembly of a fluorescent galunamide derivative and sensing of acid vapor and mechanical force stimuli

被引:50
作者
Xue, Pengchong [1 ,2 ]
Yao, Boqi [2 ]
Shen, Yanbing [2 ]
Gao, Hongqiang [2 ]
机构
[1] Tianjin Normal Univ, Coll Chem, Tianjin Key Lab Struct & Performance Funct Mol, Key Lab Inorgan Organ Hybrid Funct Mat Chem,Minis, Tianjin 300387, Peoples R China
[2] Jilin Univ, Coll Chem, 2699 Qianjin St, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
AGGREGATION-INDUCED EMISSION; ORGANIC AMINE VAPORS; PERFORMANCE LIQUID-CHROMATOGRAPHY; BETA-DIKETONATE COMPLEXES; SOLID-STATE FLUORESCENCE; VOLATILE ACID; ENHANCED EMISSION; MECHANOCHROMIC LUMINESCENCE; PIEZOCHROMIC LUMINESCENCE; RESPONSIVE FLUORESCENCE;
D O I
10.1039/c7tc03752j
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A galunamide derivative consisting of a fluorophore with benzoxazole and a cyano unit was designed and synthesized to realize a dual response to acid vapor and mechanical force. Photophysical properties and self-assembly were investigated. The dilute solution could respond to the acid stimulus, and the emission peak at 472 nm shifted to 535 nm with the addition of trifluoroacetic acid (TFA). Moreover, the derivative could self-assemble into thin nanofibers in its gel phase, and the fluorescence of the xerogel film is sensitive to TFA vapor. The emission color gradually changed from yellow to orange red upon exposure to acid vapor, and the detection limit is as low as 70 ppb for TFA. The solid exhibited a reversible fluorescence color change under the stimuli of mechanical force and solvent annealing. The UV-vis absorption and IR spectra indicate that the fluorescence color conversion can be attributed to the destruction of intermolecular hydrogen bonds and pristine p-p interaction induced by mechanical force.
引用
收藏
页码:11496 / 11503
页数:8
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