机构地区:[1]Key Laboratory for Polymeric Composite & Functional Materials of Ministry of Education,Guangdong Provincial Key Laboratory for High Performance Polymer-based Composites,Guangdong Engineering Technology Research Center for High-performance Organic and Polymer Photoelectric Functional Films,State Key Laboratory of Optoelectronic Material and Technologies,School of Chemistry,Sun Yat-sen University [2]Shenzhen China Star Optoelectronics Technology Co.,Ltd
出 处:《Chinese Journal of Polymer Science》2017年第2期282-292,共11页高分子科学(英文版)
基 金:financially supported by the National Natural Science Foundation of China(Nos.51473185,51603233 and 21672267);863 Program(No.SS2015AA031701);the Fundamental Research Funds for the Central Universities;Guangdong Science and Technology Plan(Nos.2015B090913003 and 2015B090915003)
摘 要:A polymer (poly(9,10)anthracenevinylene-alt-4,4'-(9,9-bis(4-(4'-(1,2,2'-triphenyviny)phenoxy)butyl)-9H- fluorene-2,7-diyl) dibenzaldehyde), P1) was successfully synthesized through the Wittig-Horner reaction by employing fluorene and 9,10-distyrylanthracene moieties as building blocks for backbone and tetraphenylethenes as pendant groups. Photophysical and thermal properties of the resulting polymeric emitter were fully characterized by ultraviolet-visible (UV- Vis) absorption and photoluminescence (PL) spectra, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). While P1 emits an orange-light centered at 567 nm in dilute tetrahydrofuran (THF) solution, the solid powder of the polymer exhibits strong yellow emission peaked at 541 nm. It is also found that the as-synthesized polymer shows unique property of aggregation-enhanced emission (AEE). In addition, P1 possesses high thermal stability with a decomposition temperature (Td,5%) of 430 ℃ and high morphological stability with a glass transition temperature (Tg) of 171℃. Under the stimulus of mechanical force, the emission of P1 can be changed from yellow to red (△λmax = 61 rim), showing a remarkable mechanochromism. The results from XRD analysis suggest that such mechanochromic phenomenonof PI is probably caused by the destruction of crystalline structure, which leads to the conformational planarization of the distyrylanthracene moieties forming by the polymerization and the increase of molecular conjugation of the backbone.A polymer (poly(9,10)anthracenevinylene-alt-4,4'-(9,9-bis(4-(4'-(1,2,2'-triphenyviny)phenoxy)butyl)-9H- fluorene-2,7-diyl) dibenzaldehyde), P1) was successfully synthesized through the Wittig-Horner reaction by employing fluorene and 9,10-distyrylanthracene moieties as building blocks for backbone and tetraphenylethenes as pendant groups. Photophysical and thermal properties of the resulting polymeric emitter were fully characterized by ultraviolet-visible (UV- Vis) absorption and photoluminescence (PL) spectra, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). While P1 emits an orange-light centered at 567 nm in dilute tetrahydrofuran (THF) solution, the solid powder of the polymer exhibits strong yellow emission peaked at 541 nm. It is also found that the as-synthesized polymer shows unique property of aggregation-enhanced emission (AEE). In addition, P1 possesses high thermal stability with a decomposition temperature (Td,5%) of 430 ℃ and high morphological stability with a glass transition temperature (Tg) of 171℃. Under the stimulus of mechanical force, the emission of P1 can be changed from yellow to red (△λmax = 61 rim), showing a remarkable mechanochromism. The results from XRD analysis suggest that such mechanochromic phenomenonof PI is probably caused by the destruction of crystalline structure, which leads to the conformational planarization of the distyrylanthracene moieties forming by the polymerization and the increase of molecular conjugation of the backbone.
关 键 词:Tetraphenylethene 9 10-Distyrylanthracene Aggregation-enhanced emission High thermal stability Mechanochromic polymer
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