Deep red aggregation-induced CPL emission behavior of four-component tunable AIE-active chiral polymers via two FRET pairs mechanism

被引:26
|
作者
Wang, Ziyu [1 ]
Fang, Yayun [1 ]
Tao, Xingyu [1 ]
Wang, Yuxiang [1 ]
Quan, Yiwu [1 ]
Zhang, Shuwei [2 ]
Cheng, Yixiang [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Key Lab Mesoscop Chem MOE, Nanjing 210023, Jiangsu, Peoples R China
[2] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Tunable AIE; Tunable red-AICPL; Two FRET pairs; CIRCULARLY-POLARIZED LUMINESCENCE; CONJUGATED POLYMERS; BODIPY DYES; DERIVATIVES; DICHROISM; TETRAPHENYLETHYLENE; NANOPARTICLES; ORGANIZATION; SUBSTITUTION; CHEMISTRY;
D O I
10.1016/j.polymer.2017.09.072
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two four-component chiral polymers with two Forster resonance energy transfer (FRET) pairs incorporating chiral 1,1'-binaphthyl, 4,7-di(thiophen-2-yl)-2,1,3-benzothiadiazole (DTBT), tetraphenylethene (TPE) and fluorene moieties were designed and synthesized via one-pot two-step of Pd-catalyzed Sonogashira reaction and Suzuki reaction by changing different ratios of DTBT chromophore and AIE-active TPE group. Both chiral polymers exhibit large Stokes shift (257 nm) and tunable red aggregation-induced emission (AIE) response behavior via two intramolecular FRET pairs by changing excitation wavelength. Interestingly, the chiral polymer with lower ratio of DTBT (P-1) shows obvious aggregation-induced circularly polarized luminescence (AICPL) emission signals in deep red region (around 650 nm) and higher glum, which can reach as high as +/- 2.0 x 10(-3) in THF-H2O mixtures. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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