Block copolymer self-assembly mediated aggregation induced emission for selective recognition of picric acid

被引:17
|
作者
Rasheed, Tahir [1 ]
Nabeel, Faran [1 ]
Shafi, Sameera [1 ]
Bilal, Muhammad [2 ]
Rizwan, Komal [3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Huaiyin Inst Technol, Sch Life Sci & Food Engn, Huaian 223003, Peoples R China
[3] Govt Coll Women Univ, Dept Chem, Faisalabad 38000, Pakistan
关键词
Block copolymer; Living polymerization; Photoluminescence; Explosive detection; Selectivity; Fluorescence quenching; RAFT POLYMERIZATION; ENHANCED EMISSIONS; FLUORESCENT-PROBES; AIE LUMINOGEN; QUANTUM DOTS; TETRAPHENYLETHENE; POLYMERS; CHAIN; DERIVATIVES; INTENSITY;
D O I
10.1016/j.molliq.2019.111966
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Benefiting from the excellent hydrophobic properties of polystyrene and (2-(4-vinylphenyl)ethene-1,1,2-triyl) tribenzene (PS-b-PTPEE) unit a diblock copolymer is prepared to show higher aggregation induced emission (AIE). The TPE grafted block copolymer forms homogeneous solution in common organic solvents such as THF. In aqueous solution, the copolymer self-assemble to form aggregates of nanosize. The aggregates display maximum photoluminescence (PL) in a THF/water (3:7 v/v) mixture. Fortunate introduction of TPE units into block copolymer chain makes it highly sensitive probe for picric acid (an explosive amterial) via aggregation induced emission. The nitroaromatic compound of PA was effectively quenched by possible pi-pi interactions between TPE units of PS-b-PTPEE and hydroxyl containing phenolic acid. The quenching efficiency significantly increased nonlinearly at higher quencher concentration. The present study offers details for design and synthesis of new hyperbranched polymeric fluorescent vesicle probe with high sensitivity. (C) 2019 Elsevier B.V. All rights reserved.
引用
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页数:7
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