TY - JOUR
T1 - Tunable fluorescence conjugated copolymers consisting of tetraphenylethylene and fluorene units
T2 - From aggregation-induced emission enhancement to dual-channel fluorescence response
AU - Shi, Jianbing
AU - Wu, Yanmei
AU - Sun, Shu
AU - Tong, Bin
AU - Zhi, Junge
AU - Dong, Yuping
PY - 2013/1/15
Y1 - 2013/1/15
N2 - A series of new conjugated polymers PTPExFy, which consist of tetraphenylethylene (TPE) units and fluorene (F) units, have been designed and synthesized by Suzuki cross-coupling polymerization. The polymers PTPExFy exhibited aggregation-induced emission enhancement and dual-channel fluorescence response (DCFR) when they were aggregated in solution, and these properties are related with their TPE-to-F ratio in the polymer backbone. For PTPE and PTPE0.5F0.5, the fluorescence emission was enhanced by aggregation when water was added into their THF solutions. For the copolymers PTPE0.3F0.7, PTPE0.2F0.8, and PTPE0.1F0.9, the DCFRs were observed when they were aggregated by adding water into their solution, which can be attributed to the different responses of fluorene segments and TPE segments to aggregation. The fluorene segments have an aggregation-caused quenching characteristic, whereas the TPE segments have an aggregation-induced emission characteristic. According to the fluorescence lifetime and quantum yield data of the polymer solutions, we have discovered that the polymer's natural life time increases as its TPE content increases. In the solid film, PTPE0.3F0.7 and PTPE0.2F 0.8 showed better quantum yield than other polymers, due to the combination of the excellent fluorescent property of the fluorene groups and the nonplanar conformation of the TPE groups.
AB - A series of new conjugated polymers PTPExFy, which consist of tetraphenylethylene (TPE) units and fluorene (F) units, have been designed and synthesized by Suzuki cross-coupling polymerization. The polymers PTPExFy exhibited aggregation-induced emission enhancement and dual-channel fluorescence response (DCFR) when they were aggregated in solution, and these properties are related with their TPE-to-F ratio in the polymer backbone. For PTPE and PTPE0.5F0.5, the fluorescence emission was enhanced by aggregation when water was added into their THF solutions. For the copolymers PTPE0.3F0.7, PTPE0.2F0.8, and PTPE0.1F0.9, the DCFRs were observed when they were aggregated by adding water into their solution, which can be attributed to the different responses of fluorene segments and TPE segments to aggregation. The fluorene segments have an aggregation-caused quenching characteristic, whereas the TPE segments have an aggregation-induced emission characteristic. According to the fluorescence lifetime and quantum yield data of the polymer solutions, we have discovered that the polymer's natural life time increases as its TPE content increases. In the solid film, PTPE0.3F0.7 and PTPE0.2F 0.8 showed better quantum yield than other polymers, due to the combination of the excellent fluorescent property of the fluorene groups and the nonplanar conformation of the TPE groups.
KW - aggregation-induced emission enhancement (AIEE)
KW - conjugated polymer
KW - copolymerization
KW - dual-channel fluorescence response (DCFR)
KW - fluorene
KW - luminescence
KW - tetraphenylethylene (TPE)
UR - http://www.scopus.com/inward/record.url?scp=84870979137&partnerID=8YFLogxK
U2 - 10.1002/pola.26377
DO - 10.1002/pola.26377
M3 - Article
AN - SCOPUS:84870979137
SN - 0887-624X
VL - 51
SP - 229
EP - 240
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 2
ER -