| Literature DB >> 25918903 |
Zheng-Feng Chang1, Ling-Min Jing1, Cong Wei2, Yu-Ping Dong3, Yan-Chun Ye1, Yong Sheng Zhao2, Jin-Liang Wang4.
Abstract
In this work, two rigid, multiple tetraphenylethene (TPE)-substituted, π-conjugated, snowflake-shaped luminophores BT and BPT were facilely synthesized by using a 6-fold Suzuki coupling reaction. These molecules are constructed based on the nonplanar structure of propeller-shaped hexaphenylbenzene (HPB) or benzene as core groups and TPE as end groups. As a result, they reserve the intrinsic aggregation-induced emission (AIE) property of the TPE moiety. Meanwhile, both fluorescence quantum yield and piezochromic behavior in the solid state can be tuned or switched by inserting the phenyl bridges through changing the twisting conformation. The more extended structure BPT showed a much stronger AIE effect and higher ΦF,f in the solid state in comparison with that of BT. Furthermore, an excellent optical waveguide application of these molecules was achieved. However, the revisable piezofluorochromic behavior has only appeared when BT was ground using a pestle and treated with solvent.Entities:
Keywords: aggregation; fluorescence; ligands; luminescence; self-assembly
Year: 2015 PMID: 25918903 DOI: 10.1002/chem.201406311
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236