| Literature DB >> 31206936 |
Hongwei Wu1,2, Zhao Chen3, Weijie Chi4, Anivind Kaur Bindra2, Long Gu2, Cheng Qian2, Bing Wu1, Bingbing Yue1, Guofeng Liu2, Guangbao Yang2, Liangliang Zhu1, Yanli Zhao2.
Abstract
Developing molecules with high emission efficiency both in solution and the solid state is still a great challenge, since most organic luminogens are either aggregation-caused quenching or aggregation-induced emission molecules. This dilemma was overcome by integrating planar and distorted structures with long alkyl side chains to achieve DAπAD type emitters. A linear diphenyl-diacetylene core and the charge transfer effect ensure considerable planarity of these molecules in the excited state, allowing strong emission in dilute solution (quantum yield up to 98.2 %). On the other hand, intermolecular interactions of two distorted cyanostilbene units restrict molecular vibration and rotation, and long alkyl chains reduce the quenching effect of the π-π stacking to the excimer, eventually leading to strong emission in the solid state (quantum yield up to 60.7 %).Entities:
Keywords: bioimaging; luminescence; molecular engineering; molecular stacking; noncovalent interactions
Year: 2019 PMID: 31206936 DOI: 10.1002/anie.201906507
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336