| Literature DB >> 27385550 |
Xiaofeng Chen1,2, Cheng Xu1, Tao Wang1, Cao Zhou1, Jiajun Du2, Zhongping Wang3, Hangxun Xu2, Tongqing Xie1, Guoqiang Bi1, Jun Jiang1, Xuepeng Zhang4, James N Demas5, Carl O Trindle5, Yi Luo1, Guoqing Zhang6.
Abstract
Purely organic materials with room-temperature phosphorescence (RTP) are currently under intense investigation because of their potential applications in sensing, imaging, and displaying. Inspired by certain organometallic systems, where ligand-localized phosphorescence ((3) π-π*) is mediated by ligand-to-metal or metal-to-ligand charge transfer (CT) states, we now show that donor-to-acceptor CT states from the same organic molecule can also mediate π-localized RTP. In the model system of N-substituted naphthalimides (NNIs), the relatively large energy gap between the NNI-localized (1) π-π* and (3) π-π* states of the aromatic ring can be bridged by intramolecular CT states when the NNI is chemically modified with an electron donor. These NNI-based RTP materials can be easily conjugated to both synthetic and natural macromolecules, which can be used for RTP microscopy.Entities:
Keywords: charge transfer; fluorescence; naphthalimides; organic dyes; phosphorescence
Year: 2016 PMID: 27385550 DOI: 10.1002/anie.201601252
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336