磷光
分子内力
化学
配体(生物化学)
光化学
接受者
分子
共轭体系
戒指(化学)
高分子
材料科学
荧光
立体化学
有机化学
聚合物
物理
受体
量子力学
生物化学
凝聚态物理
作者
Xiaofeng Chen,Cheng Xu,Tao Wang,Cao Zhou,Jiajun Du,Zhongping Wang,Hangxun Xu,Tongqing Xie,Guo‐Qiang Bi,Jun Jiang,Xuepeng Zhang,J. N. Demas,Carl Trindle,Yi Luo,Guoqing Zhang
标识
DOI:10.1002/anie.201601252
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI