磷光
发光
余辉
发光测量
杂原子
光化学
甲苯
化学
卤素
材料科学
光电子学
物理
荧光
有机化学
烷基
伽马射线暴
量子力学
天文
作者
Xiao Liang,Tingting Liu,Zhi‐Ping Yan,Yan Zhou,Jian Su,Xu‐Feng Luo,Zheng‐Guang Wu,Yi Wang,You‐Xuan Zheng,Jing‐Lin Zuo
标识
DOI:10.1002/ange.201909076
摘要
Abstract Pure organic materials with intrinsic room‐temperature phosphorescence typically rely on heavy atoms or heteroatoms. Two different strategies towards constructing organic room‐temperature phosphorescence (RTP) species based upon the through‐space charge transfer (TSCT) unit of [2.2]paracyclophane (PCP) were demonstrated. Materials with bromine atoms, PCP‐BrCz and PPCP‐BrCz, exhibit RTP lifetime of around 100 ms. Modulating the PCP core with non‐halogen‐containing electron‐withdrawing units, PCP‐TNTCz and PCP‐PyCNCz, successfully elongate the RTP lifetime to 313.59 and 528.00 ms, respectively, the afterglow of which is visible for several seconds under ambient conditions. The PCP‐TNTCz and PCP‐PyCNCz enantiomers display excellent circular polarized luminescence with dissymmetry factors as high as −1.2×10 −2 in toluene solutions, and decent RTP lifetime of around 300 ms for PCP‐TNTCz enantiomers in crystalline state.
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