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Prolonging Ultralong Organic Phosphorescence Lifetime to 2.5 s through Confining Rotation in Molecular Rotor
Author(s) -
Li Mengping,
Ling Kun,
Shi Huifang,
Gan Nan,
Song Lulu,
Cai Suzhi,
Cheng Zhichao,
Gu Long,
Wang Xuan,
Ma Chaoqun,
Gu Mingxing,
Wu Qi,
Bian Lifang,
Liu Mingli,
An Zhongfu,
Ma Huili,
Huang Wei
Publication year - 2019
Publication title -
advanced optical materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 91
ISSN - 2195-1071
DOI - 10.1002/adom.201800820
Subject(s) - phosphorescence , materials science , phosphor , luminescence , optoelectronics , nanotechnology , photochemistry , optics , chemistry , fluorescence , physics
Developing ultralong organic phosphorescence (UOP) materials has become a growing concern. To date, it remains a formidable challenge to prolong the lifetime of ultralong phosphorescence under ambient conditions. A series of fluoro‐substituted phenylboronic acid derivatives with UOP feature under ambient conditions is reported here. The UOP lifetime of 2,4‐difluorophenylboronic acid (24FBP) crystal is up to 2.50 s, which is the longest emission lifetime among the reported single‐component pure organic phosphors. Combining the experimental and theoretical study, upon stabilization of triplet excitons by H‐aggregation, it is reasoned that rotation confinement in molecular rotors plays a critical role in prolonging the UOP lifetime. Given the feature of ultralong luminescence, 24FBP phosphor is successfully applied to anticounterfeiting. This result will pave the way toward tuning the UOP lifetime and expanding the scope of metal‐free organic phosphorescent materials with ultralong luminescence and their applications.