| Literature DB >> 31359548 |
Nan Gan1, Xuan Wang1, Huili Ma1, Anqi Lv1, He Wang1, Qian Wang1, Mingxing Gu1, Suzhi Cai1, Yanyun Zhang1, Lishun Fu1, Meng Zhang1, Chaomin Dong1, Wei Yao1, Huifang Shi1, Zhongfu An1, Wei Huang1,2.
Abstract
Provided here is evidence showing that the stacking between triplet chromophores plays a critical role in ultralong organic phosphorescence (UOP) generation within a crystal. By varying the structure of a functional unit, and different on-off UOP behavior was observed for each structure. Remarkably, 24CPhCz, having the strongest intermolecular interaction between carbazole units exhibited the most impressive UOP with a long lifetime of 1.06 s and a phosphorescence quantum yield of 2.5 %. 34CPhCz showed dual-emission UOP and thermally activated delayed fluorescence (TADF) with a moderately decreased phosphorescence lifetime of 770 ms, while 35CPhCz only displayed TADF owing to the absence of strong electronic coupling between triplet chromophores. This study provides an explanation for UOP generation in crystal and new guidelines for obtaining UOP materials.Entities:
Keywords: crystal engineering; fluorescence; noncovalent interactions; phosphorescence; solid-state structures
Year: 2019 PMID: 31359548 DOI: 10.1002/anie.201907572
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336