| Literature DB >> 31646717 |
He Wang1, Huifang Shi1, Wenpeng Ye1, Xiaokang Yao1, Qian Wang1, Chaomin Dong1, Wenyong Jia1, Huili Ma1, Suzhi Cai1, Kaiwei Huang1, Lishun Fu1, Yanyun Zhang1, Jiahuan Zhi1, Long Gu2, Yanli Zhao2, Zhongfu An1, Wei Huang1,3.
Abstract
Amorphous purely organic phosphorescence materials with long-lived and color-tunable emission are rare. Herein, we report a concise chemical ionization strategy to endow conventional poly(4-vinylpyridine) (PVP) derivatives with ultralong organic phosphorescence (UOP) under ambient conditions. After the ionization of 1,4-butanesultone, the resulting PVP-S phosphor showed a UOP lifetime of 578.36 ms, which is 525 times longer than that of PVP polymer itself. Remarkably, multicolor UOP emission ranging from blue to red was observed with variation of the excitation wavelength, which has rarely been reported for organic luminescent materials. This finding not only provides a guideline for developing amorphous polymers with UOP properties, but also extends the scope of room-temperature phosphorescence (RTP) materials for practical applications in photoelectric fields.Entities:
Keywords: ionic bonding; multicolor emission; phosphorescence; solid-state structures; π interactions
Year: 2019 PMID: 31646717 DOI: 10.1002/anie.201911331
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336