| Literature DB >> 29417724 |
Suzhi Cai1, Huifang Shi1, Zaiyong Zhang2, Xuan Wang1, Huili Ma1, Nan Gan1, Qi Wu1, Zhichao Cheng1, Kun Ling1, Mingxing Gu1, Chaoqun Ma1, Long Gu1, Zhongfu An1, Wei Huang1,3.
Abstract
Ultralong organic phosphorescence (UOP) based on metal-free porous materials is rarely reported owing to rapid nonradiative transition under ambient conditions. In this study, hydrogen-bonded organic aromatic frameworks (HOAFs) with different pore sizes were constructed through strong intralayer π-π interactions to enable ultralong phosphorescence in metal-free porous materials under ambient conditions for the first time. Impressively, yellow UOP with a lifetime of 79.8 ms observed for PhTCz-1 lasted for several seconds upon ceasing the excitation. For PhTCz-2 and PhTCz-3, on account of oxygen-dependent phosphorescence quenching, UOP could only be visualized in N2 , thus demonstrating the potential of phosphorescent porous materials for oxygen sensing. This result not only outlines a principle for the design of new HOFs with high thermal stability, but also expands the scope of metal-free luminescent materials with the property of UOP.Entities:
Keywords: hydrogen bonds; hydrogen-bonded organic frameworks; self-assembly; ultralong organic phosphorescence; π interactions
Year: 2018 PMID: 29417724 DOI: 10.1002/anie.201800697
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336