Abstract
Ultralong organic phosphorescent materials have invoked considerable attention for their great potential in sensing, data encryption, information anti-counterfeiting and so forth. However, effective ways to achieve highly efficient ultralong organic phosphorescence (UOP) in metal-free organic materials remain a great challenge. Herein, we designed three isomers based on asymmetric triazines with various bromine substituted positions. Impressively, phosphorescence efficiency of p-BrAT in solid state can reach up to 9.7% with a long lifetime of 386 ms, which was one of the highest efficient UOP materials reported so far. Theoretical calculations further demonstrated that para-substitution exhibited the most effective radiative transition for triplet excitons. These results will provide an effective approach to achieving highly efficient UOP materials.
Original language | English |
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Pages (from-to) | 1935-1938 |
Number of pages | 4 |
Journal | Chinese Chemical Letters |
Volume | 30 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2019 |
Keywords
- Crystal engineering
- H-aggregation
- Intermolecular interactions
- Isomerism
- Ultralong organic phosphorescence (UOP)