A theoretical investigation on the thermally activated delayed fluorescence characteristics of the isomers of DTCBPy.

It has been reported that 3, 5-bis(3,6-di-tert-butyl-9H-carbazol-9-yl)-phenyl)(pyridin-4-yl)meth (DTCBPy) is an efficient thermally activated delayed fluorescence (TADF) molecule. We designed a series of the isomeric molecules (2-5) of DTCBPy (1) by changing the position of nitrogen atom in the acceptor and the substituent position of donor units. The highest occupied molecular orbitals (HOMO) of 1-5 are all delocalized over the donor units, and the lowest unoccupied molecular orbitals (LUMO) are located on the acceptor unit. As expected from frontier molecular orbital analysis, the singlet-triplet energy splitting (ΔE) values of 1-5 are in a small range from 0.087 to 0.147 eV, indicating the easy realization of reverse intersystem crossing from the lowest triplet to singlet excited states. However, the structural modification has a significant influence on the fluorescence radiative rate (k), which varies from 3.49× 10 to 2.04 × 10 s for 1-5. This work is expected to provide valuable information for synthesizing highly efficient TADF materials based on DTCBPy.