Time-dependent density functional theory study on electronic and spectroscopic properties for Ph2Bq and its complexes

Abstract

The molecular structures of the ground state and the first singlet excited state for diphenylboron analogs of Alq3 [Ph2Bq where q is 8-hydroxyquinoline (QH)] and its three derivatives were optimized with the Density Functional Theory and ab initio “configuration interaction with single excitations” method, respectively. The frontier molecular orbital characteristics of Ph2Bq were analyzed systematically in order to study the electronic transition mechanism. Electronic and spectroscopic properties of complexes have been investigated with Time-Dependent Density Functional Theory, which indicates that the emissions of Ph2Bq and its derivatives originate from the electronic π → π* transitions within the QH ligands. That means that one might tune the emission wavelengths and improve charge transfer properties through the effect of substituent on the 8-hydroxyquinoline ligand. Similar calculations were carried out for isolated QH and its three derivatives for comparison. We found that the highest occupied molecular orbital and the lowest unoccupied molecular orbital of Ph2Bq are similar to those of QH and their spectroscopic properties change similarly when they are substituted by the same group, which suggests that one can search possibility of a red or blue emission from Ph2Bq derivatives by analyzing QH and its derivatives.