Luminescent Re(i) terpyridine complexes for OLEDs: what does the DFT/TD-DFT probe reveal?

Abstract

The electronic structure and spectroscopic properties of a series of rhenium(I) terpyridine complexes were investigated using density functional theory (DFT) and time dependent density functional theory (TD-DFT) methods. The influence of different substituent groups on the optical and electronic properties of Re(I) terpyridine complexes has also been explored. The reorganization energy calculations show that the substituted Re(I) terpyridine complexes are better electron transport materials with high quantum efficiency in OLED devices due to their high electron transport mobility and low λ_electron values, whereas the unsubstituted complex shows relatively balanceable charge transfer abilities with the higher efficiency in organic light emitting devices (OLEDs). An NBO analysis reveals that n→σ* interactions are mainly responsible for the ground state stabilization of all the complexes. QTAIM results show that in all cases, Re–CO bonds are shared type transient interactions as reported in the other metal ligand complexes. The absorption is associated with ¹MLCT/¹LLCT/¹ILCT character while the emission transition has ³MLCT/³LLCT/³ILCT character as revealed by a natural transition orbital (NTO) analysis. The higher quantum yields reported for the complexes 4–6 are found to be closely related to both its smaller ΔE_S1–T1, higher μ_S1, E_T1 and moderate ³MLCT character. The calculated results show that Re(I) terpyridine complexes, particularly complexes 4–6, are suitable candidates for OLED materials.