9-Borafluoren-9-yl and diphenylboron tetracoordinate complexes of 8-quinolinolato ligands with heavy-atoms substituents: synthesis, fluorescence and application in OLED devices

Fialho, Carina B.; Cruz, Tiago.F.C.; Calhorda, Maria.José; Vieira Ferreira, Luís.F.; Pander, Piotr; Dias, Fernando B.; Maçanita, António L.; Gomes, Pedro.T.

Abstract

This work describes the synthesis and characterisation of new tetrahedral boron complexes, incorporating bromine- or iodine-substituted 8-quinolinolato chelate chromophores connected to 9-borafluoren-9-yl or diphenylboron orthogonal fragments. The molecular features and photophysical properties of these complexes are analysed in both solution and solid state. Steady-state photophysical studies reveal photoluminescence quantum yields (Φf) ranging from 0.02 to 0.15 and prompt fluorescence (PF) lifetimes (τf) between 2 and 16 ns. Time-resolved photophysical experiments show the presence of delayed fluorescence (DF) and phosphorescence at both 77 K and room temperature. The DF intensity increases with a rise in temperature. This variation is ascribed to an enhancement in the intersystem crossing (ISC) process promoted by the bromine or iodine heavy-atom effect. Investigations into the dependence of DF intensity relative to the excitation dose indicate emissions stemming either from Triplet-Triplet Annihilation (TTA), Thermally Activated Delayed Fluorescence (TADF), or a combination of these competing mechanisms. The effect is related to the size and number of heavy-atom substituents in each boron complex. A study of the DF emission intensity as a function of the excitation dose reveals that diiodo-substituted 8-quinolinolato boron complexes, whether rigid or flexible, display TADF emission. Rigid 5,7-dibromo- and 5-chloro-7-iodo-substituted 8-quinolinolato complexes exhibit a combined TADF-TTA mechanism, whereas the other complexes predominantly demonstrate pure TTA emission. DFT and TDDFT calculations showed that the ground state structures reproduced the experimental geometries and only small increases in bond lengths were observed in the excited state geometries. The low energy absorption bands displayed mainly intra-ligand π→π* (8-quinolinato) character. The fluorescence emission energies were well reproduced, while the singlet-triplet energy gaps were relatively high. Ultimately, organic light-emitting diodes (OLEDs) are fabricated using the most luminescent boron complexes. The best OLED is obtained when using complex 3a, which displays green electroluminescence (EL) (λEL = 502 nm) with maximum external quantum efficiency (EQEmax) of 2.5% and maximum luminance (Lmax) of 2200 cd m-2.

Citation

Fialho, C. B., Cruz, T., Calhorda, M., Vieira Ferreira, L., Pander, P., Dias, F. B., Maçanita, A. L., & Gomes, P. (2024). 9-Borafluoren-9-yl and diphenylboron tetracoordinate complexes of 8-quinolinolato ligands with heavy-atoms substituents: synthesis, fluorescence and application in OLED devices. Dyes and Pigments, 228, Article 112174. https://doi.org/10.1016/j.dyepig.2024.112174

• Journal Article Type: Article
• Acceptance Date: Apr 22, 2024
• Online Publication Date: Apr 24, 2024
• Publication Date: 2024-09
• Deposit Date: May 23, 2024
• Publicly Available Date: May 24, 2024
• Journal: Dyes and Pigments
• Print ISSN: 0143-7208
• Electronic ISSN: 1873-3743
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 228
• Article Number: 112174
• DOI: https://doi.org/10.1016/j.dyepig.2024.112174
• Public URL: https://durham-repository.worktribe.com/output/2433274