Herein, we report two new iridium(III) complexes (1 and 2), featuring 6-(phenyl)phenanthridine derivatives as cyclometalating (C^N) ligands and pyridyl-triazole or pyridyl-pyrazole ancillary (L^X) ligands. The synthesis of the two compounds was performed by reaction of the 6-(phenyl)-phenanthridine chloro-bridged dimer with the pyridyl-triazole/pyridyl-pyrazole (L^X) ligand. Single crystals of both complexes (1 and 2) were grown and analyzed by X-ray diffraction. Full crystallographic characterization and comparison of 1 and 2 solid-state structures is reported. Spectroscopic characterization revealed similar emissive properties for 1 (λmax = 650 nm; τdeg = 1.43 μs, QYdeg = 11.6 %) and 2 (λmax = 660 nm; τdeg = 1.45 μs, QYdeg = 12.1 %).
Synthesis and crystallographic investigation of two new neutral Ir(III) complexes bearing 6-(phenyl)phenanthridine ligands / L. Menduti, M. Mori, X. Zhou, N. Quadrio, F. Meneghetti, L. De Cola. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 582:(2025 Jul 01), pp. 122684.1-122684.9. [10.1016/j.ica.2025.122684]
Synthesis and crystallographic investigation of two new neutral Ir(III) complexes bearing 6-(phenyl)phenanthridine ligands
L. MendutiCo-primo
;M. MoriCo-primo
;F. Meneghetti
Penultimo
;L. De ColaUltimo
2025
Abstract
Herein, we report two new iridium(III) complexes (1 and 2), featuring 6-(phenyl)phenanthridine derivatives as cyclometalating (C^N) ligands and pyridyl-triazole or pyridyl-pyrazole ancillary (L^X) ligands. The synthesis of the two compounds was performed by reaction of the 6-(phenyl)-phenanthridine chloro-bridged dimer with the pyridyl-triazole/pyridyl-pyrazole (L^X) ligand. Single crystals of both complexes (1 and 2) were grown and analyzed by X-ray diffraction. Full crystallographic characterization and comparison of 1 and 2 solid-state structures is reported. Spectroscopic characterization revealed similar emissive properties for 1 (λmax = 650 nm; τdeg = 1.43 μs, QYdeg = 11.6 %) and 2 (λmax = 660 nm; τdeg = 1.45 μs, QYdeg = 12.1 %).File | Dimensione | Formato | |
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