Ladouceur, Sebastien; Fortin, Daniel; Zysman-Colman, Eli published the article 《Enhanced Luminescent Iridium(III) Complexes Bearing Aryltriazole Cyclometallated Ligands》. Keywords: yellow blue luminescence iridium cyclometalated aryltriazole bipyridine complex; DFT optimized mol structure iridium cyclometalated aryltriazole bipyridine complex; redox potential iridium cyclometalated aryltriazole bipyridine complex; crystal structure iridium cyclometalated aryltriazole bipyridine complex preparation; mol structure iridium cyclometalated aryltriazole bipyridine complex.They researched the compound: [Ir(dtbbpy)(ppy)2]PF6( cas:676525-77-2 ).Electric Literature of C40H40F6IrN4P. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:676525-77-2) here.
Herein we report the synthesis of 4-aryl-1-benzyl-1H-1,2,3-triazoles (atl), made via “”Click chem.”” and their incorporation as cyclometalating ligands into new heteroleptic iridium(III) complexes containing diimine (N∩N) ancillary ligands 2,2′-bipyridine (bpy) and 4,4′-di-tert-butyl-2,2′-bipyridine (dtBubpy). Depending on decoration, these complexes emit from the yellow to sky blue in acetonitrile (ACN) solution at room temperature (RT). Their emission energies are slightly blue-shifted and their photoluminescent quantum efficiencies are markedly higher (between 25 and 80%) than analogous (C∩N)2Ir(N∩N)+ type complexes, where C∩N is a decorated 2-phenylpyridinato ligand. This increased brilliance is in part due to the presence of the benzyl groups, which act to sterically shield the iridium metal center. X-ray crystallog. analyses of two of the atl complexes corroborate this assertion. Their electrochem. is reversible, thus making these complexes amenable for inclusion in light-emitting electrochem. cells (LEECs). A parallel computational investigation supports the exptl. findings and demonstrates that for all complexes included in this study, the HOMO is located on both the aryl fragment of the atl ligands and the iridium metal while the LUMO is located essentially exclusively on the ancillary ligand.
There is still a lot of research devoted to this compound(SMILES:[F-][P+5]([F-])([F-])([F-])([F-])[F-].CC(C)(C1=CC=[N]([Ir+3]23([C-]4=CC=CC=C4C5=CC=CC=[N]25)([C-]6=CC=CC=C6C7=CC=CC=[N]37)[N]8=CC=C(C(C)(C)C)C=C98)C9=C1)C)Electric Literature of C40H40F6IrN4P, and with the development of science, more effects of this compound(676525-77-2) can be discovered.
Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”