Cationic iridium(III) complexes bearing a bis(triazole) ancillary ligand

被引:52
作者
Donato, Loic [1 ]
Abel, Philippe [1 ]
Zysman-Colman, Eli [1 ]
机构
[1] Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
MOLECULAR-ORBITAL METHODS; EXTENDED BASIS-SETS; VALENCE BASIS-SETS; COMPACT EFFECTIVE POTENTIALS; EXPONENT BASIS-SETS; ORGANOMETALLIC COMPOUNDS; EXCITATION-ENERGIES; TRIAZOLE; EFFICIENT; 1ST-ROW;
D O I
10.1039/c3dt50334h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new heteroleptic cationic iridium complexes of the form [Ir(C boolean AND N)(btl)](+), where btl = 1,1'-benzyl-4,4'-bi-1H-1,2,3-triazolyl and C boolean AND N = 2-phenylpyridine (ppyH) (1), 1-benzyl-4-phenyl-1H-1,2,3-triazole (phtl) (2) or 1-benzyl-4-(2,4-difluorophenyl)-1H-1,2,3-triazole (dFphtl) (3), were synthesized and isolated as their hexafluorophosphate (PF6-) salts and fully characterized. The single crystal structure of 3 has been solved. Along the series from 1-3 the absorption spectra shift hypsochromically while the electrochemical gap increases from 3.25 to 3.54 to 3.88 V. Acetonitrile solutions of 1 and 2 are poorly luminescent, sky-blue emitters with predominant ligand-centered and charge transfer character, respectively. Theoretical calculations support these assignments. Complex 3 is not photostable and decomposes to solvento-based structures of the form [Ir(dFphtl)(2)(ACN)(n)](+) (n = 1, 2) through a dissociation and degradation of the btl ligand.
引用
收藏
页码:8402 / 8412
页数:11
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