4.7 Article

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

期刊

DALTON TRANSACTIONS
卷 42, 期 23, 页码 8402-8412

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3dt50334h

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资金

  1. CFI (Canadian Foundation for Innovation)
  2. NSERC (the National Sciences and Engineering Research Council of Canada)
  3. FQRNT (Le Fonds quebecois de la recherche sur la nature et les technologies)
  4. Universite de Sherbrooke

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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.

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