Co-Ligand Involvement in Ground and Excited States of Electron-Rich (Polypyridyl)PtII Complexes

The electronic absorption and luminescence properties of electron‐rich organometallic platinum(II) complexes with aromatic α‐diimine ligands [(α‐diimine)PtR2] (R = alkyl, alkynyl, Ph or Mes, Mes = 2,4,6‐trimethylphenyl) were examined. The crystal and molecular structures of [(bpy)PtMe2], [(tap)PtPh2...

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Vydané v:European journal of inorganic chemistry Ročník 2003; číslo 10; s. 1917 - 1938
Hlavní autori: Klein, Axel, Slageren, Joris van, Záliš, Stanislav
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Weinheim WILEY-VCH Verlag 01.05.2003
WILEY‐VCH Verlag
Predmet:
Crystal structure
DFT
Emission
N ligands
Optical spectroscopy
Photophysics
Platinum
Theoretical calculations
ISSN:1434-1948, 1099-0682
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Shrnutí:The electronic absorption and luminescence properties of electron‐rich organometallic platinum(II) complexes with aromatic α‐diimine ligands [(α‐diimine)PtR2] (R = alkyl, alkynyl, Ph or Mes, Mes = 2,4,6‐trimethylphenyl) were examined. The crystal and molecular structures of [(bpy)PtMe2], [(tap)PtPh2] and [(tmphen)PtMes2] were determined from single‐crystal XRD and discussed in view of intermolecular interactions that influence the emission behaviour. The combination of theoretical calculations (DFT) and spectroscopic techniques (absorption and emission) revealed the character of electronic transitions and excited states. In particular they showed that the co‐ligand involvement in the frontier orbitals is small for R = Me, but large in case of R = alkynyl, Ph or Mes. Depending on the chelate ligand and its substitution pattern, the emission efficiencies of the complexes cover a wide range from strong emission in fluid solution at ambient temperature to very weak emission in rigid matrices (glasses) at low temperatures with no emission at ambient temperature. The emission lifetimes, determined at low temperature in solvent glasses, mainly depend on the chelate ligand and not on the co‐ligands. The emission quantum yields of the complexes in solution at room temperatures are much larger for R = Mes than for R = Ph or Me. The emission bands for the complexes with unsaturated co‐ligands show slight structuring at low temperatures in contrast to the alkyl‐substituted ones. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
Bibliografia:ark:/67375/WNG-SPM8089P-B
istex:E6B80E88FAFC8C5EF5FF5BDE0ACDF833018AAD79
ArticleID:EJIC#200200617
ISSN:1434-1948
1099-0682
DOI:10.1002/ejic.200200617