Journal article

Photochemical, photophysical and redox properties of novel fulgimide derivatives with attached 2,2′-bipyridine (bpy) and [M(bpy)₃]²⁺ (M = Ru and Os) moieties

  • Jukes, Ron T. F. Van't Hoff Institute for Molecular Sciences, University of Amsterdam, The Netherlands
  • Kühni, Joël Institute of Inorganic Chemistry, University of Fribourg, Switzerland
  • Salluce, Nunzio Institute of Inorganic Chemistry, University of Fribourg, Switzerland
  • Belser, Peter Institute of Inorganic Chemistry, University of Fribourg, Switzerland
  • Cola, Luisa De Physikalisches Institut, Westfälische Wilhelms-Universität, Münster, Germany
  • Hartl, František Van't Hoff Institute for Molecular Sciences, University of Amsterdam, The Netherlands
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    26.03.2009
Published in:
  • Dalton Transactions. - 2009, p. 3993-4002
English Fulgimides monosubstituted with [M(bpy)₃]²⁺ (M = Ru, Os; bpy = 2,2′-bipyridine) chromophore units and with a single bpy group were synthesized and investigated as components of conceivable dinuclear photochromic switches of luminescence. The E-, Z- and closed-ring (C) photoisomer forms of the bpy-bound fulgimide were successfully separated by semi-preparative HPLC. The same procedure failed, however, in the case of the [M(bpy)₃]²⁺-substituted fulgimides. Energy transfer from the excited photochromic unit to the metal-bpy centre competes with the fulgimide cyclization, reducing the photocyclization quantum yields by approximately one order of magnitude compared to the non-complexed fulgimide-bpy ligand (φEC = 0.17, φEZ = 0.071, φZE = 0.15 at λexc = 334 nm). The cycloreversion of the fulgimide-bpy ligand is less efficient (φCE = 0.047 at λexc = 520 nm). The intensity of the ³MLCT-based luminescence of the metal-bpy chromophore (in MeCN, φdeaer = 6.6 × 10⁻² and τdeaer = 1.09 μs for Ru; φdeaer = 6.7 × 10⁻³ and τdeaer = 62 ns for Os) is not affected by the fulgimide photoconversion. These results and supporting spectro-electrochemical data reveal that the lowest triplet excited states of the photochromic fulgimide moiety in all its E-, Z- and closed-ring forms lie above the lowest ³MLCT levels of the attached ruthenium and osmium chromophores. The actual components are therefore unlikely to form a triad acting as functional switch of energy transfer from [Ru(bpy)₃]²⁺ to [Os(bpy)₃]²⁺ through the photochromic fulgimide bridge.
Faculty
Faculté des sciences et de médecine
Department
Département de Chimie
Language
  • English
Classification
Chemistry
License
License undefined
Identifiers
Persistent URL
https://folia.unifr.ch/unifr/documents/301161
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