4.5 Article

Synthetic Strategies for Variably Substituted Ruthenium-Imidazophenanthrolinium Complexes

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 5, Pages 750-762

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201402669

Keywords

Ruthenium; Water splitting; Ligand design; N ligands; Carbenes

Funding

  1. Graduiertenkolleg-Research Training Group [GRK 1626]
  2. Carl-Zeiss-Stiftung
  3. Elitenetzwerk Bayern
  4. graduate school molecular science Friedrich Alexander University (FAU), Erlangen-Nurnberg, Germany
  5. Deutsche Forschungsgemeinschaft (DFG) [SFB 583]

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The synthesis of several symmetric and asymmetric substituted imidazophenanthrolinium ligands and their corresponding ruthenium polypyridyl complexes was achieved by applying a newly designed synthetic concept. By testing different moieties, the advantages and limits of the synthetic approach could be defined. The substitution pattern on the imidazolium moiety has no significant influence on the structural aspects of the imidazophenanthrolinium backbone or on the photophysical properties of the ruthenium compounds. Given that imidazolium salts act as precursors for N-heterocyclic carbenes, the reported results provide the basis for the design of highly efficient oligonuclear photocatalysts.

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