Intramolecular Charge Transfer in Ruthenium Complexes [Ru(acac)2(ciq)] with Ambidentate Camphoriminoquinone (ciq) Ligands

Reaction of [Ru(acac)2(MeCN)2], acac−=acetylacetonate, with N‐phenylcamphoriminoquinone (pciq) or the new N‐(2‐thiomethylphenyl)‐camphoriminoquinone (tciq) produces complexes [Ru(acac)2(pciq)] and [Ru(acac)2(tciq)] with N,O or N,S coordination and E or Z configuration at the C=N bond, respectively....

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Bibliographic Details
Published in:Zeitschrift für anorganische und allgemeine Chemie (1950) Vol. 647; no. 5; pp. 525 - 533
Main Authors: Filippou, Vasileios, Blickle, Svenja, Bubrin, Martina, Kaim, Wolfgang
Format: Journal Article
Language:English
Published: Weinheim Wiley Subscription Services, Inc 11.03.2021
Subjects:
Camphor ligands
Charge transfer
Coordination ambivalence
Ligands
Oxidation
Ruthenium complexes
Ruthenium compounds
Spectroelectrochemistry
Structure
Valence
ISSN:0044-2313, 1521-3749
Online Access:Get full text
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Summary:Reaction of [Ru(acac)2(MeCN)2], acac−=acetylacetonate, with N‐phenylcamphoriminoquinone (pciq) or the new N‐(2‐thiomethylphenyl)‐camphoriminoquinone (tciq) produces complexes [Ru(acac)2(pciq)] and [Ru(acac)2(tciq)] with N,O or N,S coordination and E or Z configuration at the C=N bond, respectively. Oxidation state assignments in comparison with classical iminoquinone ligands are based on structural data in connection with DFT calculations. Reversible oxidation yields complex ions [RuIII(acac)2(pciq)]+ and [RuIII(acac)2(tciq)]+ as characterized by EPR, IR and UV‐vis‐NIR spectroelectrochemistry.
Bibliography:Dedicated to Professor Christoph Janiak on the Occasion of his 60th Birthday
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ISSN:0044-2313
1521-3749
DOI:10.1002/zaac.202000464