Metal/Metal Redox Isomerism Governed by Configuration |
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| Authors: | Stephan Ludwig Dr. Kai Helmdach Mareike Hüttenschmidt Elisabeth Oberem Dr. Jabor Rabeah Dr. Alexander Villinger Prof. Dr. Ralf Ludwig Prof. Dr. Wolfram W. Seidel |
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| Affiliation: | 1. Institut für Chemie, Universität Rostock, Albert-Einstein-Straße 3a, 18059 Rostock, Germany;2. Department Life, Light & Matter, Universität Rostock, Albert-Einstein-Straße 25, 18059 Rostock, Germany;3. Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert-Einstein-Strasse 29a, 18059 Rostock, Germany |
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| Abstract: | A pair of diastereomeric dinuclear complexes, [Tp′(CO)BrW{μ-η2-C,C′-κ2-S,P-C2(PPh2)S}Ru(η5-C5H5)(PPh3)], in which W and Ru are bridged by a phosphinyl(thiolato)alkyne in a side-on carbon P,S-chelate coordination mode, were synthesized, separated and fully characterized. Even though the isomers are similar in their spectroscopic properties and redox potentials, the like-isomer is oxidized at W while the unlike-isomer is oxidized at Ru, which is proven by IR, NIR and EPR-spectroscopy supported by spectro-electrochemistry and computational methods. The second oxidation of the complexes was shown to take place at the metal left unaffected in the first redox step. Finally, the tipping point could be realized in the unlike isomer of the electronically tuned thiophenolate congener [Tp′(CO)(PhS)W{μ-η2-C,C′-κ2-S,P-C2(PPh2)S}Ru(η5-C5H5)-(PPh3)], in which valence trapped WIII/RuII and WII/RuIII cationic species are at equilibrium. |
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| Keywords: | alkyne ligands bridging ligands redox chemistry redox isomerism regioselectivity |
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