Synthesis, Structure, and Reactivity of Rhodium Bipyridine Compounds: Formation of a RhII Hydrido Cluster and a RhIII Peroxido Complex
✍ Scribed by Anna Penner; Tobias Schröder; Thomas Braun; Burkhard Ziemer
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 212 KB
- Volume
- 2009
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
Abstract
Treatment of [Rh(μ‐Cl)(coe)~2~]~2~ (coe = cyclooctene) with 4,4′‐di‐tert‐butyl‐2,2′‐bipyridine (tbbpy) gives the bipyridine complex [Rh(Cl)(tbbpy)(coe)] (1). A subsequent reaction with dihydrogen results in the formation of the cluster [{Rh(Cl)(H)(tbbpy)}]~4~ (2). The reaction of [Rh(μ‐Cl)(coe)~2~]~2~ with tbbpy in thf followed by the addition of CN__t__Bu affords [Rh(Cl)(tbbpy)(CN__t__Bu)] (3). The latter reacts with O~2~ or ^18^O~2~ to yield the peroxido complexes [Rh(Cl)(O~2~)(tbbpy)(CN__t__Bu)] (4a) and [Rh(Cl)(^18^O~2~)(tbbpy)‐(CN__t__Bu)] (4b), respectively. Complexes 1–4 were characterized by X‐ray crystallography. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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## Abstract A direct and high‐yield synthetic route for a novel dodecanuclear osmium‐rhodium mixed‐metal cluster is presented. The redox properties of the cluster were examined, and it was found that the anion behaves as an “electron reservoir”. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim,