Number of the records: 1
Ambi-Valence Taken Literally: Ruthenium vs Iron Oxidation in (1,1′-Diphosphinoferrocene)ruthenium(II) Hydride and Chloride Complexes as Deduced from Spectroelectrochemistry of the Heterodimetallic “Mixed-Valent” Intermediates
- 1.
SYSNO ASEP 0349260 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Ambi-Valence Taken Literally: Ruthenium vs Iron Oxidation in (1,1′-Diphosphinoferrocene)ruthenium(II) Hydride and Chloride Complexes as Deduced from Spectroelectrochemistry of the Heterodimetallic “Mixed-Valent” Intermediates Author(s) Sixt, T. (DE)
Sieger, M. (DE)
Krafft, M. J. (DE)
Bubrin, D. (DE)
Fiedler, Jan (UFCH-W) RID, ORCID
Kaim, W. (DE)Source Title Organometallics. - : American Chemical Society - ISSN 0276-7333
Roč. 29, č. 21 (2010), s. 5511-5516Number of pages 6 s. Language eng - English Country US - United States Keywords (1,1′-Diphosphinoferrocene)ruthenium(II) ; hydride complexes ; chloriode complexes Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects GA203/09/0705 GA ČR - Czech Science Foundation (CSF) GA203/08/1157 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z40400503 - UFCH-W (2005-2011) UT WOS 000283572100103 DOI 10.1021/om1004258 Annotation Combining two different redox-active organometallic moieties, we prepared the compounds [(Cym)RuCl(dpf)](PF6), with Cym = p-cymene = 1-isopropyl-4-methylbenzene, and the diphosphinoferrocenes (dpf) 1,1′-bis(diphenylphosphino)ferrocene (dppf; complex 3), 1,1′-bis(diisopropylphosphino)ferrocene (dippf; complex 4), and 1,1′-bis(diethylphosphino)ferrocene (depf; complex 5) as well as the structurally characterized hydride complex [(C5Me5)RuH(dippf)] (2). In contrast to the case for 2, with an approximately staggered ferrocene conformation, the chloride complexes 3−5 exhibit a syn-periplanar ferrocene arrangement due to a Cl···H(C5H4) interaction in the solid and in solution. The related new compounds [(Cym)RuH(dppf)](PF6) (6) and trinuclear (μ-dpf)[(Cym)RuCl2)]2 (7−9) were also obtained and identified by 1H and 31P NMR spectroscopy. Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2011
Number of the records: 1