The title compound, [Ce(CF 3 SO 3 )(C 10 H 15 ) 2 (C 10 H 8 N 2 )], crystallizes as a bent metallocene with an inner-sphere trifluoromethanesulfonate ligand [Cg1-Ce-Cg2 = 138.91 (1) A ˚; Cg1 and Cg2 are the centroids of the cyclopentadienyl rings]. The pentamethylcyclopentadienyl rings have a slight
Bis(acetonitrile-κN)(η5-pentamethylcyclopentadienyl)(pyrimidine-κN)rhodium(III) bis(hexafluoridophosphate)
✍ Scribed by Boyer, Julie L. ;Wilson, Scott R. ;Rauchfuss, Thomas B.
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 983 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, [Rh(C 10 H 15
, where Cp* is pentamethylcyclopentadienyl, was obtained from the treatment of an acetonitrile solution of [Cp*Rh(NCMe) 3 ](PF 6 ) 2 with an excess of pyrimidine. The Rh III center is coordinated by one Cp* ring, two acetonitrile ligands and one pyrimidine ligand in a pseudo-octahedral geometry. Both PF 6 anions are disordered (site occupancies ca 0.4:0.6, and 0.3:0.4:0.3).
📜 SIMILAR VOLUMES
In the title dinuclear rhodium complex, [(- the terminal trifluoromethanesulfonate ligands adopt a trans configuration with respect to each other and the RhÁ Á ÁRh distances range from 5.5157 (8) to 5.5389 (6) A ˚. There are two and a half molecules within the asymmetric unit, one of the molecules
The cluster dication of the title compound, [Cu~2~Mo~2~(C~10~H~15~)~2~S~4~(C~5~H~5~N)~2~](ClO~4~)~2~, has [(η^5^-C~5~Me~5~)~2~Mo~2~(μ-S)~2~S~2~] units linked to Cu(py)^+^ units (py is pyridine) by Cu—S bonds and features a cubane-like [Mo~2~S~4~Cu~2~] core framework. The Cu atom shows a distorted te
In the crystal structure of the title vanadocene complex, [V( 5 -C 5 H 5 ) 2 (NCS) 2 ], the V atom has distorted tetrahedral coordination with two 5 -bonded cyclopentadienyl rings and two Nbonded thiocyanate ligands.