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
μ-Oxalato-κ2O1,O2:κ2O1′,O2′-bis[(η5-pentamethylcyclopentadienyl)(trifluoromethanesulfonato-κO)rhodium(III)]
✍ Scribed by Govindaswamy, Padavattan ;Süss-Fink, Georg ;Therrien, Bruno
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 621 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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 lying on an inversion centre. Interestingly, in one molecule, the S-O bond of a coordinated O atom is shorter than the two S-O bonds of the noncoordinated O atoms, and the corresponding Rh-O distance is significantly longer than the other M-O distances.
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)(1,10-phenanthroline-j 2 N,N 0 0 0 )copper(II)]
In the title compound, [Cu(C~2~O~4~)(C~6~H~7~NO)~2~]~__n__~, the Cu^II^ atom is six-coordinated in a slightly deformed elongated octahedral arrangement and the 3-(hydroxymethyl)pyridine ligand, surprisingly, acts as a monodentate ligand coordinated only through the N atom of the pyridine ring. The o
l-Oxalato-1j 2 O,O 0 0 0 :2j 2 O 0 0 00 0 0 ,O 0 0 00 0 00 0 0 -bis(chloro{[1-(2pyridyl-jN)ethylidene]hydrazine-jN}copper(II)
The photodecomposition product l-oxalato-1j 2 O,O 0 0 0 :2j 2 O 0 0 00 0 0 ,O 0 0 00 0 00 0 0 -bis{bis[2-(2-pyridyl)phenylj 2 C,N]iridium(III)}-acetone (1/1.974