Formation of New η5-Rhodium(III) Complexes from η5-Rh(I) Rhodacarborane-Containing Charge-Compensated Ligands

• Published in: Organometallics 2004-05, Vol.23 (10), p.2273-2280
• Main Authors: Núñez, R, Tutusaus, O, Teixidor, F, Viñas, C, Sillanpää, R, Kivekäs, R
• Format: Article
• Language: English
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/om030635h

A series of new Rh(I) half-sandwich complexes of formula [3,3-(PPh3)2-8-L-closo-3,1,2-RhC2B9H10)] (L = SMe2 (2a), SEt2 (2b), S(CH2)4 (2c), SEtPh (2d)) and [1-Me-3,3-(PPh3)2-8-L-closo-3,1,2-RhC2B9H9)] (L = SMe2 (2e), SEt2 (2f)) have been prepared by reaction of the respective monoanionic charge-compensated ligands [10-L-nido-7,8-C2B9H10]- and [7-Me-10-L-7,8-C2B9H9]- with [RhCl(PPh3)3]. Complex [3,3-(cod)-8-SMe2-closo-3,1,2-RhC2B9H10] (3) has also been prepared by reaction of K[10-SMe2-nido-7,8-C2B9H10] with [RhCl(cod)]2. Rh(I) complexes 2a−d may be easily oxidized to the corresponding Rh(III) complexes 4a−d under N2 atmosphere in some halogenated solvents such as CCl4 and CHCl3. The complexes have been fully characterized by IR and NMR spectroscopy, and the crystal structures of 2a, 3, and 4a have been elucidated by single-crystal X-ray diffraction analysis. An EPR spectrum analysis clearly evidences the formation of free radicals as intermediates in the evolution of 2a−d to 4a−d complexes. The capacity to stabilize both Rh(I) and Rh(III) oxidation states by the [10-SMe2-nido-7,8-C2B9H10]- system may be attributed to its donor capacity together with the presence of labile ligands in the molecule.