Issue 22, 1996

Oxidative addition of diferrocenyl dichalcogenides to [{Ru(η5-C5Me5)(µ3-Cl)}4]. Syntheses, crystal structures and some reactivities of [{Ru(η5-C5Me5)Cl(µ-ER)}2](E = S, Se or Te; R = ferrocenyl)

Abstract

Reaction of [{Ru(η5-C5Me5)(µ3-Cl)}4] with 2 equivalents of REER (E = S, Se or Te; R = ferrocenyl) gave novel ferrocenylchalcogenolate-bridged diruthenium complexes [{Ru(η5-C5Me5)Cl(µ-ER)}2] in good yields. Reduction of these by sodium amalgam in the presence of buta-1,3-diene afforded [{Ru(η5-C5Me5)(µ-ER)}2(µ-s-trans22′-CH2[double bond, length half m-dash]CHCH[double bond, length half m-dash]CH2)], whereas treatment with AgOSO2CF3 produced the co-ordinatively unsaturated complexes [Cl(η5-C5Me5)Ru(µ-ER)2 Ru(η5-C5Me5)][OSO2CF3]. The structures of five of the complexes have been defined by X-ray crystallography.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1996, 4307-4312

Oxidative addition of diferrocenyl dichalcogenides to [{Ru(η5-C5Me5)(µ3-Cl)}4]. Syntheses, crystal structures and some reactivities of [{Ru(η5-C5Me5)Cl(µ-ER)}2](E = S, Se or Te; R = ferrocenyl)

H. Matsuzaka, J. Qö, T. Ogino, M. Nishio, Y. Nishibayashi, Y. Ishii, S. Uemura and M. Hidai, J. Chem. Soc., Dalton Trans., 1996, 4307 DOI: 10.1039/DT9960004307

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