Abstract
Tethered arene-ruthenium complexes [RuCl2{η1:η6-Me2P(CH 2)3C6H5}], [RuCl2{η1:η6-Ph2PCH 2SiMe2C6H5}] and [RuCl2{η1:η6-Ph2P(CH 2)3(aryl)}] (aryl=2,4,6-C6H2Me3, C6Me5) have been prepared by thermal displacement of methyl o-toluate from the appropriate P-donor derivatives of [RuCl2(η6-1,2-MeC6H4CO 2Me)]2 and their structures determined by X-ray studies. The tethered complexes undergo reversible one-electron oxidation by cyclic voltammetry; the half-wave potentials are in the range 1.10-1.34 V versus AgAgCl and decrease with increasing methyl substitution on the arene.
Original language | English |
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Pages (from-to) | 7-18 |
Number of pages | 12 |
Journal | Journal of Organometallic Chemistry |
Volume | 629 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 1 Jun 2001 |