Half-sandwich ruthenium(ii) complexes with tethered arene-phosphinite ligands: synthesis, structure and application in catalytic cross dehydrogenative coupling reactions of silanes and alcohols

Abstract

The preparation of the tethered arene-ruthenium(II) complexes [RuCl₂{η⁶:κ¹(P)-C₆H₅(CH₂)_nOPR₂}] (R = Ph, n = 1 (9a), 2 (9b), 3 (9c); R = ⁱPr, n = 1 (10a), 2 (10b), 3 (10c)) from the corresponding phosphinite ligands R₂PO(CH₂)_nPh (R = Ph, n = 1 (1a), 2 (1b), 3 (1c); R = ⁱPr, n = 1 (2a), 2 (2b), 3 (2c)) is presented. Thus, in a first step, the treatment at room temperature of tetrahydrofuran solutions of dimers [{RuCl(μ-Cl)(η⁶-arene)}₂] (arene = p-cymene (3), benzene (4)) with 1-2a-c led to the clean formation of the corresponding mononuclear derivatives [RuCl₂(η⁶-p-cymene){R₂PO(CH₂)_nPh}] (5-6a-c) and [RuCl₂(η⁶-benzene){R₂PO(CH₂)_nPh}] (7-8a-c), which were isolated in 66–99% yield. The subsequent heating of 1,2-dichloroethane solutions of these compounds at 120 °C allowed the exchange of the coordinated arene. The substitution process proceeded faster with the benzene derivatives 7-8a-c, from which complexes 9-10a-c were generated in 61–82% yield after 0.5–10 h of heating. The molecular structures of [RuCl₂(η⁶-p-cymene){ⁱPr₂PO(CH₂)₃Ph}] (6c) and [RuCl₂{η⁶:κ¹(P)-C₆H₅(CH₂)_nOPⁱPr₂}] (n = 1 (10a), 2 (10b), 3 (10c)) were unequivocally confirmed by X-ray diffraction methods. In addition, complexes [RuCl₂{η⁶:κ¹(P)-C₆H₅(CH₂)_nOPR₂}] (9-10a-c) proved to be active catalysts for the dehydrogenative coupling of hydrosilanes and alcohols under mild conditions (r.t.). The best results were obtained with [RuCl₂{η⁶:κ¹(P)-C₆H₅(CH₂)₃OPⁱPr₂}] (10c), which reached TOF and TON values up to 117 600 h⁻¹ and 57 000, respectively.