A trinuclear ruthenium(II) complex with rare S,O-bridging sulfoxide ligands

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S. Francesca Lessing, Simon Lotz, H. Marita Roos and Petrus H. van Rooyen


Abstract

The trimetallic compound [Ru3(µ-mpso-S,O)2(µ-Cl)4(mpso-S[hair space])4Cl2] (mpso = C7H8OS, methyl phenyl sulfoxide) 1 was prepared from hydrated RuCl3 and methyl phenyl sulfoxide. A crystal structure determination revealed a linearly arranged molecule with three ruthenium atoms in distorted octahedral configurations with bridging chloro and S,O-mpso ligands. For the ruthenium metals with triply bridged chloro ligands, the Ru–Cl–Ru angles are 81.8(4), 82.7(1) and 83.2(1)°, and the Ru[hair space][hair space]· · ·[hair space][hair space]Ru non-bonded distance is 3.218 Å. In contrast, the Ru–Cl–Ru angle on the bridging mpso part of the molecule is 100.7(1)°, and the Ru[hair space][hair space]· · ·[hair space][hair space]Ru non-bonded distance is 3.686 Å. The configuration at sulfur on S2, S4 and S5 is opposite to that at S1, S3 and S6. In solution, the methyl resonances in the 1H and 13C NMR spectra of 1 are found in the δ ranges 3.81–2.70 and 49.7–44.9, respectively. The methyl resonances of the S,O-bridging mpso ligands are shifted upfield in the 1H NMR spectrum, but furthest downfield in the 13C NMR spectrum.


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