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Synthesis of Halfsandwich Ruthenium Complexes of Sulfinic Acid Esters [1]

  • Wolfdieter A. Schenk EMAIL logo and Nikolai Kuhnerta
Published/Copyright: June 2, 2014
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A series of halfsandwich ruthenium sulfinato complexes [CpRu(PR'3)2(SO2R)] (R = Me, CH2Ph, C2H4Ph, Ph, 4-C6H4Me; PR'3 = PMe3, 1/2 dppm) with various electronic and steric environments around the ruthenium centre, have been prepared by insertion of SO2 into a ruthenium carbon bond, by a direct ligand exchange reaction, or by oxidation of thiolato complexes with 3-chloroperoxybenzoic acid. The chiral complexes [CpRu(CO )(PPh3)(SO2R)] (R = Me, CH2Ph, Ph) were obtained similarly by oxidation of the corresponding thiolates with magnesium monoperoxyphthalate. Alkylation of the sulfinato complexes with oxonium salts [R"3O]X (R" = Me, Et; X = BF4 , PF6) gave ruthenium complexes of sulfinic acid esters, [CpRu(L)(L′)(S(O)(OR″)R)]X in high yields and, for the chiral complexes, up to 82% de. The esters may be detached from the metal by ligand exchange with acetonitrile. Stronger nucleophiles such as I- or SMe- dealkylate the coordinated sulfinic acid esters.

Received: 2000-3-20
Published Online: 2014-6-2
Published in Print: 2000-6-1

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