Half‐Sandwich Guanidinate–Osmium(II) Complexes: Synthesis and Application in the Selective Dehydration of Aldoximes

Abstract

AbstractThe novel guanidinate–osmium(II) complexes [OsCl{κ2‐(N,N′)‐C(NR)(NiPr)NHiPr}(η6‐p‐cymene)] [R = Ph (3a), 4‐C6H4F (3b), 4‐C6H4Cl (3c), 4‐C6H4CF3 (3d), 3‐C6H4CF3 (3e), 3,5‐C6H3(CF3)2 (3f), 4‐C6H4CN (3g), 4‐C6H4Me (3h), 3‐C6H4Me (3i), 2‐C6H4Me (3j), 4‐C6H4tBu (3k), 2,6‐C6H3iPr2 (3l), 2,4,6‐C6H2Me3 (3m)] have been synthesized in high yields (70–88 %) by treatment of THF solutions of the dimeric precursor [{OsCl(µ‐Cl)(η6‐p‐cymene)}2] (1) with 4 equivalents of the corresponding guanidine (iPrHN)2C=NR (2a–m) at room temperature. The easily separable guanidinium chloride salts [(iPrHN)2C(NHR)]Cl (4a–m) were also formed in these reactions. The structures of 3a, 3d, and 3h were unequivocally confirmed by X‐ray diffraction methods. Complexes 3a–m proved to be active in the catalytic dehydration of aldoximes. The best results were obtained with [OsCl{κ2‐(N,N′)‐C(N‐4‐C6H4CF3)(NiPr)NHiPr}(η6‐p‐cymene)] (3d; 5 mol‐%), which, in acetonitrile at 80 °C, was able to convert selectively a large variety of aromatic, heteroaromatic, α,β‐unsaturated, and aliphatic aldoximes into the corresponding nitriles in high yields and short reaction times.