Synthesis, structural characterization and catalytic evaluation of anionic phosphinoferrocene amidosulfonate ligands

Abstract

Triethylammonium salts of phosphinoferrocene amidosulfonates with electron-rich dialkyphosphino substituents, R2PfcCONHCH2SO3(HNEt3) (4a–c), where fc = ferrocene-1,1′-diyl, and R = i-Pr (a), cyclohexyl (Cy; b), and t-butyl (c), were synthesized from the corresponding phosphinocarboxylic acids-borane adducts, R2PfcCO2H·BH3(1a–c), via esters R2PfcCO2C6F5·BH3(2a–c) and adducts R2PfcCONHCH2SO3(HNEt3)·BH3(3a–c). Compound 4b was shown to react with [Pd(μ-Cl)(η-C3H5)]2and AgClO4to afford the zwitterionic complex [Pd(η3-C3H5) (Cy2PfcCONHCH2SO3-κ2O,P)] (5b), in which the amidosulfonate ligand coordinates as a chelating donor making use of its phosphine moiety and amide oxygen. The structures of 3b·CH2Cl2, 4b and 5b·CH2Cl2were determined by single-crystal X-ray diffraction analysis. Compounds 4a–c and their known diphenylphosphino analogue, Ph2PfcCONHCH2SO3(HNEt3) (4d), were studied as supporting ligands in Pd-catalyzed cyanation of aryl bromides with K4[Fe(CN)6] and in Suzuki–Miyaura biaryl cross-coupling performed in aqueous reaction media under mild reaction conditions. In the former reaction, the best results were achieved with a catalyst generated from [PdCl2(cod)] (cod = η2:η2-cycloocta-1,5-diene) and 2 equiv. of the least electron-rich ligand 4d in dioxane–water as a solvent. In contrast, the biaryl coupling was advantageously performed with a catalyst resulting from palladium(II) acetate and ligand 4a (1 equiv.) in the same solvent.