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Strong π-Acceptor Ligands in Rhodium-Catalyzed Hydroformylation of Ethene and 1-Octene: Operando Catalysis

机译:铑催化的乙烯和1-辛烯加氢甲酰化反应中的强π-受体配体:Operondo催化

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摘要

Strong π-acceptor N-pyrrolylphosphoramidite and pyrrolylphosphine mono- and bidentante ligands were applied in ethene hydroformylation using a stoichiometric gas mixture CO/H2/ethene 1:1:1. Very fast reactions (TOF up to 29.5 × 103 mol mol~(-1) h~(-1), 13-fold faster than triphenylphosphine) and excellent selectivities were obtained. The pyrrolylphosphine derivatives of SPANphos and Xantphos, pySPAN and pyXANT, were used in 1-octene hydroformylation. The electronic character of these ligands improved both activities and regioselectivities compared with the phenyl-substituted ligands. HPNMR and HPIR showed that both pySPAN and pyXANT favor the formation of bisequatorial [RhH(CO)2(ligand)] complexes under catalytic conditions.
机译:使用化学计量气体混合物CO / H2 /乙烯1:1:1,将强π-受体N-吡咯基亚磷酰胺和吡咯基膦单-和二齿配体应用于乙烯加氢甲酰化。获得了非常快速的反应(TOF高达29.5×103 mol mol〜(-1)h〜(-1),比三苯基膦快13倍),并且具有极好的选择性。 SPANphos和Xantphos的吡咯基膦衍生物pySPAN和pyXANT用于1-辛烯加氢甲酰化反应。与苯基取代的配体相比,这些配体的电子特性提高了活性和区域选择性。 HPNMR和HPIR表明pySPAN和pyXANT均在催化条件下有利于双水基[RhH(CO)2(配体)]配合物的形成。

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