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首页> 外文期刊>Inorganica Chimica Acta >Pd(II) and Pt(II) complexes of cyclic bidentate (S)PNP(S) ligands: Synthesis, structure and catalytic activity in the Suzuki reaction
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Pd(II) and Pt(II) complexes of cyclic bidentate (S)PNP(S) ligands: Synthesis, structure and catalytic activity in the Suzuki reaction

机译:环状双齿(S)PNP(S)配体的Pd(II)和Pt(II)配合物:铃木反应中的合成,结构和催化活性

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摘要

The synthetic approach to the novel cyclic (S)PNP(S) ligands (5a-c, R = EtO, Me, Ph), i.e. 1-thiophosphoryl-2-thioxo-1,2-azaphospholanes having different surrounding at the exocyclic phosphorus atom, has been developed. Compounds bearing two asymmetric phosphorus atoms were obtained as individual (R*,R*)- and (R*,S*)-diastereomers. Reacting with (PhCN)_2MCl_2 (M = Pd, Pt) in MeCN under ambient conditions the ligands readily form complexes MLCl_2 [6a-c (M = Pd), 7b (M = Pt)] via bidentate chelating coordination mode. The structures and stereochemistry both of the ligands and their complexes were confirmed by IR, multinuclear NMR and X-ray diffraction study. The palladium complexes demonstrated high activity as precatalysts for the Suzuki cross-coupling reaction, which was found to increase in the series 6a < 6b < 6c.
机译:合成新型环状(S)PNP(S)配体(5a-c,R = EtO,Me,Ph)的合成方法,即在环外磷处具有不同周围环境的1-硫代磷酰基-2-硫代-1,2-氮杂膦原子,已经被开发出来。获得带有两个不对称磷原子的化合物作为(R *,R *)-和(R *,S *)-非对映异构体。在环境条件下与MeCN中的(PhCN)_2MCl_2(M = Pd,Pt)反应,配体容易通过二齿螯合配位形式形成配合物MLCl_2 [6a-c(M = Pd),7b(M = Pt)]。通过IR,多核NMR和X射线衍射研究证实了配体及其配合物的结构和立体化学。钯配合物表现出很高的活性,可作为Suzuki交叉偶联反应的前催化剂,发现在6a <6b <6c系列中,钯的络合物增加。

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