首页> 外文期刊>Inorganica Chimica Acta >Synthesis and characterization of sterically hindered thiolate Pd(II) complexes of the type [Pd(SR)(2)(TMEDA)]: Examination of their catalytic properties in phosphane-free Suzuki-Miyaura cross couplings
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Synthesis and characterization of sterically hindered thiolate Pd(II) complexes of the type [Pd(SR)(2)(TMEDA)]: Examination of their catalytic properties in phosphane-free Suzuki-Miyaura cross couplings

机译:[Pd(SR)(2)(TMEDA)]型位阻硫醇盐Pd(II)配合物的合成与表征:在无膦烷的Suzuki-Miyaura交叉偶联中检查其催化性能

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摘要

The sterically hindered thiolate complexes [Pd(SR)(2)(TMEDA)] SR = SC6F5 (2), SC6F4-4-H (3), SC6H4-2-SiPh3 (4) were easily synthesized by metathetical reactions of the corresponding palladium chloro compound [Pd(Cl)(2)(TMEDA)] (1) and the lead salt of the corresponding thiol. The identity of the three species being unequivocally determined by single crystal X-ray diffraction techniques. The catalytic activity of the palladium species [Pd(SR)(2)(TMEDA)] was explored in the Suzuki-Miyaura cross coupling reactions of different p-substituted bromobenzenes.
机译:位阻硫醇盐配合物[Pd(SR)(2)(TMEDA)] SR = SC6F5(2),SC6F4-4-H(3),SC6H4-2-SiPh3(4)易于通过相应的复分解反应合成钯氯化合物[Pd(Cl)(2)(TMEDA)](1)和相应硫醇的铅盐。通过单晶X射线衍射技术可以明确确定这三个物种的身份。在不同对位取代溴苯的Suzuki-Miyaura交叉偶联反应中探索了钯类[Pd(SR)(2)(TMEDA)]的催化活性。

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