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首页> 外文期刊>Inorganic Chemistry Communications >Oxidative coupling of activated alkynes with palladium(0) olefin complexes:Side production of the highly symmetric hexamethyl mellitate species under mild conditions at low alkyne/complex molar ratios
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Oxidative coupling of activated alkynes with palladium(0) olefin complexes:Side production of the highly symmetric hexamethyl mellitate species under mild conditions at low alkyne/complex molar ratios

机译:活化炔烃与钯(0)烯烃络合物的氧化偶联:在温和条件下,低炔烃/络合物摩尔比下,高对称性六甲基甲磺酸盐物种的副产物

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摘要

The reactions of oxidative coupling of dimethylacetylene dicarboxylate (DMA) with palladium (0) olefin complexes bearing a pyr-idylthioether as ancillary ligand give rise to the corresponding palladacyclopentadienyl complexes as the main product and in some cases to the highly symmetric hexamethyl mellitate molecule,especially when a low alkyne(DMA)/complex ratio is employed.A plausible mechanism based on several pieces of experimental evidence is proposed,and the most effective complexes promoting the hexamethyl mellitate synthesis were identified.
机译:二羧酸二甲基乙炔酯(DMA)与带有吡咯基硫醚作为辅助配体的钯(0)烯烃配合物的氧化偶联反应产生相应的四环环戊二烯基配合物作为主要产物,在某些情况下会生成高度对称的六甲基甲磺酸盐分子当采用低炔烃(DMA)/配合物比率时,基于几项实验证据提出了一个合理的机理,并确定了最有效的促进六甲基乙酸甲酯合成的配合物。

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