首页> 外文期刊>Journal of the American Chemical Society >Oxidative Dinuclear Addition of a Pd~I-Pd~I Moiety to Arenes: Generation of μ-η~3:η~3-Arene-Pd~(III)_2 Species
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Oxidative Dinuclear Addition of a Pd~I-Pd~I Moiety to Arenes: Generation of μ-η~3:η~3-Arene-Pd~(III)_2 Species

机译:Pd〜I-Pd〜I部分向芳烃的氧化双核加成:μ-η〜3:η〜3-Arene-Pd〜(III)_2物种的产生

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摘要

We report the oxidative dinuclear addition of a Pd~I-Pd~I bond to arenes. The oxidative dinuclear addition products, which have a bi-π-allyl-type arene dipalladium(II) structure, were obtained from [2.2]paracydophane, anthracene, tetracene, and pentacene. A systematic study of the reaction of [Pd_2(CH_3CN)_6] [BF_4]_2 with benzene and poly-acenes showed that the larger polyacenes, tetracene and pentacene, afforded the oxidative dinuclear addition products, while benzene, naphthalene, and anthracene gave the π-sandwich Pd~I -Pd~I complexes.
机译:我们报道了Pd〜I-Pd〜I键与芳烃的氧化双核加成。具有双π-烯丙基型芳烃二铝(II)结构的氧化性双核加成产物得自[2.2]对苯二甲酰基,蒽,并四苯和并五苯。对[Pd_2(CH_3CN)_6] [BF_4] _2与苯和聚并苯的反应的系统研究表明,较大的聚并苯,并四苯和并五苯提供了氧化双核加成产物,而苯,萘和蒽则提供了氧化双核加成产物。 π夹心Pd〜I -Pd〜I络合物。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第38期|p.14908-14911|共4页
  • 作者单位

    Department of Applied Chemistry, Graduate School of Engineering, Osaka University, and PRESTO, Japan Science and Technology Agency, Suita, Osaka, 565-0871, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka University, and PRESTO, Japan Science and Technology Agency, Suita, Osaka, 565-0871, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka University, and PRESTO, Japan Science and Technology Agency, Suita, Osaka, 565-0871, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka University, and PRESTO, Japan Science and Technology Agency, Suita, Osaka, 565-0871, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:27

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