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首页> 外文期刊>Journal of the American Chemical Society >The Isomerization of Methoxy Radical: Intramolecular Hydrogen Atom Transfer Mediated through Acid Catalysis
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The Isomerization of Methoxy Radical: Intramolecular Hydrogen Atom Transfer Mediated through Acid Catalysis

机译:甲氧基自由基的异构化:通过酸催化介导的分子内氢原子转移

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摘要

The catalytic ability of water, formic acid, and sulfuric acid to facilitate the isomerization of the CH_3O radical to CH_2OH has been studied. It is shown that the activation energies for isomerization are 30.2, 25.7, 4.2, and 2.3 kcal mol~(-1), respectively, when the reaction is carried out in isolation and with water, formic acid, or sulfuric acid as a catalyst. The formation of a doubly hydrogen bonded transition state is central to lowering the activation energy and facilitating the intramolecular hydrogen atom transfer that is required for isomerization. The changes in the rate constant for the CH_3O-to-CH_2OH isomerization with acid catalysis have also been calculated at 298 K. The largest enhancement in the rate, by over 12 orders of magnitude, is with sulfuric acid. The results of the present study demonstrate the feasibility of acid catalysis of a gas-phase radical isomerization reaction that would otherwise be forbidden.
机译:研究了水,甲酸和硫酸促进CH_3O自由基异构化为CH_2OH的催化能力。结果表明,当分离反应并以水,甲酸或硫酸为催化剂进行反应时,异构化反应的活化能分别为30.2、25.7、4.2和2.3 kcal mol·(-1)。双氢键过渡态的形成对于降低活化能并促进异构化所需的分子内氢原子转移至关重要。还已经计算出在酸催化下CH_3O到CH_2OH异构化的速率常数的变化是在298 K下。最大的提高速率是硫酸,超过12个数量级。本研究的结果证明了气相自由基异构化反应中酸催化的可行性,否则将被禁止。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第7期|p.2013-2015|共3页
  • 作者单位

    Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States;

    Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0314, United States;

    Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States;

  • 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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