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Quantitative kinetic investigation of triazole-gold(Ⅰ) complex catalyzed [3,3]-rearrangement of propargyl ester

机译:三唑-金(Ⅰ)配合物催化炔丙基酯的[3,3]重排的定量动力学研究

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摘要

The triazole-gold(Ⅰ) complex catalyzed [3,3]-rearrangement of propargyl ester has been quantitatively investigated through in situ IR. First order dependence of the initial rates on [Au] and [propargyl ester] suggested that the turnover-limiting step is the associative ligand substitution. The activation enthalpy was also determined to be 7.8 kcal mol~(-1). TA-Au catalysts with different triazole derivatives were also tested, giving a linear free energy relationship with a p value of 0.74.
机译:通过原位红外定量研究了炔丙基酯的[3,3]重排催化的三唑-金(Ⅰ)配合物。初始速率对[Au]和[炔丙基酯]的一阶依赖性表明,周转限制步骤是缔合配体取代。活化焓也确定为7.8kcal mol·(-1)。还测试了具有不同三唑衍生物的TA-Au催化剂,其线性自由能关系为p值为0.74。

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  • 来源
    《Chemical Communications》 |2014年第17期|2158-2160|共3页
  • 作者单位

    C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV 26506, USA;

    C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV 26506, USA;

    C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV 26506, USA;

    Department of Medicinal Chemistry, School of Pharmacy, Shandong University, Jinan, Shandong, 250012, China;

    C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV 26506, USA;

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