...
首页> 外文期刊>Chemistry central journal >Structural effects on kinetics and a mechanistic investigation of the reaction between DMAD and N–H heterocyclic compound in the presence of triphenylarsine: spectrophotometry approach
【24h】

Structural effects on kinetics and a mechanistic investigation of the reaction between DMAD and N–H heterocyclic compound in the presence of triphenylarsine: spectrophotometry approach

机译:分光光度法在三苯基ar存在下动力学对结构的影响以及DMAD与N–H杂环化合物之间反应的机理研究

获取原文

摘要

Kinetics and a mechanistic investigation of the reaction between dimethyl acetylenedicarboxcylate (DMAD) and saccharin ( N – H heterocyclic compound) has been spectrally studied in methanol environment in the presence of triphenylarsine ( TPA ) as a catalyst. Previously, in a similar reaction, triphenylphosphine ( TTP ) (instead of triphenylarsine) has been employed as a third reactant (not catalyst) for the generation of an ylide (final product) while, in the present work the titled reaction in the presence of TPA leaded to the especial N-vinyl heterocyclic compound with different kinetics and mechanism. The reaction followed second order kinetics. In the kinetic study, activation energy and parameters (Ea, ΔH?, ΔS? and ΔG?) were determined. Also, the structural effect of the N – H heterocyclic compound was investigated on the reaction rate. The result showed that reaction rate increases in the presence of isatin ( N – H compound) that participates in the second step (step2), compared to saccharin (another N – H compound). This was a good demonstration for the second step (step2) of the reaction that could be considered as the rate- determining step (RDS). As a significant result, not only a change in the structure of the reactant ( TPA instead of TPP ) creates a different product, but also kinetics and the reaction mechanism have been changed.
机译:在甲醇环境中,以三苯基s(TPA)为催化剂,对乙酰二羧酸二甲酯(DMAD)与糖精(NH杂环化合物)之间的反应动力学和机理进行了研究。以前,在类似的反应中,三苯膦(TTP)(而不是三苯ar)已被用作第三种反应物(不是催化剂),用于生成叶立德(最终产物),而在本工作中,标题反应是在TPA导致特殊的N-乙烯基杂环化合物具有不同的动力学和机理。该反应遵循二级动力学。在动力学研究中,确定了活化能和参数(Ea,ΔH?,ΔS?和ΔG?)。同样,研究了NH杂环化合物对反应速率的结构影响。结果表明,与糖精(另一种N–H化合物)相比,在参与第二步(步骤 2 )的isatin(N–H化合物)存在下反应速率增加。这是反应的第二步(步骤 2 )的一个很好的证明,可以将其视为速率确定步骤(RDS)。结果是,不仅反应物的结构发生变化(用TPA代替TPP产生了不同的产物),而且动力学和反应机理也发生了变化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号