...
首页> 外文期刊>Oxidation Communications >KINECTIC AND MECHANISTIC INVESTIGATION OF OXIDATION OF D(+)RIBOSE BY POTASSIUM IODATE IN PRESENCE OF Rh(III) AS CATALYST IN ALKALINE MEDIUM
【24h】

KINECTIC AND MECHANISTIC INVESTIGATION OF OXIDATION OF D(+)RIBOSE BY POTASSIUM IODATE IN PRESENCE OF Rh(III) AS CATALYST IN ALKALINE MEDIUM

机译:在碱性介质中RH(III)在RH(III)存在下碘酸钾的氧化和机械调查D(+)核苷酸作为碱性培养基催化剂

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The kinetics of Rh(III)-catalysed oxidation of D(+)ribose by potassium iodate in alkaline medium has been studied at 40°C. The reaction exhibits first-order kinetics with respect to [Rh(III)] and [D(+)ribose], The order of reaction was found to be unity at low concentrations of potassium iodate and OH~- which tends to zero-order at their higher concentrations. It was found that dielectric constant of the medium and ionic strength had no effects on the rate of reaction. There is nil effect of [Cl~-] on the rate of oxidation. The reaction has been studied at four different temperatures and observed rate constant values were utilised to calculate activation energy and other activation parameters.The species, [RhCl_3(H_2O)_2OH]~- and IO_3 are postulated as the main reactive species of Rh(III) chloride and potassium iodate, respectively in alkaline medium. Sodium salts of erythronic acid and formic acid were identified as the main oxidation products of the reaction. On the basis of kinetic results, spectroscopic information and activation parameters, a suitable mechanism for the oxidation of D(+)ribose has been proposed and rate law has been derived.
机译:在40℃下,研究了在碱性培养基中通过碘酸钾进行D(+)核糖氧化的Rh(III)的催化氧化的动力学。该反应表现出关于[RH(III)]和[D(+)核糖]的一阶动力学,发现反应顺序是低浓度的碘酸钾和OH〜 - 这倾向于零阶的统一在他们更高的浓度下。发现介质和离子强度的介电常数对反应速率没有影响。 [Cl〜]对氧化率的效果。已经在四种不同温度下研究了反应,并且使用观察到的速率恒定值来计算活化能量和其他活化参数。物种[rhCl_3(H_2O)_2OH]〜 - 和IO_3被假定为RH的主要反应性物种(III )分别在碱性介质中的氯化物和碘酸钾。鉴定红酸和甲酸的钠盐作为反应的主要氧化产物。基于动力学结果,光谱信息和活化参数,已经提出了一种合适的用于氧化的D(+)核糖机制,并衍生出速率法。

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