首页> 外文期刊>Journal of Chemical and Engineering Data: the ACS Journal for Data >Spectrophotometric Determination of Acidity Constants of Alizarine Red S in Mixed Aqueous-Organic Solvents
【24h】

Spectrophotometric Determination of Acidity Constants of Alizarine Red S in Mixed Aqueous-Organic Solvents

机译:分光光度法测定混合有机溶剂中茜素红S的酸度常数。

获取原文
获取原文并翻译 | 示例
           

摘要

The effect of different organic-water mixtures on the acidity constants of alizarine red s(9,10-dihydro-3,4-dihydroxy-9,10-dioxo-2-anthracenesulfonic acid)were determined at 25 deg C and an ionic strength of 0.1 M by a multiwavelength spectrophotometric method.Two pK_a values for the-OH derivatives were determined.The organic solvents used were the amphiprotic(methanol,ethanol),dipolar aprotic(dimethyl sulfoxide),and low basic aprotic(acetonitrile).To evaluate the pH absorbance data,a resolution method based on the combination of soft-and hard-modeling is applied.The acidity constants of all related equilibria are estimated using the whole spectral fitting of the collected data using an established factor analysis model.The data analysis program DATAN was applied for determination of acidity constants.Generally,the pK_a values increase with an increase in the content of the organic solvent.This behavior can be accounted for in terms of the high stabilization of both the nonprotonated and the ionic forms of this compound by dispersion forces rather than by hydrogen bonding.There are linear relationships between acidity constants and the mole fraction of different solvents in the mixtures.The effect of solvent properties on acid-base behavior is discussed.
机译:在25℃和离子强度下测定了不同的有机水混合物对茜素红s(9,10-dihydro-3,4-dihydroxy-9,10-dioxo-2-anthracenesulfonic acid)酸度常数的影响。用多波长分光光度法测定0.1 M.-OH衍生物的两个pK_a值。使用的有机溶剂为两性质子(甲醇,乙醇),偶极非质子性(二甲基亚砜)和低碱性非质子性(乙腈)。在pH吸收数据的基础上,采用了基于软模型和硬模型相结合的解析方法。使用建立的因子分析模型,通过收集数据的整个光谱拟合来估算所有相关平衡的酸度常数。通常用DATAN程序测定酸度常数。通常,pK_a值随有机溶剂含量的增加而增加。这种现象可以用非质子化的a的高稳定性来解释。化合物的离子形式是通过分散力而不是通过氢键来实现的。酸度常数与混合物中不同溶剂的摩尔分数之间存在线性关系。讨论了溶剂性质对酸碱行为的影响。

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