• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

α-环糊精与某些胺类形成配合物的稳定常数。

Stability constants for complex formation between alpha-cyclodextrin and some amines.

作者信息

Wong A B, Lin S F, Connors K A

出版信息

J Pharm Sci. 1983 Apr;72(4):388-90. doi: 10.1002/jps.2600720417.

DOI:10.1002/jps.2600720417
PMID:6864476
Abstract

Complex formation of alpha-cyclodextrin with 15 amines (including seven 4-substituted anilines) was studied by the potentiometric method, supplemented by direct UV spectrophotometry and a competitive indicator spectrophotometric method. The data were analyzed in terms of 1:1 and 1:2 complexes (amine-cyclodextrin ratios) and the stability constants K11a, K12a, K11b, and K12b were evaluated; the subscripts indicate the stoichiometry and conjugate acid-base form. For all amines K11b was greater than K11a and K12a was 0. On the basis of the relationship of complex stability to amine structure, it was concluded that the primary binding site in anilines is the 4-substituent.

摘要

采用电位滴定法,并辅以直接紫外分光光度法和竞争指示剂分光光度法,研究了α-环糊精与15种胺(包括7种4-取代苯胺)的络合物形成情况。根据1:1和1:2络合物(胺与环糊精的比例)对数据进行分析,并评估了稳定常数K11a、K12a、K11b和K12b;下标表示化学计量比和共轭酸碱形式。对于所有胺类,K11b大于K11a,且K12a为0。根据络合物稳定性与胺结构的关系,得出苯胺中的主要结合位点是4-取代基。

相似文献

1
Stability constants for complex formation between alpha-cyclodextrin and some amines.α-环糊精与某些胺类形成配合物的稳定常数。
J Pharm Sci. 1983 Apr;72(4):388-90. doi: 10.1002/jps.2600720417.
2
Complex formation between alpha-cyclodextrin and 4-substituted phenols studied by potentiometric and competitive spectrophotometric methods.
J Pharm Sci. 1983 Nov;72(11):1333-8. doi: 10.1002/jps.2600721124.
3
Potentiometric study of molecular complexes of weak acids and bases applied to complexes of alpha-cyclodextrin with para-substituted benzoic acids.弱酸和弱碱分子络合物的电位滴定研究及其在α-环糊精与对取代苯甲酸络合物中的应用。
J Pharm Sci. 1982 Feb;71(2):217-22. doi: 10.1002/jps.2600710220.
4
Improved competitive indicator methods for the study of alpha-cyclodextrin complexes.
J Pharm Sci. 1984 Dec;73(12):1779-83. doi: 10.1002/jps.2600731230.
5
Cycloamylose complexation of adamantane derivatives.金刚烷衍生物的环糊精络合作用。
Life Sci. 1983 Jul 4;33(1):83-5. doi: 10.1016/0024-3205(83)90714-2.
6
Quantitative structure-stability relationships among inclusion complexes of cyclodextrins. I: Barbituric acid derivatives.环糊精包合物之间的定量结构-稳定性关系。I:巴比妥酸衍生物。
J Pharm Sci. 1985 Feb;74(2):211-3. doi: 10.1002/jps.2600740223.
7
Stoichiometric model of alpha-cyclodextrin complex formation.α-环糊精复合物形成的化学计量模型。
J Pharm Sci. 1980 May;69(5):564-7. doi: 10.1002/jps.2600690524.
8
Binding of substituted acetic acids to alpha-cyclodextrin in aqueous solution.取代乙酸在水溶液中与α-环糊精的结合
J Pharm Sci. 1997 Nov;86(11):1210-4. doi: 10.1021/js9702527.
9
Interaction of some benzothiadiazine diuretics with beta-cyclodextrin.某些苯并噻二嗪类利尿剂与β-环糊精的相互作用
Acta Pharm Hung. 1990 May;60(2-3):69-75.
10
trans-Cinnamic acid--alpha-cyclodextrin system as studied by solubility, spectral, and potentiometric techniques.通过溶解度、光谱和电位滴定技术研究反式肉桂酸-α-环糊精体系。
J Pharm Sci. 1980 Feb;69(2):173-9. doi: 10.1002/jps.2600690215.

引用本文的文献

1
Enantioseparation of mandelic acid derivatives by high performance liquid chromatography with substituted β-cyclodextrin as chiral mobile phase additive and evaluation of inclusion complex formation.以取代β-环糊精为手性流动相添加剂,用高效液相色谱法拆分扁桃酸衍生物并评估包合物的形成
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jul 1;962:44-51. doi: 10.1016/j.jchromb.2014.05.026. Epub 2014 May 22.
2
Determination of association constants in cyclodextrin/drug complexation using the Scatchard plot: application to beta-cyclodextrin-anilinonaphthalenesulfonates.使用Scatchard图测定环糊精/药物络合中的缔合常数:应用于β-环糊精-苯胺萘磺酸盐
Pharm Res. 1992 Dec;9(12):1568-74. doi: 10.1023/a:1015808307322.