• 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

咪唑促进过氧草酸酯化学发光的双中间体模型。

A two-intermediate model for imidazole-promoted peroxyoxalate chemiluminescence.

作者信息

Neuvonen H

机构信息

Department of Chemistry, University of Turku, Finland.

出版信息

J Biolumin Chemilumin. 1997 Sep-Oct;12(5):241-8. doi: 10.1002/(SICI)1099-1271(199709/10)12:5<241::AID-BIO449>3.0.CO;2-3.

DOI:10.1002/(SICI)1099-1271(199709/10)12:5<241::AID-BIO449>3.0.CO;2-3
PMID:9509331
Abstract

A mechanism is proposed for imidazole-catalysed peroxyoxalate chemiluminescence. The reaction model includes a sequential formation of 1-aroxalylimidazole and 1,1'-oxalyldiimidazole as light-producing reaction intermediates. The suggestion is supported by the kinetic data obtained for the reaction of imidazole with bis(4-nitrophenyl) oxalate and on the recently reported ability of 1,1'-oxalyldiimidazole to function as an efficient chemiluminescence reagent. The relative contributions of different catalytic pathways and hydrolytic side-reactions are discussed.

摘要

提出了一种咪唑催化过氧草酸酯化学发光的机制。该反应模型包括依次形成1-芳酰基咪唑和1,1'-草酰二咪唑作为发光反应中间体。咪唑与双(4-硝基苯基)草酸酯反应的动力学数据以及最近报道的1,1'-草酰二咪唑作为高效化学发光试剂的能力支持了这一观点。讨论了不同催化途径和水解副反应的相对贡献。

相似文献

1
A two-intermediate model for imidazole-promoted peroxyoxalate chemiluminescence.咪唑促进过氧草酸酯化学发光的双中间体模型。
J Biolumin Chemilumin. 1997 Sep-Oct;12(5):241-8. doi: 10.1002/(SICI)1099-1271(199709/10)12:5<241::AID-BIO449>3.0.CO;2-3.
2
Chemiluminescence characteristics of furan derivatives as blue fluorescers in peroxyoxalate-hydrogen peroxide system.过氧草酸-过氧化氢体系中呋喃衍生物作为蓝色荧光体的化学发光特性。
J Fluoresc. 2012 Sep;22(5):1209-16. doi: 10.1007/s10895-012-1060-2. Epub 2012 Jun 9.
3
Determination of C-21 ketosteroids in serum using trifluoromethanesulfonic acid catalyzed precolumn dansylation and 1,1'-oxalyldiimidazole postcolumn peroxyoxalate chemiluminescence detection.使用三氟甲磺酸催化柱前丹磺酰化和1,1'-草酰二咪唑柱后过氧草酸酯化学发光检测法测定血清中的C-21甾体酮。
Anal Chem. 1998 Dec 1;70(23):5002-9. doi: 10.1021/ac980511s.
4
Detection of substances with alcoholic or phenolic hydroxyl groups by generation of hydrogen peroxide with imidazole and peroxyoxalate chemiluminescence.
J Biolumin Chemilumin. 1995 Nov-Dec;10(6):339-44. doi: 10.1002/bio.1170100606.
5
A study of peroxyoxalate-chemiluminescence of acriflavine.吖啶黄的过氧草酸酯化学发光研究。
Spectrochim Acta A Mol Biomol Spectrosc. 2003 Feb;59(3):511-7. doi: 10.1016/s1386-1425(02)00188-9.
6
Development of a compact capillary electrophoresis-chemiluminescence system with ultra-fast peroxyoxalate reaction to monitor the hydrolysis of rhodamine 6G.开发一种紧凑的毛细管电泳-化学发光系统,采用超快过氧草酸盐反应监测罗丹明 6G 的水解。
Luminescence. 2012 Nov-Dec;27(6):482-8. doi: 10.1002/bio.1379. Epub 2011 Dec 27.
7
Influence of Imidazole and Bis(trichlorophenyl) Oxalate in the Oxalyldiimidazole Peroxyoxalate Chemiluminescence Reaction.咪唑和双(三氯苯基)草酸酯在草酰二咪唑过氧草酸酯化学发光反应中的影响。
Anal Chem. 1997 Jun 1;69(11):2109-14. doi: 10.1021/ac961225o.
8
Response surface optimized peroxyoxalate chemiluminescence of octahydro-Schiff base derivative as new luminophor and study of the quenching effect of some cations, amino acids and cholesterol.八氢席夫碱衍生物作为新型发光体的响应面优化过氧草酸酯化学发光及某些阳离子、氨基酸和胆固醇猝灭效应的研究
Luminescence. 2014 Dec;29(8):1074-81. doi: 10.1002/bio.2662. Epub 2014 Apr 10.
9
Studies on the effects of imidazole on the peroxyoxalate chemiluminescence detection system for high performance liquid chromatography.咪唑对高效液相色谱过氧草酸酯化学发光检测系统影响的研究
Biomed Chromatogr. 1990 May;4(3):100-4. doi: 10.1002/bmc.1130040305.
10
Unprecedented chemiluminescence behaviour during peroxyoxalate chemiluminescence of oxalates with fluorescent or electron-donating aryloxy groups.带有荧光或给电子芳氧基的草酸盐在过氧草酸酯化学发光过程中呈现出前所未有的化学发光行为。
Luminescence. 2006 May-Jun;21(3):164-73. doi: 10.1002/bio.901.