• 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

在手性二铑配合物存在下通过核磁共振光谱法对手性席夫碱进行手性识别。氘同位素对光学活性席夫碱及其二铑加合物的¹³C化学位移的影响。

Chiral recognition of the Schiff bases by NMR spectroscopy in the presence of a chiral dirhodium complex. Deuterium isotope effect on 13C chemical shift of the optically active Schiff bases and their dirhodium adducts.

作者信息

Rozwadowski Z

机构信息

Institute of Chemistry and Environmental Protection, Szczecin University of Technology, Al. Piastów 42, 70-065 Szczecin, Poland.

出版信息

Magn Reson Chem. 2007 Jul;45(7):605-10. doi: 10.1002/mrc.2008.

DOI:10.1002/mrc.2008
PMID:17534869
Abstract

The dirhodium method has been successfully applied in chiral recognition of the optically active Schiff bases, derivatives of ortho-hydroxyaldehydes existing in the NH-form. or at tautomeric equilibrium. The position of the equilibrium of Schiff bases as well as their adducts has been established on the basis of measurements of deuterium isotope effects on 13C chemical shifts. The presence of the proton transfer equilibrium or NH-tautomer has promoted the adduct formation. At the equilibrium state, formation of the adducts has shifted the proton transfer equilibrium towards the NH-form. The binding site was the oxygen atom of the proton donor group.

摘要

二铑方法已成功应用于对光学活性席夫碱的手性识别,这些席夫碱是存在于NH形式或处于互变异构平衡状态的邻羟基醛衍生物。席夫碱及其加合物的平衡位置已根据对13C化学位移的氘同位素效应测量确定。质子转移平衡或NH互变异构体的存在促进了加合物的形成。在平衡状态下,加合物的形成使质子转移平衡向NH形式移动。结合位点是质子供体基团的氧原子。

相似文献

1
Chiral recognition of the Schiff bases by NMR spectroscopy in the presence of a chiral dirhodium complex. Deuterium isotope effect on 13C chemical shift of the optically active Schiff bases and their dirhodium adducts.在手性二铑配合物存在下通过核磁共振光谱法对手性席夫碱进行手性识别。氘同位素对光学活性席夫碱及其二铑加合物的¹³C化学位移的影响。
Magn Reson Chem. 2007 Jul;45(7):605-10. doi: 10.1002/mrc.2008.
2
Chiral recognition of Schiff bases by 15N NMR spectroscopy in the presence of a dirhodium complex. Deuterium isotope effect on 15N chemical shift of the optically active Schiff bases and their dirhodium tetracarboxylate adducts.在二铑配合物存在下通过¹⁵N核磁共振光谱对席夫碱进行手性识别。氘同位素对光学活性席夫碱及其四羧酸二铑加合物¹⁵N化学位移的影响。
Magn Reson Chem. 2008 Oct;46(10):974-8. doi: 10.1002/mrc.2280.
3
Deuterium isotope effect on 13C chemical shifts of tetrabutylammonium salts of Schiff bases amino acids.氘同位素对席夫碱氨基酸四丁基铵盐的13C化学位移的影响。
Magn Reson Chem. 2006 Sep;44(9):881-6. doi: 10.1002/mrc.1852.
4
Solid-state NMR study of Schiff base derivatives of 2-hydroxynaphthaldehyde. Deuterium isotope effects on 15N chemical shifts in the solid state.2-羟基萘甲醛席夫碱衍生物的固态核磁共振研究。氘同位素对固态下¹⁵N化学位移的影响。
Magn Reson Chem. 2005 Jul;43(7):573-7. doi: 10.1002/mrc.1594.
5
Schiff bases of gossypol: an NMR and DFT study.棉酚席夫碱:一项核磁共振和密度泛函理论研究。
Magn Reson Chem. 2005 Apr;43(4):302-8. doi: 10.1002/mrc.1532.
6
Tautomerism of sterically hindered schiff bases. Deuterium isotope effects on 13C chemical shifts.空间位阻席夫碱的互变异构。氘同位素对碳-13化学位移的影响。
J Phys Chem A. 2005 May 26;109(20):4464-73. doi: 10.1021/jp0445977.
7
Investigations of intramolecular hydrogen bonding in three types of Schiff bases by 2H and 3H NMR isotope effects.通过2H和3H NMR同位素效应研究三种席夫碱中的分子内氢键。
Magn Reson Chem. 2004 Jun;42(6):556-60. doi: 10.1002/mrc.1375.
8
Structural investigation on phenyl- and pyridin-2-ylamino(methylene)naphthalen-2(3H)-one. Substituent effects on the NMR chemical shifts.苯氨基亚甲基萘-2(3H)-酮和吡啶-2-基亚氨基亚甲基萘-2(3H)-酮的结构研究。取代基对 NMR 化学位移的影响。
Magn Reson Chem. 2010 Aug;48(8):585-92. doi: 10.1002/mrc.2626.
9
A multinuclear magnetic resonance study of intramolecular hydrogen bonding in some Schiff and Schiff-Mannich bases in solution and in the solid state.溶液和固态下一些席夫碱和席夫-曼尼希碱分子内氢键的多核磁共振研究
Solid State Nucl Magn Reson. 2000;18(1-4):97-105. doi: 10.1006/snmr.2000.0014.
10
Theoretical NMR spectroscopic analysis of the intramolecular proton transfer mechanism in ortho-hydroxyaryl (Un-)substitued Schiff bases.邻羟基芳基(未)取代席夫碱分子内质子转移机制的理论核磁共振光谱分析
J Phys Chem A. 2008 Sep 18;112(37):8767-74. doi: 10.1021/jp802894f. Epub 2008 Aug 26.