波谱学杂志 ›› 1993, Vol. 10 ›› Issue (4): 335-341.

• 研究论文 •    下一篇

水溶液中稀土离子与甘氨酸、丝氨酸、天冬氨酸作用的13C NMR研究

任吉民, 裴奉奎, 王文韵, 倪嘉缵   

  1. 中国科学院长春应用化学研究所, 长春 130022
  • 收稿日期:1992-11-24 出版日期:1993-12-05 发布日期:2018-01-20
  • 基金资助:
    国家自然科学基金

13C NMR STUDY OF INTERACTION BETWEEN LANTHANIDE IONS AND GLYSINE,SERINE AND ASPARTIC ACID IN AQUEOUS SOLUTION

Ren Jimin, Pel Fengkui, Wang Wenyun, Ni Jiazuan   

  1. Changchun Institute of Applied Chemistry, The Chinese Academy of Sciences, Changchun 130022
  • Received:1992-11-24 Online:1993-12-05 Published:2018-01-20

摘要: 测定了酸性水溶液中甘氨酸、丝氨酸和天冬氨酸稀土络合物(Ln=La、Pr、Nd、Eu、Tb、Dy、Ho、Er、Tm和Yb)的13C诱导位移。对位移试剂的分析指出,三种氨基酸通过α-羧基以双齿形式配位于稀土,配位键长为0.23nm~0.25nm,天冬氨酸的γ-羧基也是配位基团。由本文与文献中已报道的各种氨基酸稀土络合物的13C诱导位移的系统分析表明,配体13C超精细偶合常数A值和结构因子G值有如下规律:(1)│A(C0)│<│A(Cα)│;A(C0)为正,A(Cα)为负;(2)│G(C0)│>│G(Cα)│;配体碳核的G均为负值。

关键词: 甘氨酸, 丝氨酸, 天冬氨酸, α-氨基酸, 稀土络合物, NMR

Abstract: 13C shifts of amino acids, Gly、Ser and Asp,induced by lanthanide ions,La3+、Pr3+、Nd3+、Eu3+、Tb3+、Dy3+、Ho3+、Er3+、Tm3+ and Yb3+, were measured in acidicaqueous solution. An analysis of 13C lanthanide-induced shifts (LISs) indicates that these three amino acids are bidentately coordinated to Ln through their α-carboxyl groups with Ln-0 bond length of 0.23nm~0.25nm. γ-carboxyl group is also involved in coordination for aspartic acid. By systematically analyzing 13C LISs in this paper and previously reported for various α-amino acid-Ln complexes, the following general conclusions are drawn about hyperfine coupling constant A and geometric factor G for ligand carbon nuclei:
(l)|A(C0)|<|A(Cα)|with a positive sign for A(C0) and a negative one for A(Cα); (2) G values are negative for all ligand carbon nuclei with|G(C0)|>|G(Cα)|.

Key words: Glysine, Serine, Aspartic acid, α-amino acid, Lanthanide complex, NMR