NMR in liquid crystalline solvents. Vibrational corrections on nuclear dipole-dipole interactions

被引：8

作者：

Bulthuis, J. ^{[1
]}

Maclean, C. ^{[1
]}

机构：

[1] Chem Lab Free Univ, Amsterdam, Netherlands

来源：

CHEMICAL PHYSICS LETTERS | 1970年 / 7卷 / 02期

关键词：

D O I：

10.1016/0009-2614(70)80299-8

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The deviations between experimental and calculated dipolar couplings in methylfluoride, measured by Krugh and Bernheim in a liquid crystal cannot be explained by applying vibrational corrections. It is suggested that they originate from solvent effects on the indirect couplings.

引用

页码：242 / 246

页数：5

共 21 条

[1]

ALDCUS J, 1962, SPECTROCHIM ACTA, V18, P1073

[2]

ALDCUS J, 1963, SPECTROCHIM ACTA, V19, P1567

[3] Anisotropy of the indirect nuclear spin-spin coupling constant [J].