摘要
本文测定了DMF-H_2O和DMF-D_2O体系在全部浓度范围内(摩尔分数为0~1)DMF分子中四极核 ̄(14)N的弛豫时间,讨论了弛豫的溶剂同位素效应和影响四极核弛豫的因素。研究结果表明,体系中 ̄(14)N的弛豫与溶剂水分子的动力学行为有着密切的联系,在无限稀释条件下溶质分子的运动完全受溶剂分子的控制.
In the present paper,the dynamic isotope effect of ^(14)N relaxation ofDMF/H_2O(D_2O)system is reportcd.The ^(14)N rclaxation times of DMF in DMF/H_2Oand DMF/D_2O systems have been measured through all composition range(mole fraction of DMF from 0 to 1).The solvent isotope effect on relaxation and thefactors affecting the quadrupole relaxation are discussed .The results suggcst that in thegiven system there is a close relationship between the ^(14)N relaxation and the kinetics of,solvent water.Under infinite dilutions,the kinetics of thc solute molcculcs are controlledcomplctely by the solvent molecules。
出处
《波谱学杂志》
CAS
CSCD
1994年第2期195-200,共6页
Chinese Journal of Magnetic Resonance
基金
中国科学院归国留学人员择优资助