首页> 外文期刊>Solid State Nuclear Magnetic Resonance >Molecular dynamics of n-dodecylammonium chloride in aqueous solutions investigated by 2{sup left}H NMR and 1{sup left}H NMR relaxometry
【24h】

Molecular dynamics of n-dodecylammonium chloride in aqueous solutions investigated by 2{sup left}H NMR and 1{sup left}H NMR relaxometry

机译:通过2 {Sup left} H NMR和1 {supleft} H NMR弛豫法研究水溶液中正十二烷基氯化铵的分子动力学

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Molecular dynamics in n-dodecylammonium chloride/water solutions for concentrations of 34 and 45 wt% was studied by 2{sup left}H NMR and by 1{sup left}H NMR dispersion of spin-lattice relaxation in the 2kHz-90 MHz frequency range. The system exhibits a number of lyotropic liquid crystalline phases, which differ in symmetry and involve motions characterized by a wide frequency scale. The analysis of 2{sup left}H NMR lineshapes of selectively deuterated DDAC1 molecules gave us an evidence for local trans-gauche conformational changes in the chains, whereas the dispersion of spin-lattice relaxation times T{sub}1 explored by fast field cycling method revealed fast local motions, translational diffusion and collective molecular dynamics of the chains. In particular, we have found that the order director fluctuation mechanism in smectic and nematic phases dominates spin-lattice relaxation below 1 MHz and that local motions and translational diffusion are responsible for the spin-lattice relaxation in the higher Larmor frequency range.
机译:通过2 {H} NMR和1 {H} NMR在2kHz-90 MHz频率下自旋晶格弛豫的分散研究了正十二烷基氯化铵/水溶液中浓度为34和45 wt%的分子动力学范围。该系统表现出许多溶致液晶相,它们的对称性不同,并且涉及以宽频率范围为特征的运动。对选择性氘代DDAC1分子的2 {sup left} H NMR线型的分析为我们提供了链中局部反式gauche构象变化的证据,而通过快速场循环探索了自旋晶格弛豫时间T {sub} 1的分散方法揭示了链的快速局部运动,平移扩散和集体分子动力学。特别是,我们发现近晶相和向列相中的阶数方向起伏机制主导了1 MHz以下的自旋晶格弛豫,而局部运动和平移扩散是拉莫尔频率范围较高时自旋晶格弛豫的原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号