Ni(II)离子水溶液中的场相关质子核磁共振弛豫。新的解读

J. Svoboda , T. Nilsson , J. Kowalewski , P.-O. Westlund , P.T. Larsson
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引用次数: 24

摘要

提出了溶液中顺磁性过渡金属配合物中核自旋弛豫的新模型,使电子自旋弛豫超出了雷德菲尔德极限。新颖的特点是,瞬态零场分裂(ZFS),由溶剂化壳的畸变调制,被允许是菱形对称而不是圆柱对称。该模型假设静态ZFS不存在,适用于过渡金属离子水溶液。本文研究了水溶液中质子自旋-晶格弛豫速率增强与磁场的关系,并对anS= 1体系(如Ni2+(aq))采用不同的ZFS菱形度和不同的运动条件(红场极限和慢动作状态)进行了计算。新模型还用于拟合先前报道的低pH下Ni(ClO4)2水溶液中质子弛豫的场依赖性数据[J]。Kowalewski, T. Larsson和p . o。Westlund, J。粉剂。[j].中国生物医学工程学报,2014,31(2)。在最近的理论工作的推动下,包含了菱形,提供了一个与早期hoc模型一样好的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Field-Dependent Proton NMR Relaxation in Aqueous Solutions of Ni(II) Ions. A New Interpretation

A new model is presented for nuclear-spin relaxation in paramagnetic transition metal complexes in solution, allowing the electron-spin relaxation to be outside the Redfield limit. The novel feature is that the transient zero-field splitting (ZFS), modulated by distortions of the solvation shell, is allowed to be of rhombic rather than cylindrical symmetry. The model, which assumes that the static ZFS is absent, is applicable to aqueous solutions of transition metal ions. The magnetic-field dependence of the proton spin–lattice relaxation rate enhancement in aqueous solution has been investigated, and calculations are presented for anS= 1 system such as Ni2+(aq), using different degrees of rhombicity of the ZFS and different motional conditions (Redfield limit and slow-motion regime). The new model is also applied to fit the previously reported data for the field dependence of proton relaxation in aqueous solution of Ni(ClO4)2at low pH [J. Kowalewski, T. Larsson, and P.-O. Westlund,J. Magn. Reson.74, 56 (1987)]. The inclusion of rhombicity, motivated by recent theoretical work, provides a model which performs as well as the earlierad hocmodel.

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