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Mechanism of nuclear spin initiated para-H-2 to ortho-H-2 conversion

机译:核自旋引发对位H-2向邻位H-2转化的机制

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摘要

In this paper a quantitative explanation for a diamagnetic ortho/para H-2 conversion is given. The description is based on the quantum-mechanical density matrix formalism originally developed by Alexander and Binsch for studies of exchange processes in NMR spectra. Only the nuclear spin system is treated quantum-mechanically. Employing the model of a three spin system, the reactions of the hydrogen gas with the catalysts are treated as a phenomenological rate process, described by a rate constant. Numerical calculations reveal that for nearly all possible geometrical arrangements of the three spin system an efficient spin conversion is obtained. Only in the chemically improbable case of a linear group H-X-H no spin conversion is obtained. The efficiency of the spin conversion depends strongly on the lifetime of the H-X-H complex and on the presence of exchange interactions between the two hydrogens. Even moderate exchange couplings cause a quench of the spin conversion. Thus a sufficiently strong binding of the dihydrogen to the S spin is necessary to render the quenching by the exchange interaction ineffective.
机译:在本文中,给出了反磁性正/对位H-2转换的定量解释。该描述基于亚历山大和本奇最初为研究NMR光谱中的交换过程而开发的量子力学密度矩阵形式。仅核自旋系统在量子力学上得到了处理。利用三自旋系统的模型,氢气与催化剂的反应被视为现象速率过程,用速率常数描述。数值计算表明,对于三个自旋系统的几乎所有可能的几何排列,都可以获得有效的自旋转换。仅在化学上不可能的直链基团H-X-H的情况下,不能获得自旋转化。自旋转化的效率在很大程度上取决于H-X-H络合物的寿命以及两个氢之间交换相互作用的存在。即使适度的交换偶合也会引起自旋转化的猝灭。因此,必须使二氢与S自旋足够牢固地结合,以使通过交换相互作用的猝灭无效。

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