中等分子中的13C谱分配和自旋晶格弛豫

Felix W. Wehrli
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引用次数: 19

摘要

已经测定了三种不同分子大小的分子——可待因、马钱子碱和利血平的13C自旋-晶格弛豫时间。在这三个分子中,作为各向同性重定向骨架的一部分,甲基碳的T1范围为0.15至0.23秒,对应于重定向相关时间为3 × 10−10和2 × 10−10秒。所有碳,包括第四系碳,都通过偶极子-偶极子相互作用被松弛。发现不含质子的碳的弛豫率是由双质子和邻质子控制的,因此可以进行其他技术无法获得的可靠分配。中等大小分子的完全弛豫13C傅立叶变换光谱的峰高反映自旋-自旋弛豫,从而可以对该参数进行定性估计。以3-胆甾酮的光谱为例进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
13C Spectral assignment and spin-lattice relaxation in medium-sized molecules

The individual 13C spin-lattice relaxation times in three molecules of different molecular size - codeine, brucine and reserpine - have been determined. In all three molecules, T1 for methine carbons, being part of the isotropically reorientating skeleton, ranges from 0.15 to 0.23 sec corresponding to reorientational correlation times of 3 × 10−10 and 2 × 10−10 sec. All carbons, including the quaternaries, ar shown to be relaxed through dipole-dipole interaction. The relaxation rate of non-proton-bearing carbons is found to be governed by geminal and vicinal protons thus allowing reliable assignments to be made that are unavailable from other techniques. The peak heights in completely relaxed 13C Fourier transform spectra of medium-sized molecules are shown to reflect spin-spin relaxation, thus permitting a qualitative estimate of this parameter. As an example, the spectrum of 3-cholestanone is discussed.

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