Donovan Kevin J, Allen Mary, Martin Rachel W, Shaka A J
Chemistry Department, University of California, Irvine, CA 92697-2025, USA.
J Magn Reson. 2009 Apr;197(2):237-41. doi: 10.1016/j.jmr.2008.11.016. Epub 2008 Dec 3.
Collecting a truly quantitative carbon-13 spectrum is a time-consuming chore. Very long relaxation delays, required between transients to allow the z-magnetization, M(z), of the spin with the longest T(1) to return to the equilibrium value, M(0), must precede each transient. These long delays also reduce sensitivity, as fewer transients per unit time can be acquired. In addition, sometimes T(1) is not known to within even a factor of two: a conservative guess for the relaxation delay then leads to very low sensitivity. We demonstrate a fresh method to bypass these problems and collect quantitative carbon-13 spectra by swapping the sample volume after each acquisition with a different portion where the magnetization is already equilibrated to M(0). Loading larger sample volumes of 10-20 mL into an unusually long (1520 mm) 5 mm OD. NMR tube and vertically sliding the tube between acquisitions accomplishes the swap. The relaxation delay can then be skipped altogether. The spectra are thus both quantitative, and far more sensitive. We demonstrate the moving tube technique on two small molecules (thymol and butylhydroxytoluene) and show good carbon-13 quantification. The gain in sensitivity can be as much as 10-fold for slowly-relaxing (13)C resonances. These experiments show that quantitative, sensitive carbon-13 spectra are possible whenever sufficient sample volumes are available. The method is applicable to any slow-relaxing nuclear spin species, such as (29)Si, (15)N and other low-gamma nuclei.
采集真正定量的碳 - 13谱是一项耗时的工作。在瞬态之间需要很长的弛豫延迟,以使具有最长T(1)的自旋的z轴磁化强度M(z)恢复到平衡值M(0),每次瞬态之前都必须有这样的延迟。这些长延迟也会降低灵敏度,因为每单位时间可采集的瞬态次数减少。此外,有时T(1)甚至在两倍的范围内都不清楚:对弛豫延迟进行保守猜测会导致灵敏度非常低。我们展示了一种新方法来绕过这些问题,并通过在每次采集后将样品体积与磁化强度已平衡到M(0)的不同部分进行交换来采集定量碳 - 13谱。将10 - 20 mL的较大样品体积装入一根异常长(1520 mm)、外径5 mm的核磁共振管中,并在采集之间垂直滑动该管来完成交换。然后可以完全跳过弛豫延迟。因此,所得谱图既是定量的,灵敏度也高得多。我们在两种小分子(百里酚和丁基羟基甲苯)上展示了移动管技术,并显示出良好的碳 - 13定量结果。对于弛豫缓慢的(13)C共振,灵敏度增益可达10倍。这些实验表明,只要有足够的样品体积,就可以获得定量、灵敏的碳 - 13谱。该方法适用于任何弛豫缓慢的核自旋物种,如(29)Si、(15)N和其他低γ核。