Department of Chemistry, Texas A&M University , College Station, Texas 77843-3255, United States.
Anal Chem. 2015 Nov 3;87(21):10982-7. doi: 10.1021/acs.analchem.5b02934. Epub 2015 Oct 15.
The nuclear Overhauser effect (NOE) has long been used as a selective indicator for intermolecular interactions. Due to relatively small changes of signal intensity, often on the order of several percent, quantitative NOE measurements can be challenging. Hyperpolarization of nuclear spins can dramatically increase the NOE intensity by increasing population differences, but poses its own challenge in quantifying the original polarization level. Here, we demonstrate a method for the accurate measurement of intermolecular heteronuclear cross-relaxation rates by simultaneous acquisition of signals from both nuclei. Using this method, we measure cross-relaxation rates between water protons and (19)F of trifluoroacetic acid at concentrations ranging from 23 to 72 mM. A concentration-independent value of 2.46 × 10(-4) ± 1.02 × 10(-5) s(-1) M(-1) is obtained at a temperature of 301 K and validated using a nonhyperpolarized measurement. In a broader context, accurate measurement of heteronuclear cross-relaxation rates may enable the study of intermolecular interactions including those involving macromolecules where (19)F atoms can be introduced as site-selective labels.
核奥弗豪瑟效应(NOE)长期以来一直被用作分子间相互作用的选择性指示剂。由于信号强度的变化相对较小,通常只有几个百分点,因此定量 NOE 测量可能具有挑战性。核自旋的极化可以通过增加种群差异来显著增加 NOE 强度,但在定量原始极化水平方面存在自身的挑战。在这里,我们展示了一种通过同时获取两个核信号来准确测量分子间异核交叉弛豫率的方法。使用该方法,我们测量了浓度范围为 23 至 72mM 的三氟乙酸中质子和(19)F 之间的交叉弛豫率。在 301K 的温度下,获得了一个浓度独立的值 2.46×10(-4)±1.02×10(-5)s(-1)M(-1),并使用非极化测量进行了验证。更广泛地说,异核交叉弛豫率的准确测量可以使研究包括涉及大分子的分子间相互作用成为可能,其中(19)F 原子可以作为选择性标记引入。