Department of Chemistry, New York University , New York, New York 10003, United States.
Org Lett. 2014 Mar 21;16(6):1566-9. doi: 10.1021/ol403776k. Epub 2014 Mar 6.
(13)C NMR spectroscopic integration employing short relaxation delays was evaluated as a quantitative tool to obtain ratios of diastereomers, regioisomers, constitutional isomers, mixtures of unrelated compounds, peptoids, and sugars. The results were compared to established quantitative methods such as (1)H NMR spectroscopic integration, gas chromatography, and high-performance liquid chromatography and were found to be within <3.4% of (1)H NMR spectroscopic values (most examples give results within <2%). Acquisition of the spectra took 2-30 min on as little as 10 mg of sample, proving the general utility of the technique. The simple protocol was extended to include end group analysis of low molecular weight polymers, which afforded results in accordance with (1)H NMR spectroscopy and matrix-assisted laser desorption-ionization time-of-flight spectrometry.
(13)C NMR 谱学积分采用短弛豫延迟,被评估为一种定量工具,以获得非对映异构体、区域异构体、构造异构体、无关化合物混合物、肽和糖的比例。结果与(1)H NMR 谱学积分、气相色谱和高效液相色谱等已建立的定量方法进行了比较,发现与(1)H NMR 光谱值的差异小于 <3.4%(大多数情况下结果小于 <2%)。在 10 毫克左右的样品上仅需 2-30 分钟即可获得光谱,证明了该技术的通用性。该简单方案已扩展到包括低分子量聚合物的端基分析,其结果与(1)H NMR 光谱和基质辅助激光解吸电离飞行时间质谱法一致。