顺磁性
核磁共振波谱
化学
光谱学
钆
旋转
放松(心理学)
横向弛豫优化光谱
代谢组学
自旋晶格弛豫
稳健性(进化)
二维核磁共振波谱
分析化学(期刊)
化学物理
核磁共振
氟-19核磁共振
物理
色谱法
立体化学
有机化学
凝聚态物理
社会心理学
基因
量子力学
生物化学
心理学
作者
Frans A. A. Mulder,Leonardo Tenori,Claudio Luchinat
标识
DOI:10.1002/anie.201908006
摘要
Abstract NMR spectroscopy is an indispensable technique for the determination of the chemical identity and structure of small molecules. The method is especially recognized for its robustness and intrinsically quantitative nature, and has manifested itself as a key analytical platform for diverse fields of application, ranging from chemical synthesis to metabolomics. Unfortunately, the slow recovery of nuclear spin polarization by spin‐lattice (T 1 ) relaxation causes most experimental time to be lost on idle waiting. Furthermore, truly quantitative NMR (qNMR) spectroscopy requires waiting times of 5‐times the longest T 1 in the sample, making qNMR spectroscopy slow and inefficient. We demonstrate here that co‐solute paramagnetic relaxation can mitigate these two problems simultaneously. The addition of a small amount of paramagnetic gadolinium chelate, available in the form of commercial contrast‐agent solutions, enables cheap, quantitative, and efficient high‐throughput mixture analysis.
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