Institute of Organic Chemistry, Johannes Kepler University Linz, Altenbergerstraße 69, 4040 Linz, Austria.
NIMBE, CEA, CNRS, Université Paris-Saclay, CEA/Saclay, 91191 Gif-sur-Yvette, France.
Nat Commun. 2017 Jan 9;8:13914. doi: 10.1038/ncomms13914.
The detection of minor species in the presence of large amounts of similar main components remains a key challenge in analytical chemistry, for instance, to obtain isotopic fingerprints. As an alternative to the classical NMR scheme based on coherent excitation and detection, here we introduce an approach based on spin-noise detection. Chemical shifts and transverse relaxation rates are determined using only the detection circuit. Thanks to a nonlinear effect in mixtures with small chemical shift dispersion, small signals on top of a larger one can be observed with increased sensitivity as bumps on a dip; the latter being the signature of the main magnetization. Experimental observations are underpinned by an analytical theory: the coupling between the magnetization and the coil provides an amplified detection capability of both small static magnetic field inhomogeneities and small NMR signals. This is illustrated by two-bond C/C isotopic measurements.
在存在大量类似主要成分的情况下检测次要物种仍然是分析化学中的一个关键挑战,例如,获得同位素指纹。作为基于相干激发和检测的经典 NMR 方案的替代方案,这里我们介绍了一种基于自旋噪声检测的方法。仅使用检测电路确定化学位移和横向弛豫率。由于在具有小化学位移分散的混合物中存在非线性效应,因此可以以更大的灵敏度观察到较大信号上的小信号,作为峰上的凹陷;后者是主磁化的特征。实验观察得到了分析理论的支持:磁化和线圈之间的耦合提供了对小静态磁场不均匀性和小 NMR 信号的放大检测能力。这通过二键 C/C 同位素测量得到了说明。