Ultrafast Maximum‐Quantum NMR Spectroscopy for the Analysis of Aromatic Mixtures

Maximum‐quantum (MaxQ) NMR experiments have been introduced to overcome issues related to peak overlap and high spectral density in the NMR spectra of aromatic mixtures. In MaxQ NMR, spin systems are separated on the basis of the highest‐quantum coherence that they can form. MaxQ experiments are however time consuming and methods have been introduced to accelerate them. In this article, we demonstrate the ultrafast, single‐scan acquisition of MaxQ NMR spectra using spatial encoding of the multiple‐quantum dimension. So far, the spatial encoding methodology has been applied only for the encoding of up to double‐quantum coherences, and here we show that it can be extended to higher coherence orders, to yield a massive reduction of the acquisition time of multi‐quantum spectra of aromatic mixtures, and also to monitor chemical reactions. Fast spectroscopy: Acquisition of multiple quantum spectra of an aromatic mixture in one second.