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Quick, selective NMR spectra of COH moieties in 13 C-enriched solids.
Journal of Magnetic Resonance 2019 Februrary 28
A convenient one-dimensional magic-angle spinning NMR method is presented that provides selective NMR spectra of COH moieties in uniformly 13 C-enriched organic materials. This method, termed hydroxyl-proton selection (HOPS), eliminates the magnetization of protons directly bonded to carbons by recoupling the 1 H-13 C dipolar interaction for a short time (∼70 μs), which also serves as a chemical-shift filter to suppress 1 H magnetization of CH3 groups. After cross polarization to 13 C, the signals of COH and COOH carbons are observed selectively. This makes it possible to distinguish alcohols from ethers, in particular phenols from aromatic ethers such as the furans often formed by dehydration of glucose, and carboxylic acids from carboxylates and ethers. HOPS NMR reveals that orthodiphenols are often a major component of low-temperature carbon materials. For instance, it forces the reassignment of the 143 ppm 13 C NMR signal of hydrothermal carbon to such catecholic diphenols, while a previous NMR-based structural model had attributed this peak to a central furan-furan linkage.
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