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Homonuclear Decoupling in (1)H NMR of Solids by Remote Correlation

The typical linewidths of (1)H NMR spectra of powdered organic solids at 111 kHz magic‐angle spinning (MAS) are of the order of a few hundred Hz. While this is remarkable in comparison to the tens of kHz observed in spectra of static samples, it is still the key limit to the use of (1)H in solid‐sta...

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Detalles Bibliográficos
Autores principales: Moutzouri, Pinelopi, Paruzzo, Federico M., Simões de Almeida, Bruno, Stevanato, Gabriele, Emsley, Lyndon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187420/
https://www.ncbi.nlm.nih.gov/pubmed/31967378
http://dx.doi.org/10.1002/anie.201916335
Descripción
Sumario:The typical linewidths of (1)H NMR spectra of powdered organic solids at 111 kHz magic‐angle spinning (MAS) are of the order of a few hundred Hz. While this is remarkable in comparison to the tens of kHz observed in spectra of static samples, it is still the key limit to the use of (1)H in solid‐state NMR, especially for complex systems. Here, we demonstrate a novel strategy to further improve the spectral resolution. We show that the anti‐z‐COSY experiment can be used to reduce the residual line broadening of (1)H NMR spectra of powdered organic solids. Results obtained with the anti‐z‐COSY sequence at 100 kHz MAS on thymol, β‐AspAla, and strychnine show an improvement in resolution of up to a factor of two compared to conventional spectra acquired at the same spinning rate.