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R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering

The inherent stability of methylated formamides is traced to a stabilization of the deep-lying σ-framework by resonant inelastic X-ray scattering at the nitrogen K-edge. Charge transfer from the amide nitrogen to the methyl groups underlie this stabilization mechanism that leaves the aldehyde group...

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Detalles Bibliográficos
Autores principales: Ochmann, Miguel, Vaz da Cruz, Vinícius, Eckert, Sebastian, Huse, Nils, Föhlisch, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350990/
https://www.ncbi.nlm.nih.gov/pubmed/35848855
http://dx.doi.org/10.1039/d2cc00053a
Descripción
Sumario:The inherent stability of methylated formamides is traced to a stabilization of the deep-lying σ-framework by resonant inelastic X-ray scattering at the nitrogen K-edge. Charge transfer from the amide nitrogen to the methyl groups underlie this stabilization mechanism that leaves the aldehyde group essentially unaltered and explains the stability of secondary and tertiary amides.