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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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 |
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author | Ochmann, Miguel Vaz da Cruz, Vinícius Eckert, Sebastian Huse, Nils Föhlisch, Alexander |
author_facet | Ochmann, Miguel Vaz da Cruz, Vinícius Eckert, Sebastian Huse, Nils Föhlisch, Alexander |
author_sort | Ochmann, Miguel |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9350990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-93509902022-08-29 R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering Ochmann, Miguel Vaz da Cruz, Vinícius Eckert, Sebastian Huse, Nils Föhlisch, Alexander Chem Commun (Camb) Chemistry 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. The Royal Society of Chemistry 2022-07-11 /pmc/articles/PMC9350990/ /pubmed/35848855 http://dx.doi.org/10.1039/d2cc00053a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Ochmann, Miguel Vaz da Cruz, Vinícius Eckert, Sebastian Huse, Nils Föhlisch, Alexander R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title | R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title_full | R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title_fullStr | R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title_full_unstemmed | R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title_short | R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering |
title_sort | r-group stabilization in methylated formamides observed by resonant inelastic x-ray scattering |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350990/ https://www.ncbi.nlm.nih.gov/pubmed/35848855 http://dx.doi.org/10.1039/d2cc00053a |
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