R-Group Stabilization in Methylated Formamides Observed by Resonant Inelastic X-ray Scattering
Overview
Overview
Journal
Chem Commun (Camb)
Publisher
Royal Society of Chemistry
Specialty
Chemistry
Date
2022 Jul 18
PMID
35848855
Authors
Affiliations
Affiliations
Soon will be listed here.
Abstract
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.
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Freibert A, Mendive-Tapia D, Huse N, Vendrell O J Chem Theory Comput. 2024; 20(5):2167-2180.
PMID: 38315564 PMC: 10938531. DOI: 10.1021/acs.jctc.3c01259.
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