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    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.

    Citation

    Miguel Ochmann, Vinícius Vaz da Cruz, Sebastian Eckert, Nils Huse, Alexander Föhlisch. R-Group stabilization in methylated formamides observed by resonant inelastic X-ray scattering. Chemical communications (Cambridge, England). 2022 Aug 04;58(63):8834-8837

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    PMID: 35848855

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