Inner-shell absorption spectroscopy of amino acids (Articolo in rivista)

Type
Label
  • Inner-shell absorption spectroscopy of amino acids (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Alternative label
  • Kaznacheyev K., Osanna A., Jacobsen C., Plashkevych O., Vahtras O., Agren H., Carravetta V., Hitchcock A.P. (2002)
    Inner-shell absorption spectroscopy of amino acids
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Kaznacheyev K., Osanna A., Jacobsen C., Plashkevych O., Vahtras O., Agren H., Carravetta V., Hitchcock A.P. (literal)
Pagina inizio
  • 3153 (literal)
Pagina fine
  • 3168 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 106 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
  • Molecular Modeling Lab (literal)
Note
  • ISI Web of Science (WOS) (literal)
Titolo
  • Inner-shell absorption spectroscopy of amino acids (literal)
Abstract
  • We present comprehensive measurements of the C (carbon) K edge near-edge X-ray absorption (NEXAFS) spectra of all 20 amino acids commonly occurring in nature. Qualitative trends among the spectra of amino acids with similar chemical character are identified and spectral features are compared with extensive ab initio calculations. The contributions of individual units and substitutional groups have been determined to explore their fingerprinting character using the building block concept. Several such units are found. Two that give particularly clear features in the C 1s NEXAFS spectra are the carboxyl group (which can be clearly identified by a pronounced structure due to the C 1s to pi */sub C=O/ transition with maximum at 288.65(5) eV) and modified phenol rings in aromatic amino acids (which give sharp C 1s to pi */sub C=C/ structures). The latter transitions are located around 285 eV, and their shape is specific for each aromatic amino acid. Other building blocks, such as the CNH/sub n/ group and the CH, CC, CO, CN pair bonds, are also identified, although their characteristic features are less pronounced in the C K edge spectra than the carboxyli (literal)
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