Slow ion interaction with N-methylglycine and N-acetylglycine

Autor:	Bernd A. Huber, Sergio Diaz Tendero, Jaroslav Kocisek, Dariusz Grzegorz Piekarskh, Alicja Domaracka, Fernando Martín, Lamri Adoui, Patrick Rousseau, Janina Kopyra, R. Delaunay, Manuel Alcamí
Přispěvatelé:	UAM. Departamento de Química
Jazyk:	angličtina
Rok vydání:	2015
Předmět:	chemistry.chemical_classification History Ionization Stereochemistry Diol Química Molecules Condensed matter physics Tautomer Computer Science Applications Education Amino acid Ionization of gases chemistry.chemical_compound chemistry Fragmentation (mass spectrometry) Glycine Molecule Peptide bond
Zdroj:	Biblos-e Archivo. Repositorio Institucional de la UAM instname Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
Popis:	N-acetyl glycine and N-methyl glycine molecules in the gas phase are ionized by electron exchange with slow O6+ ions at an energy of 48 keV. After ionization, the methyl and acetyl substituted glycines dissociate into fragments analogous to that resulting from ionization and fragmentation of amino acids and peptides, respectively. N-acetylglycine which contains a peptide bond also effectively tautomerizes to the diol form. Such tautomerization is typical for amino acids, however, we show that the tautomerization mechanism of the N-acetylglycine is different.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22c72407d9358032c21cd89961fefc4 https://hdl.handle.net/10486/672446 Zobrazit plný text záznamu