Slow ion interaction with N-methylglycine and N-acetylglycine
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 a...
| Autores: | , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Universidad Autónoma de Madrid |
| Repositorio: | Biblos-e Archivo. Repositorio Institucional de la UAM |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.uam.es:10486/672446 |
| Acceso en línea: | http://hdl.handle.net/10486/672446 https://dx.doi.org/10.1088/1742-6596/635/3/032054 |
| Access Level: | acceso abierto |
| Palabra clave: | Condensed matter physics Ionization Ionization of gases Molecules Química |
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Slow ion interaction with N-methylglycine and N-acetylglycineDíaz-Tendero Victoria, SergioDelaunay, RudyHuber, Bernd A.Adoui, LamriAlcamí Pertejo, ManuelMartín García, FernandoRousseau, PatrickDomaracka, AlicjaKopyra, JaninaKocisek, JaroslavPiekarski, Dariusz GrzegorzCondensed matter physicsIonizationIonization of gasesMoleculesQuímicaN-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 differentIOP Publishing Ltd.Departamento de QuímicaFacultad de Ciencias20152015-09-07research articlehttp://purl.org/coar/resource_type/c_2df8fbb1VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10486/672446https://dx.doi.org/10.1088/1742-6596/635/3/032054reponame:Biblos-e Archivo. Repositorio Institucional de la UAMinstname:Universidad Autónoma de MadridInglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:repositorio.uam.es:10486/6724462026-06-23T12:46:27Z |
| dc.title.none.fl_str_mv |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| title |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| spellingShingle |
Slow ion interaction with N-methylglycine and N-acetylglycine Díaz-Tendero Victoria, Sergio Condensed matter physics Ionization Ionization of gases Molecules Química |
| title_short |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| title_full |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| title_fullStr |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| title_full_unstemmed |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| title_sort |
Slow ion interaction with N-methylglycine and N-acetylglycine |
| dc.creator.none.fl_str_mv |
Díaz-Tendero Victoria, Sergio Delaunay, Rudy Huber, Bernd A. Adoui, Lamri Alcamí Pertejo, Manuel Martín García, Fernando Rousseau, Patrick Domaracka, Alicja Kopyra, Janina Kocisek, Jaroslav Piekarski, Dariusz Grzegorz |
| author |
Díaz-Tendero Victoria, Sergio |
| author_facet |
Díaz-Tendero Victoria, Sergio Delaunay, Rudy Huber, Bernd A. Adoui, Lamri Alcamí Pertejo, Manuel Martín García, Fernando Rousseau, Patrick Domaracka, Alicja Kopyra, Janina Kocisek, Jaroslav Piekarski, Dariusz Grzegorz |
| author_role |
author |
| author2 |
Delaunay, Rudy Huber, Bernd A. Adoui, Lamri Alcamí Pertejo, Manuel Martín García, Fernando Rousseau, Patrick Domaracka, Alicja Kopyra, Janina Kocisek, Jaroslav Piekarski, Dariusz Grzegorz |
| author2_role |
author author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Departamento de Química Facultad de Ciencias |
| dc.subject.none.fl_str_mv |
Condensed matter physics Ionization Ionization of gases Molecules Química |
| topic |
Condensed matter physics Ionization Ionization of gases Molecules Química |
| description |
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 |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015 2015-09-07 |
| dc.type.none.fl_str_mv |
research article http://purl.org/coar/resource_type/c_2df8fbb1 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10486/672446 https://dx.doi.org/10.1088/1742-6596/635/3/032054 |
| url |
http://hdl.handle.net/10486/672446 https://dx.doi.org/10.1088/1742-6596/635/3/032054 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
IOP Publishing Ltd. |
| publisher.none.fl_str_mv |
IOP Publishing Ltd. |
| dc.source.none.fl_str_mv |
reponame:Biblos-e Archivo. Repositorio Institucional de la UAM instname:Universidad Autónoma de Madrid |
| instname_str |
Universidad Autónoma de Madrid |
| reponame_str |
Biblos-e Archivo. Repositorio Institucional de la UAM |
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Biblos-e Archivo. Repositorio Institucional de la UAM |
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|
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1869404581484560384 |
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15,300719 |