GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features

Autores
Gastaca, Belén; Galletti, Gastón Hernán; Sánchez, Hernán Rubén; Pis Diez, Reinaldo; Schiavoni, María de las Mercedes; Furlong, Jorge Javier Pedro
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The mass spectral fragmentation of thiosemicarbazones synthesized from acetophenones has been studied by CG/MS. These carbonyl compounds exhibit chromatographic peaks which are not observed in aliphatic analogues or those synthesized from aldehydes. The analysis of the corresponding spectra has allowed structural assignment to the dimerization of gas phase neutral fragments. Theoretical calculations (DFT level) also provide evidence to support the experimental observations.
Centro de Estudios de Compuestos Orgánicos
Centro de Química Inorgánica
Materia
Química
Thiosemicarbazones
Mass Spectrometry Analyses
Dimerization of Thiosemicarbazones
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/119281
Acceder
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oai_identifier_str oai:sedici.unlp.edu.ar:10915/119281
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra FeaturesGastaca, BelénGalletti, Gastón HernánSánchez, Hernán RubénPis Diez, ReinaldoSchiavoni, María de las MercedesFurlong, Jorge Javier PedroQuímicaThiosemicarbazonesMass Spectrometry AnalysesDimerization of ThiosemicarbazonesThe mass spectral fragmentation of thiosemicarbazones synthesized from acetophenones has been studied by CG/MS. These carbonyl compounds exhibit chromatographic peaks which are not observed in aliphatic analogues or those synthesized from aldehydes. The analysis of the corresponding spectra has allowed structural assignment to the dimerization of gas phase neutral fragments. Theoretical calculations (DFT level) also provide evidence to support the experimental observations.Centro de Estudios de Compuestos OrgánicosCentro de Química Inorgánica2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/119281enginfo:eu-repo/semantics/altIdentifier/issn/2332-1768info:eu-repo/semantics/altIdentifier/issn/2332-1776info:eu-repo/semantics/altIdentifier/doi/10.4236/ijamsc.2015.31001info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:20:00Zoai:sedici.unlp.edu.ar:10915/119281Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:20:00.313SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
title GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
spellingShingle GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
Gastaca, Belén
Química
Thiosemicarbazones
Mass Spectrometry Analyses
Dimerization of Thiosemicarbazones
title_short GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
title_full GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
title_fullStr GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
title_full_unstemmed GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
title_sort GC/MS Analyses of Thiosemicarbazones Synthesized from Acetophenones: Thermal Decay and Mass Spectra Features
dc.creator.none.fl_str_mv Gastaca, Belén
Galletti, Gastón Hernán
Sánchez, Hernán Rubén
Pis Diez, Reinaldo
Schiavoni, María de las Mercedes
Furlong, Jorge Javier Pedro
author Gastaca, Belén
author_facet Gastaca, Belén
Galletti, Gastón Hernán
Sánchez, Hernán Rubén
Pis Diez, Reinaldo
Schiavoni, María de las Mercedes
Furlong, Jorge Javier Pedro
author_role author
author2 Galletti, Gastón Hernán
Sánchez, Hernán Rubén
Pis Diez, Reinaldo
Schiavoni, María de las Mercedes
Furlong, Jorge Javier Pedro
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Química
Thiosemicarbazones
Mass Spectrometry Analyses
Dimerization of Thiosemicarbazones
topic Química
Thiosemicarbazones
Mass Spectrometry Analyses
Dimerization of Thiosemicarbazones
dc.description.none.fl_txt_mv The mass spectral fragmentation of thiosemicarbazones synthesized from acetophenones has been studied by CG/MS. These carbonyl compounds exhibit chromatographic peaks which are not observed in aliphatic analogues or those synthesized from aldehydes. The analysis of the corresponding spectra has allowed structural assignment to the dimerization of gas phase neutral fragments. Theoretical calculations (DFT level) also provide evidence to support the experimental observations.
Centro de Estudios de Compuestos Orgánicos
Centro de Química Inorgánica
description The mass spectral fragmentation of thiosemicarbazones synthesized from acetophenones has been studied by CG/MS. These carbonyl compounds exhibit chromatographic peaks which are not observed in aliphatic analogues or those synthesized from aldehydes. The analysis of the corresponding spectra has allowed structural assignment to the dimerization of gas phase neutral fragments. Theoretical calculations (DFT level) also provide evidence to support the experimental observations.
publishDate 2015
dc.date.none.fl_str_mv 2015
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/119281
url http://sedici.unlp.edu.ar/handle/10915/119281
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/2332-1768
info:eu-repo/semantics/altIdentifier/issn/2332-1776
info:eu-repo/semantics/altIdentifier/doi/10.4236/ijamsc.2015.31001
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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score 13.22299

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