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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/119281
Ver los metadatos del registro completo
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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:UNLP2025-09-29T11:28:09Zoai: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:13292025-09-29 11:28:09.776SEDICI (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 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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