Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond

Detalhes bibliográficos
Autor(a) principal: Miguel L F Viveiros
Data de Publicação: 2012
Outros Autores: Vera L S Freitas, Nuno Vale, Jose R B Gomes, Paula Gomes, Maria D M C R Ribeiro da Silva
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://repositorio-aberto.up.pt/handle/10216/84716
Resumo: The synthesis of three new quinoxaline mono-N-oxides derivatives, namely, 2-tert-butoxycarbonyl-3-methylquinoxaline-N-oxide, 2-phenylcarbamoyl-3-ethylquinoxaline-N-oxide, and 2-carbamoyl-3-methylquinoxaline-N-oxide, from their corresponding 1,4-di-N-oxides is reported. Samples of these compounds were used for a thermochemical study, which allowed derivation of their gaseous standard molar enthalpies of formation, Delta fHmo(g), from their enthalpies of formation in the condensed phase, Delta fHmo(cr), determined by static bomb combustion calorimetry, and from their enthalpies of sublimation, Delta crgHmo, determined by Calvet microcalorimetry. Finally, combining the Delta fHmo(g) for the quinoxaline-N-oxides derived in this work with literature values for the corresponding 1,4-di-N-oxides and atomic oxygen, the bond dissociation enthalpies for cleavage of the first N-O bond in the di-N-oxides, DH1(NO), were obtained and compared with existing data. Copyright (c) 2011 John Wiley & Sons, Ltd.
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spelling Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bondQuímicaChemical sciencesThe synthesis of three new quinoxaline mono-N-oxides derivatives, namely, 2-tert-butoxycarbonyl-3-methylquinoxaline-N-oxide, 2-phenylcarbamoyl-3-ethylquinoxaline-N-oxide, and 2-carbamoyl-3-methylquinoxaline-N-oxide, from their corresponding 1,4-di-N-oxides is reported. Samples of these compounds were used for a thermochemical study, which allowed derivation of their gaseous standard molar enthalpies of formation, Delta fHmo(g), from their enthalpies of formation in the condensed phase, Delta fHmo(cr), determined by static bomb combustion calorimetry, and from their enthalpies of sublimation, Delta crgHmo, determined by Calvet microcalorimetry. Finally, combining the Delta fHmo(g) for the quinoxaline-N-oxides derived in this work with literature values for the corresponding 1,4-di-N-oxides and atomic oxygen, the bond dissociation enthalpies for cleavage of the first N-O bond in the di-N-oxides, DH1(NO), were obtained and compared with existing data. Copyright (c) 2011 John Wiley & Sons, Ltd.20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://repositorio-aberto.up.pt/handle/10216/84716eng0894-323010.1002/poc.1932Miguel L F ViveirosVera L S FreitasNuno ValeJose R B GomesPaula GomesMaria D M C R Ribeiro da Silvainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T14:39:50Zoai:repositorio-aberto.up.pt:10216/84716Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:06:17.548788Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
title Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
spellingShingle Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
Miguel L F Viveiros
Química
Chemical sciences
title_short Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
title_full Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
title_fullStr Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
title_full_unstemmed Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
title_sort Synthesis and thermochemical study of quinoxaline-N-oxides: enthalpies of dissociation of the N-O bond
author Miguel L F Viveiros
author_facet Miguel L F Viveiros
Vera L S Freitas
Nuno Vale
Jose R B Gomes
Paula Gomes
Maria D M C R Ribeiro da Silva
author_role author
author2 Vera L S Freitas
Nuno Vale
Jose R B Gomes
Paula Gomes
Maria D M C R Ribeiro da Silva
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Miguel L F Viveiros
Vera L S Freitas
Nuno Vale
Jose R B Gomes
Paula Gomes
Maria D M C R Ribeiro da Silva
dc.subject.por.fl_str_mv Química
Chemical sciences
topic Química
Chemical sciences
description The synthesis of three new quinoxaline mono-N-oxides derivatives, namely, 2-tert-butoxycarbonyl-3-methylquinoxaline-N-oxide, 2-phenylcarbamoyl-3-ethylquinoxaline-N-oxide, and 2-carbamoyl-3-methylquinoxaline-N-oxide, from their corresponding 1,4-di-N-oxides is reported. Samples of these compounds were used for a thermochemical study, which allowed derivation of their gaseous standard molar enthalpies of formation, Delta fHmo(g), from their enthalpies of formation in the condensed phase, Delta fHmo(cr), determined by static bomb combustion calorimetry, and from their enthalpies of sublimation, Delta crgHmo, determined by Calvet microcalorimetry. Finally, combining the Delta fHmo(g) for the quinoxaline-N-oxides derived in this work with literature values for the corresponding 1,4-di-N-oxides and atomic oxygen, the bond dissociation enthalpies for cleavage of the first N-O bond in the di-N-oxides, DH1(NO), were obtained and compared with existing data. Copyright (c) 2011 John Wiley & Sons, Ltd.
publishDate 2012
dc.date.none.fl_str_mv 2012
2012-01-01T00:00:00Z
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dc.identifier.uri.fl_str_mv https://repositorio-aberto.up.pt/handle/10216/84716
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 0894-3230
10.1002/poc.1932
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