Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon

Autores
Ismael, Amin; Borba, Ana; Duarte, Luís Vítor; Giuliano, Barbara Michela; Gomez Zavaglia, Andrea; Cristiano, María Lurdes Cristina
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A combined matrix isolation FTIR and theoretical DFT/B3LYP/6-311++G(3df, 3pd) study of the novel synthesised tetrazole-saccharyl conjugate 2-[1-(1H-tetrazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide [1-TE-BZT] was performed. In the gas phase, at room temperature, the compound exists as a mixture of six isomeric forms (four conformers of 1H tautomer and two conformers of 2H tautomer). According to theoretical calculations, conformers 1H were the most stable and the relative energies among the three most stable forms are lower than 4 kJ mol -1. These conformers benefit from stabilising intramolecular hydrogen bonds-like interactions involving the 1H of the tetrazole ring and the carbonyl oxygen of the saccharyl moiety. The photochemistry of 1-TE-BZT in solid argon was investigated and theoretical DFT/B3LYP/6-311++G(3df,3pd) calculations also helped in assignment of the experimental bands. A quick consumption of the compound occurred after irradiation of the matrix with UV laser light at λ = 275 nm. Three photofragmentation pathways were proposed, one leading to 2-[1-(1H-diaziren-3- yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide and molecular nitrogen, a second one giving 2-(1,1-dioxide-3-oxo-1,2-benzisothiazol-2(3H)-yl) propanenitrile and azide, and a third one involving loss of azide from the tetrazole ring and decarbonylation of the saccharyl ring of 1-TE-BZT to give acrylonitrile and 7-thia-8-azabicyclo[4.2.0] octa-1,3,5-triene 7,7 dioxide. The comparison of the relative intensities of the bands of the photoproducts obtained from the three channels allowed us to consider the latter pathway, involving an unprecedented photocleavage of the benzisothiazole (saccharyl) ring, as the preferred photodegradation channel of 1-TE-BZT.
Fil: Ismael, Amin. University of Algarve. Department of Chemistry and Pharmacy; Portugal
Fil: Borba, Ana. University of Coimbra. Department of Chemistry; Portugal
Fil: Duarte, Luís Vítor. University of Coimbra. Department of Chemistry; Portugal
Fil: Giuliano, Barbara Michela. University of Coimbra. Department of Chemistry; Portugal
Fil: Gomez Zavaglia, Andrea. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina. University of Coimbra. Department of Chemistry; Portugal
Fil: Cristiano, María Lurdes Cristina. University of Algarve. Department of Chemistry and Pharmacy; Portugal
Materia
Matrix Isolation
Molecular Structure
Photochemistry
Saccharin
Tetrazole
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/82876

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network_name_str CONICET Digital (CONICET)
spelling Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argonIsmael, AminBorba, AnaDuarte, Luís VítorGiuliano, Barbara MichelaGomez Zavaglia, AndreaCristiano, María Lurdes CristinaMatrix IsolationMolecular StructurePhotochemistrySaccharinTetrazolehttps://purl.org/becyt/ford/2.11https://purl.org/becyt/ford/2A combined matrix isolation FTIR and theoretical DFT/B3LYP/6-311++G(3df, 3pd) study of the novel synthesised tetrazole-saccharyl conjugate 2-[1-(1H-tetrazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide [1-TE-BZT] was performed. In the gas phase, at room temperature, the compound exists as a mixture of six isomeric forms (four conformers of 1H tautomer and two conformers of 2H tautomer). According to theoretical calculations, conformers 1H were the most stable and the relative energies among the three most stable forms are lower than 4 kJ mol -1. These conformers benefit from stabilising intramolecular hydrogen bonds-like interactions involving the 1H of the tetrazole ring and the carbonyl oxygen of the saccharyl moiety. The photochemistry of 1-TE-BZT in solid argon was investigated and theoretical DFT/B3LYP/6-311++G(3df,3pd) calculations also helped in assignment of the experimental bands. A quick consumption of the compound occurred after irradiation of the matrix with UV laser light at λ = 275 nm. Three photofragmentation pathways were proposed, one leading to 2-[1-(1H-diaziren-3- yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide and molecular nitrogen, a second one giving 2-(1,1-dioxide-3-oxo-1,2-benzisothiazol-2(3H)-yl) propanenitrile and azide, and a third one involving loss of azide from the tetrazole ring and decarbonylation of the saccharyl ring of 1-TE-BZT to give acrylonitrile and 7-thia-8-azabicyclo[4.2.0] octa-1,3,5-triene 7,7 dioxide. The comparison of the relative intensities of the bands of the photoproducts obtained from the three channels allowed us to consider the latter pathway, involving an unprecedented photocleavage of the benzisothiazole (saccharyl) ring, as the preferred photodegradation channel of 1-TE-BZT.Fil: Ismael, Amin. University of Algarve. Department of Chemistry and Pharmacy; PortugalFil: Borba, Ana. University of Coimbra. Department of Chemistry; PortugalFil: Duarte, Luís Vítor. University of Coimbra. Department of Chemistry; PortugalFil: Giuliano, Barbara Michela. University of Coimbra. Department of Chemistry; PortugalFil: Gomez Zavaglia, Andrea. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina. University of Coimbra. Department of Chemistry; PortugalFil: Cristiano, María Lurdes Cristina. University of Algarve. Department of Chemistry and Pharmacy; PortugalElsevier Science2012-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/82876Ismael, Amin; Borba, Ana; Duarte, Luís Vítor; Giuliano, Barbara Michela; Gomez Zavaglia, Andrea; et al.; Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon; Elsevier Science; Journal of Molecular Structure; 1025; 10-2012; 105-1160022-2860CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022286012004164info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molstruc.2012.04.081info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:05:29Zoai:ri.conicet.gov.ar:11336/82876instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:05:30.074CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
title Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
spellingShingle Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
Ismael, Amin
Matrix Isolation
Molecular Structure
Photochemistry
Saccharin
Tetrazole
title_short Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
title_full Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
title_fullStr Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
title_full_unstemmed Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
title_sort Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon
dc.creator.none.fl_str_mv Ismael, Amin
Borba, Ana
Duarte, Luís Vítor
Giuliano, Barbara Michela
Gomez Zavaglia, Andrea
Cristiano, María Lurdes Cristina
author Ismael, Amin
author_facet Ismael, Amin
Borba, Ana
Duarte, Luís Vítor
Giuliano, Barbara Michela
Gomez Zavaglia, Andrea
Cristiano, María Lurdes Cristina
author_role author
author2 Borba, Ana
Duarte, Luís Vítor
Giuliano, Barbara Michela
Gomez Zavaglia, Andrea
Cristiano, María Lurdes Cristina
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Matrix Isolation
Molecular Structure
Photochemistry
Saccharin
Tetrazole
topic Matrix Isolation
Molecular Structure
Photochemistry
Saccharin
Tetrazole
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.11
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv A combined matrix isolation FTIR and theoretical DFT/B3LYP/6-311++G(3df, 3pd) study of the novel synthesised tetrazole-saccharyl conjugate 2-[1-(1H-tetrazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide [1-TE-BZT] was performed. In the gas phase, at room temperature, the compound exists as a mixture of six isomeric forms (four conformers of 1H tautomer and two conformers of 2H tautomer). According to theoretical calculations, conformers 1H were the most stable and the relative energies among the three most stable forms are lower than 4 kJ mol -1. These conformers benefit from stabilising intramolecular hydrogen bonds-like interactions involving the 1H of the tetrazole ring and the carbonyl oxygen of the saccharyl moiety. The photochemistry of 1-TE-BZT in solid argon was investigated and theoretical DFT/B3LYP/6-311++G(3df,3pd) calculations also helped in assignment of the experimental bands. A quick consumption of the compound occurred after irradiation of the matrix with UV laser light at λ = 275 nm. Three photofragmentation pathways were proposed, one leading to 2-[1-(1H-diaziren-3- yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide and molecular nitrogen, a second one giving 2-(1,1-dioxide-3-oxo-1,2-benzisothiazol-2(3H)-yl) propanenitrile and azide, and a third one involving loss of azide from the tetrazole ring and decarbonylation of the saccharyl ring of 1-TE-BZT to give acrylonitrile and 7-thia-8-azabicyclo[4.2.0] octa-1,3,5-triene 7,7 dioxide. The comparison of the relative intensities of the bands of the photoproducts obtained from the three channels allowed us to consider the latter pathway, involving an unprecedented photocleavage of the benzisothiazole (saccharyl) ring, as the preferred photodegradation channel of 1-TE-BZT.
Fil: Ismael, Amin. University of Algarve. Department of Chemistry and Pharmacy; Portugal
Fil: Borba, Ana. University of Coimbra. Department of Chemistry; Portugal
Fil: Duarte, Luís Vítor. University of Coimbra. Department of Chemistry; Portugal
Fil: Giuliano, Barbara Michela. University of Coimbra. Department of Chemistry; Portugal
Fil: Gomez Zavaglia, Andrea. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos. Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina. University of Coimbra. Department of Chemistry; Portugal
Fil: Cristiano, María Lurdes Cristina. University of Algarve. Department of Chemistry and Pharmacy; Portugal
description A combined matrix isolation FTIR and theoretical DFT/B3LYP/6-311++G(3df, 3pd) study of the novel synthesised tetrazole-saccharyl conjugate 2-[1-(1H-tetrazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide [1-TE-BZT] was performed. In the gas phase, at room temperature, the compound exists as a mixture of six isomeric forms (four conformers of 1H tautomer and two conformers of 2H tautomer). According to theoretical calculations, conformers 1H were the most stable and the relative energies among the three most stable forms are lower than 4 kJ mol -1. These conformers benefit from stabilising intramolecular hydrogen bonds-like interactions involving the 1H of the tetrazole ring and the carbonyl oxygen of the saccharyl moiety. The photochemistry of 1-TE-BZT in solid argon was investigated and theoretical DFT/B3LYP/6-311++G(3df,3pd) calculations also helped in assignment of the experimental bands. A quick consumption of the compound occurred after irradiation of the matrix with UV laser light at λ = 275 nm. Three photofragmentation pathways were proposed, one leading to 2-[1-(1H-diaziren-3- yl)ethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide and molecular nitrogen, a second one giving 2-(1,1-dioxide-3-oxo-1,2-benzisothiazol-2(3H)-yl) propanenitrile and azide, and a third one involving loss of azide from the tetrazole ring and decarbonylation of the saccharyl ring of 1-TE-BZT to give acrylonitrile and 7-thia-8-azabicyclo[4.2.0] octa-1,3,5-triene 7,7 dioxide. The comparison of the relative intensities of the bands of the photoproducts obtained from the three channels allowed us to consider the latter pathway, involving an unprecedented photocleavage of the benzisothiazole (saccharyl) ring, as the preferred photodegradation channel of 1-TE-BZT.
publishDate 2012
dc.date.none.fl_str_mv 2012-10
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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://hdl.handle.net/11336/82876
Ismael, Amin; Borba, Ana; Duarte, Luís Vítor; Giuliano, Barbara Michela; Gomez Zavaglia, Andrea; et al.; Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon; Elsevier Science; Journal of Molecular Structure; 1025; 10-2012; 105-116
0022-2860
CONICET Digital
CONICET
url http://hdl.handle.net/11336/82876
identifier_str_mv Ismael, Amin; Borba, Ana; Duarte, Luís Vítor; Giuliano, Barbara Michela; Gomez Zavaglia, Andrea; et al.; Structure and photochemistry of a novel tetrazole-saccharyl conjugate isolated in solid argon; Elsevier Science; Journal of Molecular Structure; 1025; 10-2012; 105-116
0022-2860
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022286012004164
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molstruc.2012.04.081
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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