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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/82876
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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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1842269913614385152 |
score |
13.13397 |