Structure and spectroscopy of two new bases for building block: Terpyridine derivatives

Autores
Toledo, Dominique; Baggio, Ricardo Fortunato; Freire Espeleta, Eleonora; Vega, Andrés; Pizarro, Nancy; Moreno, Yanko
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Two new terpyridine compounds are reported: 4′-(3-methyl-2-thienyl)-4,2′:6′,4″-terpyridine, C20H15N3S, (I) and 4′-(4-quinolinyl)-4,2′:6′,4″-terpyridine, C25H17Cl3N4, (II). Both structures crystallize in centrosymmetric space groups and present weak H-bonds, which gives greater stability to their structures. Light absorption by both molecules is firmly established on the experimental and the TDDFT analysis as coming from π → π∗transitions. The fluorescence of both compounds has a small Stockes shift, which is also consistent with the emission from highly rigid molecules. Furthermore, the thermal stability observed for both compounds, until about 280 °C, making these molecules interesting candidates for use as complex ligands, which are obtained by means of solvothermal synthesis (technique with temperatures of about 150 °C).
Fil: Toledo, Dominique. Universidad de Concepción; Chile
Fil: Baggio, Ricardo Fortunato. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina
Fil: Freire Espeleta, Eleonora. Universidad Nacional de San Martín; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Vega, Andrés. Universidad Andrés Bello; Chile
Fil: Pizarro, Nancy. Universidad Andrés Bello; Chile
Fil: Moreno, Yanko. Universidad Andrés Bello; Chile
Materia
FLUORESCENCE
MOLECULAR STRUCTURE
TDDFT ANALYSIS
TERPYRIDINE
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:11336/98533
Acceder
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network_name_str CONICET Digital (CONICET)
spelling Structure and spectroscopy of two new bases for building block: Terpyridine derivativesToledo, DominiqueBaggio, Ricardo FortunatoFreire Espeleta, EleonoraVega, AndrésPizarro, NancyMoreno, YankoFLUORESCENCEMOLECULAR STRUCTURETDDFT ANALYSISTERPYRIDINEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Two new terpyridine compounds are reported: 4′-(3-methyl-2-thienyl)-4,2′:6′,4″-terpyridine, C20H15N3S, (I) and 4′-(4-quinolinyl)-4,2′:6′,4″-terpyridine, C25H17Cl3N4, (II). Both structures crystallize in centrosymmetric space groups and present weak H-bonds, which gives greater stability to their structures. Light absorption by both molecules is firmly established on the experimental and the TDDFT analysis as coming from π → π∗transitions. The fluorescence of both compounds has a small Stockes shift, which is also consistent with the emission from highly rigid molecules. Furthermore, the thermal stability observed for both compounds, until about 280 °C, making these molecules interesting candidates for use as complex ligands, which are obtained by means of solvothermal synthesis (technique with temperatures of about 150 °C).Fil: Toledo, Dominique. Universidad de Concepción; ChileFil: Baggio, Ricardo Fortunato. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; ArgentinaFil: Freire Espeleta, Eleonora. Universidad Nacional de San Martín; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Vega, Andrés. Universidad Andrés Bello; ChileFil: Pizarro, Nancy. Universidad Andrés Bello; ChileFil: Moreno, Yanko. Universidad Andrés Bello; ChileElsevier Science2015-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/98533Toledo, Dominique; Baggio, Ricardo Fortunato; Freire Espeleta, Eleonora; Vega, Andrés; Pizarro, Nancy; et al.; Structure and spectroscopy of two new bases for building block: Terpyridine derivatives; Elsevier Science; Journal of Molecular Structure; 1102; 12-2015; 18-240022-2860CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0022286015302180info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molstruc.2015.08.030info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:03:11Zoai:ri.conicet.gov.ar:11336/98533instacron: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:34982025-10-22 12:03:11.995CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
title Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
spellingShingle Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
Toledo, Dominique
FLUORESCENCE
MOLECULAR STRUCTURE
TDDFT ANALYSIS
TERPYRIDINE
title_short Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
title_full Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
title_fullStr Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
title_full_unstemmed Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
title_sort Structure and spectroscopy of two new bases for building block: Terpyridine derivatives
dc.creator.none.fl_str_mv Toledo, Dominique
Baggio, Ricardo Fortunato
Freire Espeleta, Eleonora
Vega, Andrés
Pizarro, Nancy
Moreno, Yanko
author Toledo, Dominique
author_facet Toledo, Dominique
Baggio, Ricardo Fortunato
Freire Espeleta, Eleonora
Vega, Andrés
Pizarro, Nancy
Moreno, Yanko
author_role author
author2 Baggio, Ricardo Fortunato
Freire Espeleta, Eleonora
Vega, Andrés
Pizarro, Nancy
Moreno, Yanko
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv FLUORESCENCE
MOLECULAR STRUCTURE
TDDFT ANALYSIS
TERPYRIDINE
topic FLUORESCENCE
MOLECULAR STRUCTURE
TDDFT ANALYSIS
TERPYRIDINE
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Two new terpyridine compounds are reported: 4′-(3-methyl-2-thienyl)-4,2′:6′,4″-terpyridine, C20H15N3S, (I) and 4′-(4-quinolinyl)-4,2′:6′,4″-terpyridine, C25H17Cl3N4, (II). Both structures crystallize in centrosymmetric space groups and present weak H-bonds, which gives greater stability to their structures. Light absorption by both molecules is firmly established on the experimental and the TDDFT analysis as coming from π → π∗transitions. The fluorescence of both compounds has a small Stockes shift, which is also consistent with the emission from highly rigid molecules. Furthermore, the thermal stability observed for both compounds, until about 280 °C, making these molecules interesting candidates for use as complex ligands, which are obtained by means of solvothermal synthesis (technique with temperatures of about 150 °C).
Fil: Toledo, Dominique. Universidad de Concepción; Chile
Fil: Baggio, Ricardo Fortunato. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina
Fil: Freire Espeleta, Eleonora. Universidad Nacional de San Martín; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Vega, Andrés. Universidad Andrés Bello; Chile
Fil: Pizarro, Nancy. Universidad Andrés Bello; Chile
Fil: Moreno, Yanko. Universidad Andrés Bello; Chile
description Two new terpyridine compounds are reported: 4′-(3-methyl-2-thienyl)-4,2′:6′,4″-terpyridine, C20H15N3S, (I) and 4′-(4-quinolinyl)-4,2′:6′,4″-terpyridine, C25H17Cl3N4, (II). Both structures crystallize in centrosymmetric space groups and present weak H-bonds, which gives greater stability to their structures. Light absorption by both molecules is firmly established on the experimental and the TDDFT analysis as coming from π → π∗transitions. The fluorescence of both compounds has a small Stockes shift, which is also consistent with the emission from highly rigid molecules. Furthermore, the thermal stability observed for both compounds, until about 280 °C, making these molecules interesting candidates for use as complex ligands, which are obtained by means of solvothermal synthesis (technique with temperatures of about 150 °C).
publishDate 2015
dc.date.none.fl_str_mv 2015-12
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/11336/98533
Toledo, Dominique; Baggio, Ricardo Fortunato; Freire Espeleta, Eleonora; Vega, Andrés; Pizarro, Nancy; et al.; Structure and spectroscopy of two new bases for building block: Terpyridine derivatives; Elsevier Science; Journal of Molecular Structure; 1102; 12-2015; 18-24
0022-2860
CONICET Digital
CONICET
url http://hdl.handle.net/11336/98533
identifier_str_mv Toledo, Dominique; Baggio, Ricardo Fortunato; Freire Espeleta, Eleonora; Vega, Andrés; Pizarro, Nancy; et al.; Structure and spectroscopy of two new bases for building block: Terpyridine derivatives; Elsevier Science; Journal of Molecular Structure; 1102; 12-2015; 18-24
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/https://www.sciencedirect.com/science/article/pii/S0022286015302180
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molstruc.2015.08.030
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
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
_version_ 1846782372726439936
score 12.982451

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