Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes

Autores
Pieslinger, German Eduardo; Aramburu Troselj, Bruno Martín; Cadranel, Alejandro; Baraldo Victorica, Luis Mario
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
We report here the spectroscopic properties of four very closely related mixed-valence cyanide-bridged bimetallic complexes, trans-[Ru(T)(bpy)(μ-NC)Ru(L)4(CN)]3+ (T = tris(1-pyrazolyl)methane (tpm, a) or 2,2′;6′,2″-terpyridine, (tpy, b), and L = pyridine (py, 1) or 4-methoxypyridine (MeOpy, 2)). In acetonitrile all the complexes present intervalence charge transfer (IVCT) transitions in the NIR region, but their intensities are widely different, with the intensity of the transition observed for 1a–b3+ around four times larger than that observed for 2a–b3+. This contrasting behavior can be traced to the different nature of the dπ acceptor orbitals involved in these transitions, as confirmed by (TD)DFT calculations. The spectroscopy of 1a–b3+ provides evidence that the spin density is delocalized over the two ruthenium ions, such as a narrowing of the IVCT bands that results in the resolution of the expected three bands, and a weak solvent dependence of the energy of these transitions. The spectroscopy of 2a–b3+ instead indicates that the spin density is localized on one ruthenium ion. The IVCT in these systems is particularly weak due to the configuration of the Ru(III), where the vacant orbital is perpendicular to the cyanide bridge.
Fil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Aramburu Troselj, Bruno Martín. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Cadranel, Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Materia
Cyanide-Bridged Complexes
Metal-Metal Interaction
Mixed-Valence Complexes
Intervalence Charge Transfer Band
Spectroelectrochemistry
Density Functional Theory
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/31905

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network_name_str CONICET Digital (CONICET)
spelling Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence ComplexesPieslinger, German EduardoAramburu Troselj, Bruno MartínCadranel, AlejandroBaraldo Victorica, Luis MarioCyanide-Bridged ComplexesMetal-Metal InteractionMixed-Valence ComplexesIntervalence Charge Transfer BandSpectroelectrochemistryDensity Functional Theoryhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1We report here the spectroscopic properties of four very closely related mixed-valence cyanide-bridged bimetallic complexes, trans-[Ru(T)(bpy)(μ-NC)Ru(L)4(CN)]3+ (T = tris(1-pyrazolyl)methane (tpm, a) or 2,2′;6′,2″-terpyridine, (tpy, b), and L = pyridine (py, 1) or 4-methoxypyridine (MeOpy, 2)). In acetonitrile all the complexes present intervalence charge transfer (IVCT) transitions in the NIR region, but their intensities are widely different, with the intensity of the transition observed for 1a–b3+ around four times larger than that observed for 2a–b3+. This contrasting behavior can be traced to the different nature of the dπ acceptor orbitals involved in these transitions, as confirmed by (TD)DFT calculations. The spectroscopy of 1a–b3+ provides evidence that the spin density is delocalized over the two ruthenium ions, such as a narrowing of the IVCT bands that results in the resolution of the expected three bands, and a weak solvent dependence of the energy of these transitions. The spectroscopy of 2a–b3+ instead indicates that the spin density is localized on one ruthenium ion. The IVCT in these systems is particularly weak due to the configuration of the Ru(III), where the vacant orbital is perpendicular to the cyanide bridge.Fil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Aramburu Troselj, Bruno Martín. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Cadranel, Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaAmerican Chemical Society2014-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/31905Baraldo Victorica, Luis Mario; Cadranel, Alejandro; Aramburu Troselj, Bruno Martín; Pieslinger, German Eduardo; Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes; American Chemical Society; Inorganic Chemistry; 53; 16; 7-2014; 8221-82290020-1669CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/ic5002539info:eu-repo/semantics/altIdentifier/doi/10.1021/ic5002539info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:00:06Zoai:ri.conicet.gov.ar:11336/31905instacron: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:34982025-09-10 13:00:06.901CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
title Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
spellingShingle Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
Pieslinger, German Eduardo
Cyanide-Bridged Complexes
Metal-Metal Interaction
Mixed-Valence Complexes
Intervalence Charge Transfer Band
Spectroelectrochemistry
Density Functional Theory
title_short Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
title_full Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
title_fullStr Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
title_full_unstemmed Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
title_sort Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes
dc.creator.none.fl_str_mv Pieslinger, German Eduardo
Aramburu Troselj, Bruno Martín
Cadranel, Alejandro
Baraldo Victorica, Luis Mario
author Pieslinger, German Eduardo
author_facet Pieslinger, German Eduardo
Aramburu Troselj, Bruno Martín
Cadranel, Alejandro
Baraldo Victorica, Luis Mario
author_role author
author2 Aramburu Troselj, Bruno Martín
Cadranel, Alejandro
Baraldo Victorica, Luis Mario
author2_role author
author
author
dc.subject.none.fl_str_mv Cyanide-Bridged Complexes
Metal-Metal Interaction
Mixed-Valence Complexes
Intervalence Charge Transfer Band
Spectroelectrochemistry
Density Functional Theory
topic Cyanide-Bridged Complexes
Metal-Metal Interaction
Mixed-Valence Complexes
Intervalence Charge Transfer Band
Spectroelectrochemistry
Density Functional Theory
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv We report here the spectroscopic properties of four very closely related mixed-valence cyanide-bridged bimetallic complexes, trans-[Ru(T)(bpy)(μ-NC)Ru(L)4(CN)]3+ (T = tris(1-pyrazolyl)methane (tpm, a) or 2,2′;6′,2″-terpyridine, (tpy, b), and L = pyridine (py, 1) or 4-methoxypyridine (MeOpy, 2)). In acetonitrile all the complexes present intervalence charge transfer (IVCT) transitions in the NIR region, but their intensities are widely different, with the intensity of the transition observed for 1a–b3+ around four times larger than that observed for 2a–b3+. This contrasting behavior can be traced to the different nature of the dπ acceptor orbitals involved in these transitions, as confirmed by (TD)DFT calculations. The spectroscopy of 1a–b3+ provides evidence that the spin density is delocalized over the two ruthenium ions, such as a narrowing of the IVCT bands that results in the resolution of the expected three bands, and a weak solvent dependence of the energy of these transitions. The spectroscopy of 2a–b3+ instead indicates that the spin density is localized on one ruthenium ion. The IVCT in these systems is particularly weak due to the configuration of the Ru(III), where the vacant orbital is perpendicular to the cyanide bridge.
Fil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Aramburu Troselj, Bruno Martín. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Cadranel, Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
description We report here the spectroscopic properties of four very closely related mixed-valence cyanide-bridged bimetallic complexes, trans-[Ru(T)(bpy)(μ-NC)Ru(L)4(CN)]3+ (T = tris(1-pyrazolyl)methane (tpm, a) or 2,2′;6′,2″-terpyridine, (tpy, b), and L = pyridine (py, 1) or 4-methoxypyridine (MeOpy, 2)). In acetonitrile all the complexes present intervalence charge transfer (IVCT) transitions in the NIR region, but their intensities are widely different, with the intensity of the transition observed for 1a–b3+ around four times larger than that observed for 2a–b3+. This contrasting behavior can be traced to the different nature of the dπ acceptor orbitals involved in these transitions, as confirmed by (TD)DFT calculations. The spectroscopy of 1a–b3+ provides evidence that the spin density is delocalized over the two ruthenium ions, such as a narrowing of the IVCT bands that results in the resolution of the expected three bands, and a weak solvent dependence of the energy of these transitions. The spectroscopy of 2a–b3+ instead indicates that the spin density is localized on one ruthenium ion. The IVCT in these systems is particularly weak due to the configuration of the Ru(III), where the vacant orbital is perpendicular to the cyanide bridge.
publishDate 2014
dc.date.none.fl_str_mv 2014-07
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/11336/31905
Baraldo Victorica, Luis Mario; Cadranel, Alejandro; Aramburu Troselj, Bruno Martín; Pieslinger, German Eduardo; Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes; American Chemical Society; Inorganic Chemistry; 53; 16; 7-2014; 8221-8229
0020-1669
CONICET Digital
CONICET
url http://hdl.handle.net/11336/31905
identifier_str_mv Baraldo Victorica, Luis Mario; Cadranel, Alejandro; Aramburu Troselj, Bruno Martín; Pieslinger, German Eduardo; Influence of the Electronic Configuration in the Properties of d6–d5 Mixed-Valence Complexes; American Chemical Society; Inorganic Chemistry; 53; 16; 7-2014; 8221-8229
0020-1669
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://pubs.acs.org/doi/abs/10.1021/ic5002539
info:eu-repo/semantics/altIdentifier/doi/10.1021/ic5002539
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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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