Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex

Autores
Fagalde, Florencia; Mellace, María G.; Lis, Noemi Dora; Katz, Néstor Eduardo
Año de publicación
2004
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Kinetic data for the hydrolysis reaction: [(CO)3(bpy)Re I(4-CNpy)RuIII(NH3)5]4+ + H2O → [(CO)3(bpy)ReI(4-C(O)NHpy)Ru III(NH3)5]3+ + H+ (bpy = 2,2′-bipyridine, 4-CNpy = 4-cyanopyridine and 4-C(O)NHpy = isonicotinamido), that occurs after oxidation with S2O 82- of the dinuclear species [(CO)3(bpy)Re I(4-CNpy)RuII (NH3)5]3+, have been obtained in aqueous solutions by spectrophotometric techniques. The observed rate constant, kh = (8.6 ± 0.5) × 10 -3 s-1, at 25°C, pH = 3.0 (CF3COOH) and I = 0.1 M (KCl), is ca. three times higher than the corresponding one for the mononuclear complex [(4-CNpy)RuIII(NH3)5] 3+, indicating that the catalytic effect of the Ru III(NH3)5 moiety is enhanced by coordination of the free N of 4-CNpy to the ReI(CO)3(bpy) moiety. The value of kh is even higher than that of the dinuclear complex [(trpy)(bpy)RuII (4-CNpy)RuIII(NH3) 5]5+ (trpy = 2,2′:6′,2″-terpyridine), reflecting the fact that carbonyls are much stronger π-acceptors than polypyridines.
Fil: Fagalde, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Inorgánica; Argentina
Fil: Mellace, María G.. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Fil: Lis, Noemi Dora. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Fil: Katz, Néstor Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Materia
4-CYANOPYRIDINE
CATALYSIS
DINUCLEAR COMPLEXES
MIXED-VALENT COMPLEXES
NITRILE HYDROLYSIS
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:11336/100223

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network_name_str CONICET Digital (CONICET)
spelling Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complexFagalde, FlorenciaMellace, María G.Lis, Noemi DoraKatz, Néstor Eduardo4-CYANOPYRIDINECATALYSISDINUCLEAR COMPLEXESMIXED-VALENT COMPLEXESNITRILE HYDROLYSIShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Kinetic data for the hydrolysis reaction: [(CO)3(bpy)Re I(4-CNpy)RuIII(NH3)5]4+ + H2O → [(CO)3(bpy)ReI(4-C(O)NHpy)Ru III(NH3)5]3+ + H+ (bpy = 2,2′-bipyridine, 4-CNpy = 4-cyanopyridine and 4-C(O)NHpy = isonicotinamido), that occurs after oxidation with S2O 82- of the dinuclear species [(CO)3(bpy)Re I(4-CNpy)RuII (NH3)5]3+, have been obtained in aqueous solutions by spectrophotometric techniques. The observed rate constant, kh = (8.6 ± 0.5) × 10 -3 s-1, at 25°C, pH = 3.0 (CF3COOH) and I = 0.1 M (KCl), is ca. three times higher than the corresponding one for the mononuclear complex [(4-CNpy)RuIII(NH3)5] 3+, indicating that the catalytic effect of the Ru III(NH3)5 moiety is enhanced by coordination of the free N of 4-CNpy to the ReI(CO)3(bpy) moiety. The value of kh is even higher than that of the dinuclear complex [(trpy)(bpy)RuII (4-CNpy)RuIII(NH3) 5]5+ (trpy = 2,2′:6′,2″-terpyridine), reflecting the fact that carbonyls are much stronger π-acceptors than polypyridines.Fil: Fagalde, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Inorgánica; ArgentinaFil: Mellace, María G.. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; ArgentinaFil: Lis, Noemi Dora. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; ArgentinaFil: Katz, Néstor Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; ArgentinaTaylor & Francis Ltd2004-05info: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/11336/100223Fagalde, Florencia; Mellace, María G.; Lis, Noemi Dora; Katz, Néstor Eduardo; Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex; Taylor & Francis Ltd; Journal of Coordination Chemistry; 57; 8; 5-2004; 635-6390095-8972CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1080/00958970410001689111info:eu-repo/semantics/altIdentifier/url/https://www.tandfonline.com/doi/abs/10.1080/00958970410001689111info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:13:44Zoai:ri.conicet.gov.ar:11336/100223instacron: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 13:13:44.398CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
title Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
spellingShingle Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
Fagalde, Florencia
4-CYANOPYRIDINE
CATALYSIS
DINUCLEAR COMPLEXES
MIXED-VALENT COMPLEXES
NITRILE HYDROLYSIS
title_short Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
title_full Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
title_fullStr Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
title_full_unstemmed Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
title_sort Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex
dc.creator.none.fl_str_mv Fagalde, Florencia
Mellace, María G.
Lis, Noemi Dora
Katz, Néstor Eduardo
author Fagalde, Florencia
author_facet Fagalde, Florencia
Mellace, María G.
Lis, Noemi Dora
Katz, Néstor Eduardo
author_role author
author2 Mellace, María G.
Lis, Noemi Dora
Katz, Néstor Eduardo
author2_role author
author
author
dc.subject.none.fl_str_mv 4-CYANOPYRIDINE
CATALYSIS
DINUCLEAR COMPLEXES
MIXED-VALENT COMPLEXES
NITRILE HYDROLYSIS
topic 4-CYANOPYRIDINE
CATALYSIS
DINUCLEAR COMPLEXES
MIXED-VALENT COMPLEXES
NITRILE HYDROLYSIS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Kinetic data for the hydrolysis reaction: [(CO)3(bpy)Re I(4-CNpy)RuIII(NH3)5]4+ + H2O → [(CO)3(bpy)ReI(4-C(O)NHpy)Ru III(NH3)5]3+ + H+ (bpy = 2,2′-bipyridine, 4-CNpy = 4-cyanopyridine and 4-C(O)NHpy = isonicotinamido), that occurs after oxidation with S2O 82- of the dinuclear species [(CO)3(bpy)Re I(4-CNpy)RuII (NH3)5]3+, have been obtained in aqueous solutions by spectrophotometric techniques. The observed rate constant, kh = (8.6 ± 0.5) × 10 -3 s-1, at 25°C, pH = 3.0 (CF3COOH) and I = 0.1 M (KCl), is ca. three times higher than the corresponding one for the mononuclear complex [(4-CNpy)RuIII(NH3)5] 3+, indicating that the catalytic effect of the Ru III(NH3)5 moiety is enhanced by coordination of the free N of 4-CNpy to the ReI(CO)3(bpy) moiety. The value of kh is even higher than that of the dinuclear complex [(trpy)(bpy)RuII (4-CNpy)RuIII(NH3) 5]5+ (trpy = 2,2′:6′,2″-terpyridine), reflecting the fact that carbonyls are much stronger π-acceptors than polypyridines.
Fil: Fagalde, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Inorgánica; Argentina
Fil: Mellace, María G.. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Fil: Lis, Noemi Dora. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Fil: Katz, Néstor Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
description Kinetic data for the hydrolysis reaction: [(CO)3(bpy)Re I(4-CNpy)RuIII(NH3)5]4+ + H2O → [(CO)3(bpy)ReI(4-C(O)NHpy)Ru III(NH3)5]3+ + H+ (bpy = 2,2′-bipyridine, 4-CNpy = 4-cyanopyridine and 4-C(O)NHpy = isonicotinamido), that occurs after oxidation with S2O 82- of the dinuclear species [(CO)3(bpy)Re I(4-CNpy)RuII (NH3)5]3+, have been obtained in aqueous solutions by spectrophotometric techniques. The observed rate constant, kh = (8.6 ± 0.5) × 10 -3 s-1, at 25°C, pH = 3.0 (CF3COOH) and I = 0.1 M (KCl), is ca. three times higher than the corresponding one for the mononuclear complex [(4-CNpy)RuIII(NH3)5] 3+, indicating that the catalytic effect of the Ru III(NH3)5 moiety is enhanced by coordination of the free N of 4-CNpy to the ReI(CO)3(bpy) moiety. The value of kh is even higher than that of the dinuclear complex [(trpy)(bpy)RuII (4-CNpy)RuIII(NH3) 5]5+ (trpy = 2,2′:6′,2″-terpyridine), reflecting the fact that carbonyls are much stronger π-acceptors than polypyridines.
publishDate 2004
dc.date.none.fl_str_mv 2004-05
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/11336/100223
Fagalde, Florencia; Mellace, María G.; Lis, Noemi Dora; Katz, Néstor Eduardo; Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex; Taylor & Francis Ltd; Journal of Coordination Chemistry; 57; 8; 5-2004; 635-639
0095-8972
CONICET Digital
CONICET
url http://hdl.handle.net/11336/100223
identifier_str_mv Fagalde, Florencia; Mellace, María G.; Lis, Noemi Dora; Katz, Néstor Eduardo; Nitrile hydrolysis in a rhenium(I)-ruthenium(III) dinuclear complex; Taylor & Francis Ltd; Journal of Coordination Chemistry; 57; 8; 5-2004; 635-639
0095-8972
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1080/00958970410001689111
info:eu-repo/semantics/altIdentifier/url/https://www.tandfonline.com/doi/abs/10.1080/00958970410001689111
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
dc.publisher.none.fl_str_mv Taylor & Francis Ltd
publisher.none.fl_str_mv Taylor & Francis Ltd
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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