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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/100223
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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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1842980728553340928 |
score |
12.993085 |