Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates

Autores
Gutiérrez, María M.; Alluisetti, Graciela Beatriz; Olabe Iparraguirre, Jose Antonio; Amorebieta, Valentín Tomás
Año de publicación
2009
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The substituted hydroxylamines, CH3N(H)OH (N-methylhydroxylamine) and (CH3)2NOH (N,N-dimethylhydroxylamine), disproportionate catalytically to the corresponding alkylamines and oxidation products, only in the presence of [Fe(CN)5H2O]3−. Substitution kinetic measurements suggest an initial coordination step to Fe(ii). Two parallel N- and O-coordination modes are considered with the subsequent formation of Fe(iii), free aminyl (RNCH3) and nitroxide (RN(CH3)O) radicals (R = H, CH3). With CH3N(H)OH, bound nitrosomethane, CH3NO, has been characterized by UV-visible and IR spectroscopies. The mechanism is discussed on the basis of common and differential features with respect to the disproportionation of hydroxylamine catalyzed by the same Fe-fragment.
Fil: Gutiérrez, María M.. Universidad Nacional de Mar del Plata; Argentina
Fil: Alluisetti, Graciela Beatriz. Universidad Nacional de Mar del Plata; Argentina
Fil: Olabe Iparraguirre, Jose Antonio. 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: Amorebieta, Valentín Tomás. Universidad Nacional de Mar del Plata; Argentina
Materia
Hydroxylamines
Ch3no
Ch3n
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:11336/75573
Acceder
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network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferratesGutiérrez, María M.Alluisetti, Graciela BeatrizOlabe Iparraguirre, Jose AntonioAmorebieta, Valentín TomásHydroxylaminesCh3noCh3nhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The substituted hydroxylamines, CH3N(H)OH (N-methylhydroxylamine) and (CH3)2NOH (N,N-dimethylhydroxylamine), disproportionate catalytically to the corresponding alkylamines and oxidation products, only in the presence of [Fe(CN)5H2O]3−. Substitution kinetic measurements suggest an initial coordination step to Fe(ii). Two parallel N- and O-coordination modes are considered with the subsequent formation of Fe(iii), free aminyl (RNCH3) and nitroxide (RN(CH3)O) radicals (R = H, CH3). With CH3N(H)OH, bound nitrosomethane, CH3NO, has been characterized by UV-visible and IR spectroscopies. The mechanism is discussed on the basis of common and differential features with respect to the disproportionation of hydroxylamine catalyzed by the same Fe-fragment.Fil: Gutiérrez, María M.. Universidad Nacional de Mar del Plata; ArgentinaFil: Alluisetti, Graciela Beatriz. Universidad Nacional de Mar del Plata; ArgentinaFil: Olabe Iparraguirre, Jose Antonio. 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: Amorebieta, Valentín Tomás. Universidad Nacional de Mar del Plata; ArgentinaRoyal Society of Chemistry2009-02info: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/11336/75573Gutiérrez, María M.; Alluisetti, Graciela Beatriz; Olabe Iparraguirre, Jose Antonio; Amorebieta, Valentín Tomás; Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates; Royal Society of Chemistry; Dalton Transactions; 7; 2-2009; 1187-11941477-9226CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2009/DT/b812173g#!divAbstractinfo:eu-repo/semantics/altIdentifier/doi/10.1039/b812173ginfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:34:10Zoai:ri.conicet.gov.ar:11336/75573instacron: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:34982025-09-29 10:34:10.405CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
title Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
spellingShingle Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
Gutiérrez, María M.
Hydroxylamines
Ch3no
Ch3n
title_short Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
title_full Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
title_fullStr Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
title_full_unstemmed Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
title_sort Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates
dc.creator.none.fl_str_mv Gutiérrez, María M.
Alluisetti, Graciela Beatriz
Olabe Iparraguirre, Jose Antonio
Amorebieta, Valentín Tomás
author Gutiérrez, María M.
author_facet Gutiérrez, María M.
Alluisetti, Graciela Beatriz
Olabe Iparraguirre, Jose Antonio
Amorebieta, Valentín Tomás
author_role author
author2 Alluisetti, Graciela Beatriz
Olabe Iparraguirre, Jose Antonio
Amorebieta, Valentín Tomás
author2_role author
author
author
dc.subject.none.fl_str_mv Hydroxylamines
Ch3no
Ch3n
topic Hydroxylamines
Ch3no
Ch3n
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The substituted hydroxylamines, CH3N(H)OH (N-methylhydroxylamine) and (CH3)2NOH (N,N-dimethylhydroxylamine), disproportionate catalytically to the corresponding alkylamines and oxidation products, only in the presence of [Fe(CN)5H2O]3−. Substitution kinetic measurements suggest an initial coordination step to Fe(ii). Two parallel N- and O-coordination modes are considered with the subsequent formation of Fe(iii), free aminyl (RNCH3) and nitroxide (RN(CH3)O) radicals (R = H, CH3). With CH3N(H)OH, bound nitrosomethane, CH3NO, has been characterized by UV-visible and IR spectroscopies. The mechanism is discussed on the basis of common and differential features with respect to the disproportionation of hydroxylamine catalyzed by the same Fe-fragment.
Fil: Gutiérrez, María M.. Universidad Nacional de Mar del Plata; Argentina
Fil: Alluisetti, Graciela Beatriz. Universidad Nacional de Mar del Plata; Argentina
Fil: Olabe Iparraguirre, Jose Antonio. 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: Amorebieta, Valentín Tomás. Universidad Nacional de Mar del Plata; Argentina
description The substituted hydroxylamines, CH3N(H)OH (N-methylhydroxylamine) and (CH3)2NOH (N,N-dimethylhydroxylamine), disproportionate catalytically to the corresponding alkylamines and oxidation products, only in the presence of [Fe(CN)5H2O]3−. Substitution kinetic measurements suggest an initial coordination step to Fe(ii). Two parallel N- and O-coordination modes are considered with the subsequent formation of Fe(iii), free aminyl (RNCH3) and nitroxide (RN(CH3)O) radicals (R = H, CH3). With CH3N(H)OH, bound nitrosomethane, CH3NO, has been characterized by UV-visible and IR spectroscopies. The mechanism is discussed on the basis of common and differential features with respect to the disproportionation of hydroxylamine catalyzed by the same Fe-fragment.
publishDate 2009
dc.date.none.fl_str_mv 2009-02
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/11336/75573
Gutiérrez, María M.; Alluisetti, Graciela Beatriz; Olabe Iparraguirre, Jose Antonio; Amorebieta, Valentín Tomás; Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates; Royal Society of Chemistry; Dalton Transactions; 7; 2-2009; 1187-1194
1477-9226
CONICET Digital
CONICET
url http://hdl.handle.net/11336/75573
identifier_str_mv Gutiérrez, María M.; Alluisetti, Graciela Beatriz; Olabe Iparraguirre, Jose Antonio; Amorebieta, Valentín Tomás; Catalytic disproportionation of N-alkylhydroxylamines bound to pentacyanoferrates; Royal Society of Chemistry; Dalton Transactions; 7; 2-2009; 1187-1194
1477-9226
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://pubs.rsc.org/en/content/articlelanding/2009/DT/b812173g#!divAbstract
info:eu-repo/semantics/altIdentifier/doi/10.1039/b812173g
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 Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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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score 13.070432

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