Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)

Autores
Ruiz, Gustavo Teodosio; Lappin, Alexander G.; Ferraudi, Guillermo
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The tetrasulfonated CuII(tspc)4-, tspc = 4,4´,4",4"´-phthalocyaninetetrasulfonate,  and the trisulfonated CoII(trspc)3-, trspc = n,n´,n"-phthalocyanine- trisulfonate and n, n’ and n” indicate the sulfonated positions of the various isomers, were covalently linked to a polyethyleneimine, Mn ~ 10000 and Mw ~ 25000, backbone. A fraction of the amine groups in a strand was converted to CuIIpc(-SO3)3(-SO2N<)– or CoIIpc(-SO3)2(-SO2N<)- pendants and the remaining were acetylated. Strands of the polymers, poly(K3CuIItspc) and poly(K2CoIItrspc), formed spherical bundles with diameters ~ 1000 nm for poly(K3CuIItspc) and ~ 100 nm for poly(K2CoIItrspc). The stability of the bundles is metal dependent. Poly(K2CoIItrspc) forms the most stable bundles with respect to hydrolytic and redox reactions. ESR and optical spectroscopies as well as reactions of the pendants with pulse radiolytically generated radicals, namely e-sol, C•H2OH, (CH3)2COHC•H2, CO2•-, N3• and SO4•-, revealed a distribution of pendants between isolated and aggregated forms in a bundle. The reduction of the Cu(II) to Cu(I) in aqueous solutions of the poly(K3CuIItspc) was associated with pendants present in a mostly hydrophobic environment. Unstable phthalocyanine pendants with CoIII-Carbon bonds are formed when CoIIpc(-SO3)2(-SO2N<)- reacted with C-centered radicals, (CH3)2COHC•H2 and C•H2OH. The species with CoIII-Carbon bonds were precursors in the formation of CoIpc(-SO3)2(-SO2N<)-  pendants. The redox reactions of the pendants in these polymers are compared with those of the K4CuIItspc and K3CoIItrspc.
Fil: Ruiz, Gustavo Teodosio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. University of Notre Dame; Estados Unidos
Fil: Lappin, Alexander G.. University of Notre Dame; Estados Unidos
Fil: Ferraudi, Guillermo. University of Notre Dame; Estados Unidos
Materia
Phthalocyanine-derivatized poly(ethylenimine)
Phthalocyanine radicals
Pulse radiolysis
Reaction intermediates
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:11336/275412

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network_name_str CONICET Digital (CONICET)
spelling Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)Ruiz, Gustavo TeodosioLappin, Alexander G.Ferraudi, GuillermoPhthalocyanine-derivatized poly(ethylenimine)Phthalocyanine radicalsPulse radiolysisReaction intermediateshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The tetrasulfonated CuII(tspc)4-, tspc = 4,4´,4",4"´-phthalocyaninetetrasulfonate,  and the trisulfonated CoII(trspc)3-, trspc = n,n´,n"-phthalocyanine- trisulfonate and n, n’ and n” indicate the sulfonated positions of the various isomers, were covalently linked to a polyethyleneimine, Mn ~ 10000 and Mw ~ 25000, backbone. A fraction of the amine groups in a strand was converted to CuIIpc(-SO3)3(-SO2N<)– or CoIIpc(-SO3)2(-SO2N<)- pendants and the remaining were acetylated. Strands of the polymers, poly(K3CuIItspc) and poly(K2CoIItrspc), formed spherical bundles with diameters ~ 1000 nm for poly(K3CuIItspc) and ~ 100 nm for poly(K2CoIItrspc). The stability of the bundles is metal dependent. Poly(K2CoIItrspc) forms the most stable bundles with respect to hydrolytic and redox reactions. ESR and optical spectroscopies as well as reactions of the pendants with pulse radiolytically generated radicals, namely e-sol, C•H2OH, (CH3)2COHC•H2, CO2•-, N3• and SO4•-, revealed a distribution of pendants between isolated and aggregated forms in a bundle. The reduction of the Cu(II) to Cu(I) in aqueous solutions of the poly(K3CuIItspc) was associated with pendants present in a mostly hydrophobic environment. Unstable phthalocyanine pendants with CoIII-Carbon bonds are formed when CoIIpc(-SO3)2(-SO2N<)- reacted with C-centered radicals, (CH3)2COHC•H2 and C•H2OH. The species with CoIII-Carbon bonds were precursors in the formation of CoIpc(-SO3)2(-SO2N<)-  pendants. The redox reactions of the pendants in these polymers are compared with those of the K4CuIItspc and K3CoIItrspc.Fil: Ruiz, Gustavo Teodosio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. University of Notre Dame; Estados UnidosFil: Lappin, Alexander G.. University of Notre Dame; Estados UnidosFil: Ferraudi, Guillermo. University of Notre Dame; Estados UnidosWorld Sci Publ Co Inc2010-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/275412Ruiz, Gustavo Teodosio; Lappin, Alexander G.; Ferraudi, Guillermo; Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide); World Sci Publ Co Inc; Journal Of Porphyrins And Phthalocyanines; 14; 1; 1-2010; 69-801088-4246CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.worldscientific.com/doi/abs/10.1142/S1088424610001751info:eu-repo/semantics/altIdentifier/doi/10.1142/S1088424610001751info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-12-03T09:26:26Zoai:ri.conicet.gov.ar:11336/275412instacron: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:34982025-12-03 09:26:26.464CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
title Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
spellingShingle Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
Ruiz, Gustavo Teodosio
Phthalocyanine-derivatized poly(ethylenimine)
Phthalocyanine radicals
Pulse radiolysis
Reaction intermediates
title_short Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
title_full Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
title_fullStr Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
title_full_unstemmed Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
title_sort Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide)
dc.creator.none.fl_str_mv Ruiz, Gustavo Teodosio
Lappin, Alexander G.
Ferraudi, Guillermo
author Ruiz, Gustavo Teodosio
author_facet Ruiz, Gustavo Teodosio
Lappin, Alexander G.
Ferraudi, Guillermo
author_role author
author2 Lappin, Alexander G.
Ferraudi, Guillermo
author2_role author
author
dc.subject.none.fl_str_mv Phthalocyanine-derivatized poly(ethylenimine)
Phthalocyanine radicals
Pulse radiolysis
Reaction intermediates
topic Phthalocyanine-derivatized poly(ethylenimine)
Phthalocyanine radicals
Pulse radiolysis
Reaction intermediates
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 tetrasulfonated CuII(tspc)4-, tspc = 4,4´,4",4"´-phthalocyaninetetrasulfonate,  and the trisulfonated CoII(trspc)3-, trspc = n,n´,n"-phthalocyanine- trisulfonate and n, n’ and n” indicate the sulfonated positions of the various isomers, were covalently linked to a polyethyleneimine, Mn ~ 10000 and Mw ~ 25000, backbone. A fraction of the amine groups in a strand was converted to CuIIpc(-SO3)3(-SO2N<)– or CoIIpc(-SO3)2(-SO2N<)- pendants and the remaining were acetylated. Strands of the polymers, poly(K3CuIItspc) and poly(K2CoIItrspc), formed spherical bundles with diameters ~ 1000 nm for poly(K3CuIItspc) and ~ 100 nm for poly(K2CoIItrspc). The stability of the bundles is metal dependent. Poly(K2CoIItrspc) forms the most stable bundles with respect to hydrolytic and redox reactions. ESR and optical spectroscopies as well as reactions of the pendants with pulse radiolytically generated radicals, namely e-sol, C•H2OH, (CH3)2COHC•H2, CO2•-, N3• and SO4•-, revealed a distribution of pendants between isolated and aggregated forms in a bundle. The reduction of the Cu(II) to Cu(I) in aqueous solutions of the poly(K3CuIItspc) was associated with pendants present in a mostly hydrophobic environment. Unstable phthalocyanine pendants with CoIII-Carbon bonds are formed when CoIIpc(-SO3)2(-SO2N<)- reacted with C-centered radicals, (CH3)2COHC•H2 and C•H2OH. The species with CoIII-Carbon bonds were precursors in the formation of CoIpc(-SO3)2(-SO2N<)-  pendants. The redox reactions of the pendants in these polymers are compared with those of the K4CuIItspc and K3CoIItrspc.
Fil: Ruiz, Gustavo Teodosio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. University of Notre Dame; Estados Unidos
Fil: Lappin, Alexander G.. University of Notre Dame; Estados Unidos
Fil: Ferraudi, Guillermo. University of Notre Dame; Estados Unidos
description The tetrasulfonated CuII(tspc)4-, tspc = 4,4´,4",4"´-phthalocyaninetetrasulfonate,  and the trisulfonated CoII(trspc)3-, trspc = n,n´,n"-phthalocyanine- trisulfonate and n, n’ and n” indicate the sulfonated positions of the various isomers, were covalently linked to a polyethyleneimine, Mn ~ 10000 and Mw ~ 25000, backbone. A fraction of the amine groups in a strand was converted to CuIIpc(-SO3)3(-SO2N<)– or CoIIpc(-SO3)2(-SO2N<)- pendants and the remaining were acetylated. Strands of the polymers, poly(K3CuIItspc) and poly(K2CoIItrspc), formed spherical bundles with diameters ~ 1000 nm for poly(K3CuIItspc) and ~ 100 nm for poly(K2CoIItrspc). The stability of the bundles is metal dependent. Poly(K2CoIItrspc) forms the most stable bundles with respect to hydrolytic and redox reactions. ESR and optical spectroscopies as well as reactions of the pendants with pulse radiolytically generated radicals, namely e-sol, C•H2OH, (CH3)2COHC•H2, CO2•-, N3• and SO4•-, revealed a distribution of pendants between isolated and aggregated forms in a bundle. The reduction of the Cu(II) to Cu(I) in aqueous solutions of the poly(K3CuIItspc) was associated with pendants present in a mostly hydrophobic environment. Unstable phthalocyanine pendants with CoIII-Carbon bonds are formed when CoIIpc(-SO3)2(-SO2N<)- reacted with C-centered radicals, (CH3)2COHC•H2 and C•H2OH. The species with CoIII-Carbon bonds were precursors in the formation of CoIpc(-SO3)2(-SO2N<)-  pendants. The redox reactions of the pendants in these polymers are compared with those of the K4CuIItspc and K3CoIItrspc.
publishDate 2010
dc.date.none.fl_str_mv 2010-01
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/11336/275412
Ruiz, Gustavo Teodosio; Lappin, Alexander G.; Ferraudi, Guillermo; Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide); World Sci Publ Co Inc; Journal Of Porphyrins And Phthalocyanines; 14; 1; 1-2010; 69-80
1088-4246
CONICET Digital
CONICET
url http://hdl.handle.net/11336/275412
identifier_str_mv Ruiz, Gustavo Teodosio; Lappin, Alexander G.; Ferraudi, Guillermo; Morphology and radical reactions of Cu(II) and Co(II) sulfonated phthalocyanines covalently linked to poly(ethyleneamide); World Sci Publ Co Inc; Journal Of Porphyrins And Phthalocyanines; 14; 1; 1-2010; 69-80
1088-4246
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.worldscientific.com/doi/abs/10.1142/S1088424610001751
info:eu-repo/semantics/altIdentifier/doi/10.1142/S1088424610001751
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
dc.publisher.none.fl_str_mv World Sci Publ Co Inc
publisher.none.fl_str_mv World Sci Publ Co Inc
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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