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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/275412
Ver los metadatos del registro completo
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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 |
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article |
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publishedVersion |
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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 |
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eng |
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eng |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf |
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World Sci Publ Co Inc |
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World Sci Publ Co Inc |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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