Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s
- Autores
- Froimowicz, Pablo; Belgacem, Naceur; Gandini, Alessandro; Strumia, Miriam Cristina
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A general procedure to increase the amount of photoreactive chromophore groups per oligoether chain is presented. In this work, a photoreactive macromonomer with four functionalities was synthesized by a four-step synthetic pathway with high yield. The photochemical behavior of this compound was studied with a view to obtaining polymeric networks. The significant advantage in this strategy is that the preparation of this material has as last operation, the obtaining and processing of polymer as thin film. In this way, the synthetic strategy based on assembling: (i) the polyether chains, (ii) a film forming backbone, and (iii) a photoactive moiety to be used for cross-linking, seems a viable solution to the problem of the continuous processing of materials.
Fil: Froimowicz, Pablo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnología En Polimeros y Nanotecnología. Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnología En Polimeros y Nanotecnología; Argentina
Fil: Belgacem, Naceur. Grenoble Institute Of Technology; Francia
Fil: Gandini, Alessandro. Grenoble Institute Of Technology; Francia
Fil: Strumia, Miriam Cristina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina - Materia
-
Jeffamines
Dendritic
Furan
Photochemistry
Dimerization
Cycloaddition - 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:11336/29544
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/29544 |
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Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)sFroimowicz, PabloBelgacem, NaceurGandini, AlessandroStrumia, Miriam CristinaJeffaminesDendriticFuranPhotochemistryDimerizationCycloadditionhttps://purl.org/becyt/ford/2.5https://purl.org/becyt/ford/2https://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A general procedure to increase the amount of photoreactive chromophore groups per oligoether chain is presented. In this work, a photoreactive macromonomer with four functionalities was synthesized by a four-step synthetic pathway with high yield. The photochemical behavior of this compound was studied with a view to obtaining polymeric networks. The significant advantage in this strategy is that the preparation of this material has as last operation, the obtaining and processing of polymer as thin film. In this way, the synthetic strategy based on assembling: (i) the polyether chains, (ii) a film forming backbone, and (iii) a photoactive moiety to be used for cross-linking, seems a viable solution to the problem of the continuous processing of materials.Fil: Froimowicz, Pablo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnología En Polimeros y Nanotecnología. Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnología En Polimeros y Nanotecnología; ArgentinaFil: Belgacem, Naceur. Grenoble Institute Of Technology; FranciaFil: Gandini, Alessandro. Grenoble Institute Of Technology; FranciaFil: Strumia, Miriam Cristina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaPergamon-Elsevier Science Ltd.2008-12info: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/11336/29544Froimowicz, Pablo; Belgacem, Naceur; Gandini, Alessandro; Strumia, Miriam Cristina; Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s; Pergamon-Elsevier Science Ltd.; European Polymer Journal; 44; 12; 12-2008; 4092-40970014-3057CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0014305708004734info:eu-repo/semantics/altIdentifier/doi/10.1016/j.eurpolymj.2008.09.012info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:05:05Zoai:ri.conicet.gov.ar:11336/29544instacron: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 13:05:06.198CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
title |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
spellingShingle |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s Froimowicz, Pablo Jeffamines Dendritic Furan Photochemistry Dimerization Cycloaddition |
title_short |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
title_full |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
title_fullStr |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
title_full_unstemmed |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
title_sort |
Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s |
dc.creator.none.fl_str_mv |
Froimowicz, Pablo Belgacem, Naceur Gandini, Alessandro Strumia, Miriam Cristina |
author |
Froimowicz, Pablo |
author_facet |
Froimowicz, Pablo Belgacem, Naceur Gandini, Alessandro Strumia, Miriam Cristina |
author_role |
author |
author2 |
Belgacem, Naceur Gandini, Alessandro Strumia, Miriam Cristina |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Jeffamines Dendritic Furan Photochemistry Dimerization Cycloaddition |
topic |
Jeffamines Dendritic Furan Photochemistry Dimerization Cycloaddition |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.5 https://purl.org/becyt/ford/2 https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
A general procedure to increase the amount of photoreactive chromophore groups per oligoether chain is presented. In this work, a photoreactive macromonomer with four functionalities was synthesized by a four-step synthetic pathway with high yield. The photochemical behavior of this compound was studied with a view to obtaining polymeric networks. The significant advantage in this strategy is that the preparation of this material has as last operation, the obtaining and processing of polymer as thin film. In this way, the synthetic strategy based on assembling: (i) the polyether chains, (ii) a film forming backbone, and (iii) a photoactive moiety to be used for cross-linking, seems a viable solution to the problem of the continuous processing of materials. Fil: Froimowicz, Pablo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnología En Polimeros y Nanotecnología. Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnología En Polimeros y Nanotecnología; Argentina Fil: Belgacem, Naceur. Grenoble Institute Of Technology; Francia Fil: Gandini, Alessandro. Grenoble Institute Of Technology; Francia Fil: Strumia, Miriam Cristina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina |
description |
A general procedure to increase the amount of photoreactive chromophore groups per oligoether chain is presented. In this work, a photoreactive macromonomer with four functionalities was synthesized by a four-step synthetic pathway with high yield. The photochemical behavior of this compound was studied with a view to obtaining polymeric networks. The significant advantage in this strategy is that the preparation of this material has as last operation, the obtaining and processing of polymer as thin film. In this way, the synthetic strategy based on assembling: (i) the polyether chains, (ii) a film forming backbone, and (iii) a photoactive moiety to be used for cross-linking, seems a viable solution to the problem of the continuous processing of materials. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-12 |
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/11336/29544 Froimowicz, Pablo; Belgacem, Naceur; Gandini, Alessandro; Strumia, Miriam Cristina; Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s; Pergamon-Elsevier Science Ltd.; European Polymer Journal; 44; 12; 12-2008; 4092-4097 0014-3057 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/29544 |
identifier_str_mv |
Froimowicz, Pablo; Belgacem, Naceur; Gandini, Alessandro; Strumia, Miriam Cristina; Design, synthesis and photo-cross-linking of a new photosensitive macromonomer from tetra-branched poly(ethylene oxide)s; Pergamon-Elsevier Science Ltd.; European Polymer Journal; 44; 12; 12-2008; 4092-4097 0014-3057 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0014305708004734 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.eurpolymj.2008.09.012 |
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 |
Pergamon-Elsevier Science Ltd. |
publisher.none.fl_str_mv |
Pergamon-Elsevier Science 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 |
_version_ |
1842980178057232384 |
score |
12.993085 |