Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
- Autores
- Mangione, Maria Ines; Spanevello, Rolando Angel
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.
Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina - Materia
-
Fluorenone
Carbazole
Ullmann Coupling
Dendrimers
Oled - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/6009
Ver los metadatos del registro completo
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Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reactionMangione, Maria InesSpanevello, Rolando AngelFluorenoneCarbazoleUllmann CouplingDendrimersOledhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaElsevier2014-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/6009Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-4670040-4039enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403914020474info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.11.133info:eu-repo/semantics/altIdentifier/doi/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:34:31Zoai:ri.conicet.gov.ar:11336/6009instacron: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 09:34:31.953CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
title |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
spellingShingle |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction Mangione, Maria Ines Fluorenone Carbazole Ullmann Coupling Dendrimers Oled |
title_short |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
title_full |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
title_fullStr |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
title_full_unstemmed |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
title_sort |
Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction |
dc.creator.none.fl_str_mv |
Mangione, Maria Ines Spanevello, Rolando Angel |
author |
Mangione, Maria Ines |
author_facet |
Mangione, Maria Ines Spanevello, Rolando Angel |
author_role |
author |
author2 |
Spanevello, Rolando Angel |
author2_role |
author |
dc.subject.none.fl_str_mv |
Fluorenone Carbazole Ullmann Coupling Dendrimers Oled |
topic |
Fluorenone Carbazole Ullmann Coupling Dendrimers Oled |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers. Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina Fil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina |
description |
Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-12 |
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/11336/6009 Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-467 0040-4039 |
url |
http://hdl.handle.net/11336/6009 |
identifier_str_mv |
Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-467 0040-4039 |
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/S0040403914020474 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.11.133 info:eu-repo/semantics/altIdentifier/doi/ |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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_ |
1844613067930861568 |
score |
13.070432 |