New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds

Autores
Barata Vallejo, Sebastian; Postigo, Jose Alberto
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Visible-light-photocatalyzed methods employed insynthetic transformations present attractive properties such asenvironmentally friendly, safety, availability and excellent functionalgroup tolerance. In this venue, research on the visible-lightphotocatalytic incorporation of the trifluoromethyl CF3 moiety intoorganic substrates, in particular, has contributed to a clear evolutionof the very field of photocatalysis. Outer-sphere electron transfersbetween photocatalysts and trifluoromethyl sources supply CF3radicals efficiently in clean and controlled ways, capable of effectingnumerous synthetic transformations and functionalization on organicsubstrates and compounds with pharmacological activity instraightforward manners. Although this particular area is constantlyevolving and reviewed, the last five years have experienced anoutburst of seminal and significant photocatalytic trifluoromethylationexamples that are leading the way and opening new syntheticavenues. Recent review articles on Ru- and Ir- based photocatalytictrifluoromethylation reactions have borne witness of this evolution.Although this account will show the new Ru- and Ir-basedphotocatalytic trifluoromethylations, Sections 2 and 3 will alsoillustrate other photocatalytic systems, such as organic dyes, organicsemiconductors and newly-developed all-organic photocatalysts. All the known and reviewed strategies for photocatalytictrifluoromethylation reactions of olefins and (hetero)aromaticcompounds will not be discussed but will be summarized in twoFigures (Figures 4 and 5), and new examples (2015-present) will bepresented and discussed.
Fil: Barata Vallejo, Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
Fil: Postigo, Jose Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
Materia
TRIFLUOROMETHYLATION
PHOTOCATALYSIS
ALL-ORGANIC SEMICONDUCTORS
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:11336/109053
Acceder
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spelling New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic CompoundsBarata Vallejo, SebastianPostigo, Jose AlbertoTRIFLUOROMETHYLATIONPHOTOCATALYSISALL-ORGANIC SEMICONDUCTORShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Visible-light-photocatalyzed methods employed insynthetic transformations present attractive properties such asenvironmentally friendly, safety, availability and excellent functionalgroup tolerance. In this venue, research on the visible-lightphotocatalytic incorporation of the trifluoromethyl CF3 moiety intoorganic substrates, in particular, has contributed to a clear evolutionof the very field of photocatalysis. Outer-sphere electron transfersbetween photocatalysts and trifluoromethyl sources supply CF3radicals efficiently in clean and controlled ways, capable of effectingnumerous synthetic transformations and functionalization on organicsubstrates and compounds with pharmacological activity instraightforward manners. Although this particular area is constantlyevolving and reviewed, the last five years have experienced anoutburst of seminal and significant photocatalytic trifluoromethylationexamples that are leading the way and opening new syntheticavenues. Recent review articles on Ru- and Ir- based photocatalytictrifluoromethylation reactions have borne witness of this evolution.Although this account will show the new Ru- and Ir-basedphotocatalytic trifluoromethylations, Sections 2 and 3 will alsoillustrate other photocatalytic systems, such as organic dyes, organicsemiconductors and newly-developed all-organic photocatalysts. All the known and reviewed strategies for photocatalytictrifluoromethylation reactions of olefins and (hetero)aromaticcompounds will not be discussed but will be summarized in twoFigures (Figures 4 and 5), and new examples (2015-present) will bepresented and discussed.Fil: Barata Vallejo, Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; ArgentinaFil: Postigo, Jose Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; ArgentinaWiley VCH Verlag2020-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/109053Barata Vallejo, Sebastian; Postigo, Jose Alberto; New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds; Wiley VCH Verlag; Chemistry- A European Journal; 26; 24; 4-2020; 1-100947-6539CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202000856info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202000856info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:46:25Zoai:ri.conicet.gov.ar:11336/109053instacron: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 09:46:26.155CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
title New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
spellingShingle New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
Barata Vallejo, Sebastian
TRIFLUOROMETHYLATION
PHOTOCATALYSIS
ALL-ORGANIC SEMICONDUCTORS
title_short New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
title_full New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
title_fullStr New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
title_full_unstemmed New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
title_sort New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds
dc.creator.none.fl_str_mv Barata Vallejo, Sebastian
Postigo, Jose Alberto
author Barata Vallejo, Sebastian
author_facet Barata Vallejo, Sebastian
Postigo, Jose Alberto
author_role author
author2 Postigo, Jose Alberto
author2_role author
dc.subject.none.fl_str_mv TRIFLUOROMETHYLATION
PHOTOCATALYSIS
ALL-ORGANIC SEMICONDUCTORS
topic TRIFLUOROMETHYLATION
PHOTOCATALYSIS
ALL-ORGANIC SEMICONDUCTORS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Visible-light-photocatalyzed methods employed insynthetic transformations present attractive properties such asenvironmentally friendly, safety, availability and excellent functionalgroup tolerance. In this venue, research on the visible-lightphotocatalytic incorporation of the trifluoromethyl CF3 moiety intoorganic substrates, in particular, has contributed to a clear evolutionof the very field of photocatalysis. Outer-sphere electron transfersbetween photocatalysts and trifluoromethyl sources supply CF3radicals efficiently in clean and controlled ways, capable of effectingnumerous synthetic transformations and functionalization on organicsubstrates and compounds with pharmacological activity instraightforward manners. Although this particular area is constantlyevolving and reviewed, the last five years have experienced anoutburst of seminal and significant photocatalytic trifluoromethylationexamples that are leading the way and opening new syntheticavenues. Recent review articles on Ru- and Ir- based photocatalytictrifluoromethylation reactions have borne witness of this evolution.Although this account will show the new Ru- and Ir-basedphotocatalytic trifluoromethylations, Sections 2 and 3 will alsoillustrate other photocatalytic systems, such as organic dyes, organicsemiconductors and newly-developed all-organic photocatalysts. All the known and reviewed strategies for photocatalytictrifluoromethylation reactions of olefins and (hetero)aromaticcompounds will not be discussed but will be summarized in twoFigures (Figures 4 and 5), and new examples (2015-present) will bepresented and discussed.
Fil: Barata Vallejo, Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
Fil: Postigo, Jose Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
description Visible-light-photocatalyzed methods employed insynthetic transformations present attractive properties such asenvironmentally friendly, safety, availability and excellent functionalgroup tolerance. In this venue, research on the visible-lightphotocatalytic incorporation of the trifluoromethyl CF3 moiety intoorganic substrates, in particular, has contributed to a clear evolutionof the very field of photocatalysis. Outer-sphere electron transfersbetween photocatalysts and trifluoromethyl sources supply CF3radicals efficiently in clean and controlled ways, capable of effectingnumerous synthetic transformations and functionalization on organicsubstrates and compounds with pharmacological activity instraightforward manners. Although this particular area is constantlyevolving and reviewed, the last five years have experienced anoutburst of seminal and significant photocatalytic trifluoromethylationexamples that are leading the way and opening new syntheticavenues. Recent review articles on Ru- and Ir- based photocatalytictrifluoromethylation reactions have borne witness of this evolution.Although this account will show the new Ru- and Ir-basedphotocatalytic trifluoromethylations, Sections 2 and 3 will alsoillustrate other photocatalytic systems, such as organic dyes, organicsemiconductors and newly-developed all-organic photocatalysts. All the known and reviewed strategies for photocatalytictrifluoromethylation reactions of olefins and (hetero)aromaticcompounds will not be discussed but will be summarized in twoFigures (Figures 4 and 5), and new examples (2015-present) will bepresented and discussed.
publishDate 2020
dc.date.none.fl_str_mv 2020-04
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/11336/109053
Barata Vallejo, Sebastian; Postigo, Jose Alberto; New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds; Wiley VCH Verlag; Chemistry- A European Journal; 26; 24; 4-2020; 1-10
0947-6539
CONICET Digital
CONICET
url http://hdl.handle.net/11336/109053
identifier_str_mv Barata Vallejo, Sebastian; Postigo, Jose Alberto; New Visible Light-triggered Photocatalytic Trifluoromethylation Reactions of Carbon‐carbon Multiple Bonds and (Hetero)aromatic Compounds; Wiley VCH Verlag; Chemistry- A European Journal; 26; 24; 4-2020; 1-10
0947-6539
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://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202000856
info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202000856
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 Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
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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