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Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation

Direct C-H arylation coupling is potentially a more economical and sustainable process than conventional cross-coupling. However, this method has found limited application in the synthesis of organic dyes for dye-sensitized solar cells. Although direct C-H arylation is not an universal solution to a...

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Autores principales: Yemene, Amsalu Efrem, Venkatraman, Vishwesh, Moe Almenningen, David, Hoff, Bård Helge, Gautun, Odd Reidar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288183/
https://www.ncbi.nlm.nih.gov/pubmed/32443478
http://dx.doi.org/10.3390/molecules25102349
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author Yemene, Amsalu Efrem
Venkatraman, Vishwesh
Moe Almenningen, David
Hoff, Bård Helge
Gautun, Odd Reidar
author_facet Yemene, Amsalu Efrem
Venkatraman, Vishwesh
Moe Almenningen, David
Hoff, Bård Helge
Gautun, Odd Reidar
author_sort Yemene, Amsalu Efrem
collection PubMed
description Direct C-H arylation coupling is potentially a more economical and sustainable process than conventional cross-coupling. However, this method has found limited application in the synthesis of organic dyes for dye-sensitized solar cells. Although direct C-H arylation is not an universal solution to any cross-coupling reactions, it efficiently complements conventional sp(2)−sp(2) bond formation and can provide shorter and more efficient routes to diketopyrrolopyrrole dyes. Here, we have applied palladium catalyzed direct C-H arylation in the synthesis of five new 3,6-dithienyl diketopyrrolopyrrole dyes. All prepared sensitizers display broad absorption from 350 nm up to 800 nm with high molar extinction coefficients. The dye-sensitized solar cells based on these dyes exhibit a power conversion efficiency in the range of 2.9 to 3.4%.
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spelling pubmed-72881832020-06-17 Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation Yemene, Amsalu Efrem Venkatraman, Vishwesh Moe Almenningen, David Hoff, Bård Helge Gautun, Odd Reidar Molecules Article Direct C-H arylation coupling is potentially a more economical and sustainable process than conventional cross-coupling. However, this method has found limited application in the synthesis of organic dyes for dye-sensitized solar cells. Although direct C-H arylation is not an universal solution to any cross-coupling reactions, it efficiently complements conventional sp(2)−sp(2) bond formation and can provide shorter and more efficient routes to diketopyrrolopyrrole dyes. Here, we have applied palladium catalyzed direct C-H arylation in the synthesis of five new 3,6-dithienyl diketopyrrolopyrrole dyes. All prepared sensitizers display broad absorption from 350 nm up to 800 nm with high molar extinction coefficients. The dye-sensitized solar cells based on these dyes exhibit a power conversion efficiency in the range of 2.9 to 3.4%. MDPI 2020-05-18 /pmc/articles/PMC7288183/ /pubmed/32443478 http://dx.doi.org/10.3390/molecules25102349 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yemene, Amsalu Efrem
Venkatraman, Vishwesh
Moe Almenningen, David
Hoff, Bård Helge
Gautun, Odd Reidar
Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title_full Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title_fullStr Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title_full_unstemmed Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title_short Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
title_sort synthesis of novel 3,6-dithienyl diketopyrrolopyrrole dyes by direct c-h arylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288183/
https://www.ncbi.nlm.nih.gov/pubmed/32443478
http://dx.doi.org/10.3390/molecules25102349
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