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Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials

Organic molecules and polymers with extended π-conjugation are appealing as advanced electronic materials, and have already found practical applications in thin-film transistors, light emitting diodes, and chemical sensors. Transition metal (TM)-catalyzed cross-coupling methodologies have evolved ov...

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Autores principales: Xu, Shiqing, Kim, Eun Hoo, Wei, Alexander, Negishi, Ei-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090684/
https://www.ncbi.nlm.nih.gov/pubmed/27877696
http://dx.doi.org/10.1088/1468-6996/15/4/044201
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author Xu, Shiqing
Kim, Eun Hoo
Wei, Alexander
Negishi, Ei-ichi
author_facet Xu, Shiqing
Kim, Eun Hoo
Wei, Alexander
Negishi, Ei-ichi
author_sort Xu, Shiqing
collection PubMed
description Organic molecules and polymers with extended π-conjugation are appealing as advanced electronic materials, and have already found practical applications in thin-film transistors, light emitting diodes, and chemical sensors. Transition metal (TM)-catalyzed cross-coupling methodologies have evolved over the past four decades into one of the most powerful and versatile methods for C–C bond formation, enabling the construction of a diverse and sophisticated range of π-conjugated oligomers and polymers. In this review, we focus our discussion on recent synthetic developments of several important classes of π-conjugated systems using TM-catalyzed cross-coupling reactions, with a perspective on their utility for organic electronic materials.
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spelling pubmed-50906842016-11-22 Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials Xu, Shiqing Kim, Eun Hoo Wei, Alexander Negishi, Ei-ichi Sci Technol Adv Mater Focus Articles Organic molecules and polymers with extended π-conjugation are appealing as advanced electronic materials, and have already found practical applications in thin-film transistors, light emitting diodes, and chemical sensors. Transition metal (TM)-catalyzed cross-coupling methodologies have evolved over the past four decades into one of the most powerful and versatile methods for C–C bond formation, enabling the construction of a diverse and sophisticated range of π-conjugated oligomers and polymers. In this review, we focus our discussion on recent synthetic developments of several important classes of π-conjugated systems using TM-catalyzed cross-coupling reactions, with a perspective on their utility for organic electronic materials. Taylor & Francis 2014-07-07 /pmc/articles/PMC5090684/ /pubmed/27877696 http://dx.doi.org/10.1088/1468-6996/15/4/044201 Text en © 2014 National Institute for Materials Science http://creativecommons.org/licenses/by/3.0/ Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence (http://creativecommons.org/licenses/by/3.0) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.
spellingShingle Focus Articles
Xu, Shiqing
Kim, Eun Hoo
Wei, Alexander
Negishi, Ei-ichi
Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title_full Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title_fullStr Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title_full_unstemmed Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title_short Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
title_sort pd- and ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materials
topic Focus Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090684/
https://www.ncbi.nlm.nih.gov/pubmed/27877696
http://dx.doi.org/10.1088/1468-6996/15/4/044201
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