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4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties

Palladium catalyzed Suzuki-Miyaura cross-coupling of 6,8-dibromo-4-chloroquinoline-3-carbaldehyde with arylboronic and arylvinylboronic acid derivatives in the presence of potassium carbonate in aqueous dioxane afforded the corresponding 4,6,8-triarylquinoline-3-carbaldehydes, exclusively. These pro...

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Autores principales: Mphahlele, Malose Jack, Adeloye, Adewale Olufunsho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269739/
https://www.ncbi.nlm.nih.gov/pubmed/24352028
http://dx.doi.org/10.3390/molecules181215769
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author Mphahlele, Malose Jack
Adeloye, Adewale Olufunsho
author_facet Mphahlele, Malose Jack
Adeloye, Adewale Olufunsho
author_sort Mphahlele, Malose Jack
collection PubMed
description Palladium catalyzed Suzuki-Miyaura cross-coupling of 6,8-dibromo-4-chloroquinoline-3-carbaldehyde with arylboronic and arylvinylboronic acid derivatives in the presence of potassium carbonate in aqueous dioxane afforded the corresponding 4,6,8-triarylquinoline-3-carbaldehydes, exclusively. These products were transformed into 4,6,8-triaryl-3-(4-fluorophenyl)amino)-N-(quinolin-3-yl)methylenes and their 4,6,8-triaryl-quinoline-3-methanol derivatives. The absorption and emission spectra were measured for the 4,6,8-triarylquinoline-3-carbaldehydes and their derivatives in selected solvents of different polarity.
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spelling pubmed-62697392018-12-20 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties Mphahlele, Malose Jack Adeloye, Adewale Olufunsho Molecules Article Palladium catalyzed Suzuki-Miyaura cross-coupling of 6,8-dibromo-4-chloroquinoline-3-carbaldehyde with arylboronic and arylvinylboronic acid derivatives in the presence of potassium carbonate in aqueous dioxane afforded the corresponding 4,6,8-triarylquinoline-3-carbaldehydes, exclusively. These products were transformed into 4,6,8-triaryl-3-(4-fluorophenyl)amino)-N-(quinolin-3-yl)methylenes and their 4,6,8-triaryl-quinoline-3-methanol derivatives. The absorption and emission spectra were measured for the 4,6,8-triarylquinoline-3-carbaldehydes and their derivatives in selected solvents of different polarity. MDPI 2013-12-17 /pmc/articles/PMC6269739/ /pubmed/24352028 http://dx.doi.org/10.3390/molecules181215769 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Mphahlele, Malose Jack
Adeloye, Adewale Olufunsho
4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title_full 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title_fullStr 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title_full_unstemmed 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title_short 4,6,8-Triarylquinoline-3-carbaldehyde Derivatives: Synthesis and Photophysical Properties
title_sort 4,6,8-triarylquinoline-3-carbaldehyde derivatives: synthesis and photophysical properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269739/
https://www.ncbi.nlm.nih.gov/pubmed/24352028
http://dx.doi.org/10.3390/molecules181215769
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