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Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties

In this study, we newly designed and developed a synthesis route based on the 1,3-dipolar cycloaddition of the derivatives of 4′-(1,2,3-triazol-4-yl)phenyl-2,2′:6′,2′′-terpyridine with various (hetero)aryl substituents, differing in electronic character, on a triazol ring. The obtained compounds wer...

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Detalles Bibliográficos
Autores principales: Zych, Dawid, Slodek, Aneta, Zimny, Dżastin, Golba, Sylwia, Malarz, Katarzyna, Mrozek-Wilczkiewicz, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064414/
https://www.ncbi.nlm.nih.gov/pubmed/35516389
http://dx.doi.org/10.1039/c9ra02655j
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author Zych, Dawid
Slodek, Aneta
Zimny, Dżastin
Golba, Sylwia
Malarz, Katarzyna
Mrozek-Wilczkiewicz, Anna
author_facet Zych, Dawid
Slodek, Aneta
Zimny, Dżastin
Golba, Sylwia
Malarz, Katarzyna
Mrozek-Wilczkiewicz, Anna
author_sort Zych, Dawid
collection PubMed
description In this study, we newly designed and developed a synthesis route based on the 1,3-dipolar cycloaddition of the derivatives of 4′-(1,2,3-triazol-4-yl)phenyl-2,2′:6′,2′′-terpyridine with various (hetero)aryl substituents, differing in electronic character, on a triazol ring. The obtained compounds were comprehensively characterized by UV-Vis spectroscopy and electrochemical and thermal studies. Moreover, preliminary biological tests were conducted. The investigation allowed the selection of materials with the most promising properties with particular emphasis on the nature of the substituents. In addition, theoretical studies (DFT and TD-DFT) were performed to verify the comprehensive understanding of experimental results.
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spelling pubmed-90644142022-05-04 Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties Zych, Dawid Slodek, Aneta Zimny, Dżastin Golba, Sylwia Malarz, Katarzyna Mrozek-Wilczkiewicz, Anna RSC Adv Chemistry In this study, we newly designed and developed a synthesis route based on the 1,3-dipolar cycloaddition of the derivatives of 4′-(1,2,3-triazol-4-yl)phenyl-2,2′:6′,2′′-terpyridine with various (hetero)aryl substituents, differing in electronic character, on a triazol ring. The obtained compounds were comprehensively characterized by UV-Vis spectroscopy and electrochemical and thermal studies. Moreover, preliminary biological tests were conducted. The investigation allowed the selection of materials with the most promising properties with particular emphasis on the nature of the substituents. In addition, theoretical studies (DFT and TD-DFT) were performed to verify the comprehensive understanding of experimental results. The Royal Society of Chemistry 2019-05-28 /pmc/articles/PMC9064414/ /pubmed/35516389 http://dx.doi.org/10.1039/c9ra02655j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zych, Dawid
Slodek, Aneta
Zimny, Dżastin
Golba, Sylwia
Malarz, Katarzyna
Mrozek-Wilczkiewicz, Anna
Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title_full Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title_fullStr Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title_full_unstemmed Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title_short Influence of the substituent D/A at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
title_sort influence of the substituent d/a at the 1,2,3-triazole ring on novel terpyridine derivatives: synthesis and properties
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064414/
https://www.ncbi.nlm.nih.gov/pubmed/35516389
http://dx.doi.org/10.1039/c9ra02655j
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