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Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones

New oligo- and polyenaminones with M(w) ~ 7–50 KDa were prepared in high yields by transaminative amino-enaminone polymerization of regioisomeric bis[(dimethylamino)methylidene]cyclohexanediones with alkylene and phenylenediamines. The polymers obtained are practically insoluble in aqueous and organ...

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Autores principales: Štanfel, Urša, Kotnik, Tomaž, Ričko, Sebastijan, Grošelj, Uroš, Štefane, Bogdan, Pirnat, Klemen, Žagar, Ema, Genorio, Boštjan, Svete, Jurij
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573701/
https://www.ncbi.nlm.nih.gov/pubmed/36236068
http://dx.doi.org/10.3390/polym14194120
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author Štanfel, Urša
Kotnik, Tomaž
Ričko, Sebastijan
Grošelj, Uroš
Štefane, Bogdan
Pirnat, Klemen
Žagar, Ema
Genorio, Boštjan
Svete, Jurij
author_facet Štanfel, Urša
Kotnik, Tomaž
Ričko, Sebastijan
Grošelj, Uroš
Štefane, Bogdan
Pirnat, Klemen
Žagar, Ema
Genorio, Boštjan
Svete, Jurij
author_sort Štanfel, Urša
collection PubMed
description New oligo- and polyenaminones with M(w) ~ 7–50 KDa were prepared in high yields by transaminative amino-enaminone polymerization of regioisomeric bis[(dimethylamino)methylidene]cyclohexanediones with alkylene and phenylenediamines. The polymers obtained are practically insoluble in aqueous and organic solvents and exhibit film-forming properties, UV light absorption at wavelengths below 500 nm, and redox activity. These properties indicate a promising application potential of these polymers, which could find use in optical and optoelectronic applications and in energy storage devices.
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spelling pubmed-95737012022-10-17 Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones Štanfel, Urša Kotnik, Tomaž Ričko, Sebastijan Grošelj, Uroš Štefane, Bogdan Pirnat, Klemen Žagar, Ema Genorio, Boštjan Svete, Jurij Polymers (Basel) Article New oligo- and polyenaminones with M(w) ~ 7–50 KDa were prepared in high yields by transaminative amino-enaminone polymerization of regioisomeric bis[(dimethylamino)methylidene]cyclohexanediones with alkylene and phenylenediamines. The polymers obtained are practically insoluble in aqueous and organic solvents and exhibit film-forming properties, UV light absorption at wavelengths below 500 nm, and redox activity. These properties indicate a promising application potential of these polymers, which could find use in optical and optoelectronic applications and in energy storage devices. MDPI 2022-10-01 /pmc/articles/PMC9573701/ /pubmed/36236068 http://dx.doi.org/10.3390/polym14194120 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Štanfel, Urša
Kotnik, Tomaž
Ričko, Sebastijan
Grošelj, Uroš
Štefane, Bogdan
Pirnat, Klemen
Žagar, Ema
Genorio, Boštjan
Svete, Jurij
Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title_full Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title_fullStr Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title_full_unstemmed Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title_short Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones
title_sort synthesis of optically and redox active polyenaminones from diamines and α,α’-bis[(dimethylamino)methylidene]cyclohexanediones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573701/
https://www.ncbi.nlm.nih.gov/pubmed/36236068
http://dx.doi.org/10.3390/polym14194120
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