1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers

A new cross-linkable monomer containing 1,3-diphenylethenylcarbazolyl-based hole-transporting moieties and four reactive epoxy groups, was prepared by a multistep synthesis route from 1,3-bis(2,2-diphenylethenyl)-9H-carbazol-2-ol and its application for the in situ formation of cross-linked hole tra...

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Autores principales: Daskeviciene, Maryte, Bubniene, Giedre, Malinauskas, Tadas, Jankauskas, Vygintas, Gaidelis, Valentas, Paulauskas, Valdas, Getautis, Vytautas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272464/
https://www.ncbi.nlm.nih.gov/pubmed/25996215
http://dx.doi.org/10.3390/molecules20059124
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author Daskeviciene, Maryte
Bubniene, Giedre
Malinauskas, Tadas
Jankauskas, Vygintas
Gaidelis, Valentas
Paulauskas, Valdas
Getautis, Vytautas
author_facet Daskeviciene, Maryte
Bubniene, Giedre
Malinauskas, Tadas
Jankauskas, Vygintas
Gaidelis, Valentas
Paulauskas, Valdas
Getautis, Vytautas
author_sort Daskeviciene, Maryte
collection PubMed
description A new cross-linkable monomer containing 1,3-diphenylethenylcarbazolyl-based hole-transporting moieties and four reactive epoxy groups, was prepared by a multistep synthesis route from 1,3-bis(2,2-diphenylethenyl)-9H-carbazol-2-ol and its application for the in situ formation of cross-linked hole transporting layers was investigated. A high concentration of flexible aliphatic epoxy chains ensures good solubility and makes this compound an attractive cross-linking agent. The synthesized compounds were characterized by various techniques, including differential scanning calorimetry, xerographic time of flight, and electron photoemission in air methods.
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spelling pubmed-62724642019-01-07 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers Daskeviciene, Maryte Bubniene, Giedre Malinauskas, Tadas Jankauskas, Vygintas Gaidelis, Valentas Paulauskas, Valdas Getautis, Vytautas Molecules Article A new cross-linkable monomer containing 1,3-diphenylethenylcarbazolyl-based hole-transporting moieties and four reactive epoxy groups, was prepared by a multistep synthesis route from 1,3-bis(2,2-diphenylethenyl)-9H-carbazol-2-ol and its application for the in situ formation of cross-linked hole transporting layers was investigated. A high concentration of flexible aliphatic epoxy chains ensures good solubility and makes this compound an attractive cross-linking agent. The synthesized compounds were characterized by various techniques, including differential scanning calorimetry, xerographic time of flight, and electron photoemission in air methods. MDPI 2015-05-19 /pmc/articles/PMC6272464/ /pubmed/25996215 http://dx.doi.org/10.3390/molecules20059124 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Daskeviciene, Maryte
Bubniene, Giedre
Malinauskas, Tadas
Jankauskas, Vygintas
Gaidelis, Valentas
Paulauskas, Valdas
Getautis, Vytautas
1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title_full 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title_fullStr 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title_full_unstemmed 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title_short 1,3-Diphenylethenylcarbazolyl-Based Monomer for Cross-Linked Hole Transporting Layers
title_sort 1,3-diphenylethenylcarbazolyl-based monomer for cross-linked hole transporting layers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272464/
https://www.ncbi.nlm.nih.gov/pubmed/25996215
http://dx.doi.org/10.3390/molecules20059124
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