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Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy
New conjugated polymers that incorporate dihexylanthradithiophene (DHADT) in the main chain were prepared by Stille, Sonogashira, and Yamamoto cross-coupling polymerization reactions. The polymerization chemistry is enabled by a soluble 5,11-dibromodihexylanthradithiophene monomer that is capable of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693243/ https://www.ncbi.nlm.nih.gov/pubmed/35423694 http://dx.doi.org/10.1039/d0ra09195b |
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author | Hussain, Waseem A. Plunkett, Kyle N. |
author_facet | Hussain, Waseem A. Plunkett, Kyle N. |
author_sort | Hussain, Waseem A. |
collection | PubMed |
description | New conjugated polymers that incorporate dihexylanthradithiophene (DHADT) in the main chain were prepared by Stille, Sonogashira, and Yamamoto cross-coupling polymerization reactions. The polymerization chemistry is enabled by a soluble 5,11-dibromodihexylanthradithiophene monomer that is capable of cross-coupling reactions. Five readily soluble DHADT containing polymers were prepared and characterized experimentally and computationally. These polymers possess HOMO energies of −5.18 eV to −5.43 eV and LUMO energies of −3.0 eV to −2.82 eV. The notable optical features include broad absorption and band gaps ranging from 1.62 eV to 2.15 eV. Polymers were tested in organic field effect transistors and were found to operate in the p-type regime. |
format | Online Article Text |
id | pubmed-8693243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86932432022-04-13 Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy Hussain, Waseem A. Plunkett, Kyle N. RSC Adv Chemistry New conjugated polymers that incorporate dihexylanthradithiophene (DHADT) in the main chain were prepared by Stille, Sonogashira, and Yamamoto cross-coupling polymerization reactions. The polymerization chemistry is enabled by a soluble 5,11-dibromodihexylanthradithiophene monomer that is capable of cross-coupling reactions. Five readily soluble DHADT containing polymers were prepared and characterized experimentally and computationally. These polymers possess HOMO energies of −5.18 eV to −5.43 eV and LUMO energies of −3.0 eV to −2.82 eV. The notable optical features include broad absorption and band gaps ranging from 1.62 eV to 2.15 eV. Polymers were tested in organic field effect transistors and were found to operate in the p-type regime. The Royal Society of Chemistry 2021-01-04 /pmc/articles/PMC8693243/ /pubmed/35423694 http://dx.doi.org/10.1039/d0ra09195b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Hussain, Waseem A. Plunkett, Kyle N. Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title | Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title_full | Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title_fullStr | Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title_full_unstemmed | Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title_short | Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
title_sort | synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693243/ https://www.ncbi.nlm.nih.gov/pubmed/35423694 http://dx.doi.org/10.1039/d0ra09195b |
work_keys_str_mv | AT hussainwaseema synthesisofanthradithiophenecontainingconjugatedpolymersviaacrosscouplingstrategy AT plunkettkylen synthesisofanthradithiophenecontainingconjugatedpolymersviaacrosscouplingstrategy |