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2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties
We herein report the design and synthesis of small-donor molecules, 2,1,3-benzothiadiazole derivatives (2a–d), by Stille or Suzuki reaction. The synthesized compounds were characterized by spectroscopic and electrochemical methods. The compounds 2a–d absorb the light in a wide range (the UV-green/ye...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956540/ https://www.ncbi.nlm.nih.gov/pubmed/33668393 http://dx.doi.org/10.3390/molecules26051216 |
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author | Zając, Dorota Honisz, Damian Łapkowski, Mieczysław Sołoducho, Jadwiga |
author_facet | Zając, Dorota Honisz, Damian Łapkowski, Mieczysław Sołoducho, Jadwiga |
author_sort | Zając, Dorota |
collection | PubMed |
description | We herein report the design and synthesis of small-donor molecules, 2,1,3-benzothiadiazole derivatives (2a–d), by Stille or Suzuki reaction. The synthesized compounds were characterized by spectroscopic and electrochemical methods. The compounds 2a–d absorb the light in a wide range (the UV-green/yellow light (2c)) and emit from green to red/near IR light (2c). Furthermore, these compounds show a narrow energy gap (1.75–2.38 eV), and high Ea values increasing for polymers, which prove their electron-donating nature and semiconductor properties. The measurements were enhanced by theoretical modeling. |
format | Online Article Text |
id | pubmed-7956540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79565402021-03-16 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties Zając, Dorota Honisz, Damian Łapkowski, Mieczysław Sołoducho, Jadwiga Molecules Article We herein report the design and synthesis of small-donor molecules, 2,1,3-benzothiadiazole derivatives (2a–d), by Stille or Suzuki reaction. The synthesized compounds were characterized by spectroscopic and electrochemical methods. The compounds 2a–d absorb the light in a wide range (the UV-green/yellow light (2c)) and emit from green to red/near IR light (2c). Furthermore, these compounds show a narrow energy gap (1.75–2.38 eV), and high Ea values increasing for polymers, which prove their electron-donating nature and semiconductor properties. The measurements were enhanced by theoretical modeling. MDPI 2021-02-24 /pmc/articles/PMC7956540/ /pubmed/33668393 http://dx.doi.org/10.3390/molecules26051216 Text en © 2021 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zając, Dorota Honisz, Damian Łapkowski, Mieczysław Sołoducho, Jadwiga 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title | 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title_full | 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title_fullStr | 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title_full_unstemmed | 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title_short | 2,1,3-Benzothiadiazole Small Donor Molecules: A DFT Study, Synthesis, and Optoelectronic Properties |
title_sort | 2,1,3-benzothiadiazole small donor molecules: a dft study, synthesis, and optoelectronic properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956540/ https://www.ncbi.nlm.nih.gov/pubmed/33668393 http://dx.doi.org/10.3390/molecules26051216 |
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