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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...

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Autores principales: Zając, Dorota, Honisz, Damian, Łapkowski, Mieczysław, Sołoducho, Jadwiga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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