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New Blue Donor–Acceptor Pechmann Dyes: Synthesis, Spectroscopic, Electrochemical, and Computational Studies
[Image: see text] The design, synthesis, and characterization of a new class of blue-colored thiophene-substituted Pechmann dyes are reported. Due to a distinguishing blue coloration and the capability to absorb light in one of the most photon-dense regions of the solar spectrum, such compounds are...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648098/ https://www.ncbi.nlm.nih.gov/pubmed/31459854 http://dx.doi.org/10.1021/acsomega.8b03560 |
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author | Dessì, Alessio Sinicropi, Adalgisa Mohammadpourasl, Sanaz Basosi, Riccardo Taddei, Maurizio Fabrizi de Biani, Fabrizia Calamante, Massimo Zani, Lorenzo Mordini, Alessandro Bracq, Pamela Franchi, Daniele Reginato, Gianna |
author_facet | Dessì, Alessio Sinicropi, Adalgisa Mohammadpourasl, Sanaz Basosi, Riccardo Taddei, Maurizio Fabrizi de Biani, Fabrizia Calamante, Massimo Zani, Lorenzo Mordini, Alessandro Bracq, Pamela Franchi, Daniele Reginato, Gianna |
author_sort | Dessì, Alessio |
collection | PubMed |
description | [Image: see text] The design, synthesis, and characterization of a new class of blue-colored thiophene-substituted Pechmann dyes are reported. Due to a distinguishing blue coloration and the capability to absorb light in one of the most photon-dense regions of the solar spectrum, such compounds are of great interest for application as photoactive materials in organic optoelectronics, in particular, in dye-sensitized solar cells. To achieve fine tuning of the optical and electrochemical properties, the electron-poor thiophene-bis-lactone moiety has been decorated with donor (D) and acceptor groups (A), targeting fully conjugated D–A−π–A structures. The designed structures have been investigated by means of DFT and time-dependent DFT calculations, and the most promising dyes have been synthesized. These molecules represent the very first preparation of unsymmetrical Pechmann derivatives. Optical and electrochemical properties of the new dyes have been studied by cyclic voltammetry and UV–vis and fluorescence spectroscopy. In two cases, test cells were built proving that a photocurrent can indeed be generated when using electrolytes especially formulated for narrow-band-gap dyes, although with a very low efficiency. |
format | Online Article Text |
id | pubmed-6648098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66480982019-08-27 New Blue Donor–Acceptor Pechmann Dyes: Synthesis, Spectroscopic, Electrochemical, and Computational Studies Dessì, Alessio Sinicropi, Adalgisa Mohammadpourasl, Sanaz Basosi, Riccardo Taddei, Maurizio Fabrizi de Biani, Fabrizia Calamante, Massimo Zani, Lorenzo Mordini, Alessandro Bracq, Pamela Franchi, Daniele Reginato, Gianna ACS Omega [Image: see text] The design, synthesis, and characterization of a new class of blue-colored thiophene-substituted Pechmann dyes are reported. Due to a distinguishing blue coloration and the capability to absorb light in one of the most photon-dense regions of the solar spectrum, such compounds are of great interest for application as photoactive materials in organic optoelectronics, in particular, in dye-sensitized solar cells. To achieve fine tuning of the optical and electrochemical properties, the electron-poor thiophene-bis-lactone moiety has been decorated with donor (D) and acceptor groups (A), targeting fully conjugated D–A−π–A structures. The designed structures have been investigated by means of DFT and time-dependent DFT calculations, and the most promising dyes have been synthesized. These molecules represent the very first preparation of unsymmetrical Pechmann derivatives. Optical and electrochemical properties of the new dyes have been studied by cyclic voltammetry and UV–vis and fluorescence spectroscopy. In two cases, test cells were built proving that a photocurrent can indeed be generated when using electrolytes especially formulated for narrow-band-gap dyes, although with a very low efficiency. American Chemical Society 2019-04-26 /pmc/articles/PMC6648098/ /pubmed/31459854 http://dx.doi.org/10.1021/acsomega.8b03560 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Dessì, Alessio Sinicropi, Adalgisa Mohammadpourasl, Sanaz Basosi, Riccardo Taddei, Maurizio Fabrizi de Biani, Fabrizia Calamante, Massimo Zani, Lorenzo Mordini, Alessandro Bracq, Pamela Franchi, Daniele Reginato, Gianna New Blue Donor–Acceptor Pechmann Dyes: Synthesis, Spectroscopic, Electrochemical, and Computational Studies |
title | New Blue Donor–Acceptor Pechmann Dyes: Synthesis,
Spectroscopic, Electrochemical, and Computational Studies |
title_full | New Blue Donor–Acceptor Pechmann Dyes: Synthesis,
Spectroscopic, Electrochemical, and Computational Studies |
title_fullStr | New Blue Donor–Acceptor Pechmann Dyes: Synthesis,
Spectroscopic, Electrochemical, and Computational Studies |
title_full_unstemmed | New Blue Donor–Acceptor Pechmann Dyes: Synthesis,
Spectroscopic, Electrochemical, and Computational Studies |
title_short | New Blue Donor–Acceptor Pechmann Dyes: Synthesis,
Spectroscopic, Electrochemical, and Computational Studies |
title_sort | new blue donor–acceptor pechmann dyes: synthesis,
spectroscopic, electrochemical, and computational studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648098/ https://www.ncbi.nlm.nih.gov/pubmed/31459854 http://dx.doi.org/10.1021/acsomega.8b03560 |
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