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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
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.
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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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