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Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State

While few studies show only symmetrical and poorly mono-SO(n) (n = 0–2) substituted acenes, in this study, we present a synthesis of a new group of unsymmetrical, significantly substituted derivatives, which revealed unique photophysical properties. Both sulfides (S), sulfoxides (SO) and sulfones (S...

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Autores principales: Bałczewski, Piotr, Kowalska, Emilia, Różycka-Sokołowska, Ewa, Uznański, Paweł, Wilk, Joanna, Koprowski, Marek, Owsianik, Krzysztof, Marciniak, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269563/
https://www.ncbi.nlm.nih.gov/pubmed/34201740
http://dx.doi.org/10.3390/ma14133506
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author Bałczewski, Piotr
Kowalska, Emilia
Różycka-Sokołowska, Ewa
Uznański, Paweł
Wilk, Joanna
Koprowski, Marek
Owsianik, Krzysztof
Marciniak, Bernard
author_facet Bałczewski, Piotr
Kowalska, Emilia
Różycka-Sokołowska, Ewa
Uznański, Paweł
Wilk, Joanna
Koprowski, Marek
Owsianik, Krzysztof
Marciniak, Bernard
author_sort Bałczewski, Piotr
collection PubMed
description While few studies show only symmetrical and poorly mono-SO(n) (n = 0–2) substituted acenes, in this study, we present a synthesis of a new group of unsymmetrical, significantly substituted derivatives, which revealed unique photophysical properties. Both sulfides (S), sulfoxides (SO) and sulfones (SO(2)) showed very high photochemical stabilities, unusual for these groups, during UV-irradiation at 254/365 nm (air O(2) and Ar), which was higher than any found in the literature. For the (S)/(SO) series (254 nm), the stabilities of 80–519 min. (air O(2) and Ar) were found. At 365 nm, stabilities of 124—812 min./(air O(2)) for (S)/(SO) and higher for (SO(2)) were observed. Photoluminescence lifetimes of (SO(n)) of the lower anthryl symmetry remained in the following order: (SO(2)) < (S) < (SO); those with full symmetry were in the following order: (S) < (SO) < (SO(2)). The enhanced photostability was explained with DFT/MS/Hammett’s constants, which showed the leading role of the SO(n) groups in stabilization of HOMO/LUMO frontier orbitals. The SO(n) (n = 0–2) substituted acenes turned out to be tunable violet/blue/green emitters by oxidation of S atoms and the introduction of rich substitution.
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spelling pubmed-82695632021-07-10 Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State Bałczewski, Piotr Kowalska, Emilia Różycka-Sokołowska, Ewa Uznański, Paweł Wilk, Joanna Koprowski, Marek Owsianik, Krzysztof Marciniak, Bernard Materials (Basel) Article While few studies show only symmetrical and poorly mono-SO(n) (n = 0–2) substituted acenes, in this study, we present a synthesis of a new group of unsymmetrical, significantly substituted derivatives, which revealed unique photophysical properties. Both sulfides (S), sulfoxides (SO) and sulfones (SO(2)) showed very high photochemical stabilities, unusual for these groups, during UV-irradiation at 254/365 nm (air O(2) and Ar), which was higher than any found in the literature. For the (S)/(SO) series (254 nm), the stabilities of 80–519 min. (air O(2) and Ar) were found. At 365 nm, stabilities of 124—812 min./(air O(2)) for (S)/(SO) and higher for (SO(2)) were observed. Photoluminescence lifetimes of (SO(n)) of the lower anthryl symmetry remained in the following order: (SO(2)) < (S) < (SO); those with full symmetry were in the following order: (S) < (SO) < (SO(2)). The enhanced photostability was explained with DFT/MS/Hammett’s constants, which showed the leading role of the SO(n) groups in stabilization of HOMO/LUMO frontier orbitals. The SO(n) (n = 0–2) substituted acenes turned out to be tunable violet/blue/green emitters by oxidation of S atoms and the introduction of rich substitution. MDPI 2021-06-23 /pmc/articles/PMC8269563/ /pubmed/34201740 http://dx.doi.org/10.3390/ma14133506 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bałczewski, Piotr
Kowalska, Emilia
Różycka-Sokołowska, Ewa
Uznański, Paweł
Wilk, Joanna
Koprowski, Marek
Owsianik, Krzysztof
Marciniak, Bernard
Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title_full Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title_fullStr Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title_full_unstemmed Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title_short Organosulfur Materials with High Photo- and Photo-Oxidation Stability: 10-Anthryl Sulfoxides and Sulfones and Their Photophysical Properties Dependent on the Sulfur Oxidation State
title_sort organosulfur materials with high photo- and photo-oxidation stability: 10-anthryl sulfoxides and sulfones and their photophysical properties dependent on the sulfur oxidation state
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269563/
https://www.ncbi.nlm.nih.gov/pubmed/34201740
http://dx.doi.org/10.3390/ma14133506
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