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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...
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/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. |
format | Online Article Text |
id | pubmed-8269563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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