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Beyond the Threshold: A Study of Chalcogenophene-Based Two-Photon Initiators
[Image: see text] A series of nine soluble, symmetric chalcogenophenes bearing hexyl-substituted triphenylamines, indolocarbazoles, or phenylcarbazoles was designed and synthesized as potential two-photon absorption (2PA) initiators. A detailed photophysical analysis of these molecules revealed good...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009090/ https://www.ncbi.nlm.nih.gov/pubmed/35431440 http://dx.doi.org/10.1021/acs.chemmater.1c04002 |
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author | Lunzer, Markus Beckwith, Joseph S. Chalupa-Gantner, Franziska Rosspeintner, Arnulf Licari, Giuseppe Steiger, Wolfgang Hametner, Christian Liska, Robert Fröhlich, Johannes Vauthey, Eric Ovsianikov, Aleksandr Holzer, Brigitte |
author_facet | Lunzer, Markus Beckwith, Joseph S. Chalupa-Gantner, Franziska Rosspeintner, Arnulf Licari, Giuseppe Steiger, Wolfgang Hametner, Christian Liska, Robert Fröhlich, Johannes Vauthey, Eric Ovsianikov, Aleksandr Holzer, Brigitte |
author_sort | Lunzer, Markus |
collection | PubMed |
description | [Image: see text] A series of nine soluble, symmetric chalcogenophenes bearing hexyl-substituted triphenylamines, indolocarbazoles, or phenylcarbazoles was designed and synthesized as potential two-photon absorption (2PA) initiators. A detailed photophysical analysis of these molecules revealed good 2PA properties of the series and, in particular, a strong influence of selenium on the 2PA cross sections, rendering these materials especially promising new 2PA photoinitiators. Structuring and threshold tests proved the efficiency and broad spectral versatility of two selenium-containing lead compounds as well as their applicability in an acrylate resin formulation. A comparison with commercial photoinitiators Irg369 and BAPO as well as sensitizer ITX showed that the newly designed selenium-based materials TPA-S and TPA-BBS outperform these traditional initiators by far both in terms of reactivity and dose. Moreover, by increasing the ultralow concentration of TPA-BBS, a further reduction of the polymerization threshold can be achieved, revealing the great potential of this series for application in two-photon polymerization (2PP) systems where only low laser power is available. |
format | Online Article Text |
id | pubmed-9009090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90090902022-04-14 Beyond the Threshold: A Study of Chalcogenophene-Based Two-Photon Initiators Lunzer, Markus Beckwith, Joseph S. Chalupa-Gantner, Franziska Rosspeintner, Arnulf Licari, Giuseppe Steiger, Wolfgang Hametner, Christian Liska, Robert Fröhlich, Johannes Vauthey, Eric Ovsianikov, Aleksandr Holzer, Brigitte Chem Mater [Image: see text] A series of nine soluble, symmetric chalcogenophenes bearing hexyl-substituted triphenylamines, indolocarbazoles, or phenylcarbazoles was designed and synthesized as potential two-photon absorption (2PA) initiators. A detailed photophysical analysis of these molecules revealed good 2PA properties of the series and, in particular, a strong influence of selenium on the 2PA cross sections, rendering these materials especially promising new 2PA photoinitiators. Structuring and threshold tests proved the efficiency and broad spectral versatility of two selenium-containing lead compounds as well as their applicability in an acrylate resin formulation. A comparison with commercial photoinitiators Irg369 and BAPO as well as sensitizer ITX showed that the newly designed selenium-based materials TPA-S and TPA-BBS outperform these traditional initiators by far both in terms of reactivity and dose. Moreover, by increasing the ultralow concentration of TPA-BBS, a further reduction of the polymerization threshold can be achieved, revealing the great potential of this series for application in two-photon polymerization (2PP) systems where only low laser power is available. American Chemical Society 2022-03-22 2022-04-12 /pmc/articles/PMC9009090/ /pubmed/35431440 http://dx.doi.org/10.1021/acs.chemmater.1c04002 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Lunzer, Markus Beckwith, Joseph S. Chalupa-Gantner, Franziska Rosspeintner, Arnulf Licari, Giuseppe Steiger, Wolfgang Hametner, Christian Liska, Robert Fröhlich, Johannes Vauthey, Eric Ovsianikov, Aleksandr Holzer, Brigitte Beyond the Threshold: A Study of Chalcogenophene-Based Two-Photon Initiators |
title | Beyond the Threshold: A Study of Chalcogenophene-Based
Two-Photon Initiators |
title_full | Beyond the Threshold: A Study of Chalcogenophene-Based
Two-Photon Initiators |
title_fullStr | Beyond the Threshold: A Study of Chalcogenophene-Based
Two-Photon Initiators |
title_full_unstemmed | Beyond the Threshold: A Study of Chalcogenophene-Based
Two-Photon Initiators |
title_short | Beyond the Threshold: A Study of Chalcogenophene-Based
Two-Photon Initiators |
title_sort | beyond the threshold: a study of chalcogenophene-based
two-photon initiators |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009090/ https://www.ncbi.nlm.nih.gov/pubmed/35431440 http://dx.doi.org/10.1021/acs.chemmater.1c04002 |
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