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A Modified Oxazolone Dye Dedicated to Spectroscopy and Optoelectronics
[Image: see text] Here we present a newly synthesized bifunctional organic chromophore with appealing spectroscopic and nonlinear optical features. The positions of absorption and emission maxima of the dye vary with increasing solvent polarity and exhibit positive solvatochromism. The determined ch...
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/PMC9171828/ https://www.ncbi.nlm.nih.gov/pubmed/35588394 http://dx.doi.org/10.1021/acs.joc.2c00500 |
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author | Szukalski, Adam Krawczyk, Przemysław Sahraoui, Bouchta Rosińska, Faustyna Jędrzejewska, Beata |
author_facet | Szukalski, Adam Krawczyk, Przemysław Sahraoui, Bouchta Rosińska, Faustyna Jędrzejewska, Beata |
author_sort | Szukalski, Adam |
collection | PubMed |
description | [Image: see text] Here we present a newly synthesized bifunctional organic chromophore with appealing spectroscopic and nonlinear optical features. The positions of absorption and emission maxima of the dye vary with increasing solvent polarity and exhibit positive solvatochromism. The determined change in the dipole moment upon excitation based on the Bilot and Kawski theory is 5.94 D, which corresponds to the intermolecular displacement of a charge equal to 1.24 Å. An investigated organic-based system represents a significant, repeatable, and stable over time optical signal modulation in the manner of the refractive index value. Its magnitude is varied both by optical pumping intensity as well as by external frequency modulation, which indicates that such system is an alluring and alternative core unit for optoelectronic devices and complex networks. Then, the same active system, due to the nonresonant mechanism of higher harmonics of light inducement, can provide second and third harmonic signals. According to the introduced laser line spatial modifications (parallel or perpendicular polarization directions), it is resulted in output SHG signal with magnitude varied about 100%. Its magnitude is noticeably small; however, to construct sensitive optical sensors or infrared indicators, such feature may guarantee satisfying circumstances. |
format | Online Article Text |
id | pubmed-9171828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91718282022-06-08 A Modified Oxazolone Dye Dedicated to Spectroscopy and Optoelectronics Szukalski, Adam Krawczyk, Przemysław Sahraoui, Bouchta Rosińska, Faustyna Jędrzejewska, Beata J Org Chem [Image: see text] Here we present a newly synthesized bifunctional organic chromophore with appealing spectroscopic and nonlinear optical features. The positions of absorption and emission maxima of the dye vary with increasing solvent polarity and exhibit positive solvatochromism. The determined change in the dipole moment upon excitation based on the Bilot and Kawski theory is 5.94 D, which corresponds to the intermolecular displacement of a charge equal to 1.24 Å. An investigated organic-based system represents a significant, repeatable, and stable over time optical signal modulation in the manner of the refractive index value. Its magnitude is varied both by optical pumping intensity as well as by external frequency modulation, which indicates that such system is an alluring and alternative core unit for optoelectronic devices and complex networks. Then, the same active system, due to the nonresonant mechanism of higher harmonics of light inducement, can provide second and third harmonic signals. According to the introduced laser line spatial modifications (parallel or perpendicular polarization directions), it is resulted in output SHG signal with magnitude varied about 100%. Its magnitude is noticeably small; however, to construct sensitive optical sensors or infrared indicators, such feature may guarantee satisfying circumstances. American Chemical Society 2022-05-19 2022-06-03 /pmc/articles/PMC9171828/ /pubmed/35588394 http://dx.doi.org/10.1021/acs.joc.2c00500 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 | Szukalski, Adam Krawczyk, Przemysław Sahraoui, Bouchta Rosińska, Faustyna Jędrzejewska, Beata A Modified Oxazolone Dye Dedicated to Spectroscopy and Optoelectronics |
title | A Modified Oxazolone
Dye Dedicated to Spectroscopy
and Optoelectronics |
title_full | A Modified Oxazolone
Dye Dedicated to Spectroscopy
and Optoelectronics |
title_fullStr | A Modified Oxazolone
Dye Dedicated to Spectroscopy
and Optoelectronics |
title_full_unstemmed | A Modified Oxazolone
Dye Dedicated to Spectroscopy
and Optoelectronics |
title_short | A Modified Oxazolone
Dye Dedicated to Spectroscopy
and Optoelectronics |
title_sort | modified oxazolone
dye dedicated to spectroscopy
and optoelectronics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171828/ https://www.ncbi.nlm.nih.gov/pubmed/35588394 http://dx.doi.org/10.1021/acs.joc.2c00500 |
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