A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation

The title polyaromatic chalcone compound (PyMQ-chalcone) was sequentially synthesized via a three steps synthetic procedure and well characterized. Structural illumination was achieved by 1D and 2D NMR techniques, FTIR, LCMS/MS, and SEM. Photophysical investigations showed that the emission capacity...

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Main Author: Atahan, Alparslan
Format: Text
Language:unknown
Published: Taylor & Francis 2021
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Online Access:https://dx.doi.org/10.6084/m9.figshare.13567640.v1
https://tandf.figshare.com/articles/journal_contribution/A_Novel_Polyaromatic_Chalcone_with_Multiple_Functional_Groups_Synthetic_Photophysical_and_Computational_Elucidation/13567640/1
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spelling ftdatacite:10.6084/m9.figshare.13567640.v1 2023-05-15T17:53:43+02:00 A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation Atahan, Alparslan 2021 https://dx.doi.org/10.6084/m9.figshare.13567640.v1 https://tandf.figshare.com/articles/journal_contribution/A_Novel_Polyaromatic_Chalcone_with_Multiple_Functional_Groups_Synthetic_Photophysical_and_Computational_Elucidation/13567640/1 unknown Taylor & Francis https://dx.doi.org/10.1080/10406638.2020.1871036 https://dx.doi.org/10.6084/m9.figshare.13567640 Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode cc-by-4.0 CC-BY Biophysics Biochemistry Biotechnology 39999 Chemical Sciences not elsewhere classified FOS Chemical sciences Sociology FOS Sociology 69999 Biological Sciences not elsewhere classified FOS Biological sciences Text article-journal Journal contribution ScholarlyArticle 2021 ftdatacite https://doi.org/10.6084/m9.figshare.13567640.v1 https://doi.org/10.1080/10406638.2020.1871036 https://doi.org/10.6084/m9.figshare.13567640 2021-11-05T12:55:41Z The title polyaromatic chalcone compound (PyMQ-chalcone) was sequentially synthesized via a three steps synthetic procedure and well characterized. Structural illumination was achieved by 1D and 2D NMR techniques, FTIR, LCMS/MS, and SEM. Photophysical investigations showed that the emission capacity remarkably increased by aggregation although target compound exhibited lower emission at solution state in common organic solvents. Furthermore, addition of some metal cations (such as Al 3+ and Cr 3+ ) slightly enhanced the emission in acetonitrile/water media in metal sensing studies. Lastly, density-functional theory studies were carried out by ORCA 4.2.0 software ((B3LYP; def2-TZVP basis set) to determine some electronic parameters such as HOMO–LUMO energy, total energy, dipol moment, and bond lengths, etc. Text Orca DataCite Metadata Store (German National Library of Science and Technology)
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biophysics
Biochemistry
Biotechnology
39999 Chemical Sciences not elsewhere classified
FOS Chemical sciences
Sociology
FOS Sociology
69999 Biological Sciences not elsewhere classified
FOS Biological sciences
spellingShingle Biophysics
Biochemistry
Biotechnology
39999 Chemical Sciences not elsewhere classified
FOS Chemical sciences
Sociology
FOS Sociology
69999 Biological Sciences not elsewhere classified
FOS Biological sciences
Atahan, Alparslan
A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
topic_facet Biophysics
Biochemistry
Biotechnology
39999 Chemical Sciences not elsewhere classified
FOS Chemical sciences
Sociology
FOS Sociology
69999 Biological Sciences not elsewhere classified
FOS Biological sciences
description The title polyaromatic chalcone compound (PyMQ-chalcone) was sequentially synthesized via a three steps synthetic procedure and well characterized. Structural illumination was achieved by 1D and 2D NMR techniques, FTIR, LCMS/MS, and SEM. Photophysical investigations showed that the emission capacity remarkably increased by aggregation although target compound exhibited lower emission at solution state in common organic solvents. Furthermore, addition of some metal cations (such as Al 3+ and Cr 3+ ) slightly enhanced the emission in acetonitrile/water media in metal sensing studies. Lastly, density-functional theory studies were carried out by ORCA 4.2.0 software ((B3LYP; def2-TZVP basis set) to determine some electronic parameters such as HOMO–LUMO energy, total energy, dipol moment, and bond lengths, etc.
format Text
author Atahan, Alparslan
author_facet Atahan, Alparslan
author_sort Atahan, Alparslan
title A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
title_short A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
title_full A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
title_fullStr A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
title_full_unstemmed A Novel Polyaromatic Chalcone with Multiple Functional Groups: Synthetic, Photophysical, and Computational Elucidation
title_sort novel polyaromatic chalcone with multiple functional groups: synthetic, photophysical, and computational elucidation
publisher Taylor & Francis
publishDate 2021
url https://dx.doi.org/10.6084/m9.figshare.13567640.v1
https://tandf.figshare.com/articles/journal_contribution/A_Novel_Polyaromatic_Chalcone_with_Multiple_Functional_Groups_Synthetic_Photophysical_and_Computational_Elucidation/13567640/1
genre Orca
genre_facet Orca
op_relation https://dx.doi.org/10.1080/10406638.2020.1871036
https://dx.doi.org/10.6084/m9.figshare.13567640
op_rights Creative Commons Attribution 4.0 International
https://creativecommons.org/licenses/by/4.0/legalcode
cc-by-4.0
op_rightsnorm CC-BY
op_doi https://doi.org/10.6084/m9.figshare.13567640.v1
https://doi.org/10.1080/10406638.2020.1871036
https://doi.org/10.6084/m9.figshare.13567640
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