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A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine

Though 2-arylperimidines have never been used in iridium(III) chemistry, the present study on structural, electronic and optical properties of N-unsubstituted and N-methylated 2-(2-thienyl)perimidines, supported by DFT/TDDFT calculations, has shown that these ligands are promising candidates for con...

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Autores principales: Kalle, Paulina, Kiseleva, Marina A., Tatarin, Sergei V., Smirnov, Daniil E., Zakharov, Alexander Y., Emets, Viktor V., Churakov, Andrei V., Bezzubov, Stanislav I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143831/
https://www.ncbi.nlm.nih.gov/pubmed/35630677
http://dx.doi.org/10.3390/molecules27103201
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author Kalle, Paulina
Kiseleva, Marina A.
Tatarin, Sergei V.
Smirnov, Daniil E.
Zakharov, Alexander Y.
Emets, Viktor V.
Churakov, Andrei V.
Bezzubov, Stanislav I.
author_facet Kalle, Paulina
Kiseleva, Marina A.
Tatarin, Sergei V.
Smirnov, Daniil E.
Zakharov, Alexander Y.
Emets, Viktor V.
Churakov, Andrei V.
Bezzubov, Stanislav I.
author_sort Kalle, Paulina
collection PubMed
description Though 2-arylperimidines have never been used in iridium(III) chemistry, the present study on structural, electronic and optical properties of N-unsubstituted and N-methylated 2-(2-thienyl)perimidines, supported by DFT/TDDFT calculations, has shown that these ligands are promising candidates for construction of light-harvesting iridium(III) complexes. In contrast to N-H perimidine, the N-methylated ligand gave the expected cyclometalated μ-chloro-bridged iridium(III) dimer which was readily converted to a cationic heteroleptic complex with 4,4′-dicarboxy-2,2′-bipyridine. The resulting iridium(III) dye exhibited panchromatic absorption up to 1000 nm and was tested in a dye-sensitized solar cell.
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spelling pubmed-91438312022-05-29 A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine Kalle, Paulina Kiseleva, Marina A. Tatarin, Sergei V. Smirnov, Daniil E. Zakharov, Alexander Y. Emets, Viktor V. Churakov, Andrei V. Bezzubov, Stanislav I. Molecules Article Though 2-arylperimidines have never been used in iridium(III) chemistry, the present study on structural, electronic and optical properties of N-unsubstituted and N-methylated 2-(2-thienyl)perimidines, supported by DFT/TDDFT calculations, has shown that these ligands are promising candidates for construction of light-harvesting iridium(III) complexes. In contrast to N-H perimidine, the N-methylated ligand gave the expected cyclometalated μ-chloro-bridged iridium(III) dimer which was readily converted to a cationic heteroleptic complex with 4,4′-dicarboxy-2,2′-bipyridine. The resulting iridium(III) dye exhibited panchromatic absorption up to 1000 nm and was tested in a dye-sensitized solar cell. MDPI 2022-05-17 /pmc/articles/PMC9143831/ /pubmed/35630677 http://dx.doi.org/10.3390/molecules27103201 Text en © 2022 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
Kalle, Paulina
Kiseleva, Marina A.
Tatarin, Sergei V.
Smirnov, Daniil E.
Zakharov, Alexander Y.
Emets, Viktor V.
Churakov, Andrei V.
Bezzubov, Stanislav I.
A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title_full A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title_fullStr A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title_full_unstemmed A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title_short A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine
title_sort panchromatic cyclometalated iridium dye based on 2-thienyl-perimidine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143831/
https://www.ncbi.nlm.nih.gov/pubmed/35630677
http://dx.doi.org/10.3390/molecules27103201
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