Paulina H. Marek‐Urban
Bis[1]benzothieno[1,4]thiaborins as a Platform for BODIPY Singlet Oxygen Photosensitizers
Marek‐Urban, Paulina H.; Urbanowicz, Karolina A.; Wrochna, Karolina; Pander, Piotr; Blacha‐Grzechnik, Agata; Hauer, Simone T.; Berens, Henning R. V.; Woźniak, Krzysztof; Müller, Thomas J. J.; Durka, Krzysztof
Authors
Karolina A. Urbanowicz
Karolina Wrochna
Piotr Pander piotr.h.pander@durham.ac.uk
Academic Visitor
Agata Blacha‐Grzechnik
Simone T. Hauer
Henning R. V. Berens
Krzysztof Woźniak
Thomas J. J. Müller
Krzysztof Durka
Abstract
A synthetic approach to two regioisomeric π-electron extended [1,4]thiaborins annulated with two benzothiophene units has been developed. The central thiaborin rings of the boracycles obtained exhibit different electronic properties; this is reflected in their different aromatic characters, boron Lewis acidity and UV-vis spectroscopic behavior. Thiaborins were converted to boron dipyrromethene (BODIPY) complexes. Their emission spectra exhibit two distinct bands resulting from 1LE and 1CT transitions. Strong near-infrared phosphorescence in Zeonex thin films at 77 K indicates efficient intersystem crossing and the formation of triplet states. Separation of HOMO and LUMO orbitals between boracyclic and BODIPY moieties facilitates electron transfer to a 1CT state followed by a transition to the 3LE triplet state located on the ligand. These unique properties of spiro thiaborin-BODIPY complexes were explored for their application as singlet-oxygen photosensitizers. They show excellent photocatalytic performance with singlet oxygen quantum yields reaching 77 % and full conversion of the model organic substrate achieved after 1.5 h with only 0.05 % mol catalyst load.
Citation
Marek‐Urban, P. H., Urbanowicz, K. A., Wrochna, K., Pander, P., Blacha‐Grzechnik, A., Hauer, S. T., …Durka, K. (2023). Bis[1]benzothieno[1,4]thiaborins as a Platform for BODIPY Singlet Oxygen Photosensitizers. Chemistry - A European Journal, 29(36), Article e202300680. https://doi.org/10.1002/chem.202300680
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 28, 2023 |
Online Publication Date | Mar 29, 2023 |
Publication Date | Jun 27, 2023 |
Deposit Date | Oct 10, 2023 |
Publicly Available Date | Mar 30, 2024 |
Journal | Chemistry – A European Journal |
Print ISSN | 0947-6539 |
Electronic ISSN | 1521-3765 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 29 |
Issue | 36 |
Article Number | e202300680 |
DOI | https://doi.org/10.1002/chem.202300680 |
Public URL | https://durham-repository.worktribe.com/output/1788644 |
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Copyright Statement
This is the peer reviewed version of the following article: Marek‐Urban, P. H., Urbanowicz, K. A., Wrochna, K., Pander, P., Blacha‐Grzechnik, A., Hauer, S. T., …Durka, K. (2023). Bis[1]benzothieno[1,4]thiaborins as a Platform for BODIPY Singlet Oxygen Photosensitizers. Chemistry - A European Journal, 29(36), Article e202300680, which has been published in final form at https://doi.org/10.1002/chem.202300680. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
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