Substrate Preorganization Within Photoactive Pt <sub>12</sub> L <sub>24</sub> Nanospheres for Accelerated Decarboxylation Catalysis at Low Concentrations

Photoredox catalysis with short-excited state lifetimes or in dilute conditions is challenging because the photochemical mechanism relies on collisions within the excited state of the photocatalyst. In this work, we use supramolecular substrate preorganization within Pt<sub>12</sub>L<sub>24</sub> nanospheres as strategy to perform photoredox catalysis at low concentrations. We show that Pt<sub>12</sub>L<sub>24</sub> nanospheres are efficient photocatalysts for the decarboxylative oxygenation reaction. Nanospheres with endo-functionalized guanidinium groups (Pt<sub>12</sub>LGua<sub>24</sub>) preorganize the substrate, which increases the catalytic turnover frequency by two orders of magnitude. Crucially, this preorganization ensures that Pt<sub>12</sub>LGua<sub>24</sub> retains its photocatalytic activity at extremely low concentrations (2 µM). This strategy thus overcomes the concentration limitations of photoredox catalysis and may be interesting for applications in dilute environments such as water purification and cellular photocatalysis.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-05-22
DOI
https://doi.org/10.1002/anie.202508131
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73

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article

Substrate Preorganization Within Photoactive Pt 12 L 24 Nanospheres for Accelerated Decarboxylation Catalysis at Low Concentrations

Joost N. H. Reek, Bettina Baumgartner, Rens Ham
2 citations
Angewandte Chemie International Edition
Advanced Photocatalysis Techniques
0.73
article

Substrate Preorganization Within Photoactive Pt 12 L 24 Nanospheres for Accelerated Decarboxylation Catalysis at Low Concentrations

Joost N. H. Reek, Bettina Baumgartner, Rens Ham
article en
2 citations

Abstract

Photoredox catalysis with short-excited state lifetimes or in dilute conditions is challenging because the photochemical mechanism relies on collisions within the excited state of the photocatalyst. In this work, we use supramolecular substrate preorganization within Pt<sub>12</sub>L<sub>24</sub> nanospheres as strategy to perform photoredox catalysis at low concentrations. We show that Pt<sub>12</sub>L<sub>24</sub> nanospheres are efficient photocatalysts for the decarboxylative oxygenation reaction. Nanospheres with endo-functionalized guanidinium groups (Pt<sub>12</sub>LGua<sub>24</sub>) preorganize the substrate, which increases the catalytic turnover frequency by two orders of magnitude. Crucially, this preorganization ensures that Pt<sub>12</sub>LGua<sub>24</sub> retains its photocatalytic activity at extremely low concentrations (2 µM). This strategy thus overcomes the concentration limitations of photoredox catalysis and may be interesting for applications in dilute environments such as water purification and cellular photocatalysis.

Angewandte Chemie International EditionVol. 64(31)
Centrum Wiskunde & Informatica (NL), Institute for Molecular Science (JP), Amsterdam University of Applied Sciences (NL), University of Amsterdam (NL)
Ministerie van Economische Zaken, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Ministerie van Economische Zaken en Klimaat
Clean water and sanitation
Openalex Percentile: Top 31%
Advanced Photocatalysis Techniques
0.73
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