Nature of Anti‐Dissipative High‐Energy Excited States in Quaterpyridine‐Bridged Ruthenium Complexes

High-energy excited states with slow rates for internal conversion to the lowest-energy excited state are prone to be intercepted before they dissipate energy to the medium. In a previous report, oligomeric Ru(II) photosensitizers bearing a bridging 2,2':5',3″:6″,2<sup>‴</sup>-quaterpyridine scaffold showed promising anti-dissipative behavior in photoinduced electron transfer reactivity. In here, a range of electron accepting and electron donating substituents were incorporated on the ancillary 2,2'-bipyridine ligands to modulate the excited-state dynamics. This allowed to unambiguously identify the nature of high-energy excited states and derive design guidelines for the achievement of anti-dissipative behavior in oligomeric Ru(II) polypyridines relevant for solar fuels production and photoredox catalysis.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-06-16
DOI
https://doi.org/10.1002/anie.202507738
Citations
7
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
Field-Weighted Citation Impact
3.62

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article

Nature of Anti‐Dissipative High‐Energy Excited States in Quaterpyridine‐Bridged Ruthenium Complexes

Ludovic Troian‐Gautier, Agustina Cotic, Simon De Kreijger, Alejandro Cadranel et al.
7 citations
Angewandte Chemie International Edition
Lanthanide and Transition Metal Complexes
3.62
article

Nature of Anti‐Dissipative High‐Energy Excited States in Quaterpyridine‐Bridged Ruthenium Complexes

Ludovic Troian‐Gautier, Agustina Cotic, Simon De Kreijger, Alejandro Cadranel, Benjamin Elias, Noémie Chantry, Ю.Р. Селюминова
article en
7 citations

Abstract

High-energy excited states with slow rates for internal conversion to the lowest-energy excited state are prone to be intercepted before they dissipate energy to the medium. In a previous report, oligomeric Ru(II) photosensitizers bearing a bridging 2,2':5',3″:6″,2<sup>‴</sup>-quaterpyridine scaffold showed promising anti-dissipative behavior in photoinduced electron transfer reactivity. In here, a range of electron accepting and electron donating substituents were incorporated on the ancillary 2,2'-bipyridine ligands to modulate the excited-state dynamics. This allowed to unambiguously identify the nature of high-energy excited states and derive design guidelines for the achievement of anti-dissipative behavior in oligomeric Ru(II) polypyridines relevant for solar fuels production and photoredox catalysis.

Angewandte Chemie International EditionVol. 64(33)
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Universidad de Buenos Aires (AR), International Council on Mining and Metals (GB), Walloon Excellence in Lifesciences and Biotechnology (BE), Instituto de Química y Fisicoquímica Biológicas (AR), Fundación Ciencias Exactas y Naturales (AR), UCLouvain (BE)
Université Catholique de Louvain, Deutsche Forschungsgemeinschaft, Fonds De La Recherche Scientifique - FNRS, Consejo Nacional de Investigaciones Científicas y Técnicas, Fonds pour la Formation à la Recherche dans l’Industrie et dans l’Agriculture
Affordable and clean energy
Openalex Percentile: Top 7%
Lanthanide and Transition Metal Complexes
3.62
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Nature of Anti‐Dissipative High‐Energy Excited States in Quaterpyridine‐Bridged Ruthenium Complexes — Ludovic Troian‐Gautier, Agustina Cotic, et al. · Angewandte Chemie International Edition (2025) | TGRS Research Map | TGRS