Abate PO, Cotic A, Cabrosi D, Baraldo LM, Cadranel A (2025)
Publication Type: Journal article
Publication year: 2025
Book Volume: 64
Pages Range: 21569-21580
Journal Issue: 43
DOI: 10.1021/acs.inorgchem.5c03575
With the aim of studying interligand electron transfer (ILET) with different driving forces, [Ru(tpy)(R-bpy)(CN)]+complexes with R-bpy = 4,4′-dimethylamino-2,2′-bipyridine (dMAb), 4,4′-dimethoxy-2,2′-bipyridine (dMeOb), 2,2′-bipyridine (bpy) or 4,4′-diethylester-2,2′-bipyridine (deeb) were synthesized and fully characterized using an arsenal of diffraction, electrochemical and spectroscopic techniques together with DFT/TD-DFT calculations. All the compounds studied here undergo ultrafast ILET in the picosecond or subpicosecond time scale, irrespective of the driving force or directionality of ILET, showing a typical Kasha behavior that dissipates energy before any potential bimolecular reactivity. This precludes the utilization of high-energy excited states, involving a non-LUMO excited electron, in solar-energy conversion strategies requiring diffusion-controlled reactivity.
APA:
Abate, P.O., Cotic, A., Cabrosi, D., Baraldo, L.M., & Cadranel, A. (2025). Ultrafast Dissipation via Interligand Electron Transfer in {Ru(tpy)(bpy)} Chromophores. Inorganic Chemistry, 64(43), 21569-21580. https://doi.org/10.1021/acs.inorgchem.5c03575
MLA:
Abate, Pedro O., et al. "Ultrafast Dissipation via Interligand Electron Transfer in {Ru(tpy)(bpy)} Chromophores." Inorganic Chemistry 64.43 (2025): 21569-21580.
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