Stable fluorine and chlorine decorated Thiele-like diradicaloids were synthesized and studied in solution and in thin films. Femtosecond transient absorption measurements showed, for both molecules, charge-separated states in solution, but only short-lived singlets in thin films, with no evidence of twisted or charge-separated intermediates. This suppression of excited-state dynamics reflects the strong intermolecular interactions in the solid state and limits their singlet fission potential, highlighting key design challenges for implementing diradicaloids in solid-state optoelectronic and photovoltaic devices.
From solution to thin films: unravelling excited-state behaviour in halogenated diradicaloids / Bevilacqua, M., Ciuffarin, L., Costantini, R., Schio, L., Cossaro, A., Orgiani, P., Cilento, F., Graiff, C., Tubaro, C., Baron, M., Dell'Angela, M.. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - 62:15(2026), pp. 4583-4587. [10.1039/d5cc05557a]
From solution to thin films: unravelling excited-state behaviour in halogenated diradicaloids
Ciuffarin, Luca;Costantini, Roberto;Cossaro, Albano;Cilento, Federico;Dell'Angela, Martina
2026-01-01
Abstract
Stable fluorine and chlorine decorated Thiele-like diradicaloids were synthesized and studied in solution and in thin films. Femtosecond transient absorption measurements showed, for both molecules, charge-separated states in solution, but only short-lived singlets in thin films, with no evidence of twisted or charge-separated intermediates. This suppression of excited-state dynamics reflects the strong intermolecular interactions in the solid state and limits their singlet fission potential, highlighting key design challenges for implementing diradicaloids in solid-state optoelectronic and photovoltaic devices.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


