Electronic States of 2,3-Diamino-1,4-naphthoquinone and Its N-Alkylated Derivatives

Diaminoquinones with a captodatively stabilized biradicaloid structure are candidates for singlet fission, but few such compounds are known. We report the solution spectroscopy and photophysics of 1,2,2,3-tetramethyl-2,3-dihydro-1H-naphtho[2,3-d]imidazole-4,9-dione (1): its steady-state and transien...

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Veröffentlicht in:Journal of physical chemistry. C 2019-11, Vol.124 (1)
Hauptverfasser: Wen, Jin, Turowski, Michał, Dron, Paul I., Chalupský, Jakub, Grotjahn, Robin, Maier, Toni M., Fatur, Steven M., Havlas, Zdeněk, Johnson, Justin C., Kaupp, Martin, Michl, Josef
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Sprache:eng
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Zusammenfassung:Diaminoquinones with a captodatively stabilized biradicaloid structure are candidates for singlet fission, but few such compounds are known. We report the solution spectroscopy and photophysics of 1,2,2,3-tetramethyl-2,3-dihydro-1H-naphtho[2,3-d]imidazole-4,9-dione (1): its steady-state and transient UV–visible absorption, linear dichroism in stretched poly(vinyl alcohol), and magnetic circular dichroism. We also describe the absorption spectra of the stable radical ions 1•+ and 1•– and of two parent structures, 2,3-diamino-1,4-naphthoquinone (2) and 2,3-bis(methylamino)-1,4-naphthoquinone (3). The spectra are interpreted and electronic transitions are assigned by comparison with the results of density functional theory and MS-CASPT2 calculations.
ISSN:1932-7447
1932-7455