Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules

Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shel...

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Veröffentlicht in:Synthetic metals 1997-03, Vol.85 (1), p.1651-1654
Hauptverfasser: Sedó, J., Ruiz, D., Vidal-Gancedo, J., Rovira, C., Bonvoisin, J., Launay, J.-P., Veciana, J.
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container_end_page 1654
container_issue 1
container_start_page 1651
container_title Synthetic metals
container_volume 85
creator Sedó, J.
Ruiz, D.
Vidal-Gancedo, J.
Rovira, C.
Bonvoisin, J.
Launay, J.-P.
Veciana, J.
description Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shell and anionic sites, two radical centers remain ferromagnetic ally coupled inside the molecule. The intervalence band which arises from the optical ET is clearly observed in the far NIR range and is quantitatively analyzed by means of an ad hoc model. Since these properties are rather unusual for purely organic compounds, even separately, this and similar molecules offer us a unique chance for studying the reciprocal influence between electron transfer and strong magnetic coupling in organic systems.
doi_str_mv 10.1016/S0379-6779(97)80383-9
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subjects Atomic and molecular physics
Chemical Sciences
Electrochemical methods
Electron-spin resonance
Electron-transfer
Exact sciences and technology
High-spin
Infrared spectra
Intervalence band
Molecular properties and interactions with photons
Molecular spectra
Physics
UV-Vis-NIR absorption
title Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules
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