The temperature dependence of the relaxation dynamics of a dinuclear cobalt-tetraoxolene complex undergoing photoinduced valence tautomerism is reported and discussed. Two different regimes were detected, one at low (5-20 K) and a second at higher temperatures (20-35 K). The activation energy for the low temperature regime suggests a tunnelling process assisted by lattice phonons. In the thermally activated region the activation energy is far from that expected for the total-symmetric Co-O breathing mode, thus suggesting an important role for other internal vibrational modes.

Relaxation dynamics of a photoinduced di-cobalt-tetraoxolene valence tautomer

Sangregorio C;
2007

Abstract

The temperature dependence of the relaxation dynamics of a dinuclear cobalt-tetraoxolene complex undergoing photoinduced valence tautomerism is reported and discussed. Two different regimes were detected, one at low (5-20 K) and a second at higher temperatures (20-35 K). The activation energy for the low temperature regime suggests a tunnelling process assisted by lattice phonons. In the thermally activated region the activation energy is far from that expected for the total-symmetric Co-O breathing mode, thus suggesting an important role for other internal vibrational modes.
2007
valence tautomerism; redox isomerism; photochromism; photomagnetism; semiquinone; radical ligand
INTRAMOLECULAR ELECTRON-TRANSFER; TRANSITION-METAL-COMPLEXES; O-QUINONE COMPLEXES; SPIN-CROSSOVER; DIOXOLENE ADDUCT; MAGNETIZATION; INTERCONVERSION; TEMPERATURE; LIGANDS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/131038
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