The different nature of the main excitations that contribute to the UV/Vis spectra in AQS and its derivatives, with differing charge-transfer contributions (see ESI 4, Table S1, 2 † ), mean that there is quite significant variation in peak energies between results for different functionals.
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Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple.
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