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In comparison to the strong influence of the solvent polarity on λ, we assume ΔG° to be only weakly affected by the solvent, and therefore, ΔG° is kept constant for the calculation of the potential surfaces in Figure 4.
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Interactions between the ground states that result in an energy lowering are neglected as they are supposed to be small.
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Equation 14 of this paper was corrected by us
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84
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33645512658
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note
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m1,m2 and the transition moments are similar (see eq 2).
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87
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33645523466
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note
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bridge states.
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88
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33645512467
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note
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23 may involve greater errors.
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90
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33645499710
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note
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This would be more obvious if the indices 1 and 2 of the matrix elements were exchanged.
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