“…39,41,61,76 These reports highlight the possibility of using CD spectroscopy both to follow the process, usually showing a decrease of the Cotton effect for the Z isomer 38,58,76 to assign the binding mode of both photoisomers, if they are used as ligands, by the pattern of the ICD signal. 38,39 Furthermore, we and others have reported that the chiral environment provided by DNA can influence the chiroptical properties of organic chromophores [77][78][79][80] as well as the stereochemical outcome of a photoisomerization reaction as shown, for instance, for DNA-binding diarylethenes. 29 The same experiment, however, cannot easily be repeated for azobenzenes, as the E isomer is achiral and the Z(P) and Z(M) enantiomers (interconverting helical conformers, Figure 8A) undergo fast isomerization (racemization) in solution 81 i.e.…”