Fig. 2 | Nature Communications

Fig. 2

From: Energetics of Baird aromaticity supported by inversion of photoexcited chiral [4n]annulene derivatives

Fig. 2

Optical features of Th4 COT Saddle and Th6 CDH Screw . a, b, Schematic structures of the enantiomers of Th4 COT Saddle (a) and Th6 CDH Screw (b). c, d, Electronic absorption spectra of Th4 COT Saddle (c) and Th6 CDH Screw (d) in methylcyclohexane at 25 °C. Orange- and green-colored vertical lines correspond to the wavelengths of λ = 365 and 420 nm, which were utilized for direct and sensitized photoexcitation of the molecules, respectively. e, f, Circular dichroism (CD) spectra of Th4 COT Saddle (e) and Th6 CDH Screw (f) in methylcyclohexane at 25 and –20 °C, respectively. Blue- and red-colored traces represent the spectra of compounds obtained as the first and second fractions of the chiral HPLC, respectively

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