We present the synthesis and characterization of enantiomerically pure [6]helicene o-quinones (P)-(+)-1 and (M)-(-)-1 and their application to chiroptical switching and chiral recognition. (P)-(+)-1 and (M)-(-)-1 each show a reversible one-electron reduction process in their cyclic voltammogram, which leads to the formation of the semiquinone radical anions (P)-(+)-1(•-) and (M)-(-)-1(•-), respectively. Spectroelectrochemical ECD measurements give evidence of the reversible switching between the two redox states, which is associated with large differences of the Cotton effects [Δ(Δε)] in the UV and visible regions. The reduction of (±)-1 by lithium metal provides [Li(+){(±)-1(•-)}], which was studied by EPR and ENDOR spectroscopy to reveal substantial delocalization of the spin density over the helicene backbone. DFT calculations demonstrate that the lithium hyperfine coupling A((7)Li) in [Li(+){(±)-1(•-)}] is very sensitive to the position of the lithium cation. On the basis of this observation, chiral recognition by ENDOR spectroscopy was achieved by complexation of [Li(+){(P)-(+)-1(•-)}] and [Li(+){(M)-(-)-1(•-)}] with an enantiomerically pure phosphine oxide ligand.

The synthesis of redox-active p- and o-quinones 2-phenylamino-4-phenylimino[6]helicene-1-one 1, 2-phenylamino[6]-helicene-1,4-dione 2, and 4-phenyl[6]helicene-1,2-dione 3 in their enantiopure forms by post-functionalization of (P)- and (M)-1,2-dimethoxy[6]helicene is presented. Structural characterization in solution and in the solid state was accomplished by 2D NMR spectroscopy methods and X-ray diffraction analysis, respectively. Interpretation of electrochemical redox data was accompanied by a detailed orbital picture, derived from DFT calculations. The electronic structures of compounds 1-3 were investigated by UV/Vis and electronic circular dichroism (ECD) spectroscopy, complemented by TD-DFT calculations. Quinones 1-3 were chemically reduced to study the EPR signatures of their respective radical anions. DFT methods were used for the atom assignment of the hyperfine coupling constants. The results are discussed within the context of electrochromic chiral switches and molecular recognition.

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