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The synthesis of [6]helicene para -quinone starting from the 1,4-dimethoxy-[6]helicene derivative is presented. The demethylation reaction with boron tribromide led to unexpected results. Instead of the expected para -hydroquinone, the diketone tautomeric form was isolated. In contrast to the 1,4-hydroquinone and 1,4-dihydroxynaphthalene, the stable tautomers for the [4] and [6]helicenes were the aromatic diketones. These experimental results were corroborated by calculations. Additional calculations showed that these tautomeric species were indeed the stable forms of 1,4 and 1,3-hydroquinones when present in larger aromatics, in drastic contrast with 1,2-dihydroxy-aromatics (known as catechol)., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The synthesis of several new compounds containing a chromophore and a helicenic moiety is reported. The preparation, characterisation and some physico-chemical studies are detailed. In particular, the two enantiomers of several chiral molecules of this type were separated by chiral HPLC (both analytically and in a preparative way) and their racemisation rates were determined for short-lived species. Electronic circular dichroism (ECD) and circular polarised luminescence (CPL) measurements were performed for the compounds with a very long racemisation half-life. Chiral porphyrins and Bodipys both gave ECD and CPL responses over a large area of the visible spectrum.

The preparation of several covalently linked [6]-helicene-porphyrins is reported. A fused [6]-helicene-porphyrin π-extended aromatic system was isolated, the enantiomers separated and the chiroptical properties determined. The oxidative cyclodehydrogenation proved to be very effective for six-membered fused helical systems, but not suited for the formation of five-membered fused systems.