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Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin.

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The incorporation of an azulene bridge into an aromatic hexaphyrin framework allows manipulating π-electron delocalization pathways. The palladium(ii) complex undergoes hydroxyl-triggered azulene contraction or isomerization to an oxynaphthalene unit, transforming… Click to show full abstract

The incorporation of an azulene bridge into an aromatic hexaphyrin framework allows manipulating π-electron delocalization pathways. The palladium(ii) complex undergoes hydroxyl-triggered azulene contraction or isomerization to an oxynaphthalene unit, transforming the hexaphyrin framework into meso-linked carbaporphyrins. This converts the 26π-electron pathway into the 18π one.

Keywords: transformations azulene; via azulene; switching via; azulene transformations; azulene bridged; aromaticity switching

Journal Title: Chemical communications
Year Published: 2018

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