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Thia‐bridged triarylamine hetero[4]helicenes (TBTH[4]H) are a peculiar class of geometrically stable [4]helicenes that have shown promising applications as organic electronic materials. Their structure comprises a bis‐phenothiazine moiety, with a nitrogen atom and an aromatic ring in common, forced into a helix‐shaped arrangement by four carbon–sulfur bonds. We describe a detailed study on the scope and application of the electrophilic sulfur insertion path to TBTH[4]H, with particular emphasis on the regioselective preparation of asymmetric (not dissymmetric) derivatives.

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This page is a summary of: Thia-Bridged Triarylamine Hetero[4]Helicenes: Regioselective Synthesis and Functionalization, European Journal of Organic Chemistry, November 2018, Wiley,
DOI: 10.1002/ejoc.201801493.
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