DOI: 10.1021/acs.joc.6c01417 ISSN: 0022-3263

Electronic Control of Scholl Cyclization Trajectories Enables Direct Access to Trihetero-Quasi[8]circulenes

Raseswari Dash, Parthasarathy Venkatakrishnan

Abstract

Quasi[8]circulenes remain challenging to access directly from polyaryl precursors because competing Scholl-type cyclization pathways obscure control over the annulation sequence. Here, we demonstrate that (hetero)aryl electronic programming directs oxidative cyclodehydrogenation to selectively generate S–, O–, and N-embedded quasi[8]circulenes from tailored tetrarylthiophenes. The resulting twisted π-architecture possesses induced paratropic COT cores, tunable optoelectronic properties, and persistent π-delocalized radical cations with near-infrared (NIR) absorption. Beyond hetero-quasi[8]circulenes, this work establishes electronic programming as a design principle for controlling complexity in oxidative π-framework construction.

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