Thiophene-fused aromatic belts

30 July 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Aromatic belts, ultrashort carbon nanotubes and related structures, are emerging molecular entities in the fields of organic electronics and supramolecular chemistry owing to their structural rigidity, fully fused π-conjugation, and well-defined cavity. Synthesis of aromatic belts with embedded thiophene structures, which manifest significant optoelectronic and conductive properties, has not yet been achieved. Herein, we report the synthesis of long sought-after thiophene-fused aromatic belts (thiophene belts) via one-step sulfur cross-linking reaction of partially fluorinated cycloparaphenylenes. Their unique structural features, including unidirectional columnar stacking with high dipole moment in crystals, two-dimensional layer assembly on metal surfaces, and unique photophysical properties, such as long-lifetime phosphorescence, were uncovered. These distinctive features of the thiophene belts should inspire a range of applications such as next-generation optoelectronic devices and polar materials.

Keywords

aromatic belts
fused thiophenes
cycloparaphenylenes
metal surface assembly

Supplementary materials

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