The twisted conformer of bistricyclic aromatic enes (BAEs) has a small HOMO-LUMO gap owing to the twisted double bond. In this study, we synthesized diphenoquinones fused with thiophene rings as a new twisted conformer-predominant BAE. They exhibited deep LUMO energy levels and apparent n-type semiconductor properties.
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| http://dx.doi.org/10.1039/d4cc02943g | DOI Listing |
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