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A tetracyano quinoidal tetrathiophene, having a central bi(thieno[3,4‐c]pyrrole‐4,6‐dione) acceptor, has been studied. The recovered aromaticity of the thiophenes produces a diradical species with cross‐conjugation between the inter‐dicyano and inter‐dione acceptor paths. A diradical character of y0=0.61 and a singlet–triplet gap of −2.76 kcal mol−1 were determined. Competition between the two cross‐conjugated...
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