2022
DOI: 10.1039/d2ob00800a
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Synthesis and crystal structures of unsymmetrical wave-shaped heptathienoacenes

Abstract: Three unsymmetrical wave-shaped heptathienoacenes (UHT-1, UHT-2 and UHT-3) with different isomeric locations of sulfur atoms in the two terminal thiophene rings were designed and synthesized. The synthetic strategy contains two...

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“…Another one is the high challenge of synthetic work. 10−13 Until now, a few HTs including linear, 10,11b bullhorn-shaped, 4b,11 helical, 4c,12 and wave-shaped 13 Herein, we report a novel synthetic strategy for the construction of a new family of HTs, the dragon-boat-type heptathienoacenes (DBHTs). The key synthetic step is the C− C cross-coupling between two DTTs occurring on their αand β-positions, which generates the unsymmetrical dimers of DTT (biDTT, Figure 2).…”
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confidence: 99%
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“…Another one is the high challenge of synthetic work. 10−13 Until now, a few HTs including linear, 10,11b bullhorn-shaped, 4b,11 helical, 4c,12 and wave-shaped 13 Herein, we report a novel synthetic strategy for the construction of a new family of HTs, the dragon-boat-type heptathienoacenes (DBHTs). The key synthetic step is the C− C cross-coupling between two DTTs occurring on their αand β-positions, which generates the unsymmetrical dimers of DTT (biDTT, Figure 2).…”
mentioning
confidence: 99%
“…There are two main factors to limit OFET work of HT s. One is the unobtrusive OFET performance from the limited examples of PTA and HTA ; the relative structure–property relationship is not clear. Another one is the high challenge of synthetic work. Until now, a few HT s including linear, , bull-horn-shaped, , helical, , and wave-shaped molecular skeletons (Figure ) have been constructed by the C–C bond coupling between the α–α or β–β positions of two DTT s and subsequent cyclization.…”
mentioning
confidence: 99%