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Synthesis and Properties of Thiophene-Fused Thiopyrylium Salts

机译:噻吩稠合硫钙盐的合成与性能

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A new family of thiophene-fused thiopyrylium salts has been synthesized via Lewis-acid-induced Rieche formylation, followed by an intramolecular Friedel-Crafts cyclization of a series of diarylthioethers. Moreover, in the case of diarylthioethers that bear formyl groups, Lewis-acidpromoted intramolecular cyclizations afforded novel thiophene-fused bisthiopyrylium salts in good yield. The electronic structures of the new compounds were determined experimentally by NMR and UV-vis absorption spectroscopy and theoretically investigated by density functional theory calculations. The results of our examinations revealed effective conjugation of the pi-electrons over the entire linearly fused heteroacene framework.
机译:通过路易斯 - 酸诱导的Rieche甲型合成了一种新的噻吩稠合的硫钙盐,其次是一系列二芳基醚环化的甲酸酸诱导的Rieche型甲醛。 此外,在携带甲酰基的二芳基醚的情况下,Lewis-酸性脯氨酸的分子内的环化,得到新的噻吩稠合的体积盐,良好的产率。 通过NMR和UV-Vis吸收光谱法通过NMR和UV-Vis吸收光谱法测定新化合物的电子结构,并通过密度函数理论计算进行理论研究。 我们的考试结果揭示了在整个线性融合的异烯段框架上有效地缀合PI-电子。

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