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Efficient Synthesis,Structure, and Complexation Studies of Electron‐Donating Thiacalix[n]dithienothiophene
Authors:Ryota Inoue  Dr Masashi Hasegawa  Prof Tohru Nishinaga  Dr Kenji Yoza  Prof Yasuhiro Mazaki
Institution:1. Department of Chemistry, School of Science, Kitasato University, Sagamihara, Kanagawa 252‐0373 (Japan) http://www.kitasato‐u.ac.jp/sci/resea/kagaku/HP_kinou/Index.html;2. Department of Chemistry, Graduate School of Science and Engineering, Tokyo Metropolitan University, Hachioji, Tokyo 192‐0397 (Japan);3. Bruker AXS, Yokohama, Kanagawa 221‐0022 (Japan)
Abstract:A series of thiacalixn]dithiothiophenes (n=4–10) was prepared by a facile method and X‐ray analysis was used to determine the molecular structures of square‐ (4‐mer) and pentagonal‐shaped macrocycles (5‐mer). In the cyclic voltammograms, reversible multielectron redox processes, which are due to electronic delocalization, were observed at low oxidation potentials. The cyclic 4‐mer acted as a “Janus‐head” cavitand for two C60 molecules, whereas the 5‐ and 6‐mer formed stable 1:1 complexes with C60 .
Keywords:cross‐coupling  electrochemistry  macrocycles  sulfur heterocycles  supramolecular chemistry
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