Complexation behaviour of a CT complex composed of 9,10-bis(3,5-dihydroxyphenyl)anthracene and viologen derivatives |
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Authors: | Takafumi Kinuta Kensaku Kamon Nobuo Tajima Tomohiro Sato Reiko Kuroda |
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Institution: | 1. Department of Applied Chemistry, Faculty of Science and Engineering , Kinki University , 3-4-1 Kowakae, Higashi-Osaka, Osaka, 577-8502, Japan;2. First-Principles Simulation Group, Computational Materials Science Center , NIMS , Sengen, Tsukuba, Ibaraki, 305-0047, Japan;3. JST ERATO-SORST Kuroda Chiromorphology Team , 4-7-6, Komaba, Meguro-ku, Tokyo, 153-0041, Japan;4. JST ERATO-SORST Kuroda Chiromorphology Team , 4-7-6, Komaba, Meguro-ku, Tokyo, 153-0041, Japan;5. Department of Life Sciences, Graduate School of Arts and Sciences , The University of Tokyo , 3-8-1 Komaba, Meguro-ku, Tokyo, 153-8902, Japan |
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Abstract: | A chiral charge-transfer (CT) complex was formed using achiral 9,10-bis(3,5-dihydroxyphenyl)anthracene (BDHA) as an electron donor and achiral 1,1′-dimethyl-4,4′-bipyridinium dichloride (MVCl2) as an electron acceptor. This chiral CT complex can include n-alkyl alcohol molecules as guests. On the other hand, when 1,1′-diphenyl-4,4′-bipyridinium dichloride and 1,1′-dibenzyl-4,4′-bipyridinium dichloride were used as electron acceptors, achiral CT complexes without guests were formed. It was found that the chiral crystallisation of the BDHA/MVCl2–CT host system was caused by steric and electric intermolecular interactions between host component molecules BDHA and MVCl2 during crystallisation. |
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Keywords: | 9 10-bis(3 5-dihydroxyphenyl)anthracene charge-transfer complex chiral spontaneous resolution viologen |
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