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Y. Morita, S. Maki, M. Ohmoto, H. Kitagawa, T. Okubo, T. Mitani, and K. Nakasuji, Org. Lett., 4, 2185 (2002);
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Y. Morita, T. Murata, K. Fukui, S. Yamada, K. Sato, D. Shiomi, T. Takui, H. Kitagawa, H. Yamochi, G. Saito, and K. Nakasuji, J. Org. Chem., 70, 2739 (2005).
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0032234424
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Correlation between H-bonding and electronic structure is one of the focuses of proton-coupled electron transfer system, see: R. I. Cukier and D. G. Nocera, Annu. Rev. Phys. Chem., 49, 337 (1998).
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T. J. Emge, F. M. Wiygul, J. S. Chappell, A. N. Bloch, J. P. Ferraris, D. O. Cowan, and T. J. Kistenmacher, Mol. Cryst. Liq. Cryst., 87, 137 (1982).
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T. Senga, K. Kamoshida, L. A. Kushch, G. Saito, T. Inayoshi, and I. Ono, Mol. Cryst. Liq. Cryst., 296, 97 (1997);
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18
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33750630594
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in press
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Crystal structure of DADBTTF, see: Y. Morita, E. Miyazaki, K. Fukui, S. Maki, and K. Nakasuji, Synth. Met., in press.
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Synth. Met.
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Morita, Y.1
Miyazaki, E.2
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37049111359
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J. Nakayama, E. Seki, and M. Hoshino, J. Chem. Soc., Perkin Trans. 1, 1978, 468.
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J. Chem. Soc., Perkin Trans. 1
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20
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37049111359
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1H NMR measurement did not provide the experimental information on this point, see: J. Nakayama, E. Seki, and M. Hoshino, J. Chem. Soc., Perkin Trans. 1, 1978, 468.Ref. 11
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J. Chem. Soc., Perkin Trans. 1
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Nakayama, J.1
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33845282499
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and A. Souizi, A. Robert, P. Batail, and L. Ouahab, J. Org. Chem., 52, 1610 (1987).
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Souizi, A.1
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23
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0004018410
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Wiley-WCH, Weinheim
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The reported dielectric constants of THF, MeOH, and DMSO are 7.58, 32.66, and 46.45, respectively, see: C. Reichardt, "Solvents and Solvent Effects in Organic Chemistry," Wiley-WCH, Weinheim (2003);
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Solvents and Solvent Effects in Organic Chemistry
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Reichardt, C.1
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0007895569
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S. Sakura, H. Imai, H. Anzai, and T. Moriya, Bull. Chem. Soc. Jpn., 61, 3181 (1988);
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K. Hinkelmann, K. K. Liou, and F. Wudl, J. Chem. Soc., Chem. Commun., 1989, 1744.
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J. Chem. Soc., Chem. Commun.
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Hinkelmann, K.1
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26
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33750606249
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note
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Amino groups of DADBTTF were disordered by 20% in the crystal, see: X-ray Crystallography section in Experimental.
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28
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0001294785
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T. J. Kistenmacher, T. J. Emge, A. N. Bloch, and D. O. Cowan, Acta Crystallogr., Sect. B, 38, 1193 (1982).
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Acta Crystallogr., Sect. B
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Kistenmacher, T.J.1
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21544435239
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J. S. Chappell, A. N. Bloch, W. A. Bryden, M. Maxfield, T. O. Pochler, and D. O. Cowan, J. Am. Chem. Soc., 103, 2442 (1981).
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Chappell, J.S.1
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Cowan, D.O.6
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30
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33750629976
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note
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DBTTF-F2TCNQ CT complex gives an exceptional example, see: Ref. 8.
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-
-
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31
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0035867822
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2TCNQ, was reported, see: G. Saito, S. S. Pac, and O. O. Drozdova, Synth. Met., 120, 667 (2001).
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Synth. Met.
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Saito, G.1
Pac, S.S.2
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32
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0002346789
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A few exceptional cases are also known in H-bonded CT complex of 1,6-diaminopyrene. For example, 1,6-diaminopyrene CT complex with chloranil exhibited high electric conductivity despite alternated stacking structure, see: H. Goto, T. Fujinawa, H. Asahi, T. Inabe, H. Ogata, S. Miyajima, and Y. Maruya, Bull. Chem. Soc. Jpn., 69, 85 (1996).
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Goto, H.1
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Inabe, T.4
Ogata, H.5
Miyajima, S.6
Maruya, Y.7
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33
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33750633215
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note
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3CN in solution.
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