136
M. Miyata and S. Tsuzuki
24. Tsuzuki, S., Honda, K., Uchimaru, T., Mikami, M., Tanabe, K.: Origin of attraction and directionality of the π/π interaction: model chemistry calculations of benzene dimer interaction. J.
Am. Chem. Soc. 124, 104–112 (2002)
25. Tsuzuki, S., Honda, K., Uchimaru, T., Mikami, M.: High-level ab initio computations of structures and interaction energies of naphthalene dimers: origin of attraction and its directionality.
J. Chem. Phys. 120, 647 (2004)
26. Lehn, J.M.: Supramolecular Chemistry: Concepts and Perspectives. VCH, Weinheim (1995)
27. Desiraju, G.R.: The Crystal as a Supramolecular Entity. Wiley, Chichester (1995)
28. Gardner, M.: The New Ambidextrous Universe. W. H. Freeman and Company, New York
(1999)
29. Hegstrom, R.A., Kondepudi, D.K.: Sci. Am. 262, 108 (1990)
30. Tanaka, A., Hisaki, I., Tohnai, N., Miyata, M.: Supramolecular tilt chirality derived from
symmetrical benzene molecules: handedness of the 2 1 helical assembly. Chem. Asian J. 2, 230
(2007)
31. Hisaki, I., Sasaki, T., Sakaguchi, K., Liu, W.T., Tohnai, N., Miyata, M.: Right- and lefthandedness of 2 1 symmetrical herringbone assemblies of benzene. Chem. Commun. 48, 2219
(2012)
32. Matsuura, T., Koshima, H.: J. Synth. Org. Chem. Jpn. 56, 268/466 (1998)
33. Sasaki, T., Hisaki, I., Miyano, T., Tohnai, N., Morimoto, K., Sato, H., Tsuzuki, S., Miyata,
M.: Linkage control between molecular and supramolecular chirality in 2 1 -helical hydrogenbonded networks using achiral components. Nat. Commun. 4, 1787/1–7 (2013)
34. Miyata, M.: Supramolecular chirality generated in organic crystals: stereochemical course for
conglomerates. J. Synth. Org. Chem. Jpn. 75, 503 (2017)
35. Viedma, C.: Chiral symmetry breaking during crystallization: complete chiral purity induced
by nonlinear autocatalysis and recycling. Phys. Rev. Lett. 94, 065504 (2005)
36. Sakamoto, M., Mino, T., Yoshida, Y.: Asymmetric synthesis using crystal chirality. J. Synth.
Org. Chem. Jpn. 75, 509 (2017)
37. Sasaki, T., Ida, Y., Hisaki, I., Yuge, T., Uchida, Y., Tohnai, N., Miyata, M.: Characterization of
supramolecular hidden chirality of hydrogen-bonded networks by advanced graph set analysis.
Chem. Eur. J. 20, 2478 (2014)
38. Sasaki, T., Miyata, M.: Characterization of hidden chirality: two-fold helicity in β-strands.
Symmetry (Open Access) 11, 499 (2019)
39. Cambridge Structural Database (Compound name, Identifier, Deposition Number): (Benzene,
BENZEN04, 1108753), (Naphthalene, NAPHTA15, 233928), (Anthracene, ANTCEN,
1103062), (Phenanthrene, PHENAN04, 1232369), (Pentacene, PENCEN, 1230799),
(Picene, ZZZOYC01, 1319885), (Triphenylene, TRIPHE, 1275702), (Benzo(c)phenanthrene,
BZPHAN, 1118394), (Phenanthridine, PHENAT02, 1232381), (1,5-Diiodonaphthalene,
NIFHAM, 647708)
M. Miyata and S. Tsuzuki
24. Tsuzuki, S., Honda, K., Uchimaru, T., Mikami, M., Tanabe, K.: Origin of attraction and directionality of the π/π interaction: model chemistry calculations of benzene dimer interaction. J.
Am. Chem. Soc. 124, 104–112 (2002)
25. Tsuzuki, S., Honda, K., Uchimaru, T., Mikami, M.: High-level ab initio computations of structures and interaction energies of naphthalene dimers: origin of attraction and its directionality.
J. Chem. Phys. 120, 647 (2004)
26. Lehn, J.M.: Supramolecular Chemistry: Concepts and Perspectives. VCH, Weinheim (1995)
27. Desiraju, G.R.: The Crystal as a Supramolecular Entity. Wiley, Chichester (1995)
28. Gardner, M.: The New Ambidextrous Universe. W. H. Freeman and Company, New York
(1999)
29. Hegstrom, R.A., Kondepudi, D.K.: Sci. Am. 262, 108 (1990)
30. Tanaka, A., Hisaki, I., Tohnai, N., Miyata, M.: Supramolecular tilt chirality derived from
symmetrical benzene molecules: handedness of the 2 1 helical assembly. Chem. Asian J. 2, 230
(2007)
31. Hisaki, I., Sasaki, T., Sakaguchi, K., Liu, W.T., Tohnai, N., Miyata, M.: Right- and lefthandedness of 2 1 symmetrical herringbone assemblies of benzene. Chem. Commun. 48, 2219
(2012)
32. Matsuura, T., Koshima, H.: J. Synth. Org. Chem. Jpn. 56, 268/466 (1998)
33. Sasaki, T., Hisaki, I., Miyano, T., Tohnai, N., Morimoto, K., Sato, H., Tsuzuki, S., Miyata,
M.: Linkage control between molecular and supramolecular chirality in 2 1 -helical hydrogenbonded networks using achiral components. Nat. Commun. 4, 1787/1–7 (2013)
34. Miyata, M.: Supramolecular chirality generated in organic crystals: stereochemical course for
conglomerates. J. Synth. Org. Chem. Jpn. 75, 503 (2017)
35. Viedma, C.: Chiral symmetry breaking during crystallization: complete chiral purity induced
by nonlinear autocatalysis and recycling. Phys. Rev. Lett. 94, 065504 (2005)
36. Sakamoto, M., Mino, T., Yoshida, Y.: Asymmetric synthesis using crystal chirality. J. Synth.
Org. Chem. Jpn. 75, 509 (2017)
37. Sasaki, T., Ida, Y., Hisaki, I., Yuge, T., Uchida, Y., Tohnai, N., Miyata, M.: Characterization of
supramolecular hidden chirality of hydrogen-bonded networks by advanced graph set analysis.
Chem. Eur. J. 20, 2478 (2014)
38. Sasaki, T., Miyata, M.: Characterization of hidden chirality: two-fold helicity in β-strands.
Symmetry (Open Access) 11, 499 (2019)
39. Cambridge Structural Database (Compound name, Identifier, Deposition Number): (Benzene,
BENZEN04, 1108753), (Naphthalene, NAPHTA15, 233928), (Anthracene, ANTCEN,
1103062), (Phenanthrene, PHENAN04, 1232369), (Pentacene, PENCEN, 1230799),
(Picene, ZZZOYC01, 1319885), (Triphenylene, TRIPHE, 1275702), (Benzo(c)phenanthrene,
BZPHAN, 1118394), (Phenanthridine, PHENAT02, 1232381), (1,5-Diiodonaphthalene,
NIFHAM, 647708)