372
Y. Morisaki
Kobayakawa K, Hasegawa M, Sasaki H, Endo J, Matsuzawa H, Sako K, Yoshida J, Mazaki Y (2014)
Dimeric tetrathiafulvalene linked to pseudo-ortho-[2.2]paracyclophane: chiral electrochromic
properties and use as a chiral dopant. Chem Asian J 9:2751–2754
Lunkley JL, Shirotani D, Yamanari K, Kaizaki S, Muller G (2008) Extraordinary circularly polarized luminescence activity exhibited by cesium tetrakis(3-heptafluoro-butylryl-(+)-camphorato)
Eu(III) complexes in EtOH and CHCl 3 Solutions. J Am Chem Soc 130:13814–13815
Maeda H, Bando Y (2013) Recent progress in research on stimuli-responsive circularly polarized
luminescence based on π-conjugated molecules. Pure Appl Chem 85:1967–1978
Meyer-Eppler G, Vogelsang E, Benkhäuser C, Schneider A, Schnakenburg G, Lützen A (2013)
Synthesis, chiral resolution, and absolute configuration of dissymmetric 4,12-difunctionalized
[2.2]paracyclophane. Eur J Org Chem 4523–4532
Meyer-Eppler G, Sure R, Schneider A, Schnakenburg G, Grimme S, Lützen A (2014) Synthesis,
chiral resolution, and absolute configuration of dissymmetric 4,15-difunctionalized [2.2]paracyclophanes. J Org Chem 79:6679–6687
Miyaura N, Yamada K, Suzuki A (1979) A new stereospecific cross-coupling by the palladiumcatalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett
20:3437–3440
Mizogami S, Yoshimura S (1985) Synthesis of a new crystalline polymer: polymetacyclophane. J
Chem Soc Chem Commun 1736–1738
Molina-Ontoria A, Wielopolski M, Gebhardt J, Gouloumis A, Clark T, Guldi DM, Martín N (2011)
[2,2’]paracyclophane-based π-conjugated molecular wires reveal molecular-junction behavior. J
Am Chem Soc 133:2370–2373
Morisaki Y, Chujo Y (2002) Synthesis of novel π-conjugated polymers having [2.2]paracyclophane skeleton in the main chain. extension of π-conjugated length via the through-space.
Macromolecules 35:587–589
Morisaki Y, Chujo Y (2006) Through-space conjugated polymers based on cyclophanes. Angew
Chem Int Ed 45:6430–6437
Morisaki Y, Chujo Y (2008) cyclophane-containing polymers. Prog Polym Sci 33:346–364
Morisaki Y, Chujo Y (2009) synthesis of π-stacked polymers on the basis of [2.2]paracyclophane.
Bull Chem Soc Jpn 82:1070–1082
Morisaki Y, Chujo Y (2011) Through-space conjugated polymers consisting of [2.2]paracyclophane.
Polym Chem 2:1249–1257
Morisaki Y, Chujo Y (2012) π-electron-system-layered polymers based on [2.2]paracyclophane.
Chem Lett 41:840–846
Morisaki Y, Chujo Y (2019) Planar chiral [2.2]paracyclophanes: optical resolution and transformation to optically active π-stacked molecules. Bull Chem Soc Jpn 92:265–274
Morisaki Y, Hifumi R, Lin L, Inoshita K, Chujo Y (2012a) T practical optical resolution of planar
chiral pseudo-ortho-disubstituted [2.2]paracyclophane. Chem Lett 41:990–992
Morisaki Y, Hifumi R, Lin L, Inoshita K, Chujo Y (2012b) Through-space conjugated polymers
consisting of planar chiral pseudo-ortho-linked [2.2]paracyclophane. Polym Chem 3:2727–2730
Morisaki Y, Kawakami N, Nakano T, Chujo Y (2013) Energy transfer properties of a
[2.2]paracyclophane-based through-space dimer. Chem Eur J 19:17715–17718
Morisaki Y, Kawakami N, Shibata S, Chujo Y (2014a) Through-space conjugated molecular wire
consisting of three π-electron systems. Chem Asian J 9:2891–2895
Morisaki Y, Kawakami N, Shibata S, Chujo Y (2014b) Synthesis and properties of a through-space
conjugated dimer. Chem Lett 43:426–428
Morisaki Y, Inoshita K, Chujo Y (2014c) Planar chiral through-space conjugated oligomers:
synthesis and characterization of chiroptical properties. Chem Eur J 20:8386–8390
Morisaki Y, Gon M, Sasamori T, Tokitoh N, Chujo Y (2014d) Planar chiral tetrasubstituted
[2.2]paracyclophane: optical resolution and functionalization. J Am Chem Soc 136:3350–3353
Morisaki Y, Inoshita K, Shibata S, Chujo Y (2015) Synthesis of optically active through-space
conjugated polymers consisting of planar chiral [2.2]paracyclophane and quaterthiophene. Polym
J 47:278–281
Y. Morisaki
Kobayakawa K, Hasegawa M, Sasaki H, Endo J, Matsuzawa H, Sako K, Yoshida J, Mazaki Y (2014)
Dimeric tetrathiafulvalene linked to pseudo-ortho-[2.2]paracyclophane: chiral electrochromic
properties and use as a chiral dopant. Chem Asian J 9:2751–2754
Lunkley JL, Shirotani D, Yamanari K, Kaizaki S, Muller G (2008) Extraordinary circularly polarized luminescence activity exhibited by cesium tetrakis(3-heptafluoro-butylryl-(+)-camphorato)
Eu(III) complexes in EtOH and CHCl 3 Solutions. J Am Chem Soc 130:13814–13815
Maeda H, Bando Y (2013) Recent progress in research on stimuli-responsive circularly polarized
luminescence based on π-conjugated molecules. Pure Appl Chem 85:1967–1978
Meyer-Eppler G, Vogelsang E, Benkhäuser C, Schneider A, Schnakenburg G, Lützen A (2013)
Synthesis, chiral resolution, and absolute configuration of dissymmetric 4,12-difunctionalized
[2.2]paracyclophane. Eur J Org Chem 4523–4532
Meyer-Eppler G, Sure R, Schneider A, Schnakenburg G, Grimme S, Lützen A (2014) Synthesis,
chiral resolution, and absolute configuration of dissymmetric 4,15-difunctionalized [2.2]paracyclophanes. J Org Chem 79:6679–6687
Miyaura N, Yamada K, Suzuki A (1979) A new stereospecific cross-coupling by the palladiumcatalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett
20:3437–3440
Mizogami S, Yoshimura S (1985) Synthesis of a new crystalline polymer: polymetacyclophane. J
Chem Soc Chem Commun 1736–1738
Molina-Ontoria A, Wielopolski M, Gebhardt J, Gouloumis A, Clark T, Guldi DM, Martín N (2011)
[2,2’]paracyclophane-based π-conjugated molecular wires reveal molecular-junction behavior. J
Am Chem Soc 133:2370–2373
Morisaki Y, Chujo Y (2002) Synthesis of novel π-conjugated polymers having [2.2]paracyclophane skeleton in the main chain. extension of π-conjugated length via the through-space.
Macromolecules 35:587–589
Morisaki Y, Chujo Y (2006) Through-space conjugated polymers based on cyclophanes. Angew
Chem Int Ed 45:6430–6437
Morisaki Y, Chujo Y (2008) cyclophane-containing polymers. Prog Polym Sci 33:346–364
Morisaki Y, Chujo Y (2009) synthesis of π-stacked polymers on the basis of [2.2]paracyclophane.
Bull Chem Soc Jpn 82:1070–1082
Morisaki Y, Chujo Y (2011) Through-space conjugated polymers consisting of [2.2]paracyclophane.
Polym Chem 2:1249–1257
Morisaki Y, Chujo Y (2012) π-electron-system-layered polymers based on [2.2]paracyclophane.
Chem Lett 41:840–846
Morisaki Y, Chujo Y (2019) Planar chiral [2.2]paracyclophanes: optical resolution and transformation to optically active π-stacked molecules. Bull Chem Soc Jpn 92:265–274
Morisaki Y, Hifumi R, Lin L, Inoshita K, Chujo Y (2012a) T practical optical resolution of planar
chiral pseudo-ortho-disubstituted [2.2]paracyclophane. Chem Lett 41:990–992
Morisaki Y, Hifumi R, Lin L, Inoshita K, Chujo Y (2012b) Through-space conjugated polymers
consisting of planar chiral pseudo-ortho-linked [2.2]paracyclophane. Polym Chem 3:2727–2730
Morisaki Y, Kawakami N, Nakano T, Chujo Y (2013) Energy transfer properties of a
[2.2]paracyclophane-based through-space dimer. Chem Eur J 19:17715–17718
Morisaki Y, Kawakami N, Shibata S, Chujo Y (2014a) Through-space conjugated molecular wire
consisting of three π-electron systems. Chem Asian J 9:2891–2895
Morisaki Y, Kawakami N, Shibata S, Chujo Y (2014b) Synthesis and properties of a through-space
conjugated dimer. Chem Lett 43:426–428
Morisaki Y, Inoshita K, Chujo Y (2014c) Planar chiral through-space conjugated oligomers:
synthesis and characterization of chiroptical properties. Chem Eur J 20:8386–8390
Morisaki Y, Gon M, Sasamori T, Tokitoh N, Chujo Y (2014d) Planar chiral tetrasubstituted
[2.2]paracyclophane: optical resolution and functionalization. J Am Chem Soc 136:3350–3353
Morisaki Y, Inoshita K, Shibata S, Chujo Y (2015) Synthesis of optically active through-space
conjugated polymers consisting of planar chiral [2.2]paracyclophane and quaterthiophene. Polym
J 47:278–281