10 Circularly Polarized Luminescence (CPL) Based on Planar …
371
Gleiter R, Hopf H (2004) Modern cyclophane chemistry. Wiley-VCH, Weinheim
Gon M, Morisaki Y, Chujo Y (2015a) Optically active cyclic compounds based on planar chiral
[2.2]paracyclophane: extension of the conjugated systems and chiroptical properties. J Mater
Chem C 3:521–529
Gon M, Morisaki Y, Chujo Y (2015) Highly emissive circularly polarized luminescence from
optically active conjugated dimers consisting of planar chiral [2.2]paracyclophane. Eur J Org
Chem 7756–7762
Gon M, Kozuka H, Morisaki Y, Chujo Y (2016a) Optically active cyclic compounds based on planar
chiral [2.2]paracyclophane: extension of the π-surface with naphthalene units. Asian J Org Chem
5:353–359
Gon M, Morisaki Y, Sawada R, Chujo (2016) Synthesis of optically active x-shaped conjugated compounds and dendrimers based on planar chiral [2.2]paracyclophane, leading to highly
emissive circularly polarized luminescence materials. Chem Eur J 22:2291–2298
Gon M, Sawada R, Morisaki Y, Chujo (2017) Enhancement and controlling the signal of circularly
polarized luminescence based on a planar chiral tetrasubstituted [2.2]paracyclophane framework
in aggregation system. Macromolecules 50:1790–1802
Gon M, Morisaki Y, Chujo (2017) optically active phenylethene dimers based on planar chiral
tetrasubstituted [2.2]paracyclophane. Chem Eur J 23:6323–6329
Guyard L, Audebert P (2001) Synthesis and electrochemical polymerization of bis-dithienyl
cyclophane. Electrochem Commun 3:164–167
Guyard L, Audebert P, Dolbier WR Jr, Duan JX (2002) Synthesis and electrochemical polymerization of new oligothiophene functionalized fluorocyclophanes. J Electroanal Chem 537:189–193
Haketa Y, Bando Y, Takaishi K, Uchiyama M, Muranaka A, Naito M, Shibaguchi H, Kawai T,
Maeda H (2012) Asymmetric induction in the preparation of helical receptor-anion complexes:
ion-pair formation with chiral cations. Angew Chem Int Ed 51:7967–7971
Hasegawa M, Kobayakawa K, Matsuzawa H, Nishinaga T, Hirose T, Sako K, Mazaki Y (2017)
Chem Eur J 23:3267–3271
Hasegawa M, Kobayakawa K, Nojima Y, Mazaki Y (2019) Org Biomol Chem 17:8822–8826
Hawker CJ, Fréchet JMJ (1990) Preparation of polymers with controlled molecular architecture. a
new convergent approach to dendritic macromolecules. J Am Chem Soc 112:7638–7647
Hitchcock PB, Rowlands GJ, Parmar R (2005) The synthesis of enantiomerically pure 4-substituted
[2.2]paracyclophane derivatives by sulfoxide–metal exchange. Chem Commun 4219–4221
Hopf H (2008) [2.2]paracyclophane in polymer chemistry and materials chemistry. Angew Chem
Int Ed 47:2–7
Ishioka S, Hasegawa M, Hara N, Sasaki H, Nojima Y, Imai Y, Mazaki Y (2019) Chiroptical properties
of oligophenylenes anchoring with stereogenic [2.2]paracyclophane 48:640–643
Jagtap SP, Collard DM (2010) Multitiered 2D π-stacked conjugated polymers based on pseudogeminal disubstituted [2.2]paracyclophane. J Am Chem Soc 132:12208–12209
Jiang B, Zhao XL (2004) A simple and efficient resolution of (±)-4,12dihydroxy[2.2]paracyclophane. Tetrahedron Asym 15:1141–1143
Jones PG, Hillmer J, Hopf H (2003) (S)-4,16-dihydroxymethyl-[2.2]paracyclophane bis-(1s)camphanoate. Acta Cryst E59:o24–o25
Kawai T, Kawamura K, Tsumatori H, Ishikawa M, Naito M, Fujiki M, Nakashima T (2007) Circularly polarized luminescence of a fluorescent chiral binaphthylene-perylenebiscarboxydiimide
dimer. Chem Phys Chem 8:1465:1468
Kikuchi K, Nakamura J, Nagata Y, Tsuchida H, Kakuta T, Ogoshi T, Morisaki Y (2019) Control
of circularly polarized luminescence by orientation of stacked π-electron systems. Chem Asian
J 14:1681–1685
Kimoto T, Tajima N, Fujiki M, Imai Y (2012) Control of circularly polarized luminescence by
using open- and closed-type binaphthyl derivatives with the same axial chirality. Chem Asian J
7:2836–2841
371
Gleiter R, Hopf H (2004) Modern cyclophane chemistry. Wiley-VCH, Weinheim
Gon M, Morisaki Y, Chujo Y (2015a) Optically active cyclic compounds based on planar chiral
[2.2]paracyclophane: extension of the conjugated systems and chiroptical properties. J Mater
Chem C 3:521–529
Gon M, Morisaki Y, Chujo Y (2015) Highly emissive circularly polarized luminescence from
optically active conjugated dimers consisting of planar chiral [2.2]paracyclophane. Eur J Org
Chem 7756–7762
Gon M, Kozuka H, Morisaki Y, Chujo Y (2016a) Optically active cyclic compounds based on planar
chiral [2.2]paracyclophane: extension of the π-surface with naphthalene units. Asian J Org Chem
5:353–359
Gon M, Morisaki Y, Sawada R, Chujo (2016) Synthesis of optically active x-shaped conjugated compounds and dendrimers based on planar chiral [2.2]paracyclophane, leading to highly
emissive circularly polarized luminescence materials. Chem Eur J 22:2291–2298
Gon M, Sawada R, Morisaki Y, Chujo (2017) Enhancement and controlling the signal of circularly
polarized luminescence based on a planar chiral tetrasubstituted [2.2]paracyclophane framework
in aggregation system. Macromolecules 50:1790–1802
Gon M, Morisaki Y, Chujo (2017) optically active phenylethene dimers based on planar chiral
tetrasubstituted [2.2]paracyclophane. Chem Eur J 23:6323–6329
Guyard L, Audebert P (2001) Synthesis and electrochemical polymerization of bis-dithienyl
cyclophane. Electrochem Commun 3:164–167
Guyard L, Audebert P, Dolbier WR Jr, Duan JX (2002) Synthesis and electrochemical polymerization of new oligothiophene functionalized fluorocyclophanes. J Electroanal Chem 537:189–193
Haketa Y, Bando Y, Takaishi K, Uchiyama M, Muranaka A, Naito M, Shibaguchi H, Kawai T,
Maeda H (2012) Asymmetric induction in the preparation of helical receptor-anion complexes:
ion-pair formation with chiral cations. Angew Chem Int Ed 51:7967–7971
Hasegawa M, Kobayakawa K, Matsuzawa H, Nishinaga T, Hirose T, Sako K, Mazaki Y (2017)
Chem Eur J 23:3267–3271
Hasegawa M, Kobayakawa K, Nojima Y, Mazaki Y (2019) Org Biomol Chem 17:8822–8826
Hawker CJ, Fréchet JMJ (1990) Preparation of polymers with controlled molecular architecture. a
new convergent approach to dendritic macromolecules. J Am Chem Soc 112:7638–7647
Hitchcock PB, Rowlands GJ, Parmar R (2005) The synthesis of enantiomerically pure 4-substituted
[2.2]paracyclophane derivatives by sulfoxide–metal exchange. Chem Commun 4219–4221
Hopf H (2008) [2.2]paracyclophane in polymer chemistry and materials chemistry. Angew Chem
Int Ed 47:2–7
Ishioka S, Hasegawa M, Hara N, Sasaki H, Nojima Y, Imai Y, Mazaki Y (2019) Chiroptical properties
of oligophenylenes anchoring with stereogenic [2.2]paracyclophane 48:640–643
Jagtap SP, Collard DM (2010) Multitiered 2D π-stacked conjugated polymers based on pseudogeminal disubstituted [2.2]paracyclophane. J Am Chem Soc 132:12208–12209
Jiang B, Zhao XL (2004) A simple and efficient resolution of (±)-4,12dihydroxy[2.2]paracyclophane. Tetrahedron Asym 15:1141–1143
Jones PG, Hillmer J, Hopf H (2003) (S)-4,16-dihydroxymethyl-[2.2]paracyclophane bis-(1s)camphanoate. Acta Cryst E59:o24–o25
Kawai T, Kawamura K, Tsumatori H, Ishikawa M, Naito M, Fujiki M, Nakashima T (2007) Circularly polarized luminescence of a fluorescent chiral binaphthylene-perylenebiscarboxydiimide
dimer. Chem Phys Chem 8:1465:1468
Kikuchi K, Nakamura J, Nagata Y, Tsuchida H, Kakuta T, Ogoshi T, Morisaki Y (2019) Control
of circularly polarized luminescence by orientation of stacked π-electron systems. Chem Asian
J 14:1681–1685
Kimoto T, Tajima N, Fujiki M, Imai Y (2012) Control of circularly polarized luminescence by
using open- and closed-type binaphthyl derivatives with the same axial chirality. Chem Asian J
7:2836–2841