374
Y. Morisaki
Sawada R, Gon M, Nakamura J, Morisaki Y, Chujo Y (2018) Synthesis of enantiopure planar chiral
bis-(para)-pseudo-meta-type [2.2]paracyclophanes. Chirality 30:1109–1114
Sheng Y, Ma J, Liu S, Wang Y, Zhu C, Cheng Y (2016) Strong and reversible circularly polarized
luminescence emission of a chiral 1,8-naphthalimide fluorophore induced by excimer emission
and orderly aggregation. Chem Eur J 22:9519–9522
Sonogashira K (2002) In: Negishi E (ed) Handbook of organopalladium chemistry for organic
synthesis. Wiley-Interscience, New York, pp 493–529
Takaishi K, Yamamoto S, Hinoide S, Ema T (2017) Helical oligonaphthodioxepins showing intense
Circularly Polarized Luminescence (CPL) in solution and in the solid state. Chem Eur J 23:9249–
9252
Tanaka H, Inoue Y, Mori T (2018) Circularly polarized luminescence and circular dichroisms
in small organic molecules: correlation between excitation and emission dissymmetry factors.
ChemPhotoChem 2:386–402
Tohda Y, Sonogashira K, Hagihara N (1975) A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines. Tetrahedron
Lett 16:4467–4470
Vögtle F (1993) cyclophane chemistry: synthesis, structures and reactions. John Wiley & Sons,
Chichester
Vorontsova NV, Rozenberg VI, Sergeeva EV, Vorontsov EV, Starikova ZA, Lyssenko KA,
Hopf H (2008) Symmetrically tetrasubstituted [2.2]paracyclophanes: their systematization and
regioselective synthesis of several types of bis-bifunctional derivatives by double electrophilic
substitution. Chem Eur J 14:4600–4617
Weiland KJ, Gallego A, Mayor M (2019) Beyond simple substitution patterns—symmetrically
tetrasubstituted [2.2]paracyclophanes as 3D functional materials. Eur J Org Chem 3073–3085
Wielopolski M, Molina-Ontoria A, Schubert C, Margraf JT, Krokos E, Kirschner J, Gouloumis A,
Clark T, Guldi DM, Martín N (2013) Blending through-space and through-bond π-π-coupling
in [2,2’]-paracyclophane-oligophenylenevinylene molecular wires. J Am Chem Soc 135:10372–
10381
Zhuravsky R, Starikova Z, Vorontsov E, Rozenberg V (2008) Novel Strategy for the synthesis
of chiral pseudo-ortho-substituted hydrxy[2.2]paracyclophane-based ligands from the resolved
4-bromo-12-hydroxy[2.2]paracyclophane as a parent compound. Tetrahedron Asym 19:216–222
Y. Morisaki
Sawada R, Gon M, Nakamura J, Morisaki Y, Chujo Y (2018) Synthesis of enantiopure planar chiral
bis-(para)-pseudo-meta-type [2.2]paracyclophanes. Chirality 30:1109–1114
Sheng Y, Ma J, Liu S, Wang Y, Zhu C, Cheng Y (2016) Strong and reversible circularly polarized
luminescence emission of a chiral 1,8-naphthalimide fluorophore induced by excimer emission
and orderly aggregation. Chem Eur J 22:9519–9522
Sonogashira K (2002) In: Negishi E (ed) Handbook of organopalladium chemistry for organic
synthesis. Wiley-Interscience, New York, pp 493–529
Takaishi K, Yamamoto S, Hinoide S, Ema T (2017) Helical oligonaphthodioxepins showing intense
Circularly Polarized Luminescence (CPL) in solution and in the solid state. Chem Eur J 23:9249–
9252
Tanaka H, Inoue Y, Mori T (2018) Circularly polarized luminescence and circular dichroisms
in small organic molecules: correlation between excitation and emission dissymmetry factors.
ChemPhotoChem 2:386–402
Tohda Y, Sonogashira K, Hagihara N (1975) A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines. Tetrahedron
Lett 16:4467–4470
Vögtle F (1993) cyclophane chemistry: synthesis, structures and reactions. John Wiley & Sons,
Chichester
Vorontsova NV, Rozenberg VI, Sergeeva EV, Vorontsov EV, Starikova ZA, Lyssenko KA,
Hopf H (2008) Symmetrically tetrasubstituted [2.2]paracyclophanes: their systematization and
regioselective synthesis of several types of bis-bifunctional derivatives by double electrophilic
substitution. Chem Eur J 14:4600–4617
Weiland KJ, Gallego A, Mayor M (2019) Beyond simple substitution patterns—symmetrically
tetrasubstituted [2.2]paracyclophanes as 3D functional materials. Eur J Org Chem 3073–3085
Wielopolski M, Molina-Ontoria A, Schubert C, Margraf JT, Krokos E, Kirschner J, Gouloumis A,
Clark T, Guldi DM, Martín N (2013) Blending through-space and through-bond π-π-coupling
in [2,2’]-paracyclophane-oligophenylenevinylene molecular wires. J Am Chem Soc 135:10372–
10381
Zhuravsky R, Starikova Z, Vorontsov E, Rozenberg V (2008) Novel Strategy for the synthesis
of chiral pseudo-ortho-substituted hydrxy[2.2]paracyclophane-based ligands from the resolved
4-bromo-12-hydroxy[2.2]paracyclophane as a parent compound. Tetrahedron Asym 19:216–222