66. Ray C, Bañuenlos J, Arbeloa T, Maroto BL, Moreno F, Agarrabeitia AR, Ortiz MJ, LópezArbeloa I, de la Moya S (2016) Push-pull flexibly-bridged bis(haloBODIPYs): solvent and
spacer switchable red emission. Dalton Trans 45:11839–11848
67. Morisaki Y, Gon M, Sasamori T, Tokitoh N, Chujo Y (2014) Planar chiral tetrasubstituted [2.2]
paracyclophane: optical resolution and functionalization. J Am Chem Soc 136:3350–3353
68. Gon M, Morisaki Y, Chujo Y (2015) 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
69. Gon M, Kozuka H, Morisaki Y, Chujo Y (2016) Optically active cyclic compounds based on
planar chiral [2.2] paracyclophane with naphthalene units. Asian J Org Chem 5:353–359
70. Saikawa M, Nakamura T, Uchida J, Yamamura M, Nabeshima T (2016) Synthesis of figure-ofeight helical bisBODIPY macrocycles and their chiroptical propertie. Chem Commun
52:10727–10730
71. Saikawa M, Noda T, Matsuoka R, Nakamura T, Nabeshima T (2019) Heterodinuclear group
13 element complexes of N 4 O 6 -type dipyrrin with an unsymmetrical twisted structure. Eur J
Inorg Chem 2019:766–769
72. Wang Y, Li Y, Liu S, Li F, Zhu C, Li S, Cheng Y (2016) Regulating circularly polarized
luminescence signals of chiral binaphthyl-based conjugated polymers by tuning dihedral angles
of binaphthyl moieties. Macromolecules 49:5444–5451
73. 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
74. Feuillastre S, Pauton M, Gao L, Desmarchelier A, Riives AJ, Prim D, Tondelier D, Geffroy B,
Muller G, Clavier G, Pieters G (2016) Design and synthesis of new circularly polarized
thermally activated delayed fluorescence emitters. J Am Chem Soc 138:3990–3993
75. Li J, Peng X, Huang C, Qi Q, Lai W-Y, Huang W (2018) Control of circularly polarized
luminescence from a boron ketoiminate-based π-conjugated polymer via conformational locks.
Polym Chem 9:5278–5285
76. Wu Y, Wang S, Li Z, Shenb Z, Lu H (2016) Chiral binaphthyl-linked BODIPY analogues:
synthesis and spectroscopic properties. J Mater Chem C 4:4668–4674
77. Meng F, Sheng Y, Li F, Zhu C, Quan Y, Cheng Y (2017) Reversal aggregation-induced circular
dichroism from axial chirality transfer via self-assembled helical nanowires. RSC Adv
7:15851–15856
78. Maeda C, Nagahata K, Takaishi K, Ema T (2019) Synthesis of chiral carbazole-based
BODIPYs showing circularly polarized luminescence. Chem Commun 55:3136–3139
6 BODIPY Based Emitters of Circularly Polarized Luminescence
149
spacer switchable red emission. Dalton Trans 45:11839–11848
67. Morisaki Y, Gon M, Sasamori T, Tokitoh N, Chujo Y (2014) Planar chiral tetrasubstituted [2.2]
paracyclophane: optical resolution and functionalization. J Am Chem Soc 136:3350–3353
68. Gon M, Morisaki Y, Chujo Y (2015) 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
69. Gon M, Kozuka H, Morisaki Y, Chujo Y (2016) Optically active cyclic compounds based on
planar chiral [2.2] paracyclophane with naphthalene units. Asian J Org Chem 5:353–359
70. Saikawa M, Nakamura T, Uchida J, Yamamura M, Nabeshima T (2016) Synthesis of figure-ofeight helical bisBODIPY macrocycles and their chiroptical propertie. Chem Commun
52:10727–10730
71. Saikawa M, Noda T, Matsuoka R, Nakamura T, Nabeshima T (2019) Heterodinuclear group
13 element complexes of N 4 O 6 -type dipyrrin with an unsymmetrical twisted structure. Eur J
Inorg Chem 2019:766–769
72. Wang Y, Li Y, Liu S, Li F, Zhu C, Li S, Cheng Y (2016) Regulating circularly polarized
luminescence signals of chiral binaphthyl-based conjugated polymers by tuning dihedral angles
of binaphthyl moieties. Macromolecules 49:5444–5451
73. 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
74. Feuillastre S, Pauton M, Gao L, Desmarchelier A, Riives AJ, Prim D, Tondelier D, Geffroy B,
Muller G, Clavier G, Pieters G (2016) Design and synthesis of new circularly polarized
thermally activated delayed fluorescence emitters. J Am Chem Soc 138:3990–3993
75. Li J, Peng X, Huang C, Qi Q, Lai W-Y, Huang W (2018) Control of circularly polarized
luminescence from a boron ketoiminate-based π-conjugated polymer via conformational locks.
Polym Chem 9:5278–5285
76. Wu Y, Wang S, Li Z, Shenb Z, Lu H (2016) Chiral binaphthyl-linked BODIPY analogues:
synthesis and spectroscopic properties. J Mater Chem C 4:4668–4674
77. Meng F, Sheng Y, Li F, Zhu C, Quan Y, Cheng Y (2017) Reversal aggregation-induced circular
dichroism from axial chirality transfer via self-assembled helical nanowires. RSC Adv
7:15851–15856
78. Maeda C, Nagahata K, Takaishi K, Ema T (2019) Synthesis of chiral carbazole-based
BODIPYs showing circularly polarized luminescence. Chem Commun 55:3136–3139
6 BODIPY Based Emitters of Circularly Polarized Luminescence
149