200
Y. Kubota
Chen Y, Wan L, Zhang D, Bian Y, Jiang J (2011) Modulation of the spectroscopic property of Bodipy
derivates through tuning the molecular configuration. Photochem Photobiol Sci 10:1030–1038
Chen Y, Zhao J, Guo H, Xie L (2012) Geometry relaxation-induced large Stokes shift in redemitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes. J Org
Chem 77:2192–2206
Chen JJ, Conron SM, Erwin P, Dimitriou M, McAlahney K, Thompson ME (2015) High-efficiency
BODIPY-based organic photovoltaics. ACS Appl Mater Interfaces 7:662–669
Chen P-Z, Niu L-Y, Chen Y-Z, Yang Q-Z (2017a) Difluoroboron β-diketonate dyes: spectroscopic
properties and applications. Coord Chem Rev 350:196–216
Chen N, Zhang W, Chen S, Wu Q, Yu C, Wei Y, Xu Y, Hao E, Jiao L (2017b) Sterically protected
N 2 O-type benzopyrromethene boron complexes from boronic acids with intense red/near-infrared
fluorescence. Org Lett 19:2026–2029
Chen D-G, Ranganathan R, Lin J-A, Huang C-Y, Ho M-L, Chi Y, Chou P-T (2019) Ratiometric
tuning of luminescence: interplay between the locally excited and interligand charge-transfer
states in pyrazolate-based boron compounds. J Phys Chem C 123:4022–4028
Cheng X, Li D, Zhang Z, Zhang H, Wang Y (2014) Organoboron compounds with morphologydependent NIR emissions and dual-channel fluorescent ON/OFF switching. Org Lett 16:880–883
Cherumukkil S, Vedhanarayanan B, Das G, Praveen VK, Ajayaghosh A (2018) Self-assembly of
bodipy-derived extended π-systems. Bull Chem Soc Jpn 91:100–120
Chibani S, Le Guennic B, Charaf-Eddin A, Laurenta AD, Jacquemin D (2013) Revisiting the optical
signatures of BODIPY with ab initio tools. Chem Sci 4:1950–1963
Choi S, Bouffard J, Kim Y (2014) Aggregation-induced emission enhancement of a mesotrifluoromethyl BODIPY via J-aggregation. Chem Sci 5:751–755
Chong H, Lin H-A, Shen M-Y, Liu C-Y, Zhao H, Yu H-H (2015) Step-economical syntheses
of functional BODIPY-EDOT π-conjugated materials through direct C–H arylation. Org Lett
17:3198–3201
Chua MH, Kim T, Lim ZL, Gopalakrishna TY, Ni Y, Xu J, Kim D, Wu J (2018) BODIPYbased antiaromatic macrocycles: facile synthesis by knoevenagel condensation and unusual
aggregation-enhanced two-photon absorption properties. Chem Eur J 24:2232–2241
Claessens CG, González-Rodríguez D, Torres T (2002) Subphthalocyanines: singular nonplanar
aromatic compoundssynthesis, reactivity, and physical properties. Chem Rev 102:835–853
Claessens CG, González-Rodríguez D, Rodríguez-Morgade MS, Medina A, Torres T (2014) Subphthalocyanines, subporphyrazines, and subporphyrins: singular nonplanar aromatic systems. Chem
Rev 114:2192–2277
Clarke RG, Hall MJ (2019) Chapter Three—Recent developments in the synthesis of the BODIPY
dyes. Adv Heterocycl Chem 128:181–261
Crossley DL, Cade IA, Clark ER, Escande A, Humphries MJ, King SM, Vitorica-Yrezabal I,
Ingleson MJ, Turner ML (2015) Enhancing electron affinity and tuning band gap in donor–
acceptor organic semiconductors by benzothiadiazole directed C-H borylation. Chem Sci 6:5144–
5151
Cui Y, Liu Q-D, Bai D-R, Jia W-L, Tao Y, Wang S (2005) Organoboron compounds with an 8hydroxyquinolato chelate and its derivatives: substituent effects on structures and luminescence.
Inorg Chem 44:601–609
Cui A, Peng X, Fan J, Chen X, Wu Y, Guo B (2007) Synthesis, spectral properties and photostability
of novel boron–dipyrromethene dyes. J Photochem Photobiol A 186:85–92
Culzoni MJ, de la Peña AM, Machuca A, Goicoechea HC, Babiano R (2013) Rhodamine and
BODIPY chemodosimeters and chemosensors for the detection of Hg 2+ , based on fluorescence
enhancement effects. Anal Methods 5:30–49
Curiel D, Más-Montoya M, Usea L, Espinosa A, Orenes RA, Molina P (2012) Indolocarbazole-based
ligands for ladder-type four-coordinate boron complexes. Org Lett 14:3360–3363
Daly ML, DeRosa CA, Kerr C, Morris WA, Fraser CL (2016) Blue thermally activated delayed
fluorescence from a biphenyl difluoroboron β-diketonate. RSC Adv 6:81631–81635
Y. Kubota
Chen Y, Wan L, Zhang D, Bian Y, Jiang J (2011) Modulation of the spectroscopic property of Bodipy
derivates through tuning the molecular configuration. Photochem Photobiol Sci 10:1030–1038
Chen Y, Zhao J, Guo H, Xie L (2012) Geometry relaxation-induced large Stokes shift in redemitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes. J Org
Chem 77:2192–2206
Chen JJ, Conron SM, Erwin P, Dimitriou M, McAlahney K, Thompson ME (2015) High-efficiency
BODIPY-based organic photovoltaics. ACS Appl Mater Interfaces 7:662–669
Chen P-Z, Niu L-Y, Chen Y-Z, Yang Q-Z (2017a) Difluoroboron β-diketonate dyes: spectroscopic
properties and applications. Coord Chem Rev 350:196–216
Chen N, Zhang W, Chen S, Wu Q, Yu C, Wei Y, Xu Y, Hao E, Jiao L (2017b) Sterically protected
N 2 O-type benzopyrromethene boron complexes from boronic acids with intense red/near-infrared
fluorescence. Org Lett 19:2026–2029
Chen D-G, Ranganathan R, Lin J-A, Huang C-Y, Ho M-L, Chi Y, Chou P-T (2019) Ratiometric
tuning of luminescence: interplay between the locally excited and interligand charge-transfer
states in pyrazolate-based boron compounds. J Phys Chem C 123:4022–4028
Cheng X, Li D, Zhang Z, Zhang H, Wang Y (2014) Organoboron compounds with morphologydependent NIR emissions and dual-channel fluorescent ON/OFF switching. Org Lett 16:880–883
Cherumukkil S, Vedhanarayanan B, Das G, Praveen VK, Ajayaghosh A (2018) Self-assembly of
bodipy-derived extended π-systems. Bull Chem Soc Jpn 91:100–120
Chibani S, Le Guennic B, Charaf-Eddin A, Laurenta AD, Jacquemin D (2013) Revisiting the optical
signatures of BODIPY with ab initio tools. Chem Sci 4:1950–1963
Choi S, Bouffard J, Kim Y (2014) Aggregation-induced emission enhancement of a mesotrifluoromethyl BODIPY via J-aggregation. Chem Sci 5:751–755
Chong H, Lin H-A, Shen M-Y, Liu C-Y, Zhao H, Yu H-H (2015) Step-economical syntheses
of functional BODIPY-EDOT π-conjugated materials through direct C–H arylation. Org Lett
17:3198–3201
Chua MH, Kim T, Lim ZL, Gopalakrishna TY, Ni Y, Xu J, Kim D, Wu J (2018) BODIPYbased antiaromatic macrocycles: facile synthesis by knoevenagel condensation and unusual
aggregation-enhanced two-photon absorption properties. Chem Eur J 24:2232–2241
Claessens CG, González-Rodríguez D, Torres T (2002) Subphthalocyanines: singular nonplanar
aromatic compoundssynthesis, reactivity, and physical properties. Chem Rev 102:835–853
Claessens CG, González-Rodríguez D, Rodríguez-Morgade MS, Medina A, Torres T (2014) Subphthalocyanines, subporphyrazines, and subporphyrins: singular nonplanar aromatic systems. Chem
Rev 114:2192–2277
Clarke RG, Hall MJ (2019) Chapter Three—Recent developments in the synthesis of the BODIPY
dyes. Adv Heterocycl Chem 128:181–261
Crossley DL, Cade IA, Clark ER, Escande A, Humphries MJ, King SM, Vitorica-Yrezabal I,
Ingleson MJ, Turner ML (2015) Enhancing electron affinity and tuning band gap in donor–
acceptor organic semiconductors by benzothiadiazole directed C-H borylation. Chem Sci 6:5144–
5151
Cui Y, Liu Q-D, Bai D-R, Jia W-L, Tao Y, Wang S (2005) Organoboron compounds with an 8hydroxyquinolato chelate and its derivatives: substituent effects on structures and luminescence.
Inorg Chem 44:601–609
Cui A, Peng X, Fan J, Chen X, Wu Y, Guo B (2007) Synthesis, spectral properties and photostability
of novel boron–dipyrromethene dyes. J Photochem Photobiol A 186:85–92
Culzoni MJ, de la Peña AM, Machuca A, Goicoechea HC, Babiano R (2013) Rhodamine and
BODIPY chemodosimeters and chemosensors for the detection of Hg 2+ , based on fluorescence
enhancement effects. Anal Methods 5:30–49
Curiel D, Más-Montoya M, Usea L, Espinosa A, Orenes RA, Molina P (2012) Indolocarbazole-based
ligands for ladder-type four-coordinate boron complexes. Org Lett 14:3360–3363
Daly ML, DeRosa CA, Kerr C, Morris WA, Fraser CL (2016) Blue thermally activated delayed
fluorescence from a biphenyl difluoroboron β-diketonate. RSC Adv 6:81631–81635