5 BODIPY Dyes and Their Analogues
199
Awuah SG, You Y (2012) Boron dipyrromethene (BODIPY)-based photosensitizers for photodynamic therapy. RSC Adv 2:11169–11183
Awuah SG, Polreis J, Biradar V, You Y (2011) Singlet oxygen generation by novel NIR BODIPY
dyes. Org Lett 13:3884–3887
Awuah SG, Das SK, D’Souza F, You Y (2013) Thieno–pyrrole–fused BODIPY intermediate as a
platform to multifunctional NIR agents. Chem Asian J 8:3123–3132
Bai G, Yu C, Cheng C, Hao E, Wei Y, Mu X, Jiao L (2014) Syntheses and photophysical properties
of BF 2 complexes of curcumin analogues. Org Biomol Chem 12:1618–1626
Bañuelos J (2016) BODIPY dye, the most versatile fluorophore ever? Chem Rec 16:335–348
Bañuelos J, Arbeloa FL, Martinez V, Liras M, Costela A, Morenoc IG, Arbeloa IL (2011) Difluoroboron-triaza-anthracene: a laser dye in the blue region. Theoretical simulation of alternative
difluoro-boron-diaza-aromatic systems. Phys Chem Chem Phys 13:3437–3445
Barbon SM, Staroverov VN, Gilroy JB (2015) Effect of extended π conjugation on the spectroscopic
and electrochemical properties of boron difluoride formazanate complexes. J Org Chem 80:5226–
5235
Belmonte-Vázquez JL, Avellanal-Zaballa E, Enríquez-Palacios E, Cerdán L, Esnal I, Bañuelos J,
Villegas-Gómez C, Arbeloa IL, Peña-Cabrera E (2019) Synthetic approach to readily accessible
benzofuran-fused borondipyrromethenes as red-emitting laser dyes. J Org Chem 84:2523–2541
Benstead M, Mehl GH, Boyle RW (2011) 4,4 -Difluoro-4-bora-3a,4a-diaza-s-indacenes
(BODIPYs) as components of novel light active materials. Tetrahedron 67:3573–3601
Bessette A, Hanan GS (2014) Design, synthesis and photophysical studies of dipyrromethenebased materials: insights into their applications in organic photovoltaic devices. Chem Soc Rev
43:3342–3405
Bochkov AY, Akchurin IO, Dyachenko OA, Traven VF (2013) NIR-fluorescent coumarin-fused
BODIPY dyes with large Stokes shifts. Chem Commun 49:11653–11655
Bodio E, Goze C (2019) Investigation of B-F substitution on BODIPY and aza-BODIPY dyes:
development of B-O and B-C BODIPYs. Dyes Pigm 160:700–710
Boens N, Leen V, Dehaen W (2012) Fluorescent indicators based on BODIPY. Chem Soc Rev
41:1130–1172
Boens N, Verbelen B, Dehaen W (2015) Postfunctionalization of the BODIPY core: synthesis and
spectroscopy. Eur J Org Chem 6577–6595
Bonnier C, Piers WE, Ali AAS, Thompson A, Parvez M (2009) Perfluoroaryl-substituted boron
dipyrrinato complexes. Organometallics 28:4845–4851
Bucher L, Desbois N, Harvey PD, Sharma GD, Gros CP (2017) Porphyrins and BODIPY as building
blocks for efficient donor materials in bulk heterojunction solar cells. Solar RRL 1:1700127
Bumagina NA, Kritskaya AY, Antina EV, Berezin MB, V’yugin AI (2018) Effect of alkyl, aryl, and
meso-aza substitution on the thermal stability of BODIPY. Russ J Inorg Chem 63:1326–1332
Bura T, Retailleau P, Ulrich G, Ziessel R (2011) Highly substituted bodipy dyes with spectroscopic
features sensitive to the environment. J Org Chem 76:1109–1117
Buyukcakir O, Bozdemir OA, Kolemen S, Erbas S, Akkaya EU (2009) Tetrastyryl-Bodipy dyes:
convenient synthesis and characterization of elusive near IR fluorophores. Org Lett 11:4644–4647
Chase DT, Young BS, Haley MM (2011) Incorporating BODIPY fluorophores into tetrakis(arylethynyl)benzenes. J Org Chem 76:4043–4051
Chen J, Burghart A, Derecskei-Kovacs A, Burgess K (2000) 4,4-Difluoro-4-bora-3a,4a-diaza-sindacene (BODIPY) dyes modified for extended conjugation and restricted bond rotations. J Org
Chem 65:2900–2906
Chen H-Y, Chi Y, Liu C-S, Yu J-K, Cheng Y-M, Chen K-S, Chou P-T, Peng S-M, Lee G-H, Carty
AJ, Ye S-J, Chen C-T (2005) Rational color tuning and luminescent properties of functionalized
boron-containing 2-pyridyl pyrrolide complexes. Adv Funct Mater 15:567–574
Chen J, Mizumura M, Shinokubo H, Osuka A (2009) Functionalization of boron dipyrrin (BODIPY)
dyes through iridium and rhodium catalysis: a complementary approach to α- and β-substituted
BODIPYs. Chem Eur J 15:5942–5949
199
Awuah SG, You Y (2012) Boron dipyrromethene (BODIPY)-based photosensitizers for photodynamic therapy. RSC Adv 2:11169–11183
Awuah SG, Polreis J, Biradar V, You Y (2011) Singlet oxygen generation by novel NIR BODIPY
dyes. Org Lett 13:3884–3887
Awuah SG, Das SK, D’Souza F, You Y (2013) Thieno–pyrrole–fused BODIPY intermediate as a
platform to multifunctional NIR agents. Chem Asian J 8:3123–3132
Bai G, Yu C, Cheng C, Hao E, Wei Y, Mu X, Jiao L (2014) Syntheses and photophysical properties
of BF 2 complexes of curcumin analogues. Org Biomol Chem 12:1618–1626
Bañuelos J (2016) BODIPY dye, the most versatile fluorophore ever? Chem Rec 16:335–348
Bañuelos J, Arbeloa FL, Martinez V, Liras M, Costela A, Morenoc IG, Arbeloa IL (2011) Difluoroboron-triaza-anthracene: a laser dye in the blue region. Theoretical simulation of alternative
difluoro-boron-diaza-aromatic systems. Phys Chem Chem Phys 13:3437–3445
Barbon SM, Staroverov VN, Gilroy JB (2015) Effect of extended π conjugation on the spectroscopic
and electrochemical properties of boron difluoride formazanate complexes. J Org Chem 80:5226–
5235
Belmonte-Vázquez JL, Avellanal-Zaballa E, Enríquez-Palacios E, Cerdán L, Esnal I, Bañuelos J,
Villegas-Gómez C, Arbeloa IL, Peña-Cabrera E (2019) Synthetic approach to readily accessible
benzofuran-fused borondipyrromethenes as red-emitting laser dyes. J Org Chem 84:2523–2541
Benstead M, Mehl GH, Boyle RW (2011) 4,4 -Difluoro-4-bora-3a,4a-diaza-s-indacenes
(BODIPYs) as components of novel light active materials. Tetrahedron 67:3573–3601
Bessette A, Hanan GS (2014) Design, synthesis and photophysical studies of dipyrromethenebased materials: insights into their applications in organic photovoltaic devices. Chem Soc Rev
43:3342–3405
Bochkov AY, Akchurin IO, Dyachenko OA, Traven VF (2013) NIR-fluorescent coumarin-fused
BODIPY dyes with large Stokes shifts. Chem Commun 49:11653–11655
Bodio E, Goze C (2019) Investigation of B-F substitution on BODIPY and aza-BODIPY dyes:
development of B-O and B-C BODIPYs. Dyes Pigm 160:700–710
Boens N, Leen V, Dehaen W (2012) Fluorescent indicators based on BODIPY. Chem Soc Rev
41:1130–1172
Boens N, Verbelen B, Dehaen W (2015) Postfunctionalization of the BODIPY core: synthesis and
spectroscopy. Eur J Org Chem 6577–6595
Bonnier C, Piers WE, Ali AAS, Thompson A, Parvez M (2009) Perfluoroaryl-substituted boron
dipyrrinato complexes. Organometallics 28:4845–4851
Bucher L, Desbois N, Harvey PD, Sharma GD, Gros CP (2017) Porphyrins and BODIPY as building
blocks for efficient donor materials in bulk heterojunction solar cells. Solar RRL 1:1700127
Bumagina NA, Kritskaya AY, Antina EV, Berezin MB, V’yugin AI (2018) Effect of alkyl, aryl, and
meso-aza substitution on the thermal stability of BODIPY. Russ J Inorg Chem 63:1326–1332
Bura T, Retailleau P, Ulrich G, Ziessel R (2011) Highly substituted bodipy dyes with spectroscopic
features sensitive to the environment. J Org Chem 76:1109–1117
Buyukcakir O, Bozdemir OA, Kolemen S, Erbas S, Akkaya EU (2009) Tetrastyryl-Bodipy dyes:
convenient synthesis and characterization of elusive near IR fluorophores. Org Lett 11:4644–4647
Chase DT, Young BS, Haley MM (2011) Incorporating BODIPY fluorophores into tetrakis(arylethynyl)benzenes. J Org Chem 76:4043–4051
Chen J, Burghart A, Derecskei-Kovacs A, Burgess K (2000) 4,4-Difluoro-4-bora-3a,4a-diaza-sindacene (BODIPY) dyes modified for extended conjugation and restricted bond rotations. J Org
Chem 65:2900–2906
Chen H-Y, Chi Y, Liu C-S, Yu J-K, Cheng Y-M, Chen K-S, Chou P-T, Peng S-M, Lee G-H, Carty
AJ, Ye S-J, Chen C-T (2005) Rational color tuning and luminescent properties of functionalized
boron-containing 2-pyridyl pyrrolide complexes. Adv Funct Mater 15:567–574
Chen J, Mizumura M, Shinokubo H, Osuka A (2009) Functionalization of boron dipyrrin (BODIPY)
dyes through iridium and rhodium catalysis: a complementary approach to α- and β-substituted
BODIPYs. Chem Eur J 15:5942–5949