5 BODIPY Dyes and Their Analogues
215
Umezawa K, Citterio D, Suzuki K (2014) New trends in near-infrared fluorophores for bioimaging.
Anal Sci 30:327–349
Uno H, Honda T, Kitatsuka M, Hiraoka S, Mori S, Takase M, Okujima T, Nakae T (2018) Benzenefused bis(acenaphthoBODIPY)s, stable near-infrared-selective dyes. RSC Adv 8:14072–14083
Uoyama H, Goushi K, Shizu K, Nomura H, Adachi C (2012) Highly efficient organic light-emitting
diodes from delayed fluorescence. Nature 492:234–238
Urban M, Durka K, Jankowski P, Serwatowski J, Luli´ nski S (2017) Highly fluorescent red-light
emitting bis(boranils) based on naphthalene backbone. J Org Chem 82:8234–8241
Verbelen B, Boodts S, Hofkens J, Boens N, Dehaen W (2015a) Radical C-H arylation of the BODIPY
core with aryldiazonium salts: synthesis of highly fluorescent red-shifted dyes. Angew Chem Int
Ed 54:4612–4616
Verbelen B, Rezende LCD, Boodts S, Jacobs J, Van Meervelt L, Hofkens J, Dehaen W (2015b)
Radical C-H alkylation of BODIPY dyes using potassium trifluoroborates or boronic acids. Chem
Eur J 21:12667–12675
Wakamiya A, Yamaguchi S (2015) Designs of functional π-electron materials based on the
characteristic features of boron. Bull Chem Soc Jpn 88:1357–1377
Wakamiya A, Taniguchi T, Yamaguchi S (2006) Intramolecular B-N coordination as a Scaffold for
electron-transporting materials: synthesis and properties of boryl-substituted thienylthiazoles.
Angew Chem Int Ed 45:3170–3173
Wakamiya A, Mori K, Yamaguchi S (2007) 3-boryl-2,2 -bithiophene as a versatile core skeleton
for full-color highly emissive organic solids. Angew Chem Int Ed 46:4273–4276
Wakamiya A, Murakami T, Yamaguchi S (2013) Benzene-fused BODIPY and fully-fused BODIPY
dimer: impacts of the ring-fusing at the b bond in the BODIPY skeleton†. Chem Sci 4:1002–1007
Wang D, Fan J, Gao X, Wang B, Sun S, Peng X (2009) Carboxyl BODIPY dyes from bicarboxylic
anhydrides: one-pot preparation, spectral properties, photostability, and biolabeling. J Org Chem
74:7675–7683
Wang Y-W, Descalzo AB, Shen Z, You X-Z, Rurack K (2010) Dihydronaphthalene-fused borondipyrromethene (BODIPY) dyes: insight into the electronic and conformational tuning modes of
BODIPY fluorophores. Chem Eur J 16:2887–2903
Wang D, Liu R, Chen C, Wang S, Chang J, Wu C, Zhu H, Waclawik ER (2013) Synthesis, photophysical and electrochemical properties of aza-boron-diquinomethene complexes. Dyes Pigm
99:240–249
Wang F, Guo Z, Li X, Li X, Zhao C (2014a) Development of a small molecule probe capable of
discriminating cysteine, homocysteine, and glutathione with three distinct turn-on fluorescent
outputs. Chem Eur J 20:11471–11478
Wang X, Liu H, Cui J, Wu Y, Lu H, Lu J, Liu Z, He W (2014b) New J Chem 38:1277–1283
Wang X, Wu Y, Liu Q, Li Z, Yan H, Ji C, Duan J, Liu Z (2015a) Aggregation-induced emission
(AIE) of pyridyl-enamido-based organoboron luminophores. Chem Commun 51:784–787
Wang X, Liu Q, Yan H, Liu Z, Yao M, Zhang Q, Gong S, He W (2015b) Piezochromic luminescence behaviors of two new benzothiazole–enamido boron difluoride complexes: intra- and
inter-molecular effects induced by hydrostatic compression. Chem Commun 51:7497–7500
Wang J, Li J, Chen N, Wu Y, Hao E, Wei Y, Mu X, Jiao L (2016a) Synthesis, structure and
properties of thiophene-fused BODIPYs and azaBODIPYs as near-infrared agents. New J Chem
40:5966–5975
Wang J, Wu Q, Yu C, Wei Y, Mu X, Hao E, Jiao L (2016b) Aromatic ring fused BOPHYs as stable
red fluorescent dyes. J Org Chem 81:11316–11323
Wang S, Lan H, Xiao S, Tan R, Lu Y (2017) Highly fluorescent non-conventional boron-difluoridebased π organogel with gelation-assisted piezochromism. Chem Asian J 12:198–202
Wang M, Vicente MCH, Mason D, Bobadova-Parvanova P (2018a) Stability of a series of BODIPYs
in acidic conditions: an experimental and computational study into the role of the substituents at
boron. ACS Omega 3:5502–5510
Wang T, Dou C, Liu J, Wang L (2018b) Effects of the substituents of boron atoms on conjugated
polymers containing B ← N units. Chem Eur J 24:13043–13048
215
Umezawa K, Citterio D, Suzuki K (2014) New trends in near-infrared fluorophores for bioimaging.
Anal Sci 30:327–349
Uno H, Honda T, Kitatsuka M, Hiraoka S, Mori S, Takase M, Okujima T, Nakae T (2018) Benzenefused bis(acenaphthoBODIPY)s, stable near-infrared-selective dyes. RSC Adv 8:14072–14083
Uoyama H, Goushi K, Shizu K, Nomura H, Adachi C (2012) Highly efficient organic light-emitting
diodes from delayed fluorescence. Nature 492:234–238
Urban M, Durka K, Jankowski P, Serwatowski J, Luli´ nski S (2017) Highly fluorescent red-light
emitting bis(boranils) based on naphthalene backbone. J Org Chem 82:8234–8241
Verbelen B, Boodts S, Hofkens J, Boens N, Dehaen W (2015a) Radical C-H arylation of the BODIPY
core with aryldiazonium salts: synthesis of highly fluorescent red-shifted dyes. Angew Chem Int
Ed 54:4612–4616
Verbelen B, Rezende LCD, Boodts S, Jacobs J, Van Meervelt L, Hofkens J, Dehaen W (2015b)
Radical C-H alkylation of BODIPY dyes using potassium trifluoroborates or boronic acids. Chem
Eur J 21:12667–12675
Wakamiya A, Yamaguchi S (2015) Designs of functional π-electron materials based on the
characteristic features of boron. Bull Chem Soc Jpn 88:1357–1377
Wakamiya A, Taniguchi T, Yamaguchi S (2006) Intramolecular B-N coordination as a Scaffold for
electron-transporting materials: synthesis and properties of boryl-substituted thienylthiazoles.
Angew Chem Int Ed 45:3170–3173
Wakamiya A, Mori K, Yamaguchi S (2007) 3-boryl-2,2 -bithiophene as a versatile core skeleton
for full-color highly emissive organic solids. Angew Chem Int Ed 46:4273–4276
Wakamiya A, Murakami T, Yamaguchi S (2013) Benzene-fused BODIPY and fully-fused BODIPY
dimer: impacts of the ring-fusing at the b bond in the BODIPY skeleton†. Chem Sci 4:1002–1007
Wang D, Fan J, Gao X, Wang B, Sun S, Peng X (2009) Carboxyl BODIPY dyes from bicarboxylic
anhydrides: one-pot preparation, spectral properties, photostability, and biolabeling. J Org Chem
74:7675–7683
Wang Y-W, Descalzo AB, Shen Z, You X-Z, Rurack K (2010) Dihydronaphthalene-fused borondipyrromethene (BODIPY) dyes: insight into the electronic and conformational tuning modes of
BODIPY fluorophores. Chem Eur J 16:2887–2903
Wang D, Liu R, Chen C, Wang S, Chang J, Wu C, Zhu H, Waclawik ER (2013) Synthesis, photophysical and electrochemical properties of aza-boron-diquinomethene complexes. Dyes Pigm
99:240–249
Wang F, Guo Z, Li X, Li X, Zhao C (2014a) Development of a small molecule probe capable of
discriminating cysteine, homocysteine, and glutathione with three distinct turn-on fluorescent
outputs. Chem Eur J 20:11471–11478
Wang X, Liu H, Cui J, Wu Y, Lu H, Lu J, Liu Z, He W (2014b) New J Chem 38:1277–1283
Wang X, Wu Y, Liu Q, Li Z, Yan H, Ji C, Duan J, Liu Z (2015a) Aggregation-induced emission
(AIE) of pyridyl-enamido-based organoboron luminophores. Chem Commun 51:784–787
Wang X, Liu Q, Yan H, Liu Z, Yao M, Zhang Q, Gong S, He W (2015b) Piezochromic luminescence behaviors of two new benzothiazole–enamido boron difluoride complexes: intra- and
inter-molecular effects induced by hydrostatic compression. Chem Commun 51:7497–7500
Wang J, Li J, Chen N, Wu Y, Hao E, Wei Y, Mu X, Jiao L (2016a) Synthesis, structure and
properties of thiophene-fused BODIPYs and azaBODIPYs as near-infrared agents. New J Chem
40:5966–5975
Wang J, Wu Q, Yu C, Wei Y, Mu X, Hao E, Jiao L (2016b) Aromatic ring fused BOPHYs as stable
red fluorescent dyes. J Org Chem 81:11316–11323
Wang S, Lan H, Xiao S, Tan R, Lu Y (2017) Highly fluorescent non-conventional boron-difluoridebased π organogel with gelation-assisted piezochromism. Chem Asian J 12:198–202
Wang M, Vicente MCH, Mason D, Bobadova-Parvanova P (2018a) Stability of a series of BODIPYs
in acidic conditions: an experimental and computational study into the role of the substituents at
boron. ACS Omega 3:5502–5510
Wang T, Dou C, Liu J, Wang L (2018b) Effects of the substituents of boron atoms on conjugated
polymers containing B ← N units. Chem Eur J 24:13043–13048