5 BODIPY Dyes and Their Analogues
217
Yamaguchi M, Tanaka K, Chujo Y (2018) Design of conjugated molecules presenting shortwavelength luminescence by utilizing heavier atoms of the same element group. Chem Asian
J 13:1342–1347
Yamaji M, Kato S, Tomonari K, Mamiya M, Goto K, Okamoto H, Nakamura Y, Tani F (2017)
Blue fluorescence from BF2 complexes of N, O-benzamide ligands: synthesis, structure, and
photophysical properties. Inorg Chem 56:12514–12519
Yamane H, Ohtani S, Tanaka K, Chujo Y (2017) Synthesis of furan-substituted aza-BODIPYs
having near-infrared emission. Tetrahedron Lett 58:2989–2992
Yamazawa S, Nakashima M, Suda Y, Nishiyabu R, Kubo Y (2016) 2,3-naphtho-fused BODIPYs
as near-infrared absorbing dyes. J Org Chem 81:1310–1315
Yan W, Wan X, Chen Y (2010) Phenalenyl-based boron–fluorine complexes: synthesis, crystal
structures and solid-state fluorescence properties. J Mol Struct 968:85–88
Yan W, Hong C, Long G, Yang Y, Liu Z, Bian Z, Chen Y, Huang C (2014) Synthesis, crystal
structures and photophysical properties of novel boron-containing derivatives of phenalene with
bright solid-state luminescence. Dyes Pigm 106:197–204
Yang Y, Hughes RP, Aprahamian I (2012) Visible light switching of a BF 2 -coordinated azo
compound. J Am Chem Soc 134:15221–15224
Yang SK, Shi X, Park S, Ha T, Zimmerman SC (2013) A dendritic single-molecule fluorescent
probe that is monovalent, photostable and minimally blinking. Nat Chem 5:692–697
Yang L, Liu Y, Ma C, Liu W, Li Y, Li L (2015) Naphthalene-fused BODIPY with large Stokes shift
as saturated-red fluorescent dye for living cell imaging. Dyes Pigm 122:1–5
Yang L, Liu Y, Zhou X, Wu Y, Ma C, Liu W, Zhang C (2016) Asymmetric anthracene-fused
BODIPY dye with large Stokes shift: synthesis, photophysical properties and bioimaging. Dyes
Pigm 126:232–238
Yang C, Wang X, Wang M, Xu K, Xu C (2017) Robust colloidal nanoparticles of pyrrolopyrrole
cyanine J-aggregates with bright near-infrared fluorescence in aqueous media: from spectral
tailoring to bioimaging applications. Chem Eur J 23:4310–4319
Yang J, Rousselin Y, Bucher L, Desbois N, Bolze F, Xu H-J, Gros CP (2018) Two-photon absorption
properties and structures of BODIPY and its dyad. Triad Tetrad ChemPlusChem 83:838–844
Yokoi H, Wachi N, Hiroto S, Shinokubo H (2014) Oxidation of 2-amino-substituted BODIPYs
providing pyrazine-fused BODIPY trimers. Chem Commun 50:2715–2717
Yoshii R, Nagai A, Tanaka K, Chujo Y (2013) Highly emissive boron ketoiminate derivatives as a
new class of aggregation-induced emission fluorophores. Chem Eur J 19:4506–4512
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014a) Boron diiminate with aggregation-induced emission
and crystallization-induced emission-enhancement characteristics. Chem Eur J 20:8320–8324
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014b) Functionalization of boron diiminates with unique
optical properties: multicolor tuning of crystallization-induced emission and introduction into the
main chain of conjugated polymers. J Am Chem Soc 136:18131–18139
Yoshino J, Kano N, Kawashima T (2007) Synthesis of the most intensely fluorescent azobenzene
by utilizing the B–N interaction. Chem Commun 559–561
Yoshino J, Kano N, Kawashima T (2013) Fluorescent azobenzenes and aromatic aldimines featuring
an N-B interaction. Dalton Trans 42:15826–15834
Yu C, Jiao L, Yin H, Zhou J, Pang W, Wu Y, Wang Z, Yang G, Hao E (2011) α-/β-formylated
boron–dipyrrin (BODIPY) dyes: regioselective syntheses and photophysical properties. Eur J
Org Chem 5460–5468
Yu C, Xu Y, Jiao L, Zhou J, Wang Z, Hao E (2012) Isoindole-BODIPY dyes as red to near-infrared
fluorophores. Chem Eur J 18:6437–6442
Yu C, Jiao L, Zhang P, Feng Z, Cheng C, Wei Y, Mu X, Hao E (2014) Highly fluorescent BF2
complexes of hydrazine-schiff base linked bispyrrole. Org Lett 16:3048–3051
Yu C, Hao E, Li T, Wang J, Sheng W, Wei Y, Mu X, Jiao L (2015) Dipyrrolylquinoxaline
difluoroborates with intense red solid-state fluorescence. Dalton Trans 44:13897–13905
217
Yamaguchi M, Tanaka K, Chujo Y (2018) Design of conjugated molecules presenting shortwavelength luminescence by utilizing heavier atoms of the same element group. Chem Asian
J 13:1342–1347
Yamaji M, Kato S, Tomonari K, Mamiya M, Goto K, Okamoto H, Nakamura Y, Tani F (2017)
Blue fluorescence from BF2 complexes of N, O-benzamide ligands: synthesis, structure, and
photophysical properties. Inorg Chem 56:12514–12519
Yamane H, Ohtani S, Tanaka K, Chujo Y (2017) Synthesis of furan-substituted aza-BODIPYs
having near-infrared emission. Tetrahedron Lett 58:2989–2992
Yamazawa S, Nakashima M, Suda Y, Nishiyabu R, Kubo Y (2016) 2,3-naphtho-fused BODIPYs
as near-infrared absorbing dyes. J Org Chem 81:1310–1315
Yan W, Wan X, Chen Y (2010) Phenalenyl-based boron–fluorine complexes: synthesis, crystal
structures and solid-state fluorescence properties. J Mol Struct 968:85–88
Yan W, Hong C, Long G, Yang Y, Liu Z, Bian Z, Chen Y, Huang C (2014) Synthesis, crystal
structures and photophysical properties of novel boron-containing derivatives of phenalene with
bright solid-state luminescence. Dyes Pigm 106:197–204
Yang Y, Hughes RP, Aprahamian I (2012) Visible light switching of a BF 2 -coordinated azo
compound. J Am Chem Soc 134:15221–15224
Yang SK, Shi X, Park S, Ha T, Zimmerman SC (2013) A dendritic single-molecule fluorescent
probe that is monovalent, photostable and minimally blinking. Nat Chem 5:692–697
Yang L, Liu Y, Ma C, Liu W, Li Y, Li L (2015) Naphthalene-fused BODIPY with large Stokes shift
as saturated-red fluorescent dye for living cell imaging. Dyes Pigm 122:1–5
Yang L, Liu Y, Zhou X, Wu Y, Ma C, Liu W, Zhang C (2016) Asymmetric anthracene-fused
BODIPY dye with large Stokes shift: synthesis, photophysical properties and bioimaging. Dyes
Pigm 126:232–238
Yang C, Wang X, Wang M, Xu K, Xu C (2017) Robust colloidal nanoparticles of pyrrolopyrrole
cyanine J-aggregates with bright near-infrared fluorescence in aqueous media: from spectral
tailoring to bioimaging applications. Chem Eur J 23:4310–4319
Yang J, Rousselin Y, Bucher L, Desbois N, Bolze F, Xu H-J, Gros CP (2018) Two-photon absorption
properties and structures of BODIPY and its dyad. Triad Tetrad ChemPlusChem 83:838–844
Yokoi H, Wachi N, Hiroto S, Shinokubo H (2014) Oxidation of 2-amino-substituted BODIPYs
providing pyrazine-fused BODIPY trimers. Chem Commun 50:2715–2717
Yoshii R, Nagai A, Tanaka K, Chujo Y (2013) Highly emissive boron ketoiminate derivatives as a
new class of aggregation-induced emission fluorophores. Chem Eur J 19:4506–4512
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014a) Boron diiminate with aggregation-induced emission
and crystallization-induced emission-enhancement characteristics. Chem Eur J 20:8320–8324
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014b) Functionalization of boron diiminates with unique
optical properties: multicolor tuning of crystallization-induced emission and introduction into the
main chain of conjugated polymers. J Am Chem Soc 136:18131–18139
Yoshino J, Kano N, Kawashima T (2007) Synthesis of the most intensely fluorescent azobenzene
by utilizing the B–N interaction. Chem Commun 559–561
Yoshino J, Kano N, Kawashima T (2013) Fluorescent azobenzenes and aromatic aldimines featuring
an N-B interaction. Dalton Trans 42:15826–15834
Yu C, Jiao L, Yin H, Zhou J, Pang W, Wu Y, Wang Z, Yang G, Hao E (2011) α-/β-formylated
boron–dipyrrin (BODIPY) dyes: regioselective syntheses and photophysical properties. Eur J
Org Chem 5460–5468
Yu C, Xu Y, Jiao L, Zhou J, Wang Z, Hao E (2012) Isoindole-BODIPY dyes as red to near-infrared
fluorophores. Chem Eur J 18:6437–6442
Yu C, Jiao L, Zhang P, Feng Z, Cheng C, Wei Y, Mu X, Hao E (2014) Highly fluorescent BF2
complexes of hydrazine-schiff base linked bispyrrole. Org Lett 16:3048–3051
Yu C, Hao E, Li T, Wang J, Sheng W, Wei Y, Mu X, Jiao L (2015) Dipyrrolylquinoxaline
difluoroborates with intense red solid-state fluorescence. Dalton Trans 44:13897–13905