210
Y. Kubota
Nagata Y, Chujo Y (2008) Main-chain-type N, N’-chelate organoboron aminoquinolate polymers:
synthesis, luminescence, and energy transfer behavior. Macromolecules 41:3488–3492
Nakamura M, Tahara H, Takahashi K, Nagata T, Uoyama H, Kuzuhara D, Mori S, Okujima T,
Yamada H, Uno H (2012) π-fused bis-BODIPY as a candidate for NIR dyes. Org Biomol Chem
10:6840–6849
Nawn G, Oakley SR, Majewski MB, McDonald R, Patrick BO, Hicks RG (2013) Redox-active, nearinfrared dyes based on ‘Nindigo’ (indigo-N, N’-diarylimine) boron chelate complexes. Chem Sci
4:612–621
Nepomnyashchii AB, Cho S, Rossky PJ, Bard AJ (2010) Dependence of electrochemical and
electrogenerated chemiluminescence properties on the structure of BODIPY dyes. Unusually
large separation between sequential electron transfers. J Am Chem Soc 132:17550–17559
Nepomnyashchii AB, Bröring M, Ahrens J, Bard AJ (2011) Synthesis, photophysical, electrochemical, and electrogenerated chemiluminescence studies. Multiple sequential electron transfers in
BODIPY monomers, dimers, trimers, and polymer. J Am Chem Soc 133:8633–8645
Ni Y, Wu J (2014) Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent
pH probes and bio-imaging. Org Biomol Chem 12:3774–3791
Ni Y, Zeng W, Huang K-W, Wu J (2013) Benzene-fused BODIPYs: synthesis and the impact of
fusion mode. Chem Commun 49:1217–1219
Ni Y, Kannadorai RK, Peng J, Yu SW-K, Chang Y-T, Wu J (2016a) Naphthalene-fused BODIPY
near-infrared dye as a stable contrast agent for in vivo photoacoustic imaging. Chem Commun
52:11504–11507
Ni Y, Lee S, Son M, Aratani N, Ishida M, Samanta A, Yamada H, Chang Y-T, Furuta H, Kim
D, Wu J (2016b) A diradical approach towards BODIPY-based dyes with intense near-infrared
absorption around λ = 1100 nm. Angew Chem Int Ed 55:2815–2819
Numano M, Nagami N, Nakatsuka S, Katayama T, Nakajima K, Tatsumi S, Yasuda N, Hatakeyama T
(2016) Synthesis of boronate-based benzo[fg]tetracene and benzo[hi]hexacene via demethylative
direct borylation. Chem Eur J 22:11574–11577
Oda S, Shimizu T, Katayama T, Yoshikawa H, Hatakeyama T (2019) Tetracoordinate boron-fused
double [5]helicenes as cathode active materials for lithium batteries. Org Lett 21:1770–1773
Ohtani S, Gon M, Tanaka K, Chujo Y (2017) A flexible, fused, azomethine-boron complex: thermochromic luminescence and thermosalient behavior in structural transitions between crystalline
polymorphs. Chem Eur J 23:11827–11833
Okujima T, Tomimori Y, Nakamura J, Yamada H, Uno H, Ono N (2010) Synthesis of π-expanded
BODIPYs and their fluorescent properties in the visible–near–infrared region. Tetrahedron
66:6895–6900
Ono N, Hironaga H, Ono K, Kaneko S, Murashima T, Ueda T, Tsukamura C, Ogawa T (1996) A
new synthesis of pyrroles and porphyrins fused with aromatic rings. J Chem Soc Perkin Trans
1:417–423
Ono N, Yamamoto T, Shimada N, Kuroki K, Wada M, Utsunomiya R, Yano T, Uno H, Murashima
T (2003) A new synthesis of functional dyes from 2-Acenaphtho[1,2-c]pyrrole. Heterocycles
61:433–447
Ono K, Hashizume J, Yamaguchi H, Tomura M, Nishida J, Yamashita Y (2009) Synthesis, crystal
structure, and electron-accepting property of the BF 2 complex of a dihydroxydione with a
perfluorotetracene skeleton. Org Lett 11:4326–4329
Ortiz MJ, Agarrabeitia AR, Duran-Sampedro G, Prieto JB, Lopez TA, Massad WA, Montejano HA, García NA, Arbeloa IL (2012) Synthesis and functionalization of new polyhalogenated BODIPY dyes. Study of their photophysical properties and singlet oxygen generation.
Tetrahedron 68:1153–1162
Osorio-Martínez CA, Urías-Benavides A, Gómez-Durán CFA, Bañuelos J, Esnal I, Arbeloa
IL, Peña-Cabrera E (2012) 8-AminoBODIPYs: cyanines or hemicyanines? The effect of the
coplanarity of the amino group on their optical properties. J Org Chem 77:5434–5438
Ozdemir T, Atilgan S, Kutuk I, Yildirim LT, Tulek A, Bayindir M, Akkaya EU (2009) Solid-state
emissive BODIPY dyes with bulky substituents as spacers. Org Lett 11:2105–2107
Y. Kubota
Nagata Y, Chujo Y (2008) Main-chain-type N, N’-chelate organoboron aminoquinolate polymers:
synthesis, luminescence, and energy transfer behavior. Macromolecules 41:3488–3492
Nakamura M, Tahara H, Takahashi K, Nagata T, Uoyama H, Kuzuhara D, Mori S, Okujima T,
Yamada H, Uno H (2012) π-fused bis-BODIPY as a candidate for NIR dyes. Org Biomol Chem
10:6840–6849
Nawn G, Oakley SR, Majewski MB, McDonald R, Patrick BO, Hicks RG (2013) Redox-active, nearinfrared dyes based on ‘Nindigo’ (indigo-N, N’-diarylimine) boron chelate complexes. Chem Sci
4:612–621
Nepomnyashchii AB, Cho S, Rossky PJ, Bard AJ (2010) Dependence of electrochemical and
electrogenerated chemiluminescence properties on the structure of BODIPY dyes. Unusually
large separation between sequential electron transfers. J Am Chem Soc 132:17550–17559
Nepomnyashchii AB, Bröring M, Ahrens J, Bard AJ (2011) Synthesis, photophysical, electrochemical, and electrogenerated chemiluminescence studies. Multiple sequential electron transfers in
BODIPY monomers, dimers, trimers, and polymer. J Am Chem Soc 133:8633–8645
Ni Y, Wu J (2014) Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent
pH probes and bio-imaging. Org Biomol Chem 12:3774–3791
Ni Y, Zeng W, Huang K-W, Wu J (2013) Benzene-fused BODIPYs: synthesis and the impact of
fusion mode. Chem Commun 49:1217–1219
Ni Y, Kannadorai RK, Peng J, Yu SW-K, Chang Y-T, Wu J (2016a) Naphthalene-fused BODIPY
near-infrared dye as a stable contrast agent for in vivo photoacoustic imaging. Chem Commun
52:11504–11507
Ni Y, Lee S, Son M, Aratani N, Ishida M, Samanta A, Yamada H, Chang Y-T, Furuta H, Kim
D, Wu J (2016b) A diradical approach towards BODIPY-based dyes with intense near-infrared
absorption around λ = 1100 nm. Angew Chem Int Ed 55:2815–2819
Numano M, Nagami N, Nakatsuka S, Katayama T, Nakajima K, Tatsumi S, Yasuda N, Hatakeyama T
(2016) Synthesis of boronate-based benzo[fg]tetracene and benzo[hi]hexacene via demethylative
direct borylation. Chem Eur J 22:11574–11577
Oda S, Shimizu T, Katayama T, Yoshikawa H, Hatakeyama T (2019) Tetracoordinate boron-fused
double [5]helicenes as cathode active materials for lithium batteries. Org Lett 21:1770–1773
Ohtani S, Gon M, Tanaka K, Chujo Y (2017) A flexible, fused, azomethine-boron complex: thermochromic luminescence and thermosalient behavior in structural transitions between crystalline
polymorphs. Chem Eur J 23:11827–11833
Okujima T, Tomimori Y, Nakamura J, Yamada H, Uno H, Ono N (2010) Synthesis of π-expanded
BODIPYs and their fluorescent properties in the visible–near–infrared region. Tetrahedron
66:6895–6900
Ono N, Hironaga H, Ono K, Kaneko S, Murashima T, Ueda T, Tsukamura C, Ogawa T (1996) A
new synthesis of pyrroles and porphyrins fused with aromatic rings. J Chem Soc Perkin Trans
1:417–423
Ono N, Yamamoto T, Shimada N, Kuroki K, Wada M, Utsunomiya R, Yano T, Uno H, Murashima
T (2003) A new synthesis of functional dyes from 2-Acenaphtho[1,2-c]pyrrole. Heterocycles
61:433–447
Ono K, Hashizume J, Yamaguchi H, Tomura M, Nishida J, Yamashita Y (2009) Synthesis, crystal
structure, and electron-accepting property of the BF 2 complex of a dihydroxydione with a
perfluorotetracene skeleton. Org Lett 11:4326–4329
Ortiz MJ, Agarrabeitia AR, Duran-Sampedro G, Prieto JB, Lopez TA, Massad WA, Montejano HA, García NA, Arbeloa IL (2012) Synthesis and functionalization of new polyhalogenated BODIPY dyes. Study of their photophysical properties and singlet oxygen generation.
Tetrahedron 68:1153–1162
Osorio-Martínez CA, Urías-Benavides A, Gómez-Durán CFA, Bañuelos J, Esnal I, Arbeloa
IL, Peña-Cabrera E (2012) 8-AminoBODIPYs: cyanines or hemicyanines? The effect of the
coplanarity of the amino group on their optical properties. J Org Chem 77:5434–5438
Ozdemir T, Atilgan S, Kutuk I, Yildirim LT, Tulek A, Bayindir M, Akkaya EU (2009) Solid-state
emissive BODIPY dyes with bulky substituents as spacers. Org Lett 11:2105–2107