214
Y. Kubota
Swavey S, Coladipietro M, Burbayea A, Krause JA (2016) Two-step synthetic route toward asymmetric and symmetric boron dipyrromethenes: synthesis, optical properties, and electrochemistry.
Eur J Org Chem 4429–4435
Swavey S, Quinn J, Coladipietro M, Cox KG, Brennaman MK (2017) Tuning the photophysical
properties of BODIPY dyes through extended aromatic pyrroles. RSC Adv 7:173–179
Szyszko B, Chmielewski PJ, Przewo´ znik M, Białek MJ, Kupietz K, Biało´ nska A, LatosGra˙ zy´ nski L (2019) Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): conformational switching controls
the stereochemical dynamics of the topologically chiral system. J Am Chem Soc 141:6060–6072
Tahtaoui C, Thomas C, Rohmer F, Klotz P, Duportail G, Mély Y, Bonnet D, Hibert M (2007) Convenient method to access new 4,4-dialkoxy- and 4,4-diaryloxy-diaza-s-indacene dyes: synthesis and
spectroscopic evaluation. J Org Chem 72:269–272
Tamgho I-S, Hasheminasab A, Engle JT, Nemykin VN, Ziegler CJ (2014) A new highly fluorescent
and symmetric pyrrole–BF 2 chromophore: BOPHY. J Am Chem Soc 136:5623–5626
Tanaka T, Chujo Y (2015) Recent progress of optical functional nanomaterials based on organoboron
complexes with β-diketonate, ketoiminate and diiminate. NPG Asia Mater 7:e223
Tanaka K, Yamane H, Yoshii R, Chujo Y (2013) Efficient light absorbers based on thiophene-fused
boron dipyrromethene (BODIPY) dyes. Bioorg Med Chem 21:2715–2719
Tanaka H, Inoue Y, Mori T (2018) Circularly polarized luminescence and circular dichroisms
in small organic molecules: correlation between excitation and emission dissymmetry factors.
ChemPhoto-Chem 2:386–402
Tathe AB, Sekar N (2016) Red emitting coumarin—azo dyes: synthesis, characterization, linear and
non-linear optical properties-experimental and computational approach. J Fluoresc 26:1279–1293
Tay ACY, Frogley BJ, Ware DC, Conradie J, Ghosh A, Brothers PJ (2019) Tetrahedral pegs in
square holes: stereochemistry of diboron porphyrazines and phthalocyanines. Angew Chem Int
Ed 58:3057–3061
Thivierge C, Bandichhor R, Burgess K (2007) Spectral dispersion and water solubilization of
BODIPY dyes via palladium-catalyzed C–H functionalization. Org Lett 9:2135–2138
Thorat KG, Kamble P, Mallah R, Ray AK, Sekar N (2015) Congeners of pyrromethene-567 dye:
perspectives from synthesis, photophysics, photostability, laser, and TD-DFT theory. J Org Chem
80:6152–6164
Tokoro Y, Nagai A, Chujo Y (2010) Synthesis of π-conjugated polymers containing organoboron
benzo[h]quinolate in the main chain. Macromolecules 43:6229–6233
Tomimori Y, Okujima T, Yano T, Mori S, Ono N, Yamada H, Uno H (2011) Synthesis of π-expanded
O-chelated boron–dipyrromethene as an NIR dye. Tetrahedron 67:3187–3193
Treibs A, Kreuzer F-H (1968) Difluorboryl-komplexe von di- und tripyrrylmethenen. Justus Liebigs
Ann Chem 718:208–223
Tsurumaki E, Saito S, Kim KS, Lim JM, Inokuma Y, Kim D, Osuka A (2008) Synthesis and
characterization of meso-Aryl-substituted subchlorins. J Am Chem Soc 130:438–439
Turkoglu G, Cinar ME, Ozturk T (2017) Triarylborane-based materials for OLED applications.
Molecules 22:1522
Turro NJ (1991) Modern molecular photochemistry. University Science Books, CA
Ulrich G, Goze C, Goeb S, Retailleau P, Ziessel R (2006) New fluorescent aryl- or ethynylarylboron-substituted indacenes as promising dyes. New J Chem 30:982–986
Ulrich G, Ziessel R, Harriman A (2008) The chemistry of fluorescent bodipy dyes: versatility
unsurpassed. Angew Chem Int Ed 47:1184–1201
Ulrich G, Goeb S, De Nicola A, Retailleau P, Ziessel R (2011) Chemistry at boron: synthesis
and properties of red to near-IR fluorescent dyes based on boron-substituted diisoindolomethene
frameworks. J Org Chem 76:4489–4505
Umezawa K, Nakamura Y, Makino H, Citterio D, Suzuki K (2008) Bright, color-tunable fluorescent
dyes in the visible–near-infrared region. J Am Chem Soc 130:1550–1551
Umezawa K, Matsui A, Nakamura Y, Citterio D, Suzuki K (2009) Bright, color-tunable fluorescent
dyes in the Vis/NIR region: establishment of new “tailor-made” multicolor fluorophores based
on borondipyrromethene. Chem Eur J 15:1096–1106
Y. Kubota
Swavey S, Coladipietro M, Burbayea A, Krause JA (2016) Two-step synthetic route toward asymmetric and symmetric boron dipyrromethenes: synthesis, optical properties, and electrochemistry.
Eur J Org Chem 4429–4435
Swavey S, Quinn J, Coladipietro M, Cox KG, Brennaman MK (2017) Tuning the photophysical
properties of BODIPY dyes through extended aromatic pyrroles. RSC Adv 7:173–179
Szyszko B, Chmielewski PJ, Przewo´ znik M, Białek MJ, Kupietz K, Biało´ nska A, LatosGra˙ zy´ nski L (2019) Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): conformational switching controls
the stereochemical dynamics of the topologically chiral system. J Am Chem Soc 141:6060–6072
Tahtaoui C, Thomas C, Rohmer F, Klotz P, Duportail G, Mély Y, Bonnet D, Hibert M (2007) Convenient method to access new 4,4-dialkoxy- and 4,4-diaryloxy-diaza-s-indacene dyes: synthesis and
spectroscopic evaluation. J Org Chem 72:269–272
Tamgho I-S, Hasheminasab A, Engle JT, Nemykin VN, Ziegler CJ (2014) A new highly fluorescent
and symmetric pyrrole–BF 2 chromophore: BOPHY. J Am Chem Soc 136:5623–5626
Tanaka T, Chujo Y (2015) Recent progress of optical functional nanomaterials based on organoboron
complexes with β-diketonate, ketoiminate and diiminate. NPG Asia Mater 7:e223
Tanaka K, Yamane H, Yoshii R, Chujo Y (2013) Efficient light absorbers based on thiophene-fused
boron dipyrromethene (BODIPY) dyes. Bioorg Med Chem 21:2715–2719
Tanaka H, Inoue Y, Mori T (2018) Circularly polarized luminescence and circular dichroisms
in small organic molecules: correlation between excitation and emission dissymmetry factors.
ChemPhoto-Chem 2:386–402
Tathe AB, Sekar N (2016) Red emitting coumarin—azo dyes: synthesis, characterization, linear and
non-linear optical properties-experimental and computational approach. J Fluoresc 26:1279–1293
Tay ACY, Frogley BJ, Ware DC, Conradie J, Ghosh A, Brothers PJ (2019) Tetrahedral pegs in
square holes: stereochemistry of diboron porphyrazines and phthalocyanines. Angew Chem Int
Ed 58:3057–3061
Thivierge C, Bandichhor R, Burgess K (2007) Spectral dispersion and water solubilization of
BODIPY dyes via palladium-catalyzed C–H functionalization. Org Lett 9:2135–2138
Thorat KG, Kamble P, Mallah R, Ray AK, Sekar N (2015) Congeners of pyrromethene-567 dye:
perspectives from synthesis, photophysics, photostability, laser, and TD-DFT theory. J Org Chem
80:6152–6164
Tokoro Y, Nagai A, Chujo Y (2010) Synthesis of π-conjugated polymers containing organoboron
benzo[h]quinolate in the main chain. Macromolecules 43:6229–6233
Tomimori Y, Okujima T, Yano T, Mori S, Ono N, Yamada H, Uno H (2011) Synthesis of π-expanded
O-chelated boron–dipyrromethene as an NIR dye. Tetrahedron 67:3187–3193
Treibs A, Kreuzer F-H (1968) Difluorboryl-komplexe von di- und tripyrrylmethenen. Justus Liebigs
Ann Chem 718:208–223
Tsurumaki E, Saito S, Kim KS, Lim JM, Inokuma Y, Kim D, Osuka A (2008) Synthesis and
characterization of meso-Aryl-substituted subchlorins. J Am Chem Soc 130:438–439
Turkoglu G, Cinar ME, Ozturk T (2017) Triarylborane-based materials for OLED applications.
Molecules 22:1522
Turro NJ (1991) Modern molecular photochemistry. University Science Books, CA
Ulrich G, Goze C, Goeb S, Retailleau P, Ziessel R (2006) New fluorescent aryl- or ethynylarylboron-substituted indacenes as promising dyes. New J Chem 30:982–986
Ulrich G, Ziessel R, Harriman A (2008) The chemistry of fluorescent bodipy dyes: versatility
unsurpassed. Angew Chem Int Ed 47:1184–1201
Ulrich G, Goeb S, De Nicola A, Retailleau P, Ziessel R (2011) Chemistry at boron: synthesis
and properties of red to near-IR fluorescent dyes based on boron-substituted diisoindolomethene
frameworks. J Org Chem 76:4489–4505
Umezawa K, Nakamura Y, Makino H, Citterio D, Suzuki K (2008) Bright, color-tunable fluorescent
dyes in the visible–near-infrared region. J Am Chem Soc 130:1550–1551
Umezawa K, Matsui A, Nakamura Y, Citterio D, Suzuki K (2009) Bright, color-tunable fluorescent
dyes in the Vis/NIR region: establishment of new “tailor-made” multicolor fluorophores based
on borondipyrromethene. Chem Eur J 15:1096–1106