5 BODIPY Dyes and Their Analogues
205
Jones G II, Kumar S, Klueva O, Pacheco D (2003) Photoinduced electron transfer for pyrromethene
dyes. J Phys Chem A 107:8429–8434
Kage Y, Mori S, Ide M, Saeki A, Furuta H, Shimizu S (2018) Blackening of aza-BODIPY analogues
by simple dimerization: panchromatic absorption of a pyrrolopyrrole aza-BODIPY dimer. Mater
Chem Front 2:112–120
Kaim W, Shultz A (1984) p-Phenylenediboranes: mirror images of p-phenylenediamines? Angew
Chem Int Ed 23:615–616
Kamada K, Namikawa T, Senatore S, Matthews C, Lenne P-F, Maury O, Andraud C, Ponce-Vargas
M, Le Guennic B, Jacquemin D, Agbo P, An DD, Gauny SS, Liu X, Abergel RJ, Fages F,
D´Aléo A (2016) Boron difluoride curcuminoid fluorophores with enhanced two-photon excited
fluorescence emission and versatile living-cell imaging properties. Chem Eur J 22:5219–5232
Kamkaew A, Lim SH, Lee HB, Kiew LV, Chung LY, Burgess K (2013) BODIPY dyes in
photodynamic therapy. Chem Soc Rev 42:77–88
Kang HC, Haugland RP (1995) US 5433896
Kee HL, Kirmaier C, Yu L, Thamyongkit P, Youngblood WJ, Calder ME, Ramos L, Noll BC, Bocian
DF, Scheidt WR, Birge RR, Lindsey JS, Holten D (2005) Structural control of the photodynamics
of boron–dipyrrin complexes. J Phys Chem B 109:20433–20443
Killoran J, O’Shea DF (2006) Impact of a conformationally restricted receptor on the BF 2 chelated
azadipyrromethene fluorosensing platform. Chem Commun 1503–1505
Killoran J, Allen L, Gallagher JF, Gallagher WM, O’Shea DF (2002) Synthesis of BF 2 chelates of
tetraarylazadipyrromethenes and evidence for their photodynamic therapeutic behavior. Chem
Commun 1862–1863
Kim H, Burghart A, Welch MB, Reibenspies J, Burgess K (1999) Synthesis and spectroscopic
properties of a new 4-bora-3a,4a-diaza-s-indacene (BODIPY) dye. Chem Commun 1889–1890
Kim HN, Ren WX, Kim JS, Yoon J (2012) Fluorescent and colorimetric sensors for detection of
lead, cadmium, and mercury ions. Chem Soc Rev 41:3210–3244
Kim S, Bouffard J, Kim Y (2015) Tailoring the solid-state fluorescence emission of BODIPY dyes
by meso substitution. Chem Eur J 21:17459–17465
Klfout H, Stewart A, Elkhalifa M, He H (2017) BODIPYs for dye-sensitized solar cells. ACS Appl
Mater Interfaces 9:39873–39889
Kobayashi N, Nonomura T (2002) First observation of the circular dichroism spectra of chiral
subphthalocyanines with C 3 symmetry. Tetrahedron Lett 43:4253–4255
Kobayashi N, Kondo R, Nakajima S, Osa T (1990) New route to unsymmetrical phthalocyanine
analogs by the use of structurally distorted subphthalocyanines. J Am Chem Soc 112:9640–9641
Kobayashi N, Takeuchi Y, Matsuda A (2007) meso-Aryl subporphyrins. Angew Chem Int Ed
46:758–760
Koch M, Perumal K, Blacque O, Garg JA, Saiganesh R, Kabilan S, Balasubramanian KK,
Venkatesan K (2014) Metal-free triplet phosphors with high emission efficiency and high
tenability. Angew Chem Int Ed 53:6378–6382
Köhler T, Hodgson MC, Seidel D, Veauthier JM, Meyer S, Lynch V, Boyd PDW, Brothers PJ, Sessler
JL (2004) Octaethylporphyrin and expanded porphyrin complexes containing coordinated BF 2
groups. Chem Commun 1060–1061
Kolemen S, Akkaya EU (2018) Reaction-based BODIPY probes for selective bio-imaging. Coord
Chem Rev 354:121–134
Komatsu T, Oushiki D, Takeda A, Miyamura M, Ueno T, Terai T, Hanaoka K, Urano Y, Mineno
T, Nagano T (2011) Rational design of boron dipyrromethene (BODIPY)-based photobleachingresistant fluorophores applicable to a protein dynamics study. Chem Commun 47:10055–10057
Kondakova ME, Deaton JC, Pawlik TD, Giesen DJ, Kondakov DY, Young RH, Royster TL,
Comfort DL, Shore JD (2010) Highly efficient fluorescent-phosphorescent triplet-harvesting
hybrid organic light-emitting diodes. J Appl Phys 107:014515
Kowada T, Yamaguchi S, Ohe K (2010) Highly fluorescent BODIPY dyes modulated with
spirofluorene moieties. Org Lett 12:296–299
205
Jones G II, Kumar S, Klueva O, Pacheco D (2003) Photoinduced electron transfer for pyrromethene
dyes. J Phys Chem A 107:8429–8434
Kage Y, Mori S, Ide M, Saeki A, Furuta H, Shimizu S (2018) Blackening of aza-BODIPY analogues
by simple dimerization: panchromatic absorption of a pyrrolopyrrole aza-BODIPY dimer. Mater
Chem Front 2:112–120
Kaim W, Shultz A (1984) p-Phenylenediboranes: mirror images of p-phenylenediamines? Angew
Chem Int Ed 23:615–616
Kamada K, Namikawa T, Senatore S, Matthews C, Lenne P-F, Maury O, Andraud C, Ponce-Vargas
M, Le Guennic B, Jacquemin D, Agbo P, An DD, Gauny SS, Liu X, Abergel RJ, Fages F,
D´Aléo A (2016) Boron difluoride curcuminoid fluorophores with enhanced two-photon excited
fluorescence emission and versatile living-cell imaging properties. Chem Eur J 22:5219–5232
Kamkaew A, Lim SH, Lee HB, Kiew LV, Chung LY, Burgess K (2013) BODIPY dyes in
photodynamic therapy. Chem Soc Rev 42:77–88
Kang HC, Haugland RP (1995) US 5433896
Kee HL, Kirmaier C, Yu L, Thamyongkit P, Youngblood WJ, Calder ME, Ramos L, Noll BC, Bocian
DF, Scheidt WR, Birge RR, Lindsey JS, Holten D (2005) Structural control of the photodynamics
of boron–dipyrrin complexes. J Phys Chem B 109:20433–20443
Killoran J, O’Shea DF (2006) Impact of a conformationally restricted receptor on the BF 2 chelated
azadipyrromethene fluorosensing platform. Chem Commun 1503–1505
Killoran J, Allen L, Gallagher JF, Gallagher WM, O’Shea DF (2002) Synthesis of BF 2 chelates of
tetraarylazadipyrromethenes and evidence for their photodynamic therapeutic behavior. Chem
Commun 1862–1863
Kim H, Burghart A, Welch MB, Reibenspies J, Burgess K (1999) Synthesis and spectroscopic
properties of a new 4-bora-3a,4a-diaza-s-indacene (BODIPY) dye. Chem Commun 1889–1890
Kim HN, Ren WX, Kim JS, Yoon J (2012) Fluorescent and colorimetric sensors for detection of
lead, cadmium, and mercury ions. Chem Soc Rev 41:3210–3244
Kim S, Bouffard J, Kim Y (2015) Tailoring the solid-state fluorescence emission of BODIPY dyes
by meso substitution. Chem Eur J 21:17459–17465
Klfout H, Stewart A, Elkhalifa M, He H (2017) BODIPYs for dye-sensitized solar cells. ACS Appl
Mater Interfaces 9:39873–39889
Kobayashi N, Nonomura T (2002) First observation of the circular dichroism spectra of chiral
subphthalocyanines with C 3 symmetry. Tetrahedron Lett 43:4253–4255
Kobayashi N, Kondo R, Nakajima S, Osa T (1990) New route to unsymmetrical phthalocyanine
analogs by the use of structurally distorted subphthalocyanines. J Am Chem Soc 112:9640–9641
Kobayashi N, Takeuchi Y, Matsuda A (2007) meso-Aryl subporphyrins. Angew Chem Int Ed
46:758–760
Koch M, Perumal K, Blacque O, Garg JA, Saiganesh R, Kabilan S, Balasubramanian KK,
Venkatesan K (2014) Metal-free triplet phosphors with high emission efficiency and high
tenability. Angew Chem Int Ed 53:6378–6382
Köhler T, Hodgson MC, Seidel D, Veauthier JM, Meyer S, Lynch V, Boyd PDW, Brothers PJ, Sessler
JL (2004) Octaethylporphyrin and expanded porphyrin complexes containing coordinated BF 2
groups. Chem Commun 1060–1061
Kolemen S, Akkaya EU (2018) Reaction-based BODIPY probes for selective bio-imaging. Coord
Chem Rev 354:121–134
Komatsu T, Oushiki D, Takeda A, Miyamura M, Ueno T, Terai T, Hanaoka K, Urano Y, Mineno
T, Nagano T (2011) Rational design of boron dipyrromethene (BODIPY)-based photobleachingresistant fluorophores applicable to a protein dynamics study. Chem Commun 47:10055–10057
Kondakova ME, Deaton JC, Pawlik TD, Giesen DJ, Kondakov DY, Young RH, Royster TL,
Comfort DL, Shore JD (2010) Highly efficient fluorescent-phosphorescent triplet-harvesting
hybrid organic light-emitting diodes. J Appl Phys 107:014515
Kowada T, Yamaguchi S, Ohe K (2010) Highly fluorescent BODIPY dyes modulated with
spirofluorene moieties. Org Lett 12:296–299