5 BODIPY Dyes and Their Analogues
213
Sheng W, Cui J, Ruan Z, Yan L, Wu Q, Yu C, Wei Y, Hao E, Jiao L (2017a) [a]-phenanthrene-fused
BF 2 azadipyrromethene (AzaBODIPY) dyes as bright near-infrared fluorophores. J Org Chem
82:10341–10349
Sheng W, Zheng Y-Q, Wu Q, Wu Y, Yu C, Jiao L, Hao E, Wang J-Y, Pei J (2017b) Synthesis,
properties, and semiconducting characteristics of BF2 complexes of β, β-bisphenanthrene-fused
azadipyrromethenes. Org Lett 19:2893–2896
Sheng W, Wu Y, Yu C, Bobadova-Parvanova P, Hao E, Jiao L (2018) Synthesis, crystal structure, and
the deep near-infrared absorption/emission of bright AzaBODIPY-based organic fluorophores.
Org Lett 20:2620–2623
Shimizu S, Kobayashi N (2014) Structurally-modified subphthalocyanines: molecular design
towards realization of expected properties from the electronic structure and structural features of
subphthalocyanine. Chem Commun 50:6949–6966
Shimizu S, Otaki T, Yamazaki Y, Kobayashi N (2012) Synthesis and properties of β, β-sp3hybridized subphthalocyanine analogues. Chem Commun 48:4100–4102
Shimizu S, Iino T, Araki Y, Kobayashi N (2013) Pyrrolopyrrole aza-BODIPY analogues: a facile
synthesis and intense fluorescence. Chem Commun 49:1621–1623
Shimizu S, Murayama A, Haruyama T, Iino T, Mori S, Furuta H, Kobayashi N (2015) Benzo[c,
d]indole-containing Aza-BODIPY dyes: asymmetrization-induced solid-state emission and
aggregation-induced emission enhancement as new properties of a well-known chromophore.
Chem Eur J 21:12996–13003
Shimogawa H, Mori H, Wakamiya A, Murata Y (2013) Impacts of dibenzo- and dithieno-fused
structures at the b, g bonds in the BODIPY skeleton. Chem Lett 42:986–988
Shimogawa H, Murata Y, Wakamiya A (2018) NIR-absorbing dye based on BF 2 -bridged azafulvene
dimer as a strong electron-accepting unit. Org Lett 20:5135–5138
Singh SP, Gayathri T (2014) Evolution of BODIPY dyes as potential sensitizers for dye-sensitized
solar cells. Eur J Org Chem 4689–4707
Singh RS, Yadav M, Gupta RK, Pandey R, Pandey DS (2013) Luminescent N, O-chelated chromanBF2 complexes: structural variants of BODIPY. Dalton Trans 42:1696–1707
Smithen DA, Baker AEG, Offman M, Crawford SM, Cameron TS, Thompson A (2012) Use of
F-BODIPYs as a protection strategy for dipyrrins: optimization of BF 2 removal. J Org Chem
77:3439–3453
Solomonov AV, Marfin YS, Rumyantsev EV (2019) Design and applications of dipyrrin-based
fluorescent dyes and related organic luminophores: from individual compounds to supramolecular
self-assembled systems. Dyes Pigm 162:517–542
Speck K, Magauer T (2013) The chemistry of isoindole natural products. Beilstein J Org Chem
9:2048–2078
Strickler SJ, Berg RA (1962) Relationship between absorption intensity and fluorescence lifetime
of molecules. J Chem Phys 37:814–822
Suenaga K, Tanaka K, Chujo Y (2017) Design and luminescence chromism of fused boron
complexes having constant emission efficiencies in solution and in the amorphous and crystalline
states. Eur J Org Chem 5191–5196
Sun L, Zhang F, Wang X, Qiu F, Xue M, Tregnago G, Cacialli F, Osella S, Beljonne D, Feng X
(2015) Geometric and electronic structures of boron(III)-cored dyes tailored by incorporation of
heteroatoms into ligands. Chem Asian J 10:709–714
Sun Z-B, Guo M, Zhao C-H (2016) Synthesis and properties of benzothieno[b]-fused BODIPY
dyes. J Org Chem 81:229–237
Sun Y, Qu Z, Zhou Z, Gai L, Lu H (2019) Thieno[3,2-b]thiophene fused BODIPYs: synthesis,
near-infrared luminescence and photosensitive properties. Org Biomol Chem 17:3617–3622
Sutter A, Elhabiri M, Ulrich G (2018) Fluorescent pH-responsive probes based on water-soluble
boron-dipyrromethene (BODIPY) derivatives, featuring long-wavelength emission. Chem Eur J
24:11119–11130
213
Sheng W, Cui J, Ruan Z, Yan L, Wu Q, Yu C, Wei Y, Hao E, Jiao L (2017a) [a]-phenanthrene-fused
BF 2 azadipyrromethene (AzaBODIPY) dyes as bright near-infrared fluorophores. J Org Chem
82:10341–10349
Sheng W, Zheng Y-Q, Wu Q, Wu Y, Yu C, Jiao L, Hao E, Wang J-Y, Pei J (2017b) Synthesis,
properties, and semiconducting characteristics of BF2 complexes of β, β-bisphenanthrene-fused
azadipyrromethenes. Org Lett 19:2893–2896
Sheng W, Wu Y, Yu C, Bobadova-Parvanova P, Hao E, Jiao L (2018) Synthesis, crystal structure, and
the deep near-infrared absorption/emission of bright AzaBODIPY-based organic fluorophores.
Org Lett 20:2620–2623
Shimizu S, Kobayashi N (2014) Structurally-modified subphthalocyanines: molecular design
towards realization of expected properties from the electronic structure and structural features of
subphthalocyanine. Chem Commun 50:6949–6966
Shimizu S, Otaki T, Yamazaki Y, Kobayashi N (2012) Synthesis and properties of β, β-sp3hybridized subphthalocyanine analogues. Chem Commun 48:4100–4102
Shimizu S, Iino T, Araki Y, Kobayashi N (2013) Pyrrolopyrrole aza-BODIPY analogues: a facile
synthesis and intense fluorescence. Chem Commun 49:1621–1623
Shimizu S, Murayama A, Haruyama T, Iino T, Mori S, Furuta H, Kobayashi N (2015) Benzo[c,
d]indole-containing Aza-BODIPY dyes: asymmetrization-induced solid-state emission and
aggregation-induced emission enhancement as new properties of a well-known chromophore.
Chem Eur J 21:12996–13003
Shimogawa H, Mori H, Wakamiya A, Murata Y (2013) Impacts of dibenzo- and dithieno-fused
structures at the b, g bonds in the BODIPY skeleton. Chem Lett 42:986–988
Shimogawa H, Murata Y, Wakamiya A (2018) NIR-absorbing dye based on BF 2 -bridged azafulvene
dimer as a strong electron-accepting unit. Org Lett 20:5135–5138
Singh SP, Gayathri T (2014) Evolution of BODIPY dyes as potential sensitizers for dye-sensitized
solar cells. Eur J Org Chem 4689–4707
Singh RS, Yadav M, Gupta RK, Pandey R, Pandey DS (2013) Luminescent N, O-chelated chromanBF2 complexes: structural variants of BODIPY. Dalton Trans 42:1696–1707
Smithen DA, Baker AEG, Offman M, Crawford SM, Cameron TS, Thompson A (2012) Use of
F-BODIPYs as a protection strategy for dipyrrins: optimization of BF 2 removal. J Org Chem
77:3439–3453
Solomonov AV, Marfin YS, Rumyantsev EV (2019) Design and applications of dipyrrin-based
fluorescent dyes and related organic luminophores: from individual compounds to supramolecular
self-assembled systems. Dyes Pigm 162:517–542
Speck K, Magauer T (2013) The chemistry of isoindole natural products. Beilstein J Org Chem
9:2048–2078
Strickler SJ, Berg RA (1962) Relationship between absorption intensity and fluorescence lifetime
of molecules. J Chem Phys 37:814–822
Suenaga K, Tanaka K, Chujo Y (2017) Design and luminescence chromism of fused boron
complexes having constant emission efficiencies in solution and in the amorphous and crystalline
states. Eur J Org Chem 5191–5196
Sun L, Zhang F, Wang X, Qiu F, Xue M, Tregnago G, Cacialli F, Osella S, Beljonne D, Feng X
(2015) Geometric and electronic structures of boron(III)-cored dyes tailored by incorporation of
heteroatoms into ligands. Chem Asian J 10:709–714
Sun Z-B, Guo M, Zhao C-H (2016) Synthesis and properties of benzothieno[b]-fused BODIPY
dyes. J Org Chem 81:229–237
Sun Y, Qu Z, Zhou Z, Gai L, Lu H (2019) Thieno[3,2-b]thiophene fused BODIPYs: synthesis,
near-infrared luminescence and photosensitive properties. Org Biomol Chem 17:3617–3622
Sutter A, Elhabiri M, Ulrich G (2018) Fluorescent pH-responsive probes based on water-soluble
boron-dipyrromethene (BODIPY) derivatives, featuring long-wavelength emission. Chem Eur J
24:11119–11130