5 BODIPY Dyes and Their Analogues
209
Maeda C, Todaka T, Ueda T, Ema T (2017) Synthesis of carbazole-based BODIPY dimers showing
red fluorescence in the solid state. Org Biomol Chem 15:9283–9287
Maeda C, Nagahata K, Takaishi K, Ema T (2019) Synthesis of chiral carbazole-based BODIPYs
showing circularly polarized luminescence. Chem Commun 55:3136–3139
Mao M, Song Q-H (2016) 18 F-labeling of arenes and heteroarenes for applications in positron
emission tomography. Chem Rec 16:719–733
Mao M, Zhang X, Cao L, Tong Y, Wu G (2015) Design of Bodipy based organic dyes for highefficient dye-sensitized solar cells employing double electron acceptors. Dyes Pigm 117:28–36
Marks T, Daltrozzo E, Zumbusch A (2014) Azacyanines of the pyrrolopyrrole series. Chem Eur J
20:6494–6504
Más-Montoya M, Usea L, Ferao AE, Montenegro MF, de Arellano CR, Tárraga A, Rodríguez-López
JN, Curiel D (2016) Single heteroatom fine-tuning of the emissive properties in organoboron
complexes with 7-(azaheteroaryl)indole systems. J Org Chem 81:3296–3302
Matsui A, Umezawa K, Shindo Y, Fujii T, Citterio D, Oka K, Suzuki K (2011) A near-infrared
fluorescent calcium probe: a new tool for intracellular multicolour Ca2+ imaging. Chem Commun
47:10407–10409
Meesala Y, Kavala V, Chang H-C, Kuo T-S, Yao C-F, Lee W-Z (2015) Synthesis, structures and
electrochemical and photophysical properties of anilido-benzoxazole boron difluoride (ABB)
complexes. Dalton Trans 44:1120–1129
Mei J, Leung NLC, Kwok RTK, Lam JWY, Tang BZ (2015) Aggregation-induced emission: together
we shine, united we soar! Chem Rev 115:11718–11940
Meller A, Ossko A (1972) Phthalocyaninartige bor-komplexe. Monatsh Chem 103:150–155
Michel BW, Lippert AR, Chang CJ (2012) A reaction-based fluorescent probe for selective imaging
of carbon monoxide in living cells using a palladium-mediated carbonylation. J Am Chem Soc
134:15668–15671
Min Y, Dou C, Tian H, Geng Y, Liu J, Wang L (2018) n-type azaacenes containing B ← N units.
Angew Chem Int Ed 57:2000–2004
Min Y, Dou C, Tian H, Liu J, Wang L (2019) A disk-type polyarene containing four B ← N units.
Chem Commun 55:3638–3641
Mirloup A, Huaulmé Q, Leclerc N, Lévêque P, Heiser T, Retailleau P, Ziessel R (2015) ThienylBOPHY dyes as promising templates for bulk heterojunction solar cells. Chem Commun
51:14742–14745
Monsma FJ, Barton AC, Kang HC, Brassard DL, Haughland RP, Sibley DR (1989) Characterization
of novel fluorescent ligands with high affinity for D 1 and D 2 dopaminergic receptors. J Neurochem
52:1641–1644
More AB, Mula S, Thakare S, Sekar N, Ray AK, Chattopadhyay S (2014) Masking and demasking
strategies for the BF 2 –BODIPYs as a tool for BODIPY fluorophores. J Org Chem 79:10981–
10987
Morgan GT, Tunstall RB (1924) CCLIII.—Researches on residual affinity and coordination. Part
XXI. Boron β-diketone difluorides. J Chem Soc Trans 125:1963–1967
Moriya K, Shimada R, Ono K (2019) Difluoroboron chelation to quinacridonequinone: a synthetic
method for air-sensitive 6,13-dihydroxyquinacridone via boron complexes. Chem Asian J
14:1452–1456
Mula S, Ray AK, Banerjee M, Chaudhuri T, Dasgupta K, Chattopadhyay S (2008) Design and
development of a new pyrromethene dye with improved photostability and lasing efficiency:
theoretical rationalization of photophysical and photochemical properties. J Org Chem 73:2146–
2154
Mula S, Leclerc N, Lévêque P, Retailleau P, Ulrich G (2018) Synthesis of indolo[3,2-b]carbazolebased boron complexes with tunable photophysical and electrochemical properties. J Org Chem
83:14406–14418
Murale DP, Lee KM, Kim K, Churchill DG (2011) Facile “one pot” route to the novel benzazulenetype dye class: asymmetric, derivatizable, 5-7-6 fused ring puckered half BODIPY design. Chem
Commun 47:12512–12514
209
Maeda C, Todaka T, Ueda T, Ema T (2017) Synthesis of carbazole-based BODIPY dimers showing
red fluorescence in the solid state. Org Biomol Chem 15:9283–9287
Maeda C, Nagahata K, Takaishi K, Ema T (2019) Synthesis of chiral carbazole-based BODIPYs
showing circularly polarized luminescence. Chem Commun 55:3136–3139
Mao M, Song Q-H (2016) 18 F-labeling of arenes and heteroarenes for applications in positron
emission tomography. Chem Rec 16:719–733
Mao M, Zhang X, Cao L, Tong Y, Wu G (2015) Design of Bodipy based organic dyes for highefficient dye-sensitized solar cells employing double electron acceptors. Dyes Pigm 117:28–36
Marks T, Daltrozzo E, Zumbusch A (2014) Azacyanines of the pyrrolopyrrole series. Chem Eur J
20:6494–6504
Más-Montoya M, Usea L, Ferao AE, Montenegro MF, de Arellano CR, Tárraga A, Rodríguez-López
JN, Curiel D (2016) Single heteroatom fine-tuning of the emissive properties in organoboron
complexes with 7-(azaheteroaryl)indole systems. J Org Chem 81:3296–3302
Matsui A, Umezawa K, Shindo Y, Fujii T, Citterio D, Oka K, Suzuki K (2011) A near-infrared
fluorescent calcium probe: a new tool for intracellular multicolour Ca2+ imaging. Chem Commun
47:10407–10409
Meesala Y, Kavala V, Chang H-C, Kuo T-S, Yao C-F, Lee W-Z (2015) Synthesis, structures and
electrochemical and photophysical properties of anilido-benzoxazole boron difluoride (ABB)
complexes. Dalton Trans 44:1120–1129
Mei J, Leung NLC, Kwok RTK, Lam JWY, Tang BZ (2015) Aggregation-induced emission: together
we shine, united we soar! Chem Rev 115:11718–11940
Meller A, Ossko A (1972) Phthalocyaninartige bor-komplexe. Monatsh Chem 103:150–155
Michel BW, Lippert AR, Chang CJ (2012) A reaction-based fluorescent probe for selective imaging
of carbon monoxide in living cells using a palladium-mediated carbonylation. J Am Chem Soc
134:15668–15671
Min Y, Dou C, Tian H, Geng Y, Liu J, Wang L (2018) n-type azaacenes containing B ← N units.
Angew Chem Int Ed 57:2000–2004
Min Y, Dou C, Tian H, Liu J, Wang L (2019) A disk-type polyarene containing four B ← N units.
Chem Commun 55:3638–3641
Mirloup A, Huaulmé Q, Leclerc N, Lévêque P, Heiser T, Retailleau P, Ziessel R (2015) ThienylBOPHY dyes as promising templates for bulk heterojunction solar cells. Chem Commun
51:14742–14745
Monsma FJ, Barton AC, Kang HC, Brassard DL, Haughland RP, Sibley DR (1989) Characterization
of novel fluorescent ligands with high affinity for D 1 and D 2 dopaminergic receptors. J Neurochem
52:1641–1644
More AB, Mula S, Thakare S, Sekar N, Ray AK, Chattopadhyay S (2014) Masking and demasking
strategies for the BF 2 –BODIPYs as a tool for BODIPY fluorophores. J Org Chem 79:10981–
10987
Morgan GT, Tunstall RB (1924) CCLIII.—Researches on residual affinity and coordination. Part
XXI. Boron β-diketone difluorides. J Chem Soc Trans 125:1963–1967
Moriya K, Shimada R, Ono K (2019) Difluoroboron chelation to quinacridonequinone: a synthetic
method for air-sensitive 6,13-dihydroxyquinacridone via boron complexes. Chem Asian J
14:1452–1456
Mula S, Ray AK, Banerjee M, Chaudhuri T, Dasgupta K, Chattopadhyay S (2008) Design and
development of a new pyrromethene dye with improved photostability and lasing efficiency:
theoretical rationalization of photophysical and photochemical properties. J Org Chem 73:2146–
2154
Mula S, Leclerc N, Lévêque P, Retailleau P, Ulrich G (2018) Synthesis of indolo[3,2-b]carbazolebased boron complexes with tunable photophysical and electrochemical properties. J Org Chem
83:14406–14418
Murale DP, Lee KM, Kim K, Churchill DG (2011) Facile “one pot” route to the novel benzazulenetype dye class: asymmetric, derivatizable, 5-7-6 fused ring puckered half BODIPY design. Chem
Commun 47:12512–12514