J. R. Lakowicz, Principles of fluorescence spectroscopy, Springer, New York, 3rd edn, 2006
B. Valeur and M. N. Berberan-Santos, Molecular fluorescence. Principles and applications, Wiley-VCH, Weinheim (Germany), 2nd edn, 2012
Standardization and quality assurance in fluorescence measurements, in Springer Series on Fluorescence, ed., U. Resch-Genger, Springer, Berlin, 2008
M. Sauer, J. Hofkens and J. Enderlein, Handbook of fluorescence spectroscopy and imaging. From single molecules to ensembles, Wiley-VCH, Weinheim (Germany), 2011
R. P. Haugland, The Handbook. A guide to fluorescent probes and labeling technologies, Invitrogen, Eugene, OR, 10th edn, 2005
A. Treibs F.-H. Kreuzer Difluorboryl-komplexe von di-und tripyrrylmethenen Liebigs Ann. Chem. 1968 718 208 223
A. Loudet K. Burgess BODIPY dyes and their derivatives: syntheses and spectroscopic properties Chem. Rev. 2007 107 4891 4932
G. Ulrich R. Ziessel A. Harriman The chemistry of fluorescent BODIPY dyes: versatility unsurpassed Angew. Chem., Int. Ed. 2008 47 1184 1201
K. Umezawa A. Matsui Y. Nakamura D. Citterio K. Suzuki Bright, color-tunable fluorescent dyes in the vis/NIR region: establishment of new 'tailor-made' multicolor fluorophores based on borondipyrromethene Chem.-Eur. J. 2009 15 1096 1106
L. N. Sobenina A. M. Vasil'tsov O. V. Petrova K. B. Petrushenko I. A. Ushakov G. Clavier R. Méallet-Renault A. I. Mikhaleva B. A. Trofimov General route to symmetric and asymmetric meso-CF3-3(5)-aryl(hetaryl) - and 3,5-diaryl(dihetaryl)-BODIPY dyes Org. Lett. 2011 13 2524 2527
A. Burghart H. Kim M. B. Welch L. H. Thoresen J. Reibenspies K. Burgess 3,5-Diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes: synthesis, spectroscopic, electrochemical, and structural properties J. Org. Chem. 1999 64 7813 7819
A. B. Zaitsev R. Méallet-Renault E. Y. Schmidt A. I. Mikhaleva S. Badré C. Dumas A. M. Vasil'tsov N. V. Zorina R. B. Pansu Synthesis of 2-mesityl-3-methylpyrrole via the Trofimov reaction for a new BODIPY with hindered internal rotation Tetrahedron 2005 61 2683 2688
M. Baruah W. Qin N. Basarić W. M. De Borggraeve N. Boens BODIPY-based hydroxyaryl derivatives as fluorescent pH probes J. Org. Chem. 2005 70 4152 4157
M. Baruah W. Qin R. A. L. Vallée D. Beljonne T. Rohand W. Dehaen N. Boens A highly potassium-selective ratiometric fluorescent indicator based on BODIPY azacrown ether excitable with visible light Org. Lett. 2005 7 4377 4380
T. Rohand M. Baruah W. Qin N. Boens W. Dehaen Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution Chem. Commun. 2006 266 268
W. Qin T. Rohand M. Baruah A. Stefan M. Van der Auweraer W. Dehaen N. Boens Solvent-dependent photophysical properties of borondipyrromethene dyes in solution Chem. Phys. Lett. 2006 420 562 568
T. Rohand J. Lycoops S. Smout E. Braeken M. Sliwa M. Van der Auweraer W. Dehaen W. M. De Borggraeve N. Boens Photophysics of 3,5-diphenoxy substituted BODIPY dyes in solution Photochem. Photobiol. Sci. 2007 6 1061 1066
L. Li B. Nguyen K. Burgess Functionalization of the 4,4-difluoro-4-bora- 3a,4a-diaza-s-indacene (BODIPY) core Bioorg. Med. Chem. Lett. 2008 18 3112 3116
E. Fron E. Coutiño-Gonzalez L. Pandey M. Sliwa M. Van der Auweraer F. C. De Schryver J. Thomas Z. Dong V. Leen M. Smet W. Dehaen T. Vosch Synthesis and photophysical characterization of chalcogen substituted BODIPY dyes New J. Chem. 2009 33 1490 1496
W. Qin V. Leen T. Rohand W. Dehaen P. Dedecker M. Van der Auweraer K. Robeyns L. Van Meervelt D. Beljonne B. Van Averbeke J. N. Clifford K. Driesen K. Binnemans N. Boens Synthesis, spectroscopy, crystal structure, electrochemistry, and quantum chemical and molecular dynamics calculations of a 3-anilino difluoroboron dipyrromethene dye J. Phys. Chem. A 2009 113 439 447
W. Qin V. Leen W. Dehaen J. Cui C. Xu X. Tang W. Liu T. Rohand D. Beljonne B. Van Averbeke J. N. Clifford K. Driesen K. Binnemans M. Van der Auweraer N. Boens 3,5-Dianilino substituted difluoroboron dipyrromethene: synthesis, spectroscopy, photophysics, crystal structure, electrochemistry, and quantum-chemical calculations J. Phys. Chem. C 2009 113 11731 11740
K. Cieślik-Boczula K. Burgess L. Li B. Nguyen L. Pandey W. M. De Borggraeve M. Van der Auweraer N. Boens Photophysics and stability of cyano-substituted boradiazaindacene dyes Photochem. Photobiol. Sci. 2009 8 1006 1015
V. Leen E. Braeken K. Luckermans C. Jackers M. Van der Auweraer N. Boens W. Dehaen A versatile, modular synthesis of monofunctionalized BODIPY dyes Chem. Commun. 2009 4515 4517
S. Rihn P. Retailleau N. Bugsaliewicz A. De Nicola R. Ziessel Versatile synthetic methods for the engineering of thiophene-substituted BODIPY dyes Tetrahedron Lett. 2009 50 7008 7013
L. Jiao C. Yu T. Uppal M. Liu Y. Li Y. Zhou E. Hao X. Hu M. G. H. Vicente Long wavelength red fluorescent dyes from 3,5-diiodo-BODIPYs Org. Biomol. Chem. 2010 8 2517 2519
V. Leen D. Miscoria S. Yin A. Filarowski J. M. Ngongo M. Van der Auweraer N. Boens W. Dehaen 1,7-Disubstituted boron dipyrromethene (BODIPY) dyes: synthesis and spectroscopic properties J. Org. Chem. 2011 76 8168 8176
O. Dilek S. L. Bane Synthesis and spectroscopic characterization of fluorescent boron dipyrromethene-derived hydrazones J. Fluoresc. 2011 21 347 354
L. Jiao W. Pang J. Zhou Y. Wei X. Mu G. Bai E. Hao Regioselective stepwise bromination of boron dipyrromethene (BODIPY) dyes J. Org. Chem. 2011 76 9988 9996
G. Ulrich A. Haefele P. Retailleau R. Ziessel Carbonyl derivatives of boradiazaindacene via catalytic CO insertion J. Org. Chem. 2012 77 5036 5048
T. Rohand W. Qin N. Boens W. Dehaen Palladium-catalyzed coupling reactions for the functionalization of BODIPY dyes with fluorescence spanning the visible spectrum Eur. J. Org. Chem. 2006 4658 4663
W. Qin T. Rohand W. Dehaen J. N. Clifford K. Driesen D. Beljonne B. Van Averbeke M. Van der Auweraer N. Boens Boron dipyrromethene analogs with phenyl, styryl, and ethynylphenyl substituents: synthesis, photophysics, electrochemistry, and quantum-chemical calculations J. Phys. Chem. A 2007 111 8588 8597
V. Leen T. Leemans N. Boens W. Dehaen 2- and 3-Monohalogenated BODIPY dyes and their functionalized analogues: synthesis and spectroscopy Eur. J. Org. Chem. 2011 4386 4396
T. V. Goud A. Tutar J.-F. Biellmann Synthesis of 8-heteroatom-substituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene dyes (BODIPY) Tetrahedron 2006 62 5084 5091
E. Peña-Cabrera A. Aguilar-Aguilar M. González- Domínguez E. Lager R. Zamudio-Vázquez J. Godoy-Vargas F. Villanueva-García Simple, general, and efficient synthesis of meso-substituted borondipyrromethenes from a single platform Org. Lett. 2007 9 3985 3988
J. Han O. Gonzalez A. Aguilar-Aguilar E. Peña-Cabrera K. Burgess 3- and 5-Functionalized BODIPYs via the Liebeskind-Srogl reaction Org. Biomol. Chem. 2009 7 34 36
E. Lager J. Liu A. Aguilar-Aguilar B. Z. Tang E. Peña-Cabrera Novel meso-polyarylamine-BODIPY hybrids: synthesis and study of their optical properties J. Org. Chem. 2009 74 2053 2058
C. F. A. Gómez-Durán I. García-Moreno A. Costela V. Martín R. Sastre J. Bañuelos F. López Arbeloa I. López Arbeloa E. Peña-Cabrera 8-PropargylaminoBODIPY: unprecedented blue-emitting pyrromethene dye. Synthesis, photophysics and laser properties Chem. Commun. 2010 46 5103 5105
I. J. Arroyo R. Hu B. Z. Tang F. I. López E. Peña-Cabrera 8-Alkenylborondipyrromethene dyes. General synthesis, optical properties, and preliminary study of their reactivity Tetrahedron 2011 67 7244 7250
V. Leen V. Z. Gonzalvo W. M. De Borggraeve N. Boens W. Dehaen Direct functionalization of BODIPY dyes by oxidative nucleophilic hydrogen substitution at the 3- or 3,5-positions Chem. Commun. 2010 46 4908 4910
V. Leen M. Van der Auweraer N. Boens W. Dehaen Vicarious nucleophilic substitution of α-hydrogen of BODIPY and its extension to direct ethenylation Org. Lett. 2011 13 1470 1473
C. Thivierge R. Bandichhor K. Burgess Spectral dispersion and water solubilization of BODIPY dyes via palladium-catalyzed C-H functionalization Org. Lett. 2007 9 2135 2138
J. Chen M. Mizumura H. Shinokubo A. Osuka Functionalization of boron dipyrrin (BODIPY) dyes through iridium and rhodium catalysis: a complementary approach to α- and β-substituted BODIPYs Chem.-Eur. J. 2009 15 5942 5949
I. J. Arroyo R. Hu G. Merino B. Z. Tang E. Peña-Cabrera The smallest and one of the brightest. Efficient preparation and optical description of the parent borondipyrromethene system J. Org. Chem. 2009 74 5719 5722
K. Tram H. Yan H. A. Jenkins S. Vassiliev D. Bruce The synthesis and crystal structure of unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) Dyes Pigm. 2009 82 392 395
A. Schmitt B. Hinkeldey M. Wild G. Jung Synthesis of the core compound of the BODIPY dye class: 4,4′-difluoro-4-bora-(3a,4a)-diaza-s-indacene J. Fluoresc. 2009 19 755 758
M.-c. Yee S. C. Fas M. M. Stohlmeyer T. J. Wandless K. A. Cimprich A cell-permeable, activity-based probe for protein and lipid kinases J. Biol. Chem. 2005 280 29053 29059
R. West C. Panagabko J. Atkinson Synthesis and characterization of BODIPY-α-tocopherol: a fluorescent form of vitamin E J. Org. Chem. 2010 75 2883 2892
N. Boens V. Leen W. Dehaen Fluorescent indicators based on BODIPY Chem. Soc. Rev. 2012 41 1130 1172
G. Qian Z. Y. Wang Near-infrared organic compounds and emerging applications Chem.-Asian J. 2010 5 1006 1029
F. López Arbeloa J. Banuelos V. Martinez T. Arbeloa I. Lopez Arbeloa Structural, photophysical and lasing properties of pyrromethene dyes Int. Rev. Phys. Chem. 2005 24 339 374
M. Liras J. Bañuelos Prieto M. Pintado-Sierra F. López Arbeloa I. García-Moreno A. Costela L. Infantes R. Sastre F. Amat-Guerri Synthesis, photophysical properties, and laser behavior of 3-amino and 3-acetamido BODIPY dyes Org. Lett. 2007 9 4183 4186
I. García-Moreno F. Amat-Guerri M. Liras A. Costela L. Infantes R. Sastre F. López Arbeloa J. Bañuelos Prieto I. López Arbeloa Structural changes in the BODIPY dye PM567 enhancing the laser action in liquid and solid media Adv. Funct. Mater. 2007 17 3088 3098
M. Alvarez A. Costela I. García-Moreno F. Amat-Guerri M. Liras R. Sastre F. López Arbeloa J. Bañuelos Prieto I. López Arbeloa Photophysical and laser emission studies of 8-polyphenylene-substituted BODIPY dyes in liquid solution and in solid polymeric matrices Photochem. Photobiol. Sci. 2008 7 802 813
A. Costela I. García-Moreno M. Pintado-Sierra F. Amat-Guerri M. Liras R. Sastre F. López Arbeloa J. Bañuelos Prieto I. López Arbeloa New laser dye based on the 3-styryl analog of the BODIPY dye PM567 J. Photochem. Photobiol., A 2008 198 192 199
A. Costela I. García-Moreno M. Pintado-Sierra F. Amat-Guerri R. Sastre M. Liras F. López Arbeloa J. Bañuelos Prieto I. López Arbeloa New analogues of the BODIPY dye PM597: photophysical and lasing properties in liquid solutions and in solid polymeric matrices J. Phys. Chem. A 2009 113 8118 8124
C. F. A. Gómez-Durán I. García-Moreno A. Costela V. Martín R. Sastre J. Bañuelos F. López Arbeloa I. López Arbeloa E. Peña-Cabrera 8-PropargylaminoBODIPY: unprecedented blue-emitting pyrromethene dye. Synthesis, photophysics and laser properties Chem. Commun. 2010 46 5103 5105
J. Bañuelos V. Martín C. F. A. Gómez-Durán I. J. Arroyo Córdoba E. Peña-Cabrera I. García-Moreno Á. Costela M. E. Pérez-Ojeda T. Arbeloa I. López Arbeloa New 8-amino-BODIPY derivatives: surpassing laser dyes at blue-edge wavelengths Chem.-Eur. J. 2011 17 7261 7270
M. Benstead G. H. Mehl R. W. Boyle 4,4′-Difluoro-4-bora-3a,4a- diaza-s-indacenes (BODIPYs) as components of novel light active materials Tetrahedron 2011 67 3573 3601
T. Yogo Y. Urano Y. Ishitsuka F. Maniwa T. Nagano Highly efficient and photostable photosensitizer based on BODIPY chromophore J. Am. Chem. Soc. 2005 127 12162 12163
S. Atilgan Z. Ekmekci A. L. Dogan D. Guc E. U. Akkaya Water soluble distyryl-boradiazaindacenes as efficient photosensitizers for photodynamic therapy Chem. Commun. 2006 4398 4400
S. Ozlem E. U. Akkaya Thinking outside the silicon box: molecular AND logic as an additional layer of selectivity in singlet oxygen generation for photodynamic therapy J. Am. Chem. Soc. 2009 131 48 49
S. Erbas A. Gorgulu M. Kocakusakogullari E. U. Akkaya Non-covalent functionalized SWNTs as delivery agents for novel BODIPY-based potential PDT sensitizers Chem. Commun. 2009 4956 4958
S. H. Lim C. Thivierge P. Nowak-Sliwinska J. Han H. van den Bergh G. Wagnières K. Burgess H. B. Lee In vitro and in vivo photocytotoxicity of boron dipyrromethene derivatives for photodynamic therapy J. Med. Chem. 2010 53 2865 2874
J. P. Celli B. Q. Spring I. Rizvi C. L. Evans K. S. Samkoe S. Verma B. W. Pogue T. Hasan Imaging and photodynamic therapy: mechanisms, monitoring, and optimization Chem. Rev. 2010 110 2795 2838
Y. Cakmak S. Kolemen S. Duman Y. Dede Y. Dolen B. Kilic Z. Kostereli L. T. Yildirim A. L. Dogan D. Guc E. U. Akkaya Designing excited states: theory-guided access to efficient photosensitizers for photodynamic action Angew. Chem., Int. Ed. 2011 50 11937 11941
H. He P.-C. Lo S.-L. Yeung W.-P. Fong D. K. P. Ng Preparation of unsymmetrical distyryl BODIPY derivatives and effects of the styryl substituents on their in vitro photodynamic properties Chem. Commun. 2011 47 4748 4750
H. He P.-C. Lo S.-L. Yeung W.-P. Fong D. K. P. Ng Synthesis and in vitro photodynamic activities of pegylated distyryl boron dipyrromethene derivatives J. Med. Chem. 2011 54 3097 3102
S. G. Awuah J. Polreis V. Biradar Y. You Singlet oxygen generation by novel NIR BODIPY dyes Org. Lett. 2011 13 3884 3887
L. Huang X. Yu W. Wu J. Zhao Styryl BODIPY-C60 dyads as efficient heavy-atom-free organic triplet photosensitizers Org. Lett. 2012 10 2594 2597
A. Kamkaew S. H. Lim H. B. Lee L. V. Kiew L. Y. Chung K. Burgess BODIPY dyes in photodynamic therapy Chem. Soc. Rev. 2013 42 77 88
C.-W. Wan A. Burghart J. Chen F. Bergström L. B.-Å. Johansson M. F. Wolford T. G. Kim M. R. Topp R. M. Hochstrasser K. Burgess Anthracene-BODIPY cassettes: syntheses and energy transfer Chem.-Eur. J. 2003 9 4430 4441
R. Ziessel C. Goze G. Ulrich M. Césario P. Retailleau A. Harriman J. P. Rostron Intramolecular energy transfer in pyrene-BODIPY molecular dyads and triads Chem.-Eur. J. 2005 11 7366 7378
M. D. Yilmaz O. A. Bozdemir E. U. Akkaya Light harvesting and efficient energy transfer in a boron-dipyrrin (BODIPY) functionalized perylenediimide derivative Org. Lett. 2006 8 2871 2873
A. Harriman G. Izzet R. Ziessel Rapid energy transfer in cascade-type BODIPY dyes J. Am. Chem. Soc. 2006 128 10868 10875
J.-Y. Liu H.-S. Yeung W. Xu X. Li D. K. P. Ng Highly efficient energy transfer in subphthalocyanine-BODIPY conjugates Org. Lett. 2008 10 5421 5424
R. Ziessel G. Ulrich K. J. Elliott A. Harriman Electronic energy transfer in molecular dyads built around boron-ethyne-substituted subphthalocyanines Chem.-Eur. J. 2009 15 4980 4984
G. Barin M. D. Yilmaz E. U. Akkaya Boradiazaindacene (BODIPY)-based building blocks for the construction of energy transfer cassettes Tetrahedron Lett. 2009 50 1738 1740
S. Yin V. Leen C. Jackers D. Beljonne B. Van Averbeke M. Van der Auweraer N. Boens W. Dehaen Oligo(p-phenylene ethynylene)-BODIPY derivatives: synthesis, energy transfer, and quantum-chemical calculations Chem.-Eur. J. 2011 17 13247 13257
Y. Ueno J. Jose A. Loudet C. Pérez-Bolívar P. Anzenbacher, Jr. K. Burgess Encapsulated energy-transfer cassettes with extremely well resolved fluorescent outputs J. Am. Chem. Soc. 2011 133 51 55
H. Yu Y. Xiao H. Guo X. Qian Convenient and efficient FRET platform featuring a rigid biphenyl spacer between rhodamine and BODIPY: transformation of 'turn-on' sensors into ratiometric ones with dual emission Chem.-Eur. J. 2011 17 3179 3191
D. Bai A. C. Benniston J. Hagon H. Lemmetyinen N. V. Tkachenko W. Clegg R. W. Harrington Exploring Förster electronic energy transfer in a decoupled anthracenyl-based borondipyrromethene (BODIPY) dyad Phys. Chem. Chem. Phys. 2012 14 4447 4456
T. K. Khan M. S. Shaikh M. Ravikanth Synthesis and photophysical properties of covalently linked boron dipyrromethene dyads Dyes Pigm. 2012 94 66 73
S. Hattori K. Ohkubo Y. Urano H. Sunahara T. Nagano Y. Wada N. V. Tkachenko H. Lemmetyinen S. Fukuzumi Charge separation in a nonfluorescent donor-acceptor dyad derived from boron dipyrromethene dye, leading to photocurrent generation J. Phys. Chem. B 2005 109 15368 15375
S. Erten-Ela M. D. Yilmaz B. Icli Y. Dede S. Icli E. U. Akkaya A panchromatic boradiazaindacene (BODIPY) sensitizer for dye-sensitized solar cells Org. Lett. 2008 10 3299 3302
D. Kumaresan R. P. Thummel T. Bura G. Ulrich R. Ziessel Color tuning in new metal-free organic sensitizers (BODIPYs) for dye-sensitized solar cells Chem.-Eur. J. 2009 15 6335 6339
C. Y. Lee J. T. Hupp Dye sensitized solar cells: TiO2 sensitization with a BODIPY-porphyrin antenna system Langmuir 2010 26 3760 3765
S. Kolemen O. A. Bozdemir Y. Cakmak G. Barin S. Erten-Ela M. Marszalek J.-H. Yum S. M. Zakeeruddin M. K. Nazeeruddin M. Grätzel E. U. Akkaya Optimization of distyryl-BODIPY chromophores for efficient panchromatic sensitization in dye sensitized solar cells Chem. Sci. 2011 2 949 954
J. Warnan F. Buchet Y. Pellegrin E. Blart F. Odobel Panchromatic trichromophoric sensitizer for dye-sensitized solar cells using antenna effect Org. Lett. 2011 13 3944 3947
O. A. Bozdemir S. Erbas-Cakmak O. O. Ekiz A. Dana E. U. Akkaya Towards unimolecular luminescent solar concentrators: BODIPY-based dendritic energy-transfer cascade with panchromatic absorption and monochromatized emission Angew. Chem., Int. Ed. 2011 50 10907 10912
B. Verbelen V. Leen L. Wang N. Boens W. Dehaen Direct palladium-catalysed C-H arylation of BODIPY dyes at the 3- and 3,5-positions Chem. Commun. 2012 48 9129 9131
J. Catalán Toward a generalized treatment of the solvent effect based on four empirical scales: dipolarity (SdP, a new scale), polarizability (SP), acidity (SA), and basicity (SB) of the medium J. Phys. Chem. B 2009 113 5951 5960
S. E. Braslavsky Glossary of terms used in photochemistry, 3rd ed. (IUPAC recommendations 2006) Pure Appl. Chem. 2007 79 293 465
H. L. Kee C. Kirmaier L. Yu P. Thamyongkit W. J. Youngblood M. E. Calder L. Ramos B. C. Noll D. F. Bocian W. R. Scheidt R. R. Birge J. S. Lindsey D. Holten Structural control of the photodynamics of boron-dipyrrin complexes J. Phys. Chem. B 2005 109 20433 20443
T. Yanai D. P. Tew N. C. Handy A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP) Chem. Phys. Lett. 2004 393 51 57
B. Mennucci E. Cancès J. Tomasi Evaluation of solvent effects in isotropic and anisotropic dielectrics and in ionic solutions with a unified integral equation method: theoretical bases, computational implementation, and numerical applications J. Phys. Chem. B 1997 101 10506 10517
M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski and D. J. Fox, GAUSSIAN 09 (Revision B.01), Gaussian, Inc., Wallingford CT, 2009
R. Ziessel L. Bonardi G. Ulrich Boron dipyrromethene dyes: a rational avenue for sensing and light emitting devices Dalton Trans. 2006 2913 2918
M. Landrum A. Smertenko R. Edwards P. J. Hussey P. G. Steel BODIPY probes to study peroxisome dynamics in vivo Plant J. 2010 62 529 538