[1] Treibs A, Kreuzer F H. Difluorboryl-Komplexe von di-und tripyrrylmethenen[J]. Justus Liebigs Annalen der Chemie, 1968, 718(1): 208-223
[2] Haugland R P. Handbook of molecular probes and research products molecular probes inc[M]. 9th edition, Eugene, OR: Molecular Probes, Inc., 2002
[3] Jameson E E, Cunliffe J M, Neubig R R, et al. Detection of G proteins by affinity probe capillary Electrophoresis using a fluorescently labeled GTP analogue[J]. Analytical Chemistry, 2003, 75(16): 4 297-4 304
[4] Wagner R W, Lindsey J S. Boron-Dipyrromethene dyes for incorporation in synthetic multi-pigment light-harvesting arrays[J]. Pure and Applied Chemistry, 1996, 68(7): 1 373-1 380
[5] Beer G, Rurack K, Daub J. Chiral discrimination with a fluorescent boron-dipyrromethene dye[J]. Chemical Communications, 2001 (12): 1 138-1 139
[6] Gabe Y, Urano Y, Kikuchi K, et al. Highly sensitive fluorescence probes for nitric oxide based on boron dipyrromethene chromophore rational design of potentially useful bioimaging fluorescence probe[J]. Journal of the American Chemical Society, 2004, 126(10): 3 357-3 367
[7] Golovkova T A, Kozlov D V, Neckers D C. Synthesis and properties of novel fluorescent switches[J]. The Journal of Organic Chemistry, 2005, 70(14): 5 545-5 549
[8] Lai R Y, Bard A J. Electrogenerated chemiluminescence 71. Photophysical, electrochemical, and electrogenerated chemiluminescent properties of selected dipyrromethene-BF2 dyes[J]. The Journal of Physical Chemistry B, 2003, 107(21): 5 036-5 042
[9] Hepp A, Ulrich G, Schmechel R, et al. Highly efficient energy transfer to a novel organic dye in OLED devices[J]. Synthetic Metals, 2004, 146(1): 11-15
[10] Chen T, Boyer J H, Trudell M L. Synthesis of 2,6-diethyl-3-methacroyloxymethyl-1,5,7,8-tetramethylpyrromethene-BF2 for the preparation of new solid-state laser dyes[J]. Heteroatom Chemistry, 1997, 8(1): 51-54
[11] Ambroise A, Kirmaier C, Wagner R W, et al. Weakly coupled molecular photonic wires:Synthesis and excited-state energy-transfer dynamics[J]. The Journal of Organic Chemistry, 2002, 67(11): 3 811-3 826
[12] Hattori S, Ohkubo K, Urano Y, et al. Charge separation in a nonfluorescent donor-acceptor dyad derived from boron dipyrromethene dye, leading to photocurrent generation[J]. The Journal of Physical Chemistry B, 2005, 109(32): 15 368-15 375
[13] Ziessel R, Ulrich G, Harriman A. The chemistry of Bodipy: A new El Dorado for fluorescence tools[J]. New Journal of Chemistry, 2007, 31(4): 496-501
[14] Popere B C, Della P A M, Thayumanavan S. BODIPY-based donor-acceptor π-conjugated alternating copolymers[J]. Macromolecules, 2011, 44(12): 4 767-4 776
[15] Meng G, Velayudham S, Smith A, et al. Color tuning of polyfluorene emission with BODIPY monomers[J]. Macromolecules, 2009, 42(6): 1 995-2 001
[16] Nepomnyashchii A B, Bröring M, Ahrens J, et al. Chemical and electrochemical dimerization of BODIPY compounds: Electrogenerated chemiluminescent detection of dimer formation[J]. Journal of the American Chemical Society, 2011, 133(48): 19 498-19 504
[17] Algi M P, Tirkes S, Ertan S, et al. Design and synthesis of new 4,4'-difluoro-4-bora-3a,4a-diaza-s-indacene based electrochromic polymers[J]. Electrochimica Acta, 2013, 109: 766-774
[18] Forgie J C, Skabara P J, Stibor I, et al. New redox stable low band gap conjugated polymer based on an EDOT-BODIPY-EDOT repeat unit[J]. Chemistry of Materials, 2009, 21(9): 1 784-1 786
[19] Cortizo-Lacalle D, Howells C T, Gambino S, et al. BODIPY-based conjugated polymers for broadband light sensing and harvesting applications[J]. Journal of Materials Chemistry, 2012, 22(28): 14 119-14 126
[20] Usta H, Yilmaz M D, Avestro A J, et al. BODIPY-thiophene copolymers as p-channel semiconductors for organic thin-film transistors[J]. Advanced Materials, 2013, 25(31): 4 327-4 334
[21] Alg? F, Cihaner A. An ambipolar low band gap material based on BODIPY and EDOT[J]. Organic Electronics, 2009, 10(3): 453-458
[22] Nagai A, Miyake J, Kokado K, et al. Highly luminescent BODIPY-based organoboron polymer exhibiting supramolecular self-assemble structure[J]. Journal of the American Chemical Society, 2008, 130(46): 15 276-15 278
[23] Donuru V R, Vegesna G K, Velayudham S, et al. Synthesis and optical properties of red and deep-red emissive polymeric and copolymeric BODIPY dyes[J]. Chemistry of Materials, 2009, 21(10): 2 130-2 138
[24] Thivierge C, Loudet A, Burgess K. Brilliant BODIPY-fluorene copolymers with dispersed absorption and emission maxima[J]. Macromolecules, 2011, 44(10): 4 012-4 015
[25] Kim B S, Ma B, Donuru V R, et al. Bodipy-Backboned polymers as electron donor in bulk heterojunction solar cells[J]. Chemical Communications, 2010, 46(23): 4 148-4 150
[26] He W, Jiang Y, Qin Y. Synthesis and photovoltaic properties of a low bandgap BODIPY-Pt conjugated polymer[J]. Polymer Chemistry, 2014, 5(4): 1 298-1 304
[27] Takamizu K, Inagaki A, Nomura K. Precise synthesis of poly(fluorene vinylene)s capped with chromophores: Efficient fluorescent polymers modified by conjugation length and end-groups[J]. ACS Macro Lett, 2013, 2(11): 980-984
[28] Alemdaroglu F E, Alexander S C, Ji Dongmei, et al. Poly(BODIPY)s: A new class of tunable polymeric dyes[J]. Macromolecules, 2009, 42(17): 6 529-6 536