[1]
|
Wang, E., Qiao, H., Zhou, Y.M., et al. (2015) A Novel “Turn-On” Fluorogenic Probe for Sensing Hypochlorous Acid Based on BODIPY. RSC Advances, 5, 73040-73045. https://doi.org/10.1039/C5RA14118D
|
[2]
|
Rahn, M.D. and King, T. (1995) Comparison of Laser Performance of Dye Molecules in Sol-Gel, Polycom, Ormosil, and Poly(methyl methacrylate) Host Media. Applied Optics, 34, 8260-8271. https://doi.org/10.1364/AO.34.008260
|
[3]
|
Yariv, E., Schultheiss, S. and Saraidarov, T. (2001) Efficiency and Photostability of Dye-Doped Solid-State Lasers in Different Hosts. Optical Materials, 16, 29-38. https://doi.org/10.1016/S0925-3467(00)00056-2
|
[4]
|
Costela, A., Garcıa-Moreno, I. and Sastre, R. (2003) Polymeric Solid-State Dye Lasers: Recent Developments. Physical Chemistry Chemical Physics, 5, 4745-4763. https://doi.org/10.1039/B307700B
|
[5]
|
Cerdan, L., Enciso, E., Martın, V., et al. (2012) FRET-Assisted Laser Emission in Colloidal Suspensions of Dye-Doped Latex Nanoparticles. Nature Photonics, 6, 621-626. https://doi.org/10.1038/nphoton.2012.201
|
[6]
|
Sunahara, H., Urano, Y., Kojima, H. and Nagano, T. (2007) Design and Synthesis of a Library of BODIPY-Based Environmental Polarity Sensors Utilizing Photoinduced Electron-Transfer-Controlled Fluorescence ON/OFF Switching. Journal of the American Chemical Society, 129, 5597-5604. https://doi.org/10.1021/ja068551y
|
[7]
|
Qian, X., Xiao, Y., Xu, Y., et al. (2010) “Alive” Dyes as Flu-orescent Sensors: Fluorophore, Mechanism, Receptor and Images in Living Cells. Chemical Communications, 46, 6418-6436. https://doi.org/10.1039/c0cc00686f
|
[8]
|
Miao, W., Guo, X., Yan, X., et al. (2023) Red-to-Near-Infrared Emitting pyrrolylBODIPY Dyes: Synthesis, Photophysical Properties and Bioimaging Application. Chemistry, 29, e202203832.
|
[9]
|
Loudet, A. and Burgess, K. (2007) BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties. Chemical Reviews, 107, 4891-4932. https://doi.org/10.1021/cr078381n
|
[10]
|
Ziessel, R., Ulrich, G. and Harriman, A. (2007) The Chemistry of Bodipy: A New El Dorado for Fluorescence Tools. New Journal of Chemistry, 31, 496-501. https://doi.org/10.1039/b617972j
|
[11]
|
Shen, Z., Röhr, H., Rurack, K., et al. (2004) Boron-Diindomethene (BDI) Dyes and Their Tetrahydrobicyclo Precursors—En Route to a New Class of Highly Emissive Fluorophores for the Red Spectral Range. Chemistry—A European Journal, 10, 4853-4871. https://doi.org/10.1002/chem.200400173
|
[12]
|
Baruah, M., Qin, W., Vallée, R.A.L., et al. (2005) A Highly Potas-sium-Selective Ratiometric Fluorescent Indicator Based on BODIPY Azacrown Ether Excitable with Visible Light. Or-ganic Letters, 7, 4377-4380.
https://doi.org/10.1021/ol051603o
|
[13]
|
Rohand, T., Baruah, M., Qin, W., Boens, N. and Dehaen, W. (2006) Func-tionalisation of Fluorescent BODIPY Dyes by Nucleophilic Substitution. Chemical Communications, 42, 266-268. https://doi.org/10.1039/B512756D
|
[14]
|
McDonnell, S.O. and O’Shea, D.F. (2006) Near-Infrared Sensing Proper-ties of Dimethlyamino-Substituted BF2-Aza- dipyrromethenes. Organic Letters, 8, 3493-3496. https://doi.org/10.1021/ol061171x
|
[15]
|
Jiao, C., Huang, K.-W. and Wu, J. (2011) Perylene-Fused BODIPY Dye with Near-IR Absorption/Emission and High Photostability. Organic Letters, 13, 632-635. https://doi.org/10.1021/ol102879g
|
[16]
|
Jiao, L., Yu, C., Liu, M., et al. (2010) Synthesis and Functionalization of Asymmetrical Benzo-Fused BODIPY Dyes. The Journal of Organic Chemistry, 75, 6035-6038. https://doi.org/10.1021/jo101164a
|
[17]
|
Kubota, Y., Uehara, J., Funabiki, K., et al. (2010) Strategy for the Increas-ing the Solid-State Fluorescence Intensity of Pyrromethene-BF2 Complexes. Tetrahedron Letters, 51, 6195-6198. https://doi.org/10.1016/j.tetlet.2010.09.106
|
[18]
|
Ozdemir, T., Atilgan, S., Kutuk, I., et al. (2009) Solid-State Emis-sive BODIPY Dyes with Bulky Substituents as Spacers. Organic Letters, 11, 2105-2107. https://doi.org/10.1021/ol9005568
|
[19]
|
Vu, T.T., Badré, S., Dumas-Verdes, C., et al. (2009) New Hindered BODIPY Derivatives: Solution and Amorphous State Fluorescence Properties. The Journal of Physical Chemistry C, 113, 11844-11855.
https://doi.org/10.1021/jp9019602
|
[20]
|
Badré, S., Monnier, V., Méallet-Renault, R., et al. (2006) Fluorescence of Molecular Micro- and Nanocrystals Prepared with Bodipy Derivatives. Journal of Photochemistry and Photobiology A, 183, 238-246.
https://doi.org/10.1016/j.jphotochem.2006.07.002
|
[21]
|
Treibs, A., Kreuzer, F.H. and Ann, J.L. (1968) Difluor-boryl-Komplexe von Di- und Tripyrrylmethenen. Justus Liebigs Annalen der Chemie, 718, 208-223. https://doi.org/10.1002/jlac.19687180119
|
[22]
|
Hepp, A., Ulrich, G., Schmechel, R., et al. (2004) Highly Efficient Energy Transfer to a Novel Organic Dye in OLED Devices. Synthetic Metals, 146, 11-15. https://doi.org/10.1016/j.synthmet.2004.06.016
|
[23]
|
Guggenheimer, S.C., Boyer, J.H., Thangaraj, K., et al. (1993) Efficient Laser Action from Two Cw Laser-Pumped Pyrromethene-BF2 Complexes. Applied Optics, 32, 3942-3943. https://doi.org/10.1364/AO.32.003942
|
[24]
|
Zhao, W. and Carreira, E.M. (2006) Conformationally Restricted Aza-BODIPY: Highly Fluorescent, Stable Near- Infrared Absorbing Dyes. Chemistry—A European Journal, 12, 7254-7263.
https://doi.org/10.1002/chem.200600527
|
[25]
|
Li, F., Yang, S.I., Ciringh, Y., et al. (1998) Design, Synthesis, and Photodynamics of Light-Harvesting Arrays Comprised of a Porphyrin and One, Two, or Eight Boron-Dipyrrin Acces-sory Pigments. Journal of the American Chemical Society, 120, 10001-10017. https://doi.org/10.1021/ja9812047
|
[26]
|
Bañuelos, J. (2016) BODIPY Dye, the Most Versatile Fluorophore Ever? The Chemical Record, 16, 335-348.
|
[27]
|
Zhang, D., Wen, Y., Xiao, Y., et al. (2008) Bulky 4-Tritylphenylethynyl Sub-stituted Boradiazaindacene: Pure Red Emission, Relatively Large Stokes Shift and Inhibition of Self-Quenching. Chemi-cal Communications, No. 39, 4777- 4779. https://doi.org/10.1039/b808681h
|
[28]
|
Qin, W., Baruah, M., Van der Auweraer, M., et al. (2005) Photophysical Properties of Borondipyrromethene Analogues in Solution. The Journal of Physical Chemistry A, 109, 7371-7384. https://doi.org/10.1021/jp052626n
|
[29]
|
Savoldelli, A., Meng, Q., Paolesse, R., et al. (2018) Tetrafluorobenzo-Fused BODIPY: A Platform for Regioselective Synthesis of BODIPY Dye Deriva-tives. The Journal of Organic Chemistry, 83, 6498-6507.
https://doi.org/10.1021/acs.joc.8b00789
|
[30]
|
Benniston, A.C. and Copley, G. (2009) Lighting the Way Ahead with Boron Dipyrromethene (Bodipy) Dyes. Physical Chemistry Chemical Physics, 11, 4124-4131. https://doi.org/10.1039/b901383k
|
[31]
|
Gibbs, J.H., Robins, L.T., Zhou, Z., et al. (2013) Spectroscopic, Computa-tional Modeling and Cytotoxicity of a Series of Meso-Phenyl and Meso-Thienyl-BODIPYs. Bioorganic & Medicinal Chemistry, 21, 5770-5781.
https://doi.org/10.1016/j.bmc.2013.07.017
|
[32]
|
Chu, G.M., Guerrero-Martinez, A., Fernandez, I. and Sierra, M.A. (2014) Tuning the Photophysical Properties of BODIPY Molecules by π-Conjugation with Fischer Carbene Complexes. Chemistry—A European Journal, 20, 1367-1375.
https://doi.org/10.1002/chem.201303952
|
[33]
|
Waddell, P.G., Liu, X., Zhao, T. and Cole, J.M. (2015) Rationalizing the Photophysical Properties of BODIPY Laser Dyes via Aromaticity and Electron-Donor-Based Structural Perturbations. Dyes and Pigments, 116, 74-81.
https://doi.org/10.1016/j.dyepig.2015.01.010
|
[34]
|
Zatsikha, Y.V., Maligaspe, E., Purchel, A.A., et al. (2015) Tun-ing Electronic Structure, Redox, and Photophysical Properties in Asymmetric NIR-Absorbing Organometallic BODIPYs. Inorganic Chemistry, 54, 7915-7928.
https://doi.org/10.1021/acs.inorgchem.5b00992
|
[35]
|
Thorat, K.G., Kamble, P., Mallah, R., et al. (2015) Congeners of Pyrromethene-567 Dye: Perspectives from Synthesis, Photophysics, Photostability, Laser, and TD-DFT Theory. The Journal of Organic Chemistry, 80, 6152-6164.
https://doi.org/10.1021/acs.joc.5b00654
|
[36]
|
Ulrich, G., Ziessel, R. and Harriman, A. (2008) The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed. Angewandte Chemie International Edition, 47, 1184-1201. https://doi.org/10.1002/anie.200702070
|
[37]
|
Benstead, M., Mehl, G.H. and Boyle, R.W. (2011) 4,4’-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as Components of Novel Light Active Materials. Tetrahedron, 67, 3573-3601. https://doi.org/10.1016/j.tet.2011.03.028
|
[38]
|
Boens, N., Leen, V. and Dehaen, W. (2012) Fluo-rescent Indicators Based on BODIPY. Chemical Society Reviews, 41, 1130-1172. https://doi.org/10.1039/C1CS15132K
|
[39]
|
Wan, C.W., Burghart, A., Chen, J., et al. (2003) Anthracene-BODIPY Cassettes: Syntheses and Energy Transfer. Chemistry—A European Journal, 9, 4430-4441. https://doi.org/10.1002/chem.200304754
|
[40]
|
Souza, F.D., Smith, P.M., Zandler, M.E., et al. (2004) Energy Transfer Followed by Electron Transfer in a Supramolecular Triad Composed of Boron Dipyrrin, Zinc Porphyrin, and Fullerene: A Model for the Photosynthetic Antenna-Reaction Center Complex. Journal of the American Chemical Society, 126, 7898-7907.
https://doi.org/10.1021/ja030647u
|
[41]
|
Bozdemir, O.A., Cakmak, Y., Sozmen, F., et al. (2010) Synthesis of Sym-metrical Multichromophoric Bodipy Dyes and Their Facile Transformation into Energy Transfer Cassettes. Chemistry—A European Journal, 16, 6346-6351.
https://doi.org/10.1002/chem.200903449
|
[42]
|
Iehl, J., Nierengarten, J.F., Harriman, A., et al. (2012) Artificial Light-Harvesting Arrays: Electronic Energy Migration and Trapping on a Sphere and between Spheres. Journal of the American Chemical Society, 134, 988-998.
https://doi.org/10.1021/ja206894z
|
[43]
|
Fan, J., Hu, M., Zhan, P. and Peng, X. (2013) Energy Transfer Cassettes Based on Organic Fluorophores: Construction and Applications in Ratiometric Sensing. Chemical Society Reviews, 42, 29-43. https://doi.org/10.1039/C2CS35273G
|
[44]
|
Fu, Y.L., Chong, Y.Y., Li, H., Feng, W. and Song, Q.H. (2021) Sensitive and Visual Detection of Phosgene by a TICT-Based BODIPY Dye with 8-(o-Hydroxy)aniline as the Active Site. Chemistry—A European Journal, 27, 4977.
https://doi.org/10.1002/chem.202005169
|
[45]
|
Franke, J.M., Raliski, B.K., Boggess, S.C., et al. (2019) BODIPY Fluorophores for Membrane Potential Imaging. Journal of the American Chemical Society, 141, 12824-12831. https://doi.org/10.1021/jacs.9b05912
|
[46]
|
Zhang, Y., Zheng, Y.T., Meana, Y. and Raymo, F.M. (2021) BODIPYs with Photoactivatable Fluorescence. Chemistry—A European Journal, 27, 11257-11267. https://doi.org/10.1002/chem.202101628
|