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Journal articles on the topic 'Borondipyrromethene'

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Author: Grafiati

Published: 6 September 2023

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1

Özcan, Emrah, Gürkan Keşan, Burcu Topaloğlu, Esra Tanrıverdi Eçik, Ayşegül Dere, Fahrettin Yakuphanoglu, and Bünyemin Çoşut. "Synthesis, photophysical, DFT and photodiode properties of subphthalocyanine–BODIPY dyads." New Journal of Chemistry 42, no. 7 (2018): 4972–80. http://dx.doi.org/10.1039/c7nj04568a.

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2

Chen, Lei, Yifei Jiang, Shihan Xu, Jicheng Zhang, Seung-Ryoung Jung, Jiangbo Yu, Xuanjun Zhang, and Daniel T. Chiu. "BODIPY-based near-infrared semiconducting polymer dot for selective yellow laser-excited cell imaging." RSC Advances 13, no. 22 (2023): 15121–25. http://dx.doi.org/10.1039/d3ra01083j.

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An efficient borondipyrromethene based near-infrared semiconducting polymer dot with simultaneously narrow absorption and emission bands was designed, and successfully used for selective yellow laser excited cell imaging.

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3

Hua, Qiong-Xin, Bo Xin, Zu-Jing Xiong, Wen-Liang Gong, Chong Li, Zhen-Li Huang, and Ming-Qiang Zhu. "Super-resolution imaging of self-assembly of amphiphilic photoswitchable macrocycles." Chemical Communications 53, no. 18 (2017): 2669–72. http://dx.doi.org/10.1039/c7cc00044h.

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Self-assembly of an amphiphilic photoswitchable fluorescent macrocycle methoxy-tetraethylene glycol-substituted hexaarylbiimidazole-borondipyrromethene can be observed directly under a super-resolution fluorescence microscope, with the nanoscale resolution beyond the optical diffraction limitation.

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4

Xu, Jingjing, Jingying Zhai, Yanmei Xu, Jingwei Zhu, Yu Qin, and Dechen Jiang. "A near-infrared fluorescent aza-bodipy probe for dual-wavelength detection of hydrogen peroxide in living cells." Analyst 141, no. 8 (2016): 2380–83. http://dx.doi.org/10.1039/c6an00262e.

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A boronic acid functionalized aza-borondipyrromethene dye (azaBDPBA) was applied to the dual-wavelength detection of hydrogen peroxide with high selectivity, which was loaded into cells to indicate the alteration of intracellular hydrogen peroxide during biological processes.

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5

Olivier, Jean-Hubert, Alexandre Haefele, Pascal Retailleau, and Raymond Ziessel. "Borondipyrromethene Dyes with Pentane-2,4-dione Anchors." Organic Letters 12, no. 3 (February 5, 2010): 408–11. http://dx.doi.org/10.1021/ol902386u.

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6

García-Moreno, Inmaculada, Dakui Zhang, Ángel Costela, Virginia Martín, Roberto Sastre, and Yi Xiao. "Red-edge laser action from borondipyrromethene dyes." Journal of Applied Physics 107, no. 7 (April 2010): 073105. http://dx.doi.org/10.1063/1.3327437.

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7

Mula, Soumyaditya, Stéphane Frein, Virginie Russo, Gilles Ulrich, Raymond Ziessel, Joaquín Barberá, and Robert Deschenaux. "Red and Blue Liquid-Crystalline Borondipyrromethene Dendrimers." Chemistry of Materials 27, no. 7 (March 23, 2015): 2332–42. http://dx.doi.org/10.1021/cm503577y.

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8

Qin, Wenwu, Mukulesh Baruah, Mark Van der Auweraer, Frans C. De Schryver, and Noël Boens. "Photophysical Properties of Borondipyrromethene Analogues in Solution." Journal of Physical Chemistry A 109, no. 33 (August 2005): 7371–84. http://dx.doi.org/10.1021/jp052626n.

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9

Zhao, Chunchang, Peng Feng, Jian Cao, Yulin Zhang, Xuzhe Wang, Yang Yang, Yanfen Zhang, and Jinxin Zhang. "6-Hydroxyindole-based borondipyrromethene: Synthesis and spectroscopic studies." Org. Biomol. Chem. 10, no. 2 (2012): 267–72. http://dx.doi.org/10.1039/c1ob06200j.

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10

Frein, Stéphane, Franck Camerel, Raymond Ziessel, Joaquín Barberá, and Robert Deschenaux. "Highly Fluorescent Liquid-Crystalline Dendrimers Based on Borondipyrromethene Dyes." Chemistry of Materials 21, no. 17 (September 8, 2009): 3950–59. http://dx.doi.org/10.1021/cm9008078.

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11

Qin, Wenwu, Taoufik Rohand, Mukulesh Baruah, Alina Stefan, Mark Van der Auweraer, Wim Dehaen, and Noël Boens. "Solvent-dependent photophysical properties of borondipyrromethene dyes in solution." Chemical Physics Letters 420, no. 4-6 (March 2006): 562–68. http://dx.doi.org/10.1016/j.cplett.2005.12.098.

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12

Madhu, Sheri, Santanu Kumar Basu, Sameer Jadhav, and Mangalampalli Ravikanth. "3,5-Diformyl-borondipyrromethene for selective detection of cyanide anion." Analyst 138, no. 1 (2013): 299–306. http://dx.doi.org/10.1039/c2an36407g.

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13

Banerjee, Swagata, Rimma T. Kuznetsova, and Dmitri B. Papkovsky. "Solid-state oxygen sensors based on phosphorescent diiodo-borondipyrromethene dye." Sensors and Actuators B: Chemical 212 (June 2015): 229–34. http://dx.doi.org/10.1016/j.snb.2015.02.016.

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14

Hiruta, Yuki, Hikaru Koiso, Hitoshi Ozawa, Hiroyasu Sato, Kensaku Hamada, Satoshi Yabushita, Daniel Citterio, and Koji Suzuki. "Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene." Organic Letters 17, no. 12 (June 11, 2015): 3022–25. http://dx.doi.org/10.1021/acs.orglett.5b01299.

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15

Zhao, Chunchang, Peng Feng, Jian Cao, Xuzhe Wang, Yang Yang, Yulin Zhang, Jinxing Zhang, and Yanfen Zhang. "Borondipyrromethene-derived Cu2+ sensing chemodosimeter for fast and selective detection." Organic & Biomolecular Chemistry 10, no. 15 (2012): 3104. http://dx.doi.org/10.1039/c2ob06980f.

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16

Wang, Yucai, Junxu Liao, Bangying Wang, Hongbiao Chen, Hongbin Zhao, Min Peng, and Sujuan Fan. "Synthesis and Properties of Novel Borondipyrromethene (BODIPY)-Tethered Triphenylamine Conjugates." Australian Journal of Chemistry 68, no. 10 (2015): 1485. http://dx.doi.org/10.1071/ch15026.

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A series of novel donor–acceptor type borondipyrromethene (BODIPY)-tethered triphenylamine conjugates (BDP4–8) containing one or two BODIPY cores attached to a triphenylamine scaffold at the 4- or 4,4′- positions were successfully synthesised via a mild and effective protocol. Their photophysical and electrochemical properties were investigated. The absorption spectra indicated that the meso-substituted BODIPY with triphenylamine did not give rise to an intense intramolecular charge transfer (ICT) and did not effectively extend the conjugated length compared with substitution at the 2,6- and 3,5-positions as previously reported. It is worth noticing that the asymmetric mono-BODIPY-tethered triphenylamine conjugates (BDP5, BDP7) showed an electronic distribution imbalance due to the special 3D propeller shape of triphenylamine resulting in twisted molecular space configurations. In contrast, the symmetric bis-BODIPY-tethered triphenylamine conjugates (BDP4, BDP6, and BDP8) exhibited a balanced electronic distribution. The photoluminescence spectra of these conjugates exhibited significant Stokes shifts (5300–6700 cm–1), which caused fluorescence emission spectra in near-infrared regions. Cyclic voltammograms reveal that the asymmetric mono-BODIPY-tethered triphenylamine conjugates (BDP5, BDP7) have higher LUMO energy levels and lower HOMO energy levels, thus resulting in larger bandgaps than the bis-BODIPY-tethered triphenylamine ones.

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17

Niu, Song-lin, Cédrik Massif, Gilles Ulrich, Pierre-Yves Renard, Anthony Romieu, and Raymond Ziessel. "Water-Soluble Red-Emitting Distyryl-Borondipyrromethene (BODIPY) Dyes for Biolabeling." Chemistry - A European Journal 18, no. 23 (April 27, 2012): 7229–42. http://dx.doi.org/10.1002/chem.201103613.

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18

Yoshii, Ryousuke, Atsushi Nagai, and Yoshiki Chujo. "Highly near-infrared photoluminescence from aza-borondipyrromethene-based conjugated polymers." Journal of Polymer Science Part A: Polymer Chemistry 48, no. 23 (October 5, 2010): 5348–56. http://dx.doi.org/10.1002/pola.24335.

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19

Pareek, Yogita, and Mangalampalli Ravikanth. "Synthesis and studies of covalently linked BF2-oxasmaragdyrin-BODIPY and BF2-oxasmaragdyrin-ferrocene dyads." Journal of Porphyrins and Phthalocyanines 17, no. 01n02 (January 2013): 157–64. http://dx.doi.org/10.1142/s1088424613500041.

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Covalently linked BF2 -oxasmaragdyrin-BODIPY and BF2 -oxasmaragdyrin-ferrocene dyads were synthesized by coupling of meso-triaryl oxasmaragdyrin containing meso-iodophenyl group with meso-(p-ethynylphenyl) borondipyrromethene and α-ethynyl ferrocene respectively under mild Pd(0) coupling conditions. NMR, absorption and electrochemical studies indicated that the two moieties in the dyads retain their individual characteristic features. The fluorescence studies indicated a possibility of photoinduced singlet-singlet energy transfer from BODIPY unit to BF2 -oxasmaragdyrin unit in BF2 -oxasmaragdyrin-BODIPY dyad and photoinduced electron transfer from ferrocene unit to excited state of BF2 -oxasmaragdyrin unit in BF2 -oxasmaragdyrin-ferrocene dyad.

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20

He, Yuan, Ruokun Feng, Yunrui Yi, and Zhanxiang Liu. "Recent Progress in the Research of Borondipyrromethene-Based Fluorescent Ion Chemosensor." Chinese Journal of Organic Chemistry 34, no. 11 (2014): 2236. http://dx.doi.org/10.6023/cjoc201403066.

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21

Peters, Carsten, Andreas Billich, Michael Ghobrial, Klemens Högenauer, Thomas Ullrich, and Peter Nussbaumer. "Synthesis of Borondipyrromethene (BODIPY)-Labeled Sphingosine Derivatives by Cross-metathesis Reaction." Journal of Organic Chemistry 72, no. 5 (March 2007): 1842–45. http://dx.doi.org/10.1021/jo062347b.

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22

Camerel, Franck, Laure Bonardi, Gilles Ulrich, Loïc Charbonnière, Bertrand Donnio, Cyril Bourgogne, Daniel Guillon, Pascal Retailleau, and Raymond Ziessel. "Self-Assembly of Fluorescent Amphipathic Borondipyrromethene Scaffoldings in Mesophases and Organogels." Chemistry of Materials 18, no. 21 (October 2006): 5009–21. http://dx.doi.org/10.1021/cm0611441.

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23

Ramírez-Ornelas, Diana E., Rebeca Sola-Llano, Jorge Bañuelos, Iñigo López Arbeloa, José A. Martínez-Álvarez, Héctor M. Mora-Montes, Bernardo Franco, and Eduardo Peña-Cabrera. "Synthesis, Photophysical Study, and Biological Application Analysis of Complex Borondipyrromethene Dyes." ACS Omega 3, no. 7 (July 12, 2018): 7783–97. http://dx.doi.org/10.1021/acsomega.8b00753.

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24

Shi, Peng-Cheng, Xin-Dong Jiang, Rui-Na Gao, Yuan-Yuan Dou, and Wei-Li Zhao. "Synthesis and application of Vis/NIR dialkylaminophenylbuta-1,3-dienyl borondipyrromethene dyes." Chinese Chemical Letters 26, no. 7 (July 2015): 834–38. http://dx.doi.org/10.1016/j.cclet.2014.11.010.

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25

Lu, Ziyi, Mao Liang, Panpan Dai, Kai Miao, Chunyao Zhang, Zhe Sun, and Song Xue. "A Strategy for Enhancing the Performance of Borondipyrromethene Dye-Sensitized Solar Cells." Journal of Physical Chemistry C 120, no. 45 (November 9, 2016): 25657–67. http://dx.doi.org/10.1021/acs.jpcc.6b07356.

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26

Badgurjar, Deepak, Kolanu Sudhakar, Kanika Jain, Vibha Kalantri, Yeduru Venkatesh, Naresh Duvva, Seelam Prasanthkumar, et al. "Ultrafast Intramolecular Photoinduced Energy Transfer Events in Benzothiazole–Borondipyrromethene Donor–Acceptor Dyads." Journal of Physical Chemistry C 120, no. 30 (July 20, 2016): 16305–21. http://dx.doi.org/10.1021/acs.jpcc.6b03668.

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27

Bhat, Haamid R., and Prakash C. Jha. "Intramolecular Charge Transfer: Mechanism Behind Cyanide Anion Sensing of 3,5-Diformyl-borondipyrromethene." ChemistrySelect 2, no. 9 (March 23, 2017): 2732–39. http://dx.doi.org/10.1002/slct.201601998.

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28

Kim, Raehyun, Kaiyan Lou, and Mary L. Kraft. "A new, long-wavelength borondipyrromethene sphingosine for studying sphingolipid dynamics in live cells." Journal of Lipid Research 54, no. 1 (November 4, 2012): 265–75. http://dx.doi.org/10.1194/jlr.d029207.

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29

Bai, Dan, Andrew C. Benniston, Jerry Hagon, Helge Lemmetyinen, Nikolai V. Tkachenko, William Clegg, and Ross W. Harrington. "Exploring Förster electronic energy transfer in a decoupled anthracenyl-based borondipyrromethene (bodipy) dyad." Physical Chemistry Chemical Physics 14, no. 13 (2012): 4447. http://dx.doi.org/10.1039/c2cp23868c.

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30

Nithya, R., P. Kolandaivel, and K. Senthilkumar. "Understanding the absorption and emission spectra of borondipyrromethene dye and its substituted analogues." Molecular Physics 110, no. 8 (April 20, 2012): 445–56. http://dx.doi.org/10.1080/00268976.2012.655792.

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31

Sevinç, Gökhan, Betül Küçüköz, Halil Yılmaz, Gökhan Şirikçi, H. Gul Yaglioglu, Mustafa Hayvalı, and Ayhan Elmali. "Explanation of pH probe mechanism in borondipyrromethene-benzimidazole compound using ultrafast spectroscopy technique." Sensors and Actuators B: Chemical 193 (March 2014): 737–44. http://dx.doi.org/10.1016/j.snb.2013.12.043.

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32

Baruah, Mukulesh, Wenwu Qin, Cristina Flors, Johan Hofkens, Renaud A. L. Vallée, David Beljonne, Mark Van der Auweraer, Wim M. De Borggraeve, and Noël Boens. "Solvent and pH Dependent Fluorescent Properties of a Dimethylaminostyryl Borondipyrromethene Dye in Solution." Journal of Physical Chemistry A 110, no. 18 (May 2006): 5998–6009. http://dx.doi.org/10.1021/jp054878u.

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33

Goze, Christine, Gilles Ulrich, Laura J. Mallon, Ben D. Allen, Anthony Harriman, and Raymond Ziessel. "Synthesis and Photophysical Properties of Borondipyrromethene Dyes Bearing Aryl Substituents at the Boron Center." Journal of the American Chemical Society 128, no. 31 (August 2006): 10231–39. http://dx.doi.org/10.1021/ja062405a.

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34

Zhao, Chunchang, Yulin Zhang, Peng Feng, and Jian Cao. "Development of a borondipyrromethene-based Zn2+fluorescent probe: solvent effects on modulation sensing ability." Dalton Trans. 41, no. 3 (2012): 831–38. http://dx.doi.org/10.1039/c1dt10797f.

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35

Giribabu, Lingamallu, Kanika Jain, Kolanu Sudhakar, Naresh Duvva, and Raghu Chitta. "Light induced intramolecular electron and energy transfer events in rigidly linked borondipyrromethene: Corrole Dyad." Journal of Luminescence 177 (September 2016): 209–18. http://dx.doi.org/10.1016/j.jlumin.2016.03.038.

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36

Gotor, R., A. M. Costero, P. Gaviña, and Salvador Gil. "Ratiometric double channel borondipyrromethene based chemodosimeter for the selective detection of nerve agent mimics." Dyes and Pigments 108 (September 2014): 76–83. http://dx.doi.org/10.1016/j.dyepig.2014.04.011.

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37

Zhang, Yang, Yeting Zheng, Andrea Tomassini, Ambarish Kumar Singh, and Françisco M. Raymo. "Photoactivatable BODIPYs for Live-Cell PALM." Molecules 28, no. 6 (March 7, 2023): 2447. http://dx.doi.org/10.3390/molecules28062447.

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Photoactivated localization microscopy (PALM) relies on fluorescence photoactivation and single-molecule localization to overcome optical diffraction and reconstruct images of biological samples with spatial resolution at the nanoscale. The implementation of this subdiffraction imaging method, however, requires fluorescent probes with photochemical and photophysical properties specifically engineered to enable the localization of single photoactivated molecules with nanometer precision. The synthetic versatility and outstanding photophysical properties of the borondipyrromethene (BODIPY) chromophore are ideally suited to satisfy these stringent requirements. Specifically, synthetic manipulations of the BODIPY scaffold can be invoked to install photolabile functional groups and photoactivate fluorescence under photochemical control. Additionally, targeting ligands can be incorporated in the resulting photoactivatable fluorophores (PAFs) to label selected subcellular components in live cells. Indeed, photoactivatable BODIPYs have already allowed the sub-diffraction imaging of diverse cellular substructures in live cells using PALM and can evolve into invaluable analytical probes for bioimaging applications.

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38

Yu, Yan-Hong, Ana B Descalzo, Zhen Shen, Holger Röhr, Quan Liu, Yan-Wei Wang, Monika Spieles, Yi-Zhi Li, Knut Rurack, and Xiao-Zeng You. "Mono- and Di(dimethylamino)styryl-Substituted Borondipyrromethene and Borondiindomethene Dyes with Intense Near-Infrared Fluorescence." Chemistry – An Asian Journal 1, no. 1-2 (July 17, 2006): 176–87. http://dx.doi.org/10.1002/asia.200600042.

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39

Ziessel, Raymond, Ben D Allen, Dorota B Rewinska, and Anthony Harriman. "Selective Triplet-State Formation during Charge Recombination in a Fullerene/Bodipy Molecular Dyad (Bodipy=Borondipyrromethene)." Chemistry - A European Journal 15, no. 30 (July 27, 2009): 7382–93. http://dx.doi.org/10.1002/chem.200900440.

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40

Tutel, Yusuf, Gökhan Sevinç, Betül Küçüköz, Elif Akhuseyin Yildiz, Ahmet Karatay, Fatih Mehmet Dumanoğulları, Halil Yılmaz, Mustafa Hayvali, and Ayhan Elmali. "Ultrafast Electron/Energy Transfer and Intersystem Crossing Mechanisms in BODIPY-Porphyrin Compounds." Processes 9, no. 2 (February 8, 2021): 312. http://dx.doi.org/10.3390/pr9020312.

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Meso-substituted borondipyrromethene (BODIPY)-porphyrin compounds that include free base porphyrin with two different numbers of BODIPY groups (BDP-TTP and 3BDP-TTP) were designed and synthesized to analyze intramolecular energy transfer mechanisms of meso-substituted BODIPY-porphyrin dyads and the effect of the different numbers of BODIPY groups connected to free-base porphyrin on the energy transfer mechanism. Absorption spectra of BODIPY-porphyrin conjugates showed wide absorption features in the visible region, and that is highly valuable to increase light-harvesting efficiency. Fluorescence spectra of the studied compounds proved that BODIPY emission intensity decreased upon the photoexcitation of the BODIPY core, due to the energy transfer from BODIPY unit to porphyrin. In addition, ultrafast pump-probe spectroscopy measurements indicated that the energy transfer of the 3BDP-TTP compound (about 3 ps) is faster than the BDP-TTP compound (about 22 ps). Since the BODIPY core directly binds to the porphyrin unit, rapid energy transfer was seen for both compounds. Thus, the energy transfer rate increased with an increasing number of BODIPY moiety connected to free-base porphyrin.

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41

Arroyo, Ismael J., Rongrong Hu, Gabriel Merino, Ben Zhong Tang, and Eduardo Peña-Cabrera. "The Smallest and One of the Brightest. Efficient Preparation and Optical Description of the Parent Borondipyrromethene System." Journal of Organic Chemistry 74, no. 15 (August 7, 2009): 5719–22. http://dx.doi.org/10.1021/jo901014w.

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42

Benniston, Andrew C., Songjie Yang, Helge Lemmetyinen, and Nikolai V. Tkachenko. "Complexation Enhanced Excited-State Deactivation by Lithium Ion Coordination to a Borondipyrromethene (Bodipy) Donor-Bridge-Acceptor Dyad." European Journal of Organic Chemistry 2013, no. 30 (September 4, 2013): 6859–69. http://dx.doi.org/10.1002/ejoc.201300867.

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43

Trieflinger, Christian, Knut Rurack, and J�rg Daub. "?Turn ON/OFF your LOV light?: Borondipyrromethene-Flavin Dyads as Biomimetic Switches Derived from the LOV Domain." Angewandte Chemie International Edition 44, no. 15 (April 8, 2005): 2288–91. http://dx.doi.org/10.1002/anie.200462377.

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44

Bai, Dan, Andrew C. Benniston, Jerry Hagon, Helge Lemmetyinen, Nikolai V. Tkachenko, and Ross W. Harrington. "Tuning the Förster overlap integral: energy transfer over 20 Ångstroms from a pyrene-based donor to borondipyrromethene (Bodipy)." Physical Chemistry Chemical Physics 15, no. 24 (2013): 9854. http://dx.doi.org/10.1039/c3cp50173f.

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45

Alamiry, Mohammed A. H., Andrew C. Benniston, Jerry Hagon, Thomas P. L. Winstanley, Helge Lemmetyinen, and Nikolai V. Tkachenko. "The fluorine effect: photophysical properties of borondipyrromethene (bodipy) dyes appended at the meso position with fluorinated aryl groups." RSC Advances 2, no. 11 (2012): 4944. http://dx.doi.org/10.1039/c2ra20219k.

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46

Chan, Li, Joshua Teo, Kevin Tan, Keitaro Sou, Wei Kwan, and Chi-Lik Lee. "Near Infrared Fluorophore-Tagged Chloroquine in Plasmodium falciparum Diagnostic Imaging." Molecules 23, no. 10 (October 14, 2018): 2635. http://dx.doi.org/10.3390/molecules23102635.

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Chloroquine was among the first of several effective drug treatments against malaria until the onset of chloroquine resistance. In light of diminished clinical efficacy of chloroquine as an antimalarial therapeutic, there is potential in efforts to adapt chloroquine for other clinical applications, such as in combination therapies and in diagnostics. In this context, we designed and synthesized a novel asymmetrical squaraine dye coupled with chloroquine (SQR1-CQ). In this study, SQR1-CQ was used to label live Plasmodium falciparum (P. falciparum) parasite cultures of varying sensitivities towards chloroquine. SQR1-CQ positively stained ring, mature trophozoite and schizont stages of both chloroquine–sensitive and chloroquine–resistant P. falciparum strains. In addition, SQR1-CQ exhibited significantly higher fluorescence, when compared to the commercial chloroquine-BODIPY (borondipyrromethene) conjugate CQ-BODIPY. We also achieved successful SQR1-CQ labelling of P. falciparum directly on thin blood smear preparations. Drug efficacy experiments measuring half-maximal inhibitory concentration (IC50) showed lower concentration of effective inhibition against resistant strain K1 by SQR1-CQ compared to conventional chloroquine. Taken together, the versatile and highly fluorescent labelling capability of SQR1-CQ and promising preliminary IC50 findings makes it a great candidate for further development as diagnostic tool with drug efficacy against chloroquine-resistant P. falciparum.

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47

Qin, Wenwu, Mukulesh Baruah, Wim M. De Borggraeve, and Noël Boens. "Photophysical properties of an on/off fluorescent pH indicator excitable with visible light based on a borondipyrromethene-linked phenol." Journal of Photochemistry and Photobiology A: Chemistry 183, no. 1-2 (September 2006): 190–97. http://dx.doi.org/10.1016/j.jphotochem.2006.03.015.

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48

He, Xiaoyan, Andrew C. Benniston, Helge Lemmetyinen, and Nikolai V. Tkachenko. "Charge Shift/Recombination and Triplet Formation in a Molecular Dyad based on a Borondipyrromethene (Bodipy) and an Expanded Acridinium Cation." ChemPhotoChem 2, no. 3 (January 5, 2018): 277–82. http://dx.doi.org/10.1002/cptc.201700184.

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49

Umezawa, Keitaro, Akihiro Matsui, Yuki Nakamura, Daniel Citterio, and Koji Suzuki. "Bright, Color-Tunable Fluorescent Dyes in the Vis/NIR Region: Establishment of New “Tailor-Made” Multicolor Fluorophores Based on Borondipyrromethene." Chemistry - A European Journal 15, no. 5 (December 30, 2008): 1096–106. http://dx.doi.org/10.1002/chem.200801906.

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50

Benniston, Andrew C., Sophie Clift, Jerry Hagon, Helge Lemmetyinen, Nikolai V. Tkachenko, William Clegg, and Ross W. Harrington. "Effect on Charge Transfer and Charge Recombination by Insertion of a Naphthalene-Based Bridge in Molecular Dyads Based on Borondipyrromethene (Bodipy)." ChemPhysChem 13, no. 16 (August 21, 2012): 3672–81. http://dx.doi.org/10.1002/cphc.201200510.

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