Статті в журналах з теми "Borondipyrromethene"
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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.
Повний текст джерелаChen, 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.
Повний текст джерелаHua, 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.
Повний текст джерелаXu, 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.
Повний текст джерелаOlivier, 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.
Повний текст джерелаGarcía-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.
Повний текст джерелаMula, 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.
Повний текст джерелаQin, 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.
Повний текст джерелаZhao, 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.
Повний текст джерелаFrein, 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.
Повний текст джерелаQin, 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.
Повний текст джерелаMadhu, 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.
Повний текст джерелаBanerjee, 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.
Повний текст джерелаHiruta, 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.
Повний текст джерелаZhao, 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.
Повний текст джерелаWang, 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.
Повний текст джерелаNiu, 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.
Повний текст джерелаYoshii, 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.
Повний текст джерелаPareek, 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.
Повний текст джерелаHe, 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.
Повний текст джерелаPeters, 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.
Повний текст джерелаCamerel, 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.
Повний текст джерелаRamírez-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.
Повний текст джерелаShi, 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.
Повний текст джерелаLu, 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.
Повний текст джерелаBadgurjar, 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.
Повний текст джерелаBhat, 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.
Повний текст джерелаKim, 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.
Повний текст джерелаBai, 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.
Повний текст джерелаNithya, 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.
Повний текст джерелаSevinç, 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.
Повний текст джерелаBaruah, 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.
Повний текст джерелаGoze, 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.
Повний текст джерелаZhao, 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.
Повний текст джерелаGiribabu, 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.
Повний текст джерелаGotor, 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.
Повний текст джерелаZhang, 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.
Повний текст джерелаYu, 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.
Повний текст джерелаZiessel, 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.
Повний текст джерелаTutel, 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.
Повний текст джерелаArroyo, 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.
Повний текст джерелаBenniston, 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.
Повний текст джерелаTrieflinger, 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.
Повний текст джерелаBai, 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.
Повний текст джерелаAlamiry, 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.
Повний текст джерелаChan, 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.
Повний текст джерелаQin, 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.
Повний текст джерелаHe, 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.
Повний текст джерелаUmezawa, 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.
Повний текст джерелаBenniston, 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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