Artículos de revistas sobre el tema "Perylene"
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Lentijo, S., J. E. Expósito, G. Aullón, J. A. Miguel y P. Espinet. "Highly fluorescent complexes with 3-isocyanoperylene and N-(2,5-di-tert-butylphenyl)-9-isocyano-perylene-3,4-dicarboximide". Dalton Trans. 43, n.º 28 (2014): 10885–97. http://dx.doi.org/10.1039/c4dt01016g.
Texto completoLoewe, Robert S., Kin-ya Tomizaki, Fabien Chevalier y Jonathan S. Lindsey. "Synthesis of perylene-porphyrin dyads for light-harvesting studies". Journal of Porphyrins and Phthalocyanines 06, n.º 10 (octubre de 2002): 626–42. http://dx.doi.org/10.1142/s1088424602000774.
Texto completoMauri, Luca, Alessia Colombo, Claudia Dragonetti, Francesco Fagnani y Dominique Roberto. "Iridium and Ruthenium Complexes Bearing Perylene Ligands". Molecules 27, n.º 22 (16 de noviembre de 2022): 7928. http://dx.doi.org/10.3390/molecules27227928.
Texto completoNakano, Masahiro, Kyohei Nakano, Kazuo Takimiya y Keisuke Tajima. "Two isomeric perylenothiophene diimides: physicochemical properties and applications in organic semiconducting devices". Journal of Materials Chemistry C 7, n.º 8 (2019): 2267–75. http://dx.doi.org/10.1039/c8tc05577g.
Texto completoGutman, Ivan, Boris Furtula, Jelena Djurdjevic, Rradmila Kovacevic y Sonja Stankovic. "Annelated perylenes: Benzenoid molecules violating the Kekulé-structure-based cyclic conjugation models". Journal of the Serbian Chemical Society 70, n.º 8-9 (2005): 1023–32. http://dx.doi.org/10.2298/jsc0509023g.
Texto completoDuncan, Katelyn M., Donald L. Kellis, Jonathan S. Huff, Matthew S. Barclay, Jeunghoon Lee, Daniel B. Turner, Paul H. Davis, Bernard Yurke, William B. Knowlton y Ryan D. Pensack. "Symmetry Breaking Charge Transfer in DNA-Templated Perylene Dimer Aggregates". Molecules 27, n.º 19 (5 de octubre de 2022): 6612. http://dx.doi.org/10.3390/molecules27196612.
Texto completoFang, Xiangdong. "BN-Embedded Perylenes". Molecules 26, n.º 23 (25 de noviembre de 2021): 7148. http://dx.doi.org/10.3390/molecules26237148.
Texto completoLiu, Yu, Han Zhong, Yu Qin, Yan Zhang, Xinfeng Liu y Tao Zhang. "Non-covalent hydrophilization of reduced graphene oxide used as a paclitaxel vehicle". RSC Advances 6, n.º 36 (2016): 30184–93. http://dx.doi.org/10.1039/c6ra04349f.
Texto completoNagasawa, Yuya, Takeshi Koyama y Susumu Okada. "Energetics and electronic structures of perylene confined in carbon nanotubes". Royal Society Open Science 5, n.º 6 (junio de 2018): 180359. http://dx.doi.org/10.1098/rsos.180359.
Texto completoCremer, Jens y Peter Bäuerle. "Perylene-Oligothiophene-Perylene Triads for Photovoltaic Applications". European Journal of Organic Chemistry 2005, n.º 17 (septiembre de 2005): 3715–23. http://dx.doi.org/10.1002/ejoc.200500147.
Texto completoPapadopoulos, Ilias, David Gutiérrez-Moreno, Yifan Bo, Rubén Casillas, Phillip M. Greißel, Timothy Clark, Fernando Fernández-Lázaro y Dirk M. Guldi. "Altering singlet fission pathways in perylene-dimers; perylene-diimide versus perylene-monoimide". Nanoscale 14, n.º 13 (2022): 5194–203. http://dx.doi.org/10.1039/d1nr08523a.
Texto completoSuzuki, Akira, Munetaka Akita y Michito Yoshizawa. "Amphiphilic tribranched scaffolds with polyaromatic panels that wrap perylene stacks displaying unusual emissions". Chemical Communications 52, n.º 65 (2016): 10024–27. http://dx.doi.org/10.1039/c6cc04823d.
Texto completoTucker, Sheryl A., William E. Acree, John C. Fetzer y Reginald H. Mitchell. "Polycyclic Aromatic Hydrocarbon Solute Probes. Part X: Evaluation of Select Hydrogenated Pyrene, Benzo[ghi]perylene, and Naphthacene Derivatives as Possible Solvent Polarity Probes". Applied Spectroscopy 47, n.º 7 (julio de 1993): 1040–45. http://dx.doi.org/10.1366/0003702934415200.
Texto completoWojciechowski, Jonathan P., Adam D. Martin, Mohan Bhadbhade, James E. A. Webb y Pall Thordarson. "Halogen bonding influences perylene-core twists in non-core substituted perylene tetraesters". CrystEngComm 18, n.º 24 (2016): 4513–17. http://dx.doi.org/10.1039/c6ce00929h.
Texto completoAlmuhana, Asia R. Y., Philipp Langer, Sarah L. Griffin, Rhys W. Lodge, Graham A. Rance y Neil R. Champness. "Retention of perylene diimide optical properties in solid-state materials through tethering to nanodiamonds". Journal of Materials Chemistry C 9, n.º 32 (2021): 10317–23. http://dx.doi.org/10.1039/d1tc02577e.
Texto completoWangatia, Lodrick Makokha, Bin Sun, Ting Zeng y Meifang Zhu. "Reactive bay functionalized perylene monoimide-polyhedral oligomeric silsesquioxane organic electronic dye". Materials Science-Poland 33, n.º 1 (1 de marzo de 2015): 113–21. http://dx.doi.org/10.1515/msp-2015-0016.
Texto completoDeng, Qingyuan, Enbao Zhou, Yongwei Huang, Weixia Qing, Haiyan Zhai, Zhonghua Liu y Zhixiang Wei. "Chalcogen-substitution modulated supramolecular chirality and gas sensing properties in perylenediimides". Chemical Communications 55, n.º 30 (2019): 4379–82. http://dx.doi.org/10.1039/c9cc01443h.
Texto completoWang, Gang, Weina Wang, Rong Miao, Congdi Shang, Meixia He, Haonan Peng, Gang He y Yu Fang. "A perylene bisimide derivative with pyrene and cholesterol as modifying structures: synthesis and fluorescence behavior". Physical Chemistry Chemical Physics 18, n.º 17 (2016): 12221–30. http://dx.doi.org/10.1039/c6cp01447j.
Texto completoKozma, E., W. Mróz, A. Andicsová Eckstein, V. Lukeš, F. Galeotti, A. Šišková, M. Danko y M. Catellani. "A joint experimental and theoretical study on the electro-optical properties of 1,6- and 1,7-fluorenyl disubstituted perylene diimide isomers". New Journal of Chemistry 42, n.º 2 (2018): 1061–66. http://dx.doi.org/10.1039/c7nj03860g.
Texto completoXu, Xu, Yuqi Li, Zhongqiang Xiong, Jin Yang, Lulu Pan, Yunyun Wu, Chun Wei y Shaorong Lu. "Preparation and model of high-performance shape-memory polyurethane with hydroxylated perylene bisimide". RSC Advances 6, n.º 111 (2016): 110329–36. http://dx.doi.org/10.1039/c6ra24393b.
Texto completoDraper, Emily R., James J. Walsh, Tom O. McDonald, Martijn A. Zwijnenburg, Petra J. Cameron, Alexander J. Cowan y Dave J. Adams. "Air-stable photoconductive films formed from perylene bisimide gelators". J. Mater. Chem. C 2, n.º 28 (2014): 5570–75. http://dx.doi.org/10.1039/c4tc00744a.
Texto completoSchmidt, Rüdiger, Peter Osswald, Martin Könemann y Frank Würthner. "Synthetic Routes to Core-fluorinated Perylene Bisimide Dyes and their Properties". Zeitschrift für Naturforschung B 64, n.º 6 (1 de junio de 2009): 735–46. http://dx.doi.org/10.1515/znb-2009-0621.
Texto completoNiide, Teppei, Kyohei Ozawa, Hikaru Nakazawa, Daniel Oliveira, Hitoshi Kasai, Mari Onodera, Ryutaro Asano, Izumi Kumagai y Mitsuo Umetsu. "Organic crystal-binding peptides: morphology control and one-pot formation of protein-displaying organic crystals". Nanoscale 7, n.º 47 (2015): 20155–63. http://dx.doi.org/10.1039/c5nr06471f.
Texto completoKozlov, A. V., L. R. Sizov, D. V. Revina, A. Yu Rybkin y N. S. Goryachev. "Photophysical and Photochemical Properties of Perylene–(Cyanine Dye) Dyad in the VIS–NIR Spectrum Region". Журнал физической химии 97, n.º 5 (1 de mayo de 2023): 602–6. http://dx.doi.org/10.31857/s0044453723050138.
Texto completoYang, X., H. J. Räder, A. Rouhanipour y K. Müllen. "Soft Deposition of Organic Macromolecules with Fast Atom Bombardment Mass Spectrometry". European Journal of Mass Spectrometry 11, n.º 3 (junio de 2005): 287–93. http://dx.doi.org/10.1255/ejms.762.
Texto completoYang, Lin, Shu Chen, Jing Zhang, Junting Wang, Min Zhang, Xiandui Dong y Peng Wang. "Judicious engineering of a metal-free perylene dye for high-efficiency dye sensitized solar cells: the control of excited state and charge carrier dynamics". Journal of Materials Chemistry A 5, n.º 7 (2017): 3514–22. http://dx.doi.org/10.1039/c6ta10506h.
Texto completoKohl, Miroslav, Fouzy Alafid, Marek Bouška, Anna Krejčová, Yash Raycha, Andréa Kalendová, Radim Hrdina y Ladislav Burgert. "New Corrosion Inhibitors Based on Perylene Units in Epoxy Ester Resin Coatings". Coatings 12, n.º 7 (29 de junio de 2022): 923. http://dx.doi.org/10.3390/coatings12070923.
Texto completoLeowanawat, Pawaret, Agnieszka Nowak-Król y Frank Würthner. "Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling". Organic Chemistry Frontiers 3, n.º 5 (2016): 537–44. http://dx.doi.org/10.1039/c6qo00047a.
Texto completoSun, Yan, Tongfei Zuo, Fang Guo, Jing Sun, Ziwei Liu y Guowang Diao. "Perylene dye-functionalized silver nanoparticles serving as pH-dependent metal sensor systems". RSC Advances 7, n.º 39 (2017): 24215–20. http://dx.doi.org/10.1039/c7ra03264a.
Texto completoVentura, Barbara, Heinz Langhals, Bernd Böck y Lucia Flamigni. "Phosphorescent perylene imides". Chemical Communications 48, n.º 35 (2012): 4226. http://dx.doi.org/10.1039/c2cc30948c.
Texto completoSwager, Timothy y Kosuke Yoshinaga. "Fluorofluorescent Perylene Bisimides". Synlett 29, n.º 19 (31 de julio de 2018): 2509–14. http://dx.doi.org/10.1055/s-0037-1610224.
Texto completoMarkoulides, Marios S., Chiara Venturini, David Neumeyer y André Gourdon. "Oxidative cyclodehydrogenation of a perylene derivative: different reagents give different products". New Journal of Chemistry 39, n.º 8 (2015): 6498–503. http://dx.doi.org/10.1039/c5nj00808e.
Texto completoBaba, Koichi, Sayaka Konta, Daniel Oliveira, Kenji Sugai, Tsunenobu Onodera, Akito Masuhara, Hitoshi Kasai, Hidetoshi Oikawa y Hachiro Nakanishi. "Perylene and Perylene-Derivative Nano-Cocrystals: Preparation and Physicochemical Property". Japanese Journal of Applied Physics 51 (19 de noviembre de 2012): 125201. http://dx.doi.org/10.1143/jjap.51.125201.
Texto completoBaba, Koichi, Sayaka Konta, Daniel Oliveira, Kenji Sugai, Tsunenobu Onodera, Akito Masuhara, Hitoshi Kasai, Hidetoshi Oikawa y Hachiro Nakanishi. "Perylene and Perylene-Derivative Nano-Cocrystals: Preparation and Physicochemical Property". Japanese Journal of Applied Physics 51, n.º 12R (1 de diciembre de 2012): 125201. http://dx.doi.org/10.7567/jjap.51.125201.
Texto completoMikhnovets, Igor E., Jiří Holoubek, Irina S. Panina, Jan Kotouček, Daniil A. Gvozdev, Stepan P. Chumakov, Maxim S. Krasilnikov et al. "Alkyl Derivatives of Perylene Photosensitizing Antivirals: Towards Understanding the Influence of Lipophilicity". International Journal of Molecular Sciences 24, n.º 22 (18 de noviembre de 2023): 16483. http://dx.doi.org/10.3390/ijms242216483.
Texto completoAhmad, Shargeel, Jinxuan Liu, Wei Ji y Licheng Sun. "Metal–Organic Framework Thin Film-Based Dye Sensitized Solar Cells with Enhanced Photocurrent". Materials 11, n.º 10 (1 de octubre de 2018): 1868. http://dx.doi.org/10.3390/ma11101868.
Texto completoZhang, Fengxia, Xianqiang Huang, Xiaofeng Wei, Huixue Ren, Tianyi Jiang, Xuemei Li, Junsen Wu y Yongshan Ma. "Synthesis and properties of bay unilaterally extended and mono-substituted perylene diimides". Journal of Chemical Research 44, n.º 1-2 (14 de noviembre de 2019): 60–66. http://dx.doi.org/10.1177/1747519819886502.
Texto completoMameri, Samir, Joanna R. Siekierzycka y Albert M. Brouwer. "Artificial miniaturized luminescent materials based on perylene-covered glass surfaces". New Journal of Chemistry 41, n.º 14 (2017): 6083–88. http://dx.doi.org/10.1039/c7nj01337j.
Texto completoBalashova, T. V., S. K. Polyakova, A. A. Fagin, V. A. Ilichev, K. A. Kozhanov, E. V. Baranov, G. K. Fukin y M. N. Bochkarev. "The First Perylene Complexes of Neodymium and Dysprosium". Координационная химия 49, n.º 5 (1 de mayo de 2023): 259–68. http://dx.doi.org/10.31857/s0132344x22600291.
Texto completoVoskoboynikov, Alexander, Bogdan Guzeev, Dmitry Mladentsev, Mikhail Sharikov, Georgy Goryunov y Dmitry Uborsky. "Synthesis of Perylene-Tagged Internal and External Electron Donors for Magnesium Dichloride Supported Ziegler–Natta Catalysts". Synthesis 51, n.º 06 (6 de noviembre de 2018): 1399–407. http://dx.doi.org/10.1055/s-0037-1611085.
Texto completoPiryatinski, Yuri P., Markiian B. Malynovskyi, Maryna M. Sevryukova, Anatoli B. Verbitsky, Olga A. Kapush, Aleksey G. Rozhin y Petro M. Lutsyk. "Mixing of Excitons in Nanostructures Based on a Perylene Dye with CdTe Quantum Dots". Materials 16, n.º 2 (6 de enero de 2023): 552. http://dx.doi.org/10.3390/ma16020552.
Texto completoLiang, Meng, Jun Yin, Kadali Chaitanya y Xue-Hai Ju. "Theoretical investigations on charge transfer properties of fluorinated perylene diimides". Journal of Theoretical and Computational Chemistry 15, n.º 03 (mayo de 2016): 1650027. http://dx.doi.org/10.1142/s0219633616500279.
Texto completoRoa-Linares, Vicky C., Ana C. Mesa-Arango, Ramón J. Zaragozá y Miguel A. González-Cardenete. "Antifungal Activity of Amphiphilic Perylene Bisimides". Molecules 27, n.º 20 (14 de octubre de 2022): 6890. http://dx.doi.org/10.3390/molecules27206890.
Texto completoWei, Hui Min, Nan Zhao, Nan Jiang, Wen Feng Duan y Bao Xiang Gao. "The Synthesis and Electro-Optical Properties of Perylene Dicarboximide Dimer with Electron Withdrawing Groups". Advanced Materials Research 936 (junio de 2014): 950–54. http://dx.doi.org/10.4028/www.scientific.net/amr.936.950.
Texto completoDatars, W. R., T. R. Chien y P. K. Ummat. "Properties of perylene reacted with AsF5". Canadian Journal of Physics 73, n.º 11-12 (1 de noviembre de 1995): 653–57. http://dx.doi.org/10.1139/p95-097.
Texto completoSalzillo, Tommaso, Raffaele G. Della Valle, Elisabetta Venuti, Aldo Brillante, Gabriele Kociok-Köhn, Daniele Di Nuzzo, Matteo Masino y Alberto Girlando. "(Perylene)3-(TCNQF1)2: Yet Another Member in the Series of Perylene–TCNQFx Polymorphic Charge Transfer Crystals". Crystals 10, n.º 3 (6 de marzo de 2020): 177. http://dx.doi.org/10.3390/cryst10030177.
Texto completoFujimoto, Keisuke, Masaki Takahashi, Seiichiro Izawa y Masahiro Hiramoto. "Development of Perylene-Based Non-Fullerene Acceptors through Bay-Functionalization Strategy". Materials 13, n.º 9 (6 de mayo de 2020): 2148. http://dx.doi.org/10.3390/ma13092148.
Texto completoAlves, Alessandro L., Simone V. Bernardino, Carlos H. Stadtlober, Edivandro Girotto, Giliandro Farias, Rodney M. do Nascimento, Sergio F. Curcio et al. "Charge carrier transport in perylene-based and pyrene-based columnar liquid crystals". Beilstein Journal of Organic Chemistry 19 (16 de noviembre de 2023): 1755–65. http://dx.doi.org/10.3762/bjoc.19.128.
Texto completoTakahashi, Masaki, Yousuke Suzuki, Yasunori Ichihashi, Mitsuji Yamashita y Hideki Kawai. "1,3,8,10-Tetrahydro-2,9-diazadibenzo[cd,lm]perylenes: synthesis of reduced perylene bisimide analogues". Tetrahedron Letters 48, n.º 3 (enero de 2007): 357–59. http://dx.doi.org/10.1016/j.tetlet.2006.11.100.
Texto completoHu, Xiao Jun, Xin Yan Hu y Zhi Zhang. "A New Approach to Fluorescent Chemosensor of Cu2+ Ion". Applied Mechanics and Materials 513-517 (febrero de 2014): 65–69. http://dx.doi.org/10.4028/www.scientific.net/amm.513-517.65.
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