Articoli di riviste sul tema "Organic electron donors (OEDs)"
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Cha, Judy J. "Intercalation and Functionalization in 2D Materials". ECS Meeting Abstracts MA2023-01, n. 13 (28 agosto 2023): 1306. http://dx.doi.org/10.1149/ma2023-01131306mtgabs.
Murphy, John A. "ChemInform Abstract: Organic Electron Donors". ChemInform 43, n. 37 (16 agosto 2012): no. http://dx.doi.org/10.1002/chin.201237244.
Broggi, Julie, Marion Rollet, Jean-Louis Clément, Gabriel Canard, Thierry Terme, Didier Gigmes e Patrice Vanelle. "Polymerization Initiated by Organic Electron Donors". Angewandte Chemie International Edition 55, n. 20 (8 aprile 2016): 5994–99. http://dx.doi.org/10.1002/anie.201600327.
Broggi, Julie, Marion Rollet, Jean-Louis Clément, Gabriel Canard, Thierry Terme, Didier Gigmes e Patrice Vanelle. "Polymerization Initiated by Organic Electron Donors". Angewandte Chemie 128, n. 20 (8 aprile 2016): 6098–103. http://dx.doi.org/10.1002/ange.201600327.
Broggi, Julie, Thierry Terme e Patrice Vanelle. "Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis". Angewandte Chemie International Edition 53, n. 2 (24 novembre 2013): 384–413. http://dx.doi.org/10.1002/anie.201209060.
Zhou, Shengze, Hardeep Farwaha e John A. Murphy. "The Development of Organic Super Electron Donors". CHIMIA International Journal for Chemistry 66, n. 6 (27 giugno 2012): 418–24. http://dx.doi.org/10.2533/chimia.2012.418.
Rohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie International Edition 58, n. 33 (12 agosto 2019): 11454–58. http://dx.doi.org/10.1002/anie.201905814.
Lowe, Grace A. "Enabling artificial photosynthesis systems with molecular recycling: A review of photo- and electrochemical methods for regenerating organic sacrificial electron donors". Beilstein Journal of Organic Chemistry 19 (8 agosto 2023): 1198–215. http://dx.doi.org/10.3762/bjoc.19.88.
Murphy, John A. "Discovery and Development of Organic Super-Electron-Donors". Journal of Organic Chemistry 79, n. 9 (25 marzo 2014): 3731–46. http://dx.doi.org/10.1021/jo500071u.
Rohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Corrigendum: Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie International Edition 58, n. 43 (21 ottobre 2019): 15183. http://dx.doi.org/10.1002/anie.201910425.
Rohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Berichtigung: Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie 131, n. 43 (14 ottobre 2019): 15325. http://dx.doi.org/10.1002/ange.201910425.
Broggi, Julie, Thierry Terme e Patrice Vanelle. "ChemInform Abstract: Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis". ChemInform 45, n. 19 (23 aprile 2014): no. http://dx.doi.org/10.1002/chin.201419251.
Anderson, Greg M., Iain Cameron, John A. Murphy e Tell Tuttle. "Predicting the reducing power of organic super electron donors". RSC Advances 6, n. 14 (2016): 11335–43. http://dx.doi.org/10.1039/c5ra26483a.
Kushto, Gary P., Antti J. Makinen e Paul A. Lane. "Organic Photovoltaic Cells Using Group 10 Metallophthalocyanine Electron Donors". IEEE Journal of Selected Topics in Quantum Electronics 16, n. 6 (novembre 2010): 1552–59. http://dx.doi.org/10.1109/jstqe.2010.2052354.
Guidi, Vanina V., Zhou Jin, Devin Busse, William B. Euler e Brett L. Lucht. "Bis(phosphine Imide)s: Easily Tunable Organic Electron Donors". Journal of Organic Chemistry 70, n. 19 (settembre 2005): 7737–43. http://dx.doi.org/10.1021/jo051196u.
Zhou, Shengze, Hardeep Farwaha e John A. Murphy. "ChemInform Abstract: The Development of Organic Super Electron Donors". ChemInform 43, n. 44 (4 ottobre 2012): no. http://dx.doi.org/10.1002/chin.201244258.
YAMASHITA, Yoshiro. "Novel electron acceptors and donors containing fused-heterocycles." Journal of Synthetic Organic Chemistry, Japan 47, n. 12 (1989): 1108–17. http://dx.doi.org/10.5059/yukigoseikyokaishi.47.1108.
Hoffman, Robert V. "THE OXIDATION OF ELECTRON DONORS WITH SULFONYL PEROXIDES". Organic Preparations and Procedures International 18, n. 3 (giugno 1986): 179–201. http://dx.doi.org/10.1080/00304948609458139.
Doni, Eswararao, e John A. Murphy. "Evolution of neutral organic super-electron-donors and their applications". Chem. Commun. 50, n. 46 (2014): 6073–87. http://dx.doi.org/10.1039/c3cc48969h.
Li, Shuixing, Zhongqiang Zhang, Minmin Shi, Chang-Zhi Li e Hongzheng Chen. "Molecular electron acceptors for efficient fullerene-free organic solar cells". Physical Chemistry Chemical Physics 19, n. 5 (2017): 3440–58. http://dx.doi.org/10.1039/c6cp07465k.
Garnier, Jean, Douglas W. Thomson, Shengze Zhou, Phillip I. Jolly, Leonard E. A. Berlouis e John A. Murphy. "Hybrid super electron donors – preparation and reactivity". Beilstein Journal of Organic Chemistry 8 (3 luglio 2012): 994–1002. http://dx.doi.org/10.3762/bjoc.8.112.
Murphy, John A. "ChemInform Abstract: Discovery and Development of Organic Super-Electron-Donors". ChemInform 45, n. 28 (26 giugno 2014): no. http://dx.doi.org/10.1002/chin.201428243.
Martin, Julien D., e C. Adam Dyker. "Facile preparation and isolation of neutral organic electron donors based on 4-dimethylaminopyridine". Canadian Journal of Chemistry 96, n. 6 (giugno 2018): 522–25. http://dx.doi.org/10.1139/cjc-2017-0526.
Wonner, P., T. Steinke e S. M. Huber. "Activation of Quinolines by Cationic Chalcogen Bond Donors". Synlett 30, n. 14 (9 agosto 2019): 1673–78. http://dx.doi.org/10.1055/s-0039-1690110.
Santos, Fabiano S., Elamparuthi Ramasamy, V. Ramamurthy e Fabiano S. Rodembusch. "Correction: Photoinduced electron transfer across an organic molecular wall: octa acid encapsulated ESIPT dyes as electron donors". Photochemical & Photobiological Sciences 16, n. 8 (2017): 1335. http://dx.doi.org/10.1039/c7pp90026k.
Sandanayaka, Atula S. D., Hisahiro Sasabe, Toshikazu Takata e Osamu Ito. "Photoinduced electron transfer processes of fullerene rotaxanes containing various electron-donors". Journal of Photochemistry and Photobiology C: Photochemistry Reviews 11, n. 2-3 (settembre 2010): 73–92. http://dx.doi.org/10.1016/j.jphotochemrev.2010.05.001.
Seel, Catharina Julia, Antonín Králík, Melanie Hacker, Annika Frank, Burkhard König e Tanja Gulder. "Atom-Economic Electron Donors for Photobiocatalytic Halogenations". ChemCatChem 10, n. 18 (25 luglio 2018): 3960–63. http://dx.doi.org/10.1002/cctc.201800886.
Onitsch, Christine, Arnulf Rosspeintner, Gonzalo Angulo, Markus Griesser, Milan Kivala, Brian Frank, François Diederich e Georg Gescheidt. "Donor-Substituted Diphenylacetylene Derivatives Act as Electron Donors and Acceptors". Journal of Organic Chemistry 76, n. 14 (15 luglio 2011): 5628–35. http://dx.doi.org/10.1021/jo2005022.
Bryce, Martin R., Malcolm A. Coffin e William Clegg. "New vinylogous tetrathiafulvalene .pi.-electron donors with peripheral alkylseleno substitution". Journal of Organic Chemistry 57, n. 6 (marzo 1992): 1696–99. http://dx.doi.org/10.1021/jo00032a018.
Miao, Junhui, Bin Meng, Jun Liu e Lixiang Wang. "Small-Molecule Donor/Polymer Acceptor Type Organic Solar Cells: Effect of Terminal Groups of Small-Molecule Donors". Organic Materials 01, n. 01 (novembre 2019): 088–94. http://dx.doi.org/10.1055/s-0039-3401017.
Jiang, Xudong, Yunhua Xu, Xiaohui Wang, Yang Wu, Guitao Feng, Cheng Li, Wei Ma e Weiwei Li. "Non-fullerene organic solar cells based on diketopyrrolopyrrole polymers as electron donors and ITIC as an electron acceptor". Physical Chemistry Chemical Physics 19, n. 11 (2017): 8069–75. http://dx.doi.org/10.1039/c7cp00494j.
Dyachenko, V. I., B. L. Tumanskii, Yu I. Lyakhovetskii, N. M. Loim, R. G. Gasanov, N. N. Bubnov, A. F. Kolomiets e A. V. Fokin. "One-electron transfer in the reactions of polyfluoroketones with organic donors". Bulletin of the Russian Academy of Sciences Division of Chemical Science 41, n. 3 (marzo 1992): 599. http://dx.doi.org/10.1007/bf00863099.
Torres, Isabela C., Kanika S. Inglett e K. R. Reddy. "Heterotrophic microbial activity in lake sediments: effects of organic electron donors". Biogeochemistry 104, n. 1-3 (30 giugno 2010): 165–81. http://dx.doi.org/10.1007/s10533-010-9494-6.
Tintori, Guillaume, Pierre Nabokoff, Ruqaya Buhaibeh, David Bergé-Lefranc, Sébastien Redon, Julie Broggi e Patrice Vanelle. "Base-Free Generation of Organic Electron Donors from Air-Stable Precursors". Angewandte Chemie 130, n. 12 (15 febbraio 2018): 3202–7. http://dx.doi.org/10.1002/ange.201713079.
Wang, Hua-Jing, Jing Shi, Ming Fang, Zhe Li e Qing-Xiang Guo. "Design of new neutral organic super-electron donors: a theoretical study". Journal of Physical Organic Chemistry 23, n. 1 (21 agosto 2009): 75–83. http://dx.doi.org/10.1002/poc.1590.
Tintori, Guillaume, Pierre Nabokoff, Ruqaya Buhaibeh, David Bergé-Lefranc, Sébastien Redon, Julie Broggi e Patrice Vanelle. "Base-Free Generation of Organic Electron Donors from Air-Stable Precursors". Angewandte Chemie International Edition 57, n. 12 (15 febbraio 2018): 3148–53. http://dx.doi.org/10.1002/anie.201713079.
Lazareva, N. F., e I. M. Lazarev. "α-Silyl amines as electron donors: application in synthetic organic chemistry". Russian Chemical Bulletin 73, n. 4 (aprile 2024): 761–86. http://dx.doi.org/10.1007/s11172-024-4191-0.
Wang, Jinfeng, Siwei Liu, Kai Chang, Qiuyan Liao, Sheng Li, Hongwei Han, Qianqian Li e Zhen Li. "Synergy effect of electronic characteristics and spatial configurations of electron donors on photovoltaic performance of organic dyes". Journal of Materials Chemistry C 8, n. 41 (2020): 14453–61. http://dx.doi.org/10.1039/d0tc02556a.
Doni, Eswararao, e John A. Murphy. "Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors". Org. Chem. Front. 1, n. 9 (2014): 1072–76. http://dx.doi.org/10.1039/c4qo00202d.
Zhou, T. F., X. Y. Ma, W. X. Han, X. P. Guo, R. Q. Gu, L. J. Yu, J. Li, Y. M. Zhao e Tao Wang. "D–D–A dyes with phenothiazine–carbazole/triphenylamine as double donors in photopolymerization under 455 nm and 532 nm laser beams". Polymer Chemistry 7, n. 31 (2016): 5039–49. http://dx.doi.org/10.1039/c6py00918b.
Molina-Ontoria, Agustín, María Gallego, Luís Echegoyen, Emilio M. Pérez e Nazario Martín. "Organic solar cells based on bowl-shaped small-molecules". RSC Advances 5, n. 40 (2015): 31541–46. http://dx.doi.org/10.1039/c5ra02073e.
Miyaji, Tsutomu, Takanori Suzuki, Tsuneyuki Okubo, Akihisa Okada, Yoshiro Yamashita e Tsutomu Miyashi. "Benzidine Type Electron Donors Fused with 1,2,5-Chalcogenadiazole Units". HETEROCYCLES 35, n. 1 (1993): 395. http://dx.doi.org/10.3987/com-92-s34.
Tintori, Guillaume, Arona Fall, Nadhrata Assani, Yuxi Zhao, David Bergé-Lefranc, Sébastien Redon, Patrice Vanelle e Julie Broggi. "Generation of powerful organic electron donors by water-assisted decarboxylation of benzimidazolium carboxylates". Organic Chemistry Frontiers 8, n. 6 (2021): 1197–205. http://dx.doi.org/10.1039/d0qo01488e.
Paleti, Sri Harish Kumar, Nicola Gasparini, Christos L. Chochos e Derya Baran. "High performance conjugated terpolymers as electron donors in nonfullerene organic solar cells". Journal of Materials Chemistry C 8, n. 38 (2020): 13422–29. http://dx.doi.org/10.1039/d0tc01379j.
Uchiyama, Takayuki, Takashi Sano, Yoshiko Okada-Shudo e Varun Vohra. "Durable organic solar cells produced by in situ encapsulation of an air-sensitive natural organic semiconductor by the fullerene derivative and the metal oxide layer". Journal of Materials Chemistry C 8, n. 21 (2020): 7162–69. http://dx.doi.org/10.1039/d0tc00379d.
Brancaleon, Lorenzo, Darryl Brousmiche e Linda J. Johnston. "Article". Canadian Journal of Chemistry 77, n. 5-6 (1 giugno 1999): 787–91. http://dx.doi.org/10.1139/v99-060.
Sun, Jian-Ke, Ya-Jun Zhang, Gui-Peng Yu, Jie Zhang, Markus Antonietti e Jiayin Yuan. "Three birds, one stone – photo-/piezo-/chemochromism in one conjugated nanoporous ionic organic network". Journal of Materials Chemistry C 6, n. 34 (2018): 9065–70. http://dx.doi.org/10.1039/c8tc01324a.
Quinton, Cassandre, Valérie Alain-Rizzo, Cécile Dumas-Verdes, Gilles Clavier, Laurence Vignau e Pierre Audebert. "Triphenylamine/tetrazine based π-conjugated systems as molecular donors for organic solar cells". New Journal of Chemistry 39, n. 12 (2015): 9700–9713. http://dx.doi.org/10.1039/c5nj02097b.
Rueping, Magnus, Pavlo Nikolaienko, Yury Lebedev e Alina Adams. "Metal-free reduction of the greenhouse gas sulfur hexafluoride, formation of SF5 containing ion pairs and the application in fluorinations". Green Chemistry 19, n. 11 (2017): 2571–75. http://dx.doi.org/10.1039/c7gc00877e.
Yang, Zhenqing, Changjin Shao e Dapeng Cao. "Screening donor groups of organic dyes for dye-sensitized solar cells". RSC Advances 5, n. 29 (2015): 22892–98. http://dx.doi.org/10.1039/c4ra17261b.