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