Статті в журналах з теми "Organic electron donors"
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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 (August 8, 2023): 1198–215. http://dx.doi.org/10.3762/bjoc.19.88.
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 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 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 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 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, Feng, Jing-Hui He, Quan Liu, Pei-Yang Gu, Hua Li, Guo-Qin Xu, Qing-Feng Xu, and Jian-Mei Lu. "Tuning memory performances from WORM to flash or DRAM by structural tailoring with different donor moieties." J. Mater. Chem. C 2, no. 36 (2014): 7674–80. http://dx.doi.org/10.1039/c4tc00943f.
Повний текст джерелаXu, Tongle, Yuying Chang, Cenqi Yan, Qianguang Yang, Zhipeng Kan, Ranbir Singh, Manish Kumar, Gang Li, Shirong Lu, and Tainan Duan. "Fluorinated oligothiophene donors for high-performance nonfullerene small-molecule organic solar cells." Sustainable Energy & Fuels 4, no. 6 (2020): 2680–85. http://dx.doi.org/10.1039/d0se00335b.
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 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 джерелаPayne, Rayford B., Darren M. Gentry, Barbara J. Rapp-Giles, Laurence Casalot, and Judy D. Wall. "Uranium Reduction by Desulfovibrio desulfuricans Strain G20 and a Cytochrome c3 Mutant." Applied and Environmental Microbiology 68, no. 6 (June 2002): 3129–32. http://dx.doi.org/10.1128/aem.68.6.3129-3132.2002.
Повний текст джерелаSaputra, Beny, Agus Sutanto, Mia Cholvistaria, Suprayitno Suprayitno, and Nala Rahmawati. "IDENTIFIKASI BAKTERI PEREDUKSI SULFAT PADA KAWAH AIR PANAS NIRWANA SUOH LAMPUNG BARAT." BIOLOVA 2, no. 2 (August 30, 2021): 122–27. http://dx.doi.org/10.24127/biolova.v2i2.1089.
Повний текст джерелаNocera, Giuseppe, and John A. Murphy. "Ground State Cross-Coupling of Haloarenes with Arenes Initiated by Organic Electron Donors, Formed in situ: An Overview." Synthesis 52, no. 03 (September 13, 2019): 327–36. http://dx.doi.org/10.1055/s-0039-1690614.
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 джерелаMurata, Tsuyoshi, Kazuki Kariyazono, Shusaku Ukai, Akira Ueda, Yuki Kanzaki, Daisuke Shiomi, Kazunobu Sato, Takeji Takui, and Yasushi Morita. "Trioxotriangulene with carbazole: a donor–acceptor molecule showing strong near-infrared absorption exceeding 1000 nm." Organic Chemistry Frontiers 6, no. 17 (2019): 3107–15. http://dx.doi.org/10.1039/c9qo00663j.
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 джерелаYamashita, Yoshiro, and Masaaki Tomura. "Highly polarized electron donors, acceptors and donor–acceptor compounds for organic conductors." Journal of Materials Chemistry 8, no. 9 (1998): 1933–44. http://dx.doi.org/10.1039/a803151g.
Повний текст джерелаZhao, Yuan, Huan Wang, Weixuan Zeng, Shengpeng Xia, Feng Zhou, Hui Chen, Feng He, and Chuluo Yang. "Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells." Journal of Materials Chemistry A 6, no. 17 (2018): 8101–8. http://dx.doi.org/10.1039/c8ta01353e.
Повний текст джерелаLiu, Shi-Yong, Jae Woong Jung, Chang-Zhi Li, Jiang Huang, Jianyuan Zhang, Hongzheng Chen, and Alex K. Y. Jen. "Three-dimensional molecular donors combined with polymeric acceptors for high performance fullerene-free organic photovoltaic devices." Journal of Materials Chemistry A 3, no. 44 (2015): 22162–69. http://dx.doi.org/10.1039/c5ta06639e.
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 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 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 джерелаHimmel, Hans-Jörg. "Guanidines as Reagents in Proton-Coupled Electron-Transfer Reactions and Redox Catalysts." Synlett 29, no. 15 (June 8, 2018): 1957–77. http://dx.doi.org/10.1055/s-0037-1610156.
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 джерелаSethio, Daniel, Vytor Oliveira, and Elfi Kraka. "Quantitative Assessment of Tetrel Bonding Utilizing Vibrational Spectroscopy." Molecules 23, no. 11 (October 25, 2018): 2763. http://dx.doi.org/10.3390/molecules23112763.
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 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 джерелаTruong, K. D., A. D. Bandrauk, J. ZAUHAR, and C. Carlose. "Vibrational spectra of two new organic semiconductors: tetrathiafulvalene (TTF) and tetramethyltetraselenafulvalene (TMTSF) salts of paranitrophenylmalononitrile (PNMA)." Canadian Journal of Chemistry 69, no. 5 (May 1, 1991): 901–7. http://dx.doi.org/10.1139/v91-132.
Повний текст джерелаMohamed El Amine, Boudia, Yi Zhou, Hongying Li, Qiuwang Wang, Jun Xi, and Cunlu Zhao. "Latest Updates of Single-Junction Organic Solar Cells up to 20% Efficiency." Energies 16, no. 9 (May 4, 2023): 3895. http://dx.doi.org/10.3390/en16093895.
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 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 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 джерелаGalani, Andriani, Daniel Mamais, Constantinos Noutsopoulos, Petra Anastopoulou, and Alexia Varouxaki. "Biotic and Abiotic Biostimulation for the Reduction of Hexavalent Chromium in Contaminated Aquifers." Water 14, no. 1 (January 4, 2022): 89. http://dx.doi.org/10.3390/w14010089.
Повний текст джерелаDavydov, Alexandr S., and Ivan I. Ukrainskii. "Electron states and electron transport in quasi-one-dimensional molecular systems." Canadian Journal of Chemistry 63, no. 7 (July 1, 1985): 1899–903. http://dx.doi.org/10.1139/v85-314.
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 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 джерелаDell’Armi, Edoardo, Marta Maria Rossi, Lucia Taverna, Marco Petrangeli Papini, and Marco Zeppilli. "Evaluation of the Bioelectrochemical Approach and Different Electron Donors for Biological Trichloroethylene Reductive Dechlorination." Toxics 10, no. 1 (January 13, 2022): 37. http://dx.doi.org/10.3390/toxics10010037.
Повний текст джерелаDeng, Qinghui, Keju Wang, Wang Xu, Xinfan Yu, Jie Feng, Shuangfei Li, and Huirong Chen. "Enhancement of Microbial and Metabolic Mechanisms in an Aerobic Bioreactor with Immobilized Microflora by Simple and Complex Electron Donors." Water 15, no. 14 (July 12, 2023): 2548. http://dx.doi.org/10.3390/w15142548.
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 джерелаSierra-Alvarez, R., F. Guerrero, P. Rowlette, S. Freeman, and J. A. Field. "Comparison of chemo-, hetero- and mixotrophic denitrification in laboratory-scale UASBs." Water Science and Technology 52, no. 1-2 (July 1, 2005): 337–42. http://dx.doi.org/10.2166/wst.2005.0536.
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 джерелаChen, Yao, Weigang Zhu, Jianglin Wu, Yan Huang, Antonio Facchetti, and Tobin J. Marks. "Recent Advances in Squaraine Dyes for Bulk-Heterojunction Organic Solar Cells." Organic Photonics and Photovoltaics 6, no. 1 (January 1, 2019): 1–16. http://dx.doi.org/10.1515/oph-2019-0001.
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