Artigos de revistas sobre o tema "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 (8 de agosto de 2023): 1198–215. http://dx.doi.org/10.3762/bjoc.19.88.
Texto completo da fonteMurphy, John A. "ChemInform Abstract: Organic Electron Donors". ChemInform 43, n.º 37 (16 de agosto de 2012): no. http://dx.doi.org/10.1002/chin.201237244.
Texto completo da fonteGarnier, 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 de julho de 2012): 994–1002. http://dx.doi.org/10.3762/bjoc.8.112.
Texto completo da fonteBroggi, 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.º 20 (8 de abril de 2016): 5994–99. http://dx.doi.org/10.1002/anie.201600327.
Texto completo da fonteBroggi, 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.º 20 (8 de abril de 2016): 6098–103. http://dx.doi.org/10.1002/ange.201600327.
Texto completo da fonteMartin, 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.º 6 (junho de 2018): 522–25. http://dx.doi.org/10.1139/cjc-2017-0526.
Texto completo da fonteBroggi, Julie, Thierry Terme e Patrice Vanelle. "Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis". Angewandte Chemie International Edition 53, n.º 2 (24 de novembro de 2013): 384–413. http://dx.doi.org/10.1002/anie.201209060.
Texto completo da fonteZhou, Feng, Jing-Hui He, Quan Liu, Pei-Yang Gu, Hua Li, Guo-Qin Xu, Qing-Feng Xu e Jian-Mei Lu. "Tuning memory performances from WORM to flash or DRAM by structural tailoring with different donor moieties". J. Mater. Chem. C 2, n.º 36 (2014): 7674–80. http://dx.doi.org/10.1039/c4tc00943f.
Texto completo da fonteXu, Tongle, Yuying Chang, Cenqi Yan, Qianguang Yang, Zhipeng Kan, Ranbir Singh, Manish Kumar, Gang Li, Shirong Lu e Tainan Duan. "Fluorinated oligothiophene donors for high-performance nonfullerene small-molecule organic solar cells". Sustainable Energy & Fuels 4, n.º 6 (2020): 2680–85. http://dx.doi.org/10.1039/d0se00335b.
Texto completo da fonteZhou, Shengze, Hardeep Farwaha e John A. Murphy. "The Development of Organic Super Electron Donors". CHIMIA International Journal for Chemistry 66, n.º 6 (27 de junho de 2012): 418–24. http://dx.doi.org/10.2533/chimia.2012.418.
Texto completo da fonteRohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie International Edition 58, n.º 33 (12 de agosto de 2019): 11454–58. http://dx.doi.org/10.1002/anie.201905814.
Texto completo da fonteOnitsch, 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.º 14 (15 de julho de 2011): 5628–35. http://dx.doi.org/10.1021/jo2005022.
Texto completo da fontePayne, Rayford B., Darren M. Gentry, Barbara J. Rapp-Giles, Laurence Casalot e Judy D. Wall. "Uranium Reduction by Desulfovibrio desulfuricans Strain G20 and a Cytochrome c3 Mutant". Applied and Environmental Microbiology 68, n.º 6 (junho de 2002): 3129–32. http://dx.doi.org/10.1128/aem.68.6.3129-3132.2002.
Texto completo da fonteSaputra, Beny, Agus Sutanto, Mia Cholvistaria, Suprayitno Suprayitno e Nala Rahmawati. "IDENTIFIKASI BAKTERI PEREDUKSI SULFAT PADA KAWAH AIR PANAS NIRWANA SUOH LAMPUNG BARAT". BIOLOVA 2, n.º 2 (30 de agosto de 2021): 122–27. http://dx.doi.org/10.24127/biolova.v2i2.1089.
Texto completo da fonteNocera, Giuseppe, e John A. Murphy. "Ground State Cross-Coupling of Haloarenes with Arenes Initiated by Organic Electron Donors, Formed in situ: An Overview". Synthesis 52, n.º 03 (13 de setembro de 2019): 327–36. http://dx.doi.org/10.1055/s-0039-1690614.
Texto completo da fonteMiao, 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.º 01 (novembro de 2019): 088–94. http://dx.doi.org/10.1055/s-0039-3401017.
Texto completo da fonteMurata, Tsuyoshi, Kazuki Kariyazono, Shusaku Ukai, Akira Ueda, Yuki Kanzaki, Daisuke Shiomi, Kazunobu Sato, Takeji Takui e Yasushi Morita. "Trioxotriangulene with carbazole: a donor–acceptor molecule showing strong near-infrared absorption exceeding 1000 nm". Organic Chemistry Frontiers 6, n.º 17 (2019): 3107–15. http://dx.doi.org/10.1039/c9qo00663j.
Texto completo da fonteMurphy, John A. "Discovery and Development of Organic Super-Electron-Donors". Journal of Organic Chemistry 79, n.º 9 (25 de março de 2014): 3731–46. http://dx.doi.org/10.1021/jo500071u.
Texto completo da fonteRohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Corrigendum: Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie International Edition 58, n.º 43 (21 de outubro de 2019): 15183. http://dx.doi.org/10.1002/anie.201910425.
Texto completo da fonteRohrbach, Simon, Rushabh S. Shah, Tell Tuttle e John A. Murphy. "Berichtigung: Neutral Organic Super Electron Donors Made Catalytic". Angewandte Chemie 131, n.º 43 (14 de outubro de 2019): 15325. http://dx.doi.org/10.1002/ange.201910425.
Texto completo da fonteBroggi, Julie, Thierry Terme e Patrice Vanelle. "ChemInform Abstract: Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis". ChemInform 45, n.º 19 (23 de abril de 2014): no. http://dx.doi.org/10.1002/chin.201419251.
Texto completo da fonteYamashita, Yoshiro, e Masaaki Tomura. "Highly polarized electron donors, acceptors and donor–acceptor compounds for organic conductors". Journal of Materials Chemistry 8, n.º 9 (1998): 1933–44. http://dx.doi.org/10.1039/a803151g.
Texto completo da fonteZhao, Yuan, Huan Wang, Weixuan Zeng, Shengpeng Xia, Feng Zhou, Hui Chen, Feng He e 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, n.º 17 (2018): 8101–8. http://dx.doi.org/10.1039/c8ta01353e.
Texto completo da fonteLiu, Shi-Yong, Jae Woong Jung, Chang-Zhi Li, Jiang Huang, Jianyuan Zhang, Hongzheng Chen e 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, n.º 44 (2015): 22162–69. http://dx.doi.org/10.1039/c5ta06639e.
Texto completo da fonteAnderson, Greg M., Iain Cameron, John A. Murphy e Tell Tuttle. "Predicting the reducing power of organic super electron donors". RSC Advances 6, n.º 14 (2016): 11335–43. http://dx.doi.org/10.1039/c5ra26483a.
Texto completo da fonteLi, 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.º 5 (2017): 3440–58. http://dx.doi.org/10.1039/c6cp07465k.
Texto completo da fonteDoni, Eswararao, e John A. Murphy. "Evolution of neutral organic super-electron-donors and their applications". Chem. Commun. 50, n.º 46 (2014): 6073–87. http://dx.doi.org/10.1039/c3cc48969h.
Texto completo da fonteHimmel, Hans-Jörg. "Guanidines as Reagents in Proton-Coupled Electron-Transfer Reactions and Redox Catalysts". Synlett 29, n.º 15 (8 de junho de 2018): 1957–77. http://dx.doi.org/10.1055/s-0037-1610156.
Texto completo da fonteKushto, 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.º 6 (novembro de 2010): 1552–59. http://dx.doi.org/10.1109/jstqe.2010.2052354.
Texto completo da fonteGuidi, 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.º 19 (setembro de 2005): 7737–43. http://dx.doi.org/10.1021/jo051196u.
Texto completo da fonteZhou, Shengze, Hardeep Farwaha e John A. Murphy. "ChemInform Abstract: The Development of Organic Super Electron Donors". ChemInform 43, n.º 44 (4 de outubro de 2012): no. http://dx.doi.org/10.1002/chin.201244258.
Texto completo da fonteSethio, Daniel, Vytor Oliveira e Elfi Kraka. "Quantitative Assessment of Tetrel Bonding Utilizing Vibrational Spectroscopy". Molecules 23, n.º 11 (25 de outubro de 2018): 2763. http://dx.doi.org/10.3390/molecules23112763.
Texto completo da fonteSantos, 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.º 8 (2017): 1335. http://dx.doi.org/10.1039/c7pp90026k.
Texto completo da fonteWang, 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.º 41 (2020): 14453–61. http://dx.doi.org/10.1039/d0tc02556a.
Texto completo da fonteTruong, K. D., A. D. Bandrauk, J. ZAUHAR e C. Carlose. "Vibrational spectra of two new organic semiconductors: tetrathiafulvalene (TTF) and tetramethyltetraselenafulvalene (TMTSF) salts of paranitrophenylmalononitrile (PNMA)". Canadian Journal of Chemistry 69, n.º 5 (1 de maio de 1991): 901–7. http://dx.doi.org/10.1139/v91-132.
Texto completo da fonteMohamed El Amine, Boudia, Yi Zhou, Hongying Li, Qiuwang Wang, Jun Xi e Cunlu Zhao. "Latest Updates of Single-Junction Organic Solar Cells up to 20% Efficiency". Energies 16, n.º 9 (4 de maio de 2023): 3895. http://dx.doi.org/10.3390/en16093895.
Texto completo da fonteZhou, 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.º 31 (2016): 5039–49. http://dx.doi.org/10.1039/c6py00918b.
Texto completo da fonteJiang, 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.º 11 (2017): 8069–75. http://dx.doi.org/10.1039/c7cp00494j.
Texto completo da fonteYAMASHITA, Yoshiro. "Novel electron acceptors and donors containing fused-heterocycles." Journal of Synthetic Organic Chemistry, Japan 47, n.º 12 (1989): 1108–17. http://dx.doi.org/10.5059/yukigoseikyokaishi.47.1108.
Texto completo da fonteHoffman, Robert V. "THE OXIDATION OF ELECTRON DONORS WITH SULFONYL PEROXIDES". Organic Preparations and Procedures International 18, n.º 3 (junho de 1986): 179–201. http://dx.doi.org/10.1080/00304948609458139.
Texto completo da fonteGalani, Andriani, Daniel Mamais, Constantinos Noutsopoulos, Petra Anastopoulou e Alexia Varouxaki. "Biotic and Abiotic Biostimulation for the Reduction of Hexavalent Chromium in Contaminated Aquifers". Water 14, n.º 1 (4 de janeiro de 2022): 89. http://dx.doi.org/10.3390/w14010089.
Texto completo da fonteDavydov, Alexandr S., e Ivan I. Ukrainskii. "Electron states and electron transport in quasi-one-dimensional molecular systems". Canadian Journal of Chemistry 63, n.º 7 (1 de julho de 1985): 1899–903. http://dx.doi.org/10.1139/v85-314.
Texto completo da fonteMurphy, John A. "ChemInform Abstract: Discovery and Development of Organic Super-Electron-Donors". ChemInform 45, n.º 28 (26 de junho de 2014): no. http://dx.doi.org/10.1002/chin.201428243.
Texto completo da fonteDoni, Eswararao, e John A. Murphy. "Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors". Org. Chem. Front. 1, n.º 9 (2014): 1072–76. http://dx.doi.org/10.1039/c4qo00202d.
Texto completo da fonteDell’Armi, Edoardo, Marta Maria Rossi, Lucia Taverna, Marco Petrangeli Papini e Marco Zeppilli. "Evaluation of the Bioelectrochemical Approach and Different Electron Donors for Biological Trichloroethylene Reductive Dechlorination". Toxics 10, n.º 1 (13 de janeiro de 2022): 37. http://dx.doi.org/10.3390/toxics10010037.
Texto completo da fonteDeng, Qinghui, Keju Wang, Wang Xu, Xinfan Yu, Jie Feng, Shuangfei Li e Huirong Chen. "Enhancement of Microbial and Metabolic Mechanisms in an Aerobic Bioreactor with Immobilized Microflora by Simple and Complex Electron Donors". Water 15, n.º 14 (12 de julho de 2023): 2548. http://dx.doi.org/10.3390/w15142548.
Texto completo da fonteRueping, 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.º 11 (2017): 2571–75. http://dx.doi.org/10.1039/c7gc00877e.
Texto completo da fonteSierra-Alvarez, R., F. Guerrero, P. Rowlette, S. Freeman e J. A. Field. "Comparison of chemo-, hetero- and mixotrophic denitrification in laboratory-scale UASBs". Water Science and Technology 52, n.º 1-2 (1 de julho de 2005): 337–42. http://dx.doi.org/10.2166/wst.2005.0536.
Texto completo da fonteTintori, 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.º 6 (2021): 1197–205. http://dx.doi.org/10.1039/d0qo01488e.
Texto completo da fonteChen, Yao, Weigang Zhu, Jianglin Wu, Yan Huang, Antonio Facchetti e Tobin J. Marks. "Recent Advances in Squaraine Dyes for Bulk-Heterojunction Organic Solar Cells". Organic Photonics and Photovoltaics 6, n.º 1 (1 de janeiro de 2019): 1–16. http://dx.doi.org/10.1515/oph-2019-0001.
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