Добірка наукової літератури з теми "Organic electron donors"
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Статті в журналах з теми "Organic electron donors"
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 джерелаДисертації з теми "Organic electron donors"
Schonebeck, Franziska. "Super electron donors powerful reductions performed by neutral organic molecules." Thesis, University of Strathclyde, 2007. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=21732.
Повний текст джерелаCumine, Florimond. "Studies on organic electron donors and their applications in chemistry." Thesis, University of Strathclyde, 2017. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=29432.
Повний текст джерелаBuker, Nicholas D. "Guanidine donors in nonlinear optical chromophores /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/8669.
Повний текст джерелаChua, Jonathan. "Exploring new reactions with Organic Electron Donors and the complexities of the Birch reduction." Thesis, University of Strathclyde, 2016. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=26437.
Повний текст джерелаAnderson, Greg. "Towards the rational development of organic super electron donors for transition metal-free biaryl coupling." Thesis, University of Strathclyde, 2016. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=27424.
Повний текст джерелаTyree, William Stuart. "Correlation of Structure and Magnetic Properties in Charge-Transfer Salt Molecular Magnets Composed of Decamethylmetallocene Electron Donors and Organic Electron Acceptors." Thesis, Virginia Tech, 2005. http://hdl.handle.net/10919/34436.
Повний текст джерелаMaster of Science
Xu, Yunhua. "Synthesis and Photoinduced Electron Transfer of Donor-Sensitizer-Acceptor Systems." Doctoral thesis, Stockholm : Department of Organic Chemistry, Stockholm University, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-411.
Повний текст джерелаZhao, Yuxi. "Synthèse de donneurs d’électrons organiques : application en synthèse organique et chimie des polymères." Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0156.
Повний текст джерелаOrganic electron donors (OEDs) with exceptionally negative redox potentials have attracted considerable attention in organic synthesis as powerful reducers. They enable the spontaneous transfer of one or two electrons to organic substrates, to form radical or anionic intermediates. Nevertheless, the structural diversity of OEDs is limited and their application scope quite narrow. In this thesis, we first developed novel libraries of OEDs in order to identify new families of organic reducers, broaden the range of redox potentials and access new reducing reactivities. Appropriate structural modulations on seven categories of iminium salts gave access to powerful OED with various reducing abilities. It also allowed to rationalize the factors governing single- or double-electron transfers according to the OED structures and the reaction conditions. A more thorough mechanistic investigation was conducted to formally confirm the active electron donor species at work.Finally, OEDs also appeared to be remarkable organic redox initiating systems for both free radical and anionic polymerization reactions. While the anionic propagation was promoted by direct reduction of the monomer, simple addition of a competing oxidant with a higher reduction potential allowed to switch to a clean free radical propagation process. Scope investigation exhibited excellent applicability of these self-initiating polymerization strategies, which enabled the preparation of a large array of (co-)polymers with high added values
Fall, Arona. "Donneurs d’électrons organiques : développement d’un nouveau système catalytique photoredox." Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0607.
Повний текст джерелаDuring this last decade, the reactivity of enamine-based organic electron donor (OED) has been widely explored in electron transfer processes. With exceptionally negative redox potentials, OEDs spontaneously promote single (SET) or double electron transfer (DET) to an organic substrate, to form radical or anionic intermediates. However, the use of stoichiometric amount of OEDs limits their competitivity compared to their organometallic and organic catalysts. This thesis project consisted in developing a new catalytic system with OEDs. Different strategies were envisaged. In a first method a catalytic amount of OED would initiate the electron transfer to reduce the substrate. The oxidation of the generated radical intermediate would allow the regeneration of OED. Unfortunately, this strategy was unsuccessful. The second strategy would consist in regenerating the OED from its air-stable oxidized form OED2+ and a sacrificial electron donor (tertiary amine, sodium dithionite or Rongalite®) under photoactivation. Several optimizing steps allowed the development of a new efficient catalytic photoredox system with the oxidized form as photocatalyst and Rongalite® as sacrificial electron donor. This new photoredox catalytic system was applied to the reduction of various functionals groups (sulfone, aryl halide and triflate) by single electron transfer (SET) and double electron transfer (DET). The reactivity of the photocatalytic system was also explored in radical addition reactions
Turek, Amanda Katherine. "Activation of Electron-Deficient Quinones Through Hydrogen-Bond-Donor-Coupled Electron Transfer." Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845499.
Повний текст джерелаChemistry and Chemical Biology
Книги з теми "Organic electron donors"
Kapinus, E. I. Fotonika molekuli͡a︡rnykh kompleksov. Kiev: Nauk. dumka, 1988.
Знайти повний текст джерелаOgura, F., and Y. Aso. Design of Novel Chalcogen-Containing Organic Metals: Extensively Conjugated Electron Donors and Acceptors with Reduced On-site Coulomb Repulsion. Taylor & Francis Group, 1992.
Знайти повний текст джерелаSolymar, L., D. Walsh, and R. R. A. Syms. Semiconductors. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198829942.003.0008.
Повний текст джерелаKirchman, David L. Processes in anoxic environments. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789406.003.0011.
Повний текст джерелаClarke, Andrew. Metabolism. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199551668.003.0008.
Повний текст джерелаRaven, John. Phytoplankton Productivity. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199233267.003.0003.
Повний текст джерелаBronson, Vincent. Guide to DIY Homemade Yoghurt: Fermentation Is an Enzyme-Catalyzed, Energy-generating Process in Which Organic Compounds Act As Both Donors and Acceptors of Electrons. Independently Published, 2021.
Знайти повний текст джерелаЧастини книг з теми "Organic electron donors"
Graja, A., V. N. Semkin, N. G. Spitsina, and S. Król. "Electron Donor-Acceptor Interactions of C60 with Tetraphenylphosphonium and Tetraphenylarsonium Halides." In Electrical and Related Properties of Organic Solids, 259–78. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5790-2_15.
Повний текст джерелаWróbel, Danuta, and Bolesław Barszcz. "Quantum Dot and Fullerene with Organic Chromophores as Electron-Donor-Acceptor Systems." In Challenges and Advances in Computational Chemistry and Physics, 97–122. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-01355-4_3.
Повний текст джерелаNewton, Marshall D. "Electronic Coupling of Donor—Acceptor Sites Mediated by Homologous Unsaturated Organic Bridges." In ACS Symposium Series, 196–218. Washington, DC: American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0844.ch015.
Повний текст джерелаSchubert, Marcel, Johannes Frisch, Sybille Allard, Eduard Preis, Ullrich Scherf, Norbert Koch, and Dieter Neher. "Tuning Side Chain and Main Chain Order in a Prototypical Donor–Acceptor Copolymer: Implications for Optical, Electronic, and Photovoltaic Characteristics." In Elementary Processes in Organic Photovoltaics, 243–65. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28338-8_10.
Повний текст джерелаWilliams, Jack M., K. Douglas Carlson, Aravinda M. Kini, H. Hau Wang, Urs Geiser, John A. Schlueter, Arthur J. Schultz, et al. "Structure-Property Relationships in Radical-Cation (Electron-Donor Molecule) and Anion-Based (Including Fullerides) Organic Superconductors and their Use in the Design of New Materials." In Materials and Crystallographic Aspects of HTc-Superconductivity, 539–51. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1064-8_26.
Повний текст джерелаClark, K. F., D. Dimitrova, and J. A. Murphy. "2.1 Organic Electron Donors in Electron-Transfer Reactions." In Free Radicals: Fundamentals and Applications in Organic Synthesis 2. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-233-00233.
Повний текст джерела"Conjugated Polymers as Electron Donors in Organic Solar Cells." In Organic Solar Cells, 24–39. CRC Press, 2017. http://dx.doi.org/10.1201/b18072-5.
Повний текст джерелаCook, Michael, and Philippa Cranwell. "Nucleophilic substitution." In Organic Chemistry, edited by Elizabeth Page. Oxford University Press, 2017. http://dx.doi.org/10.1093/hesc/9780198729518.003.0003.
Повний текст джерелаOgura, Fumio, and Kazuo Takimiya. "Preparation of organic conductors." In Organoselenium Chemistry, 257–78. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780198501411.003.0014.
Повний текст джерелаLeonties, Anca R., Ludmila Aricov, and Adina Raducan. "Electron Transfer." In Fundamental and Biomedical Aspects of Redox Processes, 344–68. IGI Global, 2023. http://dx.doi.org/10.4018/978-1-6684-7198-2.ch016.
Повний текст джерелаТези доповідей конференцій з теми "Organic electron donors"
Gu, Qinying, and Dan Credgington. "Organic Photovoltaics Incorporating Electron Donors with Small Exchange Energy." In 1st International Conference on Advances in Organic and Hybrid Electronic Materials. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.aohm.2019.040.
Повний текст джерелаSheats, John E., Andrew Jones, Albert Lang, Felicia Bland та Elizabeth Hernandez. "Organotransition Metal Complexes as π Acceptors in Non-linear Optical Materials". У Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.22.
Повний текст джерелаTian, Mingzhen, Baozhu Luo, Wenlian Li, Shihua Huang, and Jiaqi Yu. "Persistent Photon-gated Spectral Holeburning In A New Donor-Acceptor Electron Transfer System." In Persistent Spectral Hole Burning: Science and Applications. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/pshb.1991.fa7.
Повний текст джерелаEhrlich, J., A. Heikal, Z. Y. Hu, I. Y. S. Lee, S. R. Marder, J. W. Perry, H. Röckel, and X. L. Wu. "Nonlinear Spectroscopy and Applications of Two-Photon Absorbing Molecules." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.tha.3.
Повний текст джерелаJiang, Min-hua, Xu-tang Tao, Duo-rong Yuan, Nan Zhang, and Dong Xu. "The Exploration of New Organic Crystals for Semiconductor Laser Second-Harmonic Generation." In Nonlinear Optics. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/nlo.1992.md31.
Повний текст джерелаAhrens, Michael J., Michael J. Fuller, and Michael R. Wasielewski. "Aminated and cyanated perylene mono- and diimides: Liquid crystalline electron donors and acceptors for organic photonics and electronics." In Frontiers in Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/fio.2003.tuj5.
Повний текст джерелаRovira, C., J. Veciana, J. Tarres, N. SantaIo, E. Molins, M. Mas, D. O. Cowan, S. Yang, and E. Canadell. "Towards tridimensional organic metals. synthesis and study of mlrlti sulfur /spl pi/-electron donors and their charge transfer complexes and salts." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835659.
Повний текст джерелаPatel, J. "Role of Plasma-Induced Liquid Chemistry for the Reduction Mechanism of Silver Ions to form Silver Nanostructures." In Functional Materials and Applied Physics. Materials Research Forum LLC, 2022. http://dx.doi.org/10.21741/9781644901878-7.
Повний текст джерелаCha, Myoungsik, Akira Otomo, William E. Torruellas, George I. Stegeman, David Beljonne, Jean Luc Brédas, Winfried H. G. Horsthuis, and Guus R. Möhlmann. "Nonlinear Spectroscopy of DANS Side Chain Polymers." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.ma.5.
Повний текст джерелаZyss, Joseph, Ifor Samuel, Céline FIORINI, Fabrice Charra, and Jean-Michel Nunzi. "Permanent All Optical Poling of An Octupolar Dye." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.tue.1.
Повний текст джерелаЗвіти організацій з теми "Organic electron donors"
Rittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.
Повний текст джерелаForsythe, Eric, Jianmin Shi, and David Morton. Next Generation Highly Conducting Organic Films Using Novel Donor-Acceptor Molecules for Opto-Electronic Applications. Fort Belvoir, VA: Defense Technical Information Center, June 2009. http://dx.doi.org/10.21236/ada499643.
Повний текст джерелаChefetz, Benny, Baoshan Xing, Leor Eshed-Williams, Tamara Polubesova, and Jason Unrine. DOM affected behavior of manufactured nanoparticles in soil-plant system. United States Department of Agriculture, January 2016. http://dx.doi.org/10.32747/2016.7604286.bard.
Повний текст джерела