Literatura científica selecionada sobre o tema "Organic electron donors"
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Artigos de revistas sobre o assunto "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 (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 fonteTeses / dissertações sobre o assunto "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.
Texto completo da fonteCumine, 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.
Texto completo da fonteBuker, Nicholas D. "Guanidine donors in nonlinear optical chromophores /". Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/8669.
Texto completo da fonteChua, 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.
Texto completo da fonteAnderson, 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.
Texto completo da fonteTyree, 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.
Texto completo da fonteMaster 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.
Texto completo da fonteZhao, 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.
Texto completo da fonteOrganic 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.
Texto completo da fonteDuring 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.
Texto completo da fonteChemistry and Chemical Biology
Livros sobre o assunto "Organic electron donors"
Kapinus, E. I. Fotonika molekuli͡a︡rnykh kompleksov. Kiev: Nauk. dumka, 1988.
Encontre o texto completo da fonteOgura, F., e 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.
Encontre o texto completo da fonteSolymar, L., D. Walsh e R. R. A. Syms. Semiconductors. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198829942.003.0008.
Texto completo da fonteKirchman, David L. Processes in anoxic environments. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789406.003.0011.
Texto completo da fonteClarke, Andrew. Metabolism. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199551668.003.0008.
Texto completo da fonteRaven, John. Phytoplankton Productivity. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199233267.003.0003.
Texto completo da fonteBronson, 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.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Organic electron donors"
Graja, A., V. N. Semkin, N. G. Spitsina e 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.
Texto completo da fonteWróbel, Danuta, e 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.
Texto completo da fonteNewton, 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.
Texto completo da fonteSchubert, Marcel, Johannes Frisch, Sybille Allard, Eduard Preis, Ullrich Scherf, Norbert Koch e 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.
Texto completo da fonteWilliams, 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.
Texto completo da fonteClark, K. F., D. Dimitrova e 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.
Texto completo da fonte"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.
Texto completo da fonteCook, Michael, e Philippa Cranwell. "Nucleophilic substitution". In Organic Chemistry, editado por Elizabeth Page. Oxford University Press, 2017. http://dx.doi.org/10.1093/hesc/9780198729518.003.0003.
Texto completo da fonteOgura, Fumio, e 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.
Texto completo da fonteLeonties, Anca R., Ludmila Aricov e 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.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Organic electron donors"
Gu, Qinying, e 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.
Texto completo da fonteSheats, John E., Andrew Jones, Albert Lang, Felicia Bland e Elizabeth Hernandez. "Organotransition Metal Complexes as π Acceptors in Non-linear Optical Materials". In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.22.
Texto completo da fonteTian, Mingzhen, Baozhu Luo, Wenlian Li, Shihua Huang e 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.
Texto completo da fonteEhrlich, J., A. Heikal, Z. Y. Hu, I. Y. S. Lee, S. R. Marder, J. W. Perry, H. Röckel e 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.
Texto completo da fonteJiang, Min-hua, Xu-tang Tao, Duo-rong Yuan, Nan Zhang e 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.
Texto completo da fonteAhrens, Michael J., Michael J. Fuller e 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.
Texto completo da fonteRovira, C., J. Veciana, J. Tarres, N. SantaIo, E. Molins, M. Mas, D. O. Cowan, S. Yang e 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.
Texto completo da fontePatel, 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.
Texto completo da fonteCha, Myoungsik, Akira Otomo, William E. Torruellas, George I. Stegeman, David Beljonne, Jean Luc Brédas, Winfried H. G. Horsthuis e 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.
Texto completo da fonteZyss, Joseph, Ifor Samuel, Céline FIORINI, Fabrice Charra e 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.
Texto completo da fonteRelatórios de organizações sobre o assunto "Organic electron donors"
Rittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.
Texto completo da fonteForsythe, Eric, Jianmin Shi e David Morton. Next Generation Highly Conducting Organic Films Using Novel Donor-Acceptor Molecules for Opto-Electronic Applications. Fort Belvoir, VA: Defense Technical Information Center, junho de 2009. http://dx.doi.org/10.21236/ada499643.
Texto completo da fonteChefetz, Benny, Baoshan Xing, Leor Eshed-Williams, Tamara Polubesova e Jason Unrine. DOM affected behavior of manufactured nanoparticles in soil-plant system. United States Department of Agriculture, janeiro de 2016. http://dx.doi.org/10.32747/2016.7604286.bard.
Texto completo da fonte