Добірка наукової літератури з теми "Heteroatomic radical"
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Статті в журналах з теми "Heteroatomic radical"
Han, Yuxuan, and Xiuling Cui. "Copper-Catalyzed Enantioselective Radical Heteroatomic S—O Cross-Coupling." Chinese Journal of Organic Chemistry 43, no. 3 (2023): 1201. http://dx.doi.org/10.6023/cjoc202300013.
Повний текст джерелаLinker, Torsten. "Addition of Heteroatom Radicals to endo-Glycals †." Chemistry 2, no. 1 (February 20, 2020): 80–92. http://dx.doi.org/10.3390/chemistry2010008.
Повний текст джерелаDi Vaira, Massimo, Piero Stoppioni, Stefano Midollini, Franco Laschi, and Piero Zanello. "H+ addition to the heteroatomic CoP3 cluster. Synthesis of the radical CoP3+ cluster and electrochemical study." Polyhedron 10, no. 18 (January 1991): 2123–29. http://dx.doi.org/10.1016/s0277-5387(00)86131-8.
Повний текст джерелаRhodes, Christopher J., Harry Morris, Hikmet Agirbas, Mark Standing, and Yaming Zhang. "Distonic isomerisations of imine radical cations: aspects of the reactivity of heteroatomic subunits damaged by ionising radiation." Journal of the Chemical Society, Perkin Transactions 2, no. 6 (1998): 1375–80. http://dx.doi.org/10.1039/a801066h.
Повний текст джерелаTaniguchi, Tsuyoshi. "Recent Advances in Reactions of Heteroatom-Centered Radicals." Synthesis 49, no. 16 (July 26, 2017): 3511–34. http://dx.doi.org/10.1055/s-0036-1588481.
Повний текст джерелаOgawa, Akiya, and Yuki Yamamoto. "Multicomponent Reactions between Heteroatom Compounds and Unsaturated Compounds in Radical Reactions." Molecules 28, no. 17 (August 30, 2023): 6356. http://dx.doi.org/10.3390/molecules28176356.
Повний текст джерелаRenaud, Philippe, Alice Beauseigneur, Andrea Brecht-Forster, Barbara Becattini, Vincent Darmency, Sarkunam Kandhasamy, Florian Montermini, et al. "Boron: A key element in radical reactions." Pure and Applied Chemistry 79, no. 2 (January 1, 2007): 223–33. http://dx.doi.org/10.1351/pac200779020223.
Повний текст джерелаKawaguchi, Shin-ichi, Akiya Ogawa, Yuki Sato, and Akihiro Nomoto. "Photoinduced Coupling Reaction of Diphenyl(2,4,6-trimethylbenzoyl)phosphine Oxide with Interelement Compounds: Application to the Synthesis of Thio- or Selenophosphinates." Synthesis 49, no. 16 (July 4, 2017): 3558–67. http://dx.doi.org/10.1055/s-0036-1588867.
Повний текст джерелаGuo, Weisi, Qian Wang, and Jieping Zhu. "Visible light photoredox-catalysed remote C–H functionalisation enabled by 1,5-hydrogen atom transfer (1,5-HAT)." Chemical Society Reviews 50, no. 13 (2021): 7359–77. http://dx.doi.org/10.1039/d0cs00774a.
Повний текст джерелаKubo, Takashi. "Synthesis, Physical Properties, and Reactivity of Stable, π-Conjugated, Carbon-Centered Radicals". Molecules 24, № 4 (13 лютого 2019): 665. http://dx.doi.org/10.3390/molecules24040665.
Повний текст джерелаДисертації з теми "Heteroatomic radical"
Wickenden, Jason. "Development of heteroatom radical based synthetic strategies." Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/45730.
Повний текст джерелаNabokoff, Pierre. "Synthèses de précurseurs organiques de radicaux hétéroatomiques pour la préparation de matériaux hybrides." Electronic Thesis or Diss., Aix-Marseille, 2020. http://theses.univ-amu.fr.lama.univ-amu.fr/201218_NABOKOFF_575sxytx526xlluw827l449jumhkc_TH.pdf.
Повний текст джерелаThe aim of this work was to investigate the influence of the nanocofinement on the behaviour of organic substrates embedded in mesoporous silicas. This research hinged on two parts. The first study focused on the efficiency of the fragmentation reaction of confined alkoxyamines, under thermal or photochemical activation. Thanks to the comparison with the very same reactions in solution, the quantitative EPR measurements showed that the confinement of organic precursors had no effect on the efficiency of these reactions. Secondly, organic-inorganic hybrid materials were synthesized. These mesoporous silicas were functionalized with diazene radical precursors. Upon 360 nm irradiation, they generated heteroatomic radicals. Different materials were prepared, including one which enabled to form a face-to-face pair of different radicals, i.e. an aryloxyl radical in front of an arylsulfanyl radical. Studies carried out by continuous and pulsed wave EPR enabled to highlight the high stability of these confined paramagnetic species and to measure their relaxation times
Brulay, Guillaume. "Optimisation de la quantité de radicaux générés dans les silices hybrides mésoporeuses : synthèse, caractérisation, application." Electronic Thesis or Diss., Aix-Marseille, 2022. http://www.theses.fr/2022AIXM0575.
Повний текст джерелаThe aim of this work was the development of hybrid mesoporous silicas composed with high concentration of embedded transient radicals in order to use them as polarizing agent in DNP-NMR. First of all, quantitative yield in paramagnetic centers were obtained from unimolecular processed carried out under photoirradiation. The synthesis and optimization of photolysis conditions allowed to obtain functionalized silicas by transient radicals from good to quantitative yields. The reactivity difference of radical precursors was rationalized by the fragmentation mechanism and environmental constraints inside the walls of the silica structure which provided high yields. Polyradical systems were characterized by EPR spectroscopy. High life-time allows the evaluation of these new "persistent" radical species as polarizing agent for DNP-NMR
Buquoi, John Q. III. "Multicomponent Radical Reactions Incorporating Heteroatom-Carbon Bonds Via Polarity-Reversal Cascades." The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1574348050305556.
Повний текст джерелаKayahara, Eiichi. "Studies on the Precision Control of Polymer Structure Based on Heteroatom-Mediated Living Radical Polymerization Reaction." 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142245.
Повний текст джерелаUeno, Ryota. "Development of the Reactions of sp3-Carbon Radicals Adjacent to a Heteroatom with Aromatic Compoun." 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225416.
Повний текст джерелаTsai, Yi-Wen, and 蔡依雯. "Synthesis of heteroatom-doped carbon dots with tunable luminescence properties for bioimaging and free radical scavenging." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/yg29wt.
Повний текст джерела國立臺灣科技大學
化學工程系
107
Herein, we combined with nano-synthesis technology and biomedical applications. We present an aqueous based facile microwave-assisted synthesis of carbon quantum dots, which has short synthesis time, low toxicity, water dispersibility and biocompatibility. These advantages are beneficial for biological application. The red, yellow, green and blue fluorescent carbon dots were successfully synthesized by adjusting the heteroatomic doping and changing the purification method. Furthermore, we applied these carbon dots for in vitro antioxidant activity and bioimaging. Part Ⅰ: Antioxidant activity of phosphorous and manganese element co-doped red magnetofluorescent carbon dots P-phenylenediamine was used as carbon precursor. Doping phosphorous (P) heteroatom into Cdots could enhance the quantum yield. Furthermore, doping manganese (Mn) could impart magnetic property to carbon dots. The red fluorescent carbon dots were successfully synthesized by one-pot microwave method. In this study, the application of antioxidant property for PMn@Cdots was carried out by using DPPH, •OH and O2-•, respectively. The result was compared with ascorbic acid and it showed that PMn@Cdots also have good antioxidant property. Furthermore, in the protective activity result of H2O2-induced cell death model, it was found that PMn@Cdots-HA could reduce intracellular ROS levels and protect cells from oxidative stress.
Manna, Sabyasachi. "Construction of C-C Bonds by Photocatalysis via Radical Addition Cascade Cyclization (RACC): Synthesis of Heteroatom-Containing Small Molecules." Thesis, 2022. https://etd.iisc.ac.in/handle/2005/6050.
Повний текст джерелаRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds." Thesis, 2014. http://etd.iisc.ac.in/handle/2005/3479.
Повний текст джерелаRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds." Thesis, 2014. http://etd.iisc.ernet.in/2005/3479.
Повний текст джерелаКниги з теми "Heteroatomic radical"
Fischer, H., ed. Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-45824-1.
Повний текст джерелаFischer, H., ed. Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0.
Повний текст джерелаFischer, H., ed. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria. Berlin/Heidelberg: Springer-Verlag, 1997. http://dx.doi.org/10.1007/b52381.
Повний текст джерелаFischer, H., ed. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals II. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b34135.
Повний текст джерелаFischer, H., ed. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals I. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b86661.
Повний текст джерелаDavies, Alwyn G. Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Springer Berlin / Heidelberg, 2009.
Знайти повний текст джерелаDohrmann, J. K., and R. F. C. Claridge. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria (Numerical Data & Functional Relationships in Science & Technology). Springer, 1997.
Знайти повний текст джерелаHoward, J. A., H. B. Stegmann, D. Klotz, G. Deuschle, and P. Tordo. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals I / Heteroatomzentrierte (Z > 7) Radikale und ausgewählte Anionradikale I (Numerical ... Relationships in Science & Technology). Springer, 1988.
Знайти повний текст джерелаRadicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals II / Heteroatomzentrierte (Z > 7) Radikale und ausgewählte Anionradikale II (Numerical ... Relationships in Science & Technology). Springer, 1987.
Знайти повний текст джерелаЧастини книг з теми "Heteroatomic radical"
Claridge, R. F. C. "14 Radicals centered on other heteroatoms." In Landolt-Börnstein - Group II Molecules and Radicals, 126. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-45824-1_9.
Повний текст джерелаFischer, H. "I General introduction." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 1–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_1.
Повний текст джерелаDavies, A. G. "16.2.1.7 Tetrasubstituted 1,2-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 93–107. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_10.
Повний текст джерелаDavies, A. G. "16.2.1.8 Imino-1,2-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 108–13. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_11.
Повний текст джерелаDavies, A. G. "16.2.2.1 Unsubstituted 1,4-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 114–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_12.
Повний текст джерелаDavies, A. G. "16.2.2.2 Monosubstituted 1,4-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 116–22. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_13.
Повний текст джерелаDavies, A. G. "16.2.2.3 Disubstituted 1,4-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 123–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_14.
Повний текст джерелаDavies, A. G. "16.2.2.4 Trisubstituted 1,4-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 128–31. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_15.
Повний текст джерелаDavies, A. G. "16.2.2.5 Tetrasubstituted 1,4-benzosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 132–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_16.
Повний текст джерелаDavies, A. G. "16.3 1,4-Naphthosemiquinones." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 141–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_17.
Повний текст джерела