Auswahl der wissenschaftlichen Literatur zum Thema „Heteroatomic radical“
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Zeitschriftenartikel zum Thema "Heteroatomic radical"
Han, Yuxuan, und Xiuling Cui. „Copper-Catalyzed Enantioselective Radical Heteroatomic S—O Cross-Coupling“. Chinese Journal of Organic Chemistry 43, Nr. 3 (2023): 1201. http://dx.doi.org/10.6023/cjoc202300013.
Der volle Inhalt der QuelleLinker, Torsten. „Addition of Heteroatom Radicals to endo-Glycals †“. Chemistry 2, Nr. 1 (20.02.2020): 80–92. http://dx.doi.org/10.3390/chemistry2010008.
Der volle Inhalt der QuelleDi Vaira, Massimo, Piero Stoppioni, Stefano Midollini, Franco Laschi und Piero Zanello. „H+ addition to the heteroatomic CoP3 cluster. Synthesis of the radical CoP3+ cluster and electrochemical study“. Polyhedron 10, Nr. 18 (Januar 1991): 2123–29. http://dx.doi.org/10.1016/s0277-5387(00)86131-8.
Der volle Inhalt der QuelleRhodes, Christopher J., Harry Morris, Hikmet Agirbas, Mark Standing und 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, Nr. 6 (1998): 1375–80. http://dx.doi.org/10.1039/a801066h.
Der volle Inhalt der QuelleTaniguchi, Tsuyoshi. „Recent Advances in Reactions of Heteroatom-Centered Radicals“. Synthesis 49, Nr. 16 (26.07.2017): 3511–34. http://dx.doi.org/10.1055/s-0036-1588481.
Der volle Inhalt der QuelleOgawa, Akiya, und Yuki Yamamoto. „Multicomponent Reactions between Heteroatom Compounds and Unsaturated Compounds in Radical Reactions“. Molecules 28, Nr. 17 (30.08.2023): 6356. http://dx.doi.org/10.3390/molecules28176356.
Der volle Inhalt der QuelleRenaud, 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, Nr. 2 (01.01.2007): 223–33. http://dx.doi.org/10.1351/pac200779020223.
Der volle Inhalt der QuelleKawaguchi, Shin-ichi, Akiya Ogawa, Yuki Sato und 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, Nr. 16 (04.07.2017): 3558–67. http://dx.doi.org/10.1055/s-0036-1588867.
Der volle Inhalt der QuelleGuo, Weisi, Qian Wang und Jieping Zhu. „Visible light photoredox-catalysed remote C–H functionalisation enabled by 1,5-hydrogen atom transfer (1,5-HAT)“. Chemical Society Reviews 50, Nr. 13 (2021): 7359–77. http://dx.doi.org/10.1039/d0cs00774a.
Der volle Inhalt der QuelleKubo, Takashi. „Synthesis, Physical Properties, and Reactivity of Stable, π-Conjugated, Carbon-Centered Radicals“. Molecules 24, Nr. 4 (13.02.2019): 665. http://dx.doi.org/10.3390/molecules24040665.
Der volle Inhalt der QuelleDissertationen zum Thema "Heteroatomic radical"
Wickenden, Jason. „Development of heteroatom radical based synthetic strategies“. Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/45730.
Der volle Inhalt der QuelleNabokoff, 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.
Der volle Inhalt der QuelleThe 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.
Der volle Inhalt der QuelleThe 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.
Der volle Inhalt der QuelleKayahara, 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.
Der volle Inhalt der QuelleUeno, 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.
Der volle Inhalt der QuelleTsai, Yi-Wen, und 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.
Der volle Inhalt der Quelle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.
Der volle Inhalt der QuelleRokade, Balaji Vasantrao. „Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds“. Thesis, 2014. http://etd.iisc.ac.in/handle/2005/3479.
Der volle Inhalt der QuelleRokade, Balaji Vasantrao. „Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds“. Thesis, 2014. http://etd.iisc.ernet.in/2005/3479.
Der volle Inhalt der QuelleBücher zum Thema "Heteroatomic radical"
Fischer, H., Hrsg. 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.
Der volle Inhalt der QuelleFischer, H., Hrsg. 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.
Der volle Inhalt der QuelleFischer, H., Hrsg. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria. Berlin/Heidelberg: Springer-Verlag, 1997. http://dx.doi.org/10.1007/b52381.
Der volle Inhalt der QuelleFischer, H., Hrsg. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals II. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b34135.
Der volle Inhalt der QuelleFischer, H., Hrsg. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals I. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b86661.
Der volle Inhalt der QuelleDavies, Alwyn G. Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Springer Berlin / Heidelberg, 2009.
Den vollen Inhalt der Quelle findenDohrmann, J. K., und R. F. C. Claridge. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria (Numerical Data & Functional Relationships in Science & Technology). Springer, 1997.
Den vollen Inhalt der Quelle findenHoward, J. A., H. B. Stegmann, D. Klotz, G. Deuschle und 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.
Den vollen Inhalt der Quelle findenRadicals 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.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "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.
Der volle Inhalt der QuelleFischer, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
Der volle Inhalt der QuelleDavies, 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.
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