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Artykuły w czasopismach na temat "Heteroatomic radical"
Han, Yuxuan, i 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.
Pełny tekst źródłaLinker, Torsten. "Addition of Heteroatom Radicals to endo-Glycals †". Chemistry 2, nr 1 (20.02.2020): 80–92. http://dx.doi.org/10.3390/chemistry2010008.
Pełny tekst źródłaDi Vaira, Massimo, Piero Stoppioni, Stefano Midollini, Franco Laschi i Piero Zanello. "H+ addition to the heteroatomic CoP3 cluster. Synthesis of the radical CoP3+ cluster and electrochemical study". Polyhedron 10, nr 18 (styczeń 1991): 2123–29. http://dx.doi.org/10.1016/s0277-5387(00)86131-8.
Pełny tekst źródłaRhodes, Christopher J., Harry Morris, Hikmet Agirbas, Mark Standing i 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.
Pełny tekst źródłaTaniguchi, 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.
Pełny tekst źródłaOgawa, Akiya, i 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.
Pełny tekst źródłaRenaud, Philippe, Alice Beauseigneur, Andrea Brecht-Forster, Barbara Becattini, Vincent Darmency, Sarkunam Kandhasamy, Florian Montermini i in. "Boron: A key element in radical reactions". Pure and Applied Chemistry 79, nr 2 (1.01.2007): 223–33. http://dx.doi.org/10.1351/pac200779020223.
Pełny tekst źródłaKawaguchi, Shin-ichi, Akiya Ogawa, Yuki Sato i 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 (4.07.2017): 3558–67. http://dx.doi.org/10.1055/s-0036-1588867.
Pełny tekst źródłaGuo, Weisi, Qian Wang i 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.
Pełny tekst źródłaKubo, 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.
Pełny tekst źródłaRozprawy doktorskie na temat "Heteroatomic radical"
Wickenden, Jason. "Development of heteroatom radical based synthetic strategies". Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/45730.
Pełny tekst źródłaNabokoff, 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.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaKayahara, 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.
Pełny tekst źródłaUeno, 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.
Pełny tekst źródłaTsai, Yi-Wen, i 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.
Pełny tekst źródła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.
Pełny tekst źródłaRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds". Thesis, 2014. http://etd.iisc.ac.in/handle/2005/3479.
Pełny tekst źródłaRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds". Thesis, 2014. http://etd.iisc.ernet.in/2005/3479.
Pełny tekst źródłaKsiążki na temat "Heteroatomic radical"
Fischer, H., red. 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.
Pełny tekst źródłaFischer, H., red. 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.
Pełny tekst źródłaFischer, H., red. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria. Berlin/Heidelberg: Springer-Verlag, 1997. http://dx.doi.org/10.1007/b52381.
Pełny tekst źródłaFischer, H., red. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals II. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b34135.
Pełny tekst źródłaFischer, H., red. Radicals Centered on Heteroatoms with Z > 7 and Selected Anion Radicals I. Berlin/Heidelberg: Springer-Verlag, 1988. http://dx.doi.org/10.1007/b86661.
Pełny tekst źródłaDavies, Alwyn G. Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Springer Berlin / Heidelberg, 2009.
Znajdź pełny tekst źródłaDohrmann, J. K., i R. F. C. Claridge. Radicals Centered on Other Heteroatoms. Proton Transfer Equilibria (Numerical Data & Functional Relationships in Science & Technology). Springer, 1997.
Znajdź pełny tekst źródłaHoward, J. A., H. B. Stegmann, D. Klotz, G. Deuschle i 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.
Znajdź pełny tekst źródłaRadicals 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.
Znajdź pełny tekst źródłaCzęści książek na temat "Heteroatomic radical"
Claridge, R. F. C. "14 Radicals centered on other heteroatoms". W 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.
Pełny tekst źródłaFischer, H. "I General introduction". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.1.7 Tetrasubstituted 1,2-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.1.8 Imino-1,2-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.2.1 Unsubstituted 1,4-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.2.2 Monosubstituted 1,4-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.2.3 Disubstituted 1,4-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.2.4 Trisubstituted 1,4-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.2.2.5 Tetrasubstituted 1,4-benzosemiquinones". W 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.
Pełny tekst źródłaDavies, A. G. "16.3 1,4-Naphthosemiquinones". W 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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