Relevant bibliographies by topics / Bis-amidoxime

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Bis-amidoxime'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Bis-amidoxime"

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Piechowicz, Marek, R. Chiarizia, and L. Soderholm. "Insight into selectivity: uptake studies of radionuclides 90Sr2+, 137Cs+, and 233UO22+ with bis-amidoxime polymers." Dalton Transactions 47, no. 15 (2018): 5348–58. http://dx.doi.org/10.1039/c7dt04935h.

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Gup, Ramazan, H. Korkmaz Alpoguz, and A. Dincer Beduk. "Synthesis and Extraction Properties of 1,2-Bis(amidoxime) Derivatives." Collection of Czechoslovak Chemical Communications 67, no. 2 (2002): 209–18. http://dx.doi.org/10.1135/cccc20020209.

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Four 1,2-bis(amidoxime)s bearing benzoate groups were synthesized. Their complexing properties were studied by the liquid-liquid extraction of selected alkali (Na+ and K+) and transition metals (Hg2+, Cu2+, Pb2+ and Ni2+). It has been observed that all ligands show a high affinity to Cu2+ and Hg2+ ions, whereas almost no affinity to alkali metals.
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Vukovic, Sinisa, and Benjamin P. Hay. "De Novo Structure-Based Design of Bis-amidoxime Uranophiles." Inorganic Chemistry 52, no. 13 (June 19, 2013): 7805–10. http://dx.doi.org/10.1021/ic401089u.

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Werner, M., J. Berner, and P. G. Jones. "Bis(acetato)bis(pyridine-2-amidoxime-N,N')nickel(II)–Ethanol (1/2)." Acta Crystallographica Section C Crystal Structure Communications 52, no. 1 (January 15, 1996): 72–74. http://dx.doi.org/10.1107/s0108270195009413.

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He, Dianxiong, Ni Tan, Xiaomei Luo, Xuechun Yang, Kang Ji, Jingwen Han, Can Chen, and Yaqing Liu. "Preparation, uranium (VI) absorption and reuseability of marine fungus mycelium modified by the bis-amidoxime-based groups." Radiochimica Acta 108, no. 1 (December 18, 2019): 37–49. http://dx.doi.org/10.1515/ract-2018-3063.

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Abstract Bis-amidoxime-based claw-like-functionalized marine fungus material (ZZF51-GPTS-DCDA-AM) was prepared for study to absorb the low concentration uranium (VI) from aqueous solution. A series of characterization methods such as SEM, TGA and FT-IR were applied for the functionalized materials before and after modification and adsorption. The experimental results suggested that the amidoxime groups were successfully grafted onto the surface of mycelium powder and provided the special binding sites for the absorption of uranium (VI). In the absorption research, uranium (VI) initial concentration, pH and equilibrium time were optimized as 40 mg L−1, 6.0, and 110 min by L43 orthogonal experiment, respectively, and the maximum absorption capacity of the prepared material was 370.85 mg g−1 under the optimum batch conditions. After five cycling process, the desorption rate and regeneration efficiency of the modified mycelium were found to be 80.29 % and 94.51 %, respectively, which indicated that the material had an adequately high reusability property as a cleanup tool. The well known Langmuir and Freundlich isotherm adsorption model fitting found that the modified materials had both monolayer and bilayer adsorption to uranium (VI) ions. Simultaneously, the pseudo-second-order model was better to illustrated the adsorption kinetics process. The enhanced adsorption capacity of uranium (VI) by the modified fungus materials over raw biomass was mainly owing to the strong chelation of amidoxime groups and uranium (VI) ions.
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Gup, Ramazan, H. Korkmaz Alpoguz, and A. Dincer Beduk. "ChemInform Abstract: Synthesis and Extraction Properties of 1,2-Bis(Amidoxime) Derivatives." ChemInform 33, no. 32 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200232080.

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Berger, Olivier, Stéphanie Ortial, Sharon Wein, Séverine Denoyelle, Françoise Bressolle, Thierry Durand, Roger Escale, Henri J. Vial, and Yen Vo-Hoang. "Evaluation of amidoxime derivatives as prodrug candidates of potent bis-cationic antimalarials." Bioorganic & Medicinal Chemistry Letters 29, no. 16 (August 2019): 2203–7. http://dx.doi.org/10.1016/j.bmcl.2019.06.045.

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A. Pearse, George, Paul R. Raithby, and Jack Lewis. "Synthesis and X-ray crystal structure of pyridine-2-amidoxime, C6H7N3O, and aqua-bis-(pyridine-2-amidoxime)copper(II) chloride, [Cu(C6H7N3O)(H2O)]Cl2." Polyhedron 8, no. 3 (January 1989): 301–4. http://dx.doi.org/10.1016/s0277-5387(00)80418-0.

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Stemper, Jérémy, Wei Tuo, Eva Mazarío, Ahmed S. Helal, Alexandre Djurovic, Claude Lion, Jean-Michel El Hage Chahine, François Maurel, Miryana Hémadi, and Thierry Le Gall. "Synthesis of bis(amidoxime)s and evaluation of their properties as uranyl-complexing agents." Tetrahedron 74, no. 21 (May 2018): 2641–49. http://dx.doi.org/10.1016/j.tet.2018.04.016.

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10

Piechowicz, Marek, Carter W. Abney, Nathan C. Thacker, James C. Gilhula, Youfu Wang, Samuel S. Veroneau, Aiguo Hu, and Wenbin Lin. "Successful Coupling of a Bis-Amidoxime Uranophile with a Hydrophilic Backbone for Selective Uranium Sequestration." ACS Applied Materials & Interfaces 9, no. 33 (August 15, 2017): 27894–904. http://dx.doi.org/10.1021/acsami.7b04656.

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Dissertations / Theses on the topic "Bis-amidoxime"

1

Degardin, Mélissa. "Synthèse et activités antipaludiques de bis-alkylamidines N-monosubstituées, bis-alkylguanidines et de leurs bioprécurseurs de type amidoxime et O-dérivés." Montpellier 2, 2009. http://www.theses.fr/2009MON20165.

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Des stratégies prodrogues amidoxime et oxadiazolone ont été appliquées à de nouvelles drogues bis-alkylamidines N-monosubstituées que nous avons synthétisées selon une nouvelle stratégie divergente basée sur l'utilisation de la bis-alkyloxadiazolone N-substituée comme intermédiaire de synthèse. Des dérivés N-alkylsulfonyles de bis-alkylamidoximes ont été développés dans le but d'obtenir des structures stables in vitro tout en conservant de fortes activités orales. Enfin, de nouvelles drogues bis-alkylguanidines ont été synthétisées ainsi que leurs bioprécurseurs N-hydroxyguanidines, aminooxadiazolones et iminooxadiazolidinones. Les activités antipaludiques in vitro et in vivo des composés obtenus ont été évaluées
Amidoxime and oxadiazolone prodrug strategies have been applied to new N-monosubstituted bis-alkylamidine drugs which were synthesised by a new divergent strategy based on the use of the N-substitued bis-alkyloxadiazolone as an intermediate. Bis-alkylamidoxime N-alkylsulfonyles derivatives have been developed to obtain in vitro stable structures preserving potent oral activities. Finally, new bis-alkylguanidine drugs were synthesised as well as their bioprecursors N-hydroxyguanidines, aminooxadiazolones and iminooxadiazolidinones. In vitro and in vivo antiplasmodial activities of the obtained compounds were evaluated
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