Добірка наукової літератури з теми "Polypyridyl Oxovanadium(IV) Complexes"
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Статті в журналах з теми "Polypyridyl Oxovanadium(IV) Complexes"
Banerjee, Samya, Ila Pant, Imran Khan, Puja Prasad, Akhtar Hussain, Paturu Kondaiah, and Akhil R. Chakravarty. "Remarkable enhancement in photocytotoxicity and hydrolytic stability of curcumin on binding to an oxovanadium(iv) moiety." Dalton Transactions 44, no. 9 (2015): 4108–22. http://dx.doi.org/10.1039/c4dt02165g.
Повний текст джерелаYuan, Caixia, Liping Lu, Yanbo Wu, Zhiwei Liu, Maolin Guo, Shu Xing, Xueqi Fu, and Miaoli Zhu. "Synthesis, characterization, and protein tyrosine phosphatases inhibition activities of oxovanadium(IV) complexes with Schiff base and polypyridyl derivatives." Journal of Inorganic Biochemistry 104, no. 9 (September 2010): 978–86. http://dx.doi.org/10.1016/j.jinorgbio.2010.05.003.
Повний текст джерелаLu, Liping, Jinjun Yue, Caixia Yuan, Miaoli Zhu, Hong Han, Zhiwei Liu, and Maolin Guo. "Ternary oxovanadium(IV) complexes with amino acid-Schiff base and polypyridyl derivatives: Synthesis, characterization, and protein tyrosine phosphatase 1B inhibition." Journal of Inorganic Biochemistry 105, no. 10 (October 2011): 1323–28. http://dx.doi.org/10.1016/j.jinorgbio.2011.07.008.
Повний текст джерелаYuan, Caixia, Liping Lu, Xiaoli Gao, Yanbo Wu, Maolin Guo, Ying Li, Xueqi Fu, and Miaoli Zhu. "Ternary oxovanadium(IV) complexes of ONO-donor Schiff base and polypyridyl derivatives as protein tyrosine phosphatase inhibitors: synthesis, characterization, and biological activities." JBIC Journal of Biological Inorganic Chemistry 14, no. 6 (March 17, 2009): 841–51. http://dx.doi.org/10.1007/s00775-009-0496-6.
Повний текст джерелаOhde, Christian, Christian Limberg, Reinhard Stösser, and Serhiy Demeshko. "Oxovanadium(IV) Silsesquioxane Complexes." Inorganic Chemistry 49, no. 5 (March 2010): 2479–85. http://dx.doi.org/10.1021/ic902392y.
Повний текст джерелаBaran, Enrique J. "OXOVANADIUM(IV) COMPLEXES OF CARBOHYDRATES." Journal of Carbohydrate Chemistry 20, no. 9 (December 31, 2001): 769–88. http://dx.doi.org/10.1081/car-100108656.
Повний текст джерелаWilliams, Patricia A. M., Evelina G. Ferrer, and Enrique J. Baran. "OXOVANADIUM(IV) COMPLEXES OF CAPTOPRIL." Journal of Coordination Chemistry 42, no. 4 (November 1, 1997): 261–69. http://dx.doi.org/10.1080/00958979708022856.
Повний текст джерелаPandya, Bhavna J., and Pabitra K. Bhattacharya. "Binary and ternary complexes of oxovanadium(IV) and homobinuclear double-bridged oxovanadium(IV) complexes." Transition Metal Chemistry 12, no. 5 (October 1987): 398–400. http://dx.doi.org/10.1007/bf01171645.
Повний текст джерелаMishra, Mahendra Kumar, Ruchita Tripathi, Pandeya Kb та Tripathi Ip. "α-AMYLASE INHIBITION AND ELECTROCHEMICAL BEHAVIOR OF SOME OXOVANADIUM (IV) COMPLEXES OF L-AMINO ACIDS". Asian Journal of Pharmaceutical and Clinical Research 11, № 8 (7 серпня 2018): 218. http://dx.doi.org/10.22159/ajpcr.2018.v11i8.25800.
Повний текст джерелаHasan, M. F., A. M. Seyam, and H. A. Hodali. "Oxovanadium(IV) Complexes with Azooxime Ligands." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 26, no. 2 (February 1, 1996): 181–89. http://dx.doi.org/10.1080/00945719608004257.
Повний текст джерелаДисертації з теми "Polypyridyl Oxovanadium(IV) Complexes"
Choudhary, Nosheen Fatima. "The chemistry of oxovanadium(IV) tetradentate Schiff base complexes." Thesis, University of Sussex, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244319.
Повний текст джерелаWalmsley, Ryan Steven. "An investigation into the antidiabetic and catalytic properties of oxovanadium(IV) complexes." Thesis, Rhodes University, 2012. http://hdl.handle.net/10962/d1004978.
Повний текст джерелаAlvino, De la Sota Nora, and Calderón Javier Pacheco. "Diseño de Agentes Antidiabéticos de Vanadio: Desarrollo y Avances Recientes." Revista de Química, 2007. http://repositorio.pucp.edu.pe/index/handle/123456789/100688.
Повний текст джерелаDesign of Vanadium Antidiabetic Agents: Development and Recent AdvancesThe discovery of the enhanced hypoglycemic activity of bis(maltolate)oxovanadiu m (IV) (BMOV) compared to simplevanadium salts stimulated the design, synthesis and both in vitro and in vivo evaluation of a large variety of oxovanadium (IV)complexes with different organic ligands for their potential use as antidiabetic drugs that may be able to substitute, either partially or totally, the daily insulin injections used in the treatment of type 1 diabetes mellitus or the orally available hypoglycemic drugs usually used in combined therapy for type 2 diabetes.Recently, a close BMOV analogue, an ethyl substitute, has already successfully completed the phase 1 clinical trial in humans. The design of new types of complexes and the development of alternative delivery methods represent an active research field today.
Lima, Silvânia Marilene de. "Novos catalisadores à base de oxovanádio (IV) e Cucurbit[6]urila." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/59/59138/tde-01092009-111752/.
Повний текст джерелаCucurbiturils are versatile molecules used in several branches of chemistry. These molecular cages form a family of homologues from the condensation of glycoluril and formaldehyde in acidic medium. Their applications range from catalysis, photochemistry, organic and inorganic synthesis, materials and supramolecular chemistry. Particularly cucurbit[6]uril, or simply CB[6], is a very symmetrical molecule, which posesses coordination points on its portals, especially with hard acids. Due to this characteristic, it was possible to synthesize a new complex, with a vanadyl, VO2+, catalytic center bonded to the extremity of the cavitand. The access to the catalytic center of this molecule should be determined by the entrance of the substrate inside the macrocycle, which is limited by its volume and by solvophobicity, because the cavity is strongly hydrophobic. The structure of this new complex could not be completely solved yet, because it was impossible to obtain a single crystal for X-rays diffraction analysis. The solid state characterization techniques indicated that this new complex has its metallic center in a rectangular-base pyramid configuration. This was shown by the spectroscopic evidences which point to a d1 ion in a C2V symmetry. Attempts were made to synthesize both mono and binuclear species, but all the techniques we have used have demonstrated that only the former one was obtained. The first catalytic tests for hydrocarbons convertion in mild conditions have shown good results towards for linear substrates and no activity at all towards more volumous cyclic molecules. The results we have obtained indicate that the alkane oxidation reactions with these complexes occur inside the cavity along the (V=O)2+ ion dz2 orbital , and not on its superior moiety on the vanadyl oxygen atom.
Bouhsina, Saâd. "Pouvoir complexant des sucres acides avec les ions métalliques. Complexation de l'acide lactobionique avec les ions cuivre(II) et oxovanadium(IV)." Lille 1, 1991. http://www.theses.fr/1991LIL10174.
Повний текст джерела何嘉麗 and Clare Ho. "Reactivities and kinetic studies on high valent ruthenium(IV), (V) and(VI) oxo complexes of chelating tertiary amine, polypyridyl andporphyrinato ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1991. http://hub.hku.hk/bib/B31232577.
Повний текст джерелаHo, Clare. "Reactivities and kinetic studies on high valent ruthenium(IV), (V) and (VI) oxo complexes of chelating tertiary amine, polypyridyl and porphyrinato ligands /." [Hong Kong : University of Hong Kong], 1991. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13154102.
Повний текст джерелаZhou, Ying. "Oxovanadium(IV) and (V) complexes with naturally-occurring molecules." Thesis, 1993. http://hdl.handle.net/2429/2608.
Повний текст джерелаHon, Sang-Wen, and 洪三文. "Catalytic Asymmetric Coupling of 2-Naphthols by Chiral Tridentate Oxovanadium(IV) Complexes." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/62659171488582496658.
Повний текст джерела國立臺灣師範大學
化學研究所
89
A series of chiral oxovanadium(IV) complexes derived from tridentate N-3,5-substituted and N-3,4-benzo- and N-5,6-benzo-salicylidene-α-amino acids can serve as efficient catalysts for the enantioselective oxidative couplings of various 3-,6-,7-substituted- 2-naphthols under O2. We take the reseach about the solvent effect,cooxidant effect,amino acid effect….and so on in detail. Our catalyst in the coupling reaction of 2-naphthol is the best methodology as we know. The best scenario involves the use of a vanadyl complex arising from 2-hydroxy-1-naphtholaldehyde and valine (or phenylalanine) in CCl4, leading to BINOLs in good yields (75-100%) and with enantioselectivities of up to 68%.
Prasad, Puja. "Studies on Near-IR Light Photocytotoxic Oxovanadium Complexes." Thesis, 2013. http://etd.iisc.ernet.in/2005/3379.
Повний текст джерелаЧастини книг з теми "Polypyridyl Oxovanadium(IV) Complexes"
Thompson, Katherine H., Barry D. Liboiron, Graeme R. Hanson, and Chris Orvig. "In Vivo Coordination Chemistry and Biolocalization of Bis(ligand)oxovanadium(IV) Complexes for Diabetes Treatment." In ACS Symposium Series, 384–99. Washington, DC: American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0903.ch021.
Повний текст джерелаThompson, K. H., J. H. McNeill, and C. Orvig. "Design of New Oxovanadium (IV) Complexes for Treatment of Diabetes. Biovailability, Speciation, and Tissue Targeting Considerations." In Trace Elements in Man and Animals 10, 539. New York, NY: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47466-2_172.
Повний текст джерелаSakurai, Hiromu. "Structure-Activity Relationship and Molecular Action Mechanism in the Family of Antidiabeticbis(Picolinato)oxovanadium(IV) Complexes." In Vanadium: The Versatile Metal, 110–20. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0974.ch009.
Повний текст джерелаТези доповідей конференцій з теми "Polypyridyl Oxovanadium(IV) Complexes"
Puri, Rojila. "Synthesis and characterization of some mixed-ligand oxovanadium (IV) complexes of carbodithioate ligands and 1,10- phenanthroline or 2,2′–bipyridyl." In INTERNATIONAL CONFERENCE ON ADVANCES IN MULTI-DISCIPLINARY SCIENCES AND ENGINEERING RESEARCH: ICAMSER-2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0095311.
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