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Статті в журналах з теми "Paladium and Copper Complexes"
Friedrich, Manfred, Juan Carlos Gálvez-Ruiz, Thomas M. Klapötke, Peter Mayer, Birgit Weber, and Jan J. Weigand. "BTA Copper Complexes." Inorganic Chemistry 44, no. 22 (October 2005): 8044–52. http://dx.doi.org/10.1021/ic050657r.
Повний текст джерелаWoollard-Shore, John G., Jason P. Holland, Michael W. Jones, and Jonathan R. Dilworth. "Nitritereduction by copper complexes." Dalton Trans. 39, no. 6 (2010): 1576–85. http://dx.doi.org/10.1039/b913463h.
Повний текст джерелаNakamura, Minoru, and Hitoshi Iwasaki. "Copper complexes in silicon." Journal of Applied Physics 86, no. 10 (November 15, 1999): 5372–75. http://dx.doi.org/10.1063/1.371613.
Повний текст джерелаZhao, Hong, Zhi-Rong Qu, Qiong Ye, Brendan F. Abrahams, Yi-Ping Wang, Zhi-Guo Liu, Ziling Xue, Ren-Gen Xiong, and Xiao-Zeng You. "Ferroelectric Copper Quinine Complexes." Chemistry of Materials 15, no. 22 (November 2003): 4166–68. http://dx.doi.org/10.1021/cm034301u.
Повний текст джерелаWhitmire, Kenton H., J. Chris Hutchison, Anna Gardberg, and Chris Edwards. "Triethanolamine complexes of copper." Inorganica Chimica Acta 294, no. 2 (November 1999): 153–62. http://dx.doi.org/10.1016/s0020-1693(99)00274-1.
Повний текст джерелаBlower, P. J., J. S. Lewis, J. L. J. Dearling, B. C. Rooney, L. Kelland, H. Coley, and J. Zweit. "34. Copper diphosphine complexes." Nuclear Medicine Communications 18, no. 4 (April 1997): 298. http://dx.doi.org/10.1097/00006231-199704000-00036.
Повний текст джерелаBoudakgi, Amer, Julia Jezierska, and Bozena N. Kolarz. "Amidoxime polymers - copper complexes." Makromolekulare Chemie. Macromolecular Symposia 59, no. 1 (June 1992): 343–52. http://dx.doi.org/10.1002/masy.19920590128.
Повний текст джерелаYarykin, N. A., and J. Weber. "Identification of copper-copper and copper-hydrogen complexes in silicon." Semiconductors 47, no. 2 (February 2013): 275–78. http://dx.doi.org/10.1134/s1063782613020231.
Повний текст джерелаBirdsall, W. J., and Bruce A. Weber. "Copper(I) and Copper(II) Complexes of Creatinine." Journal of Coordination Chemistry 22, no. 3 (December 1990): 205–8. http://dx.doi.org/10.1080/00958979009408216.
Повний текст джерелаGarc�a-Onrubia, Azucena, Pilar Souza, Jos� R. Masaguer, and Agueda Arquero. "Copper(II) and copper(I) complexes of benzenecarbothioamides." Transition Metal Chemistry 13, no. 5 (October 1988): 384–87. http://dx.doi.org/10.1007/bf01225133.
Повний текст джерелаДисертації з теми "Paladium and Copper Complexes"
Broch, Fernanda. "Síntese, cristalografia e propriedades de ligantes triazenos mono e biscatenados e derivados complexos de Cu(II), Ni(II) e Pd(II)." Universidade Federal de Santa Maria, 2013. http://repositorio.ufsm.br/handle/1/4248.
Повний текст джерелаTriazenes are a class of compounds characterized by the presence of a diazoamino functional group (N=N N) showing remarkable ability to support the stereochemical requisites of a wide variety of metal transition complexes. They act as versatile ligands in coordination chemistry when deprotonated and have relevant biological and synthetic porperties. This work presents the synthesis and investigation of molecular and crystal structure of a new series of monotriazenes [3-(4-phenyldiazenyl)-1-(2-fluorophenyl)triazene (2b); 1-(2-chlorophenyl)-3-(4-phenyldiazenyl)triazeno (2c), 1-(2-bromophenyl)-3-(4-phenyldiazenyl)triazene (2d); 3-(4-phenyldiazenyl)-1-(2-iodophenyl) triazene (2e); 1,3-bis-(3-methoxy-4-methylbenzoate)triazene (2g)] and substituted 1,4-bis (phenyltriazenyl)butanes, C6H5N(H)=N-N(CH2)4-N=NN(H)C6H5, [1,4-bis(4-ethyl-benzoato triazenyl) butane (5a), 1,4-bis(2-fluorophenyltriazenyl)butane (5b), 1,4-bis(2-clorophenyltriazenyl)butane (5c), 1,4-bis(2-bromophenyltriazenyl)butane (5d), 1,4-bis(2-iodophenyltriazenyl)butane (5e), 1,4-bis(4-amidophenyltriazenyll)butane (5f)]. The insertion of groups on phenyl rings attached to the triazene chains makes the environment significantly more interesting coordination providing the supramolecular array through noncovalent intermolecular interactions and self-organizatinal units of primary molecule. The metal ions used for complexation are salts of Ni2+, Cu2+ and Pd2+ and they were chosen due to the attracting biological relevance, magnetic properties, catalytic yielding. Nine metal complexes unpublished were synthesized [trans-[PdII(C6H5NNC6H4NNNC6H4Cl)2(C5H5N)2] (3c) [(PdII (R1R2C6H3NNNC6H3R1R2)(PPh3)2Cl) DMSO] [R1 = 4-C(O)OCH3, R2 = 3-OCH3] (3g) [CuII (RC6H5NNN(CH2)4NNNC6H5R)]2 [R = C2H5C(O)O (6a), R = F (6b), R = NH2C(O) (6f)], [NiII (RC6H5NNN(CH2)4NNNC6H5R)]2 [R = F (7b) R = Cl (7c) R = Br (7d) R = NH2C(O) (7f)]. The synthesis and characterization of these compounds is justified by the exploration of the reactivity, the coordinative behavior and by the understanding of the interactions between different ligands and metal centers. The structural analysis of the synthesized compounds by X-ray diffraction on single crystal in the solid state were performed for characterization of interactions in the crystal. Thus, a thorough understanding of the relationship between the crystal structure and supramolecular organization is analyzed. Besides the structural analysis of compounds, elemental analysis CHN, infrared, nuclear magnetic resonance and ultraviolet-visible spectroscopies and mass spectrometry were also carried out for characterization. The physical chemical properties were investigated through thermogravimetric analysis and magnetic susceptibility.
Triazenos são importantes membros da família de compostos nitrogenados de cadeia aberta, caracterizados por conter o grupo funcional [N═N─N] e apresentam diferentes propriedades de coordenação a metais de transição. São compostos fracamente ácidos e quando desprotonados atuam como ótimos ligantes na química de coordenação apresentando grande importância sintética e biológica. Nessa tese, foi inicialmente desenvolvida a síntese de uma série inédita de compostos triazenos monocatenados [3-(4-fenildiazenil)-1-(2-fluorofenil)triazeno (2b); 1-(2-clorofenil)-3-(4-fenildiazenil)triazeno (2c); 1-(2-bromofenil)-3-(4-fenildiazenil)triazeno (2d); 3-(4-fenildiazenil)-1-(2-iodofenil)triazeno (2e); 1,3-bis(3-metoxi-4-metilbenzoato)triazeno (2g)] e de compostos triazenos biscatenados derivados do 1,4-bis(feniltriazenido)butano, C6H5N(H)N=N-(CH2)4-N=N-N(H)C6H5, [1,4-bis(etil-4-benzoatotriazenil) butano (5a); 1,4-bis(2-fluorofeniltriazenido)butano (5b); 1,4-bis(2-clorofeniltriazenido)butano (5c); 1,4-bis(2-bromofeniltriazenido)butano (5d); 1,4-bis(2-iodofeniltriazenido)butano (5e); 1,4-bis(4-amidofeniltriazenido)butano (5f)]. A inserção de grupamentos substituintes nos anéis fenila na cadeia triazenídica tornam o ambiente de coordenação significativamente mais interessante, propiciando o aumento da ocorrência de interações intermoleculares não covalentes e impondo a auto-organização de unidades moleculares primárias no estado sólido. Os metais escolhidos para complexação foram sais de Ni2+, Cu2+ e Pd2+ em virtude de atraírem atenção como objeto de estudos relacionados com medicina, propriedades magnéticas e catálise obtendo-se como resultados deste trabalho nove complexos metálicos inéditos [trans-[PdII(C6H5NNC6H4NNNC6H4Cl)2(C5H5N)2] (3c); [(PdII(R1R2C6H3NNNC6H3R1R2)(PPh3)2Cl)·DMSO] [R1 = 4-C(O)OCH3, R2 = 3-OCH3] (3g); [CuII(RC6H5NNN(CH2)4NNNC6H5R)]2 [R = C2H5C(O)O (6a); R = F (6b); R = NH2C(O) (6f)] ; [NiII(RC6H5NNN(CH2)4NNNC6H5R)]2 [R = F (7b); R = Cl (7c); R = Br (7d); R = NH2C(O) (7f)]. A síntese, e a caracterização desses novos compostos estão relacionadas à exploração da reatividade, ao comportamento coordenativo e a compreensão das interações entre os diferentes centros metálicos e os ligantes. Efetuou-se um estudo estrutural no estado sólido para a caracterização das interações presentes nas estruturas cristalinas dos compostos sintetizados e a ferramenta utilizada foi à difração de raios X em monocristal. Dessa forma aprofundou-se a compreensão da relação entre a estrutura cristalina e sua organização supramolecular. Além do método de difração de raios X de monocristal os compostos foram caracterizados por espectroscopia de infravermelho, espectroscopia de ressonância magnética nuclear, 1H e 13C, espectroscopia ultravioleta e visível, espectrometria de massas e análise elementar CHN. As propriedades físico-químicas foram investigadas através de análise termogravimétrica e susceptibilidade magnética.
Dearling, Jason L. J. "Hypoxia targeting copper complexes." Thesis, University of Kent, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297352.
Повний текст джерелаLu, Qin. "Copper complexes of polyazacryptands." Thesis, Open University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298997.
Повний текст джерелаSalaudeen, Abibat Abisola. "Switchable iron and copper complexes." Thesis, University of Leeds, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522980.
Повний текст джерелаHeslop, Julia M. "Copper complexes with potential radiopharmaceutical applications." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418800.
Повний текст джерелаAshfield, Laura. "Copper complexes with potential biomedical applications." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426384.
Повний текст джерелаTrotter, Katherine D. "Copper complexes as putative contrast agents." Thesis, University of Strathclyde, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538815.
Повний текст джерелаTaylor, Michelle K. "Copper complexes as putative imaging agents." Thesis, University of Strathclyde, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424316.
Повний текст джерелаHueting, Rebekka. "Radiolabelled copper complexes for cancer imaging." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:47438968-6aa3-41f5-82b4-9121dc327b53.
Повний текст джерелаKarabaeva, Kanykey E. "Photochemistry of dipyridyl-phenanthrenedioxin-copper complexes." Bowling Green State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1530026213399288.
Повний текст джерелаКниги з теми "Paladium and Copper Complexes"
Sorenson, John R. J., ed. Biology of Copper Complexes. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1.
Повний текст джерелаJ, Sorenson John R., ed. Biology of copper complexes. Clifton, N.J: Humana Press, 1987.
Знайти повний текст джерелаMcMaster, Jonathan. Copper and Zinc complexes of bi-imidazole ligands. Manchester: University of Manchester, 1995.
Знайти повний текст джерелаHiggs, Timothy Charles. Synthesis of polyimidazole ligands and their copper complexes. Manchester: University of Manchester, 1994.
Знайти повний текст джерелаJoost, Maximilian. Synthesis and Original Reactivity of Copper and Gold Complexes. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18690-0.
Повний текст джерелаBhalla, Rajiv. Copper and zinc complexes of Bis- and Tris-imidazole ligands. Manchester: University ofManchester, 1995.
Знайти повний текст джерелаNishikawa, Michihiro. Photofunctionalization of Molecular Switch Based on Pyrimidine Ring Rotation in Copper Complexes. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54625-2.
Повний текст джерелаBlusch, Lina K. The Siamese-Twin Porphyrin and Its Copper and Nickel Complexes: A Non-Innocent Twist. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01674-0.
Повний текст джерела1941-, Rainsford K. D., ed. Copper and zinc in inflammatory and degenerative diseases. Dordrecht: Kluwer Academic Publishers, 1998.
Знайти повний текст джерелаJezierska, Julia. Badanie metodą elektronowego rezonansu paramagnetycznego struktury kompleksów miedzi (II) ze szczególnym uwzględnieniem procesów polimeryzacji i ligandów polimerycznych. Wrocław: Wydawn. Uniwersytetu Wrocławskiego, 1993.
Знайти повний текст джерелаЧастини книг з теми "Paladium and Copper Complexes"
Ardizzoia, G. A., G. La Monica, C. W. Liu, and John P. Fackler. "Pyrazolato Copper(I) Complexes." In Inorganic Syntheses, 299–302. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132623.ch53.
Повний текст джерелаBlusch, Lina K. "Nickel and Copper Complexes." In Springer Theses, 67–92. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01674-0_5.
Повний текст джерелаCarvalho, Luciana da Costa. "Copper-Organic Complexes Synthetized Electrochemically." In Beyond Copper Soaps, 13–39. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-97892-1_3.
Повний текст джерелаLoven, Dean P. "Copper and Copper Enzymes in the Development and Treatment of Cancer." In Biology of Copper Complexes, 387–98. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_29.
Повний текст джерелаCarvalho, Luciana da Costa. "Copper-Organic Complexes in Cultural Heritage." In Beyond Copper Soaps, 1–4. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-97892-1_1.
Повний текст джерелаSorenson, John R. J. "A Physiological Basis for Pharmacological Activities of Copper Complexes: An Hypothesis." In Biology of Copper Complexes, 3–16. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_1.
Повний текст джерелаFields, Meira. "Dietary Simple Sugars Increase the Severity of Copper Deficiency in Experimental Animals." In Biology of Copper Complexes, 127–40. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_10.
Повний текст джерелаKeen, Carl L., Michael S. Clegg, Fay Ferrell, Glenn C. Hunter, and Michael A. Dubick. "Hypertension Induced Alterations in Copper and Zinc Metabolism: A Link to Vascular Disease?" In Biology of Copper Complexes, 141–53. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_11.
Повний текст джерелаAnderson, Alfred W. "Manifestations of Copper Deficiency in Dairy Cattle." In Biology of Copper Complexes, 155–63. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_12.
Повний текст джерелаJohnson, J. L., N. R. Schneider, A. R. Doster, M. P. Carlson, and H. W. Leipold. "Observations on Biological Effects of Low Dietary Copper in Nebraska Beef Cattle." In Biology of Copper Complexes, 165–74. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_13.
Повний текст джерелаТези доповідей конференцій з теми "Paladium and Copper Complexes"
Freitag, Marina. "Copper Complexes for Dye-sensitized Solar Cells." In 10th International Conference on Hybrid and Organic Photovoltaics. Valencia: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.hopv.2018.138.
Повний текст джерелаEdis, Zehra, Samir Haj Bloukh, Hamed Abu Sara, Radhika Raheja, Richie Bandareh, and Guido Reiss. "Antimicrobial copper complexes with polymeric pentaiodide chains." In 7th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11602.
Повний текст джерелаZink, Daniel M., Daniel Volz, Larissa Bergmann, Martin Nieger, Stefan Bräse, Hartmut Yersin, and Thomas Baumann. "Novel oligonuclear copper complexes featuring exciting luminescent characteristics." In SPIE Organic Photonics + Electronics, edited by Franky So and Chihaya Adachi. SPIE, 2013. http://dx.doi.org/10.1117/12.2028619.
Повний текст джерелаAlí-Torres, Jorge, Jean-Didier Marechal, Andrea Mirats, Cristina Rodríguez-Rodríguez, Luis Rodríguez-Santiago, and Mariona Sodupe. "Computational simulations of copper complexes relevant to Alzheimer's disease." In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2014 (ICCMSE 2014). AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4897688.
Повний текст джерелаDwivedi, Shikha, S. K. Joshi, V. K. Hinge, B. D. Shrivastava, J. Prasad, and K. Srivastava. "XAFS study of benzimidazole mixed ligand complexes of copper." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098748.
Повний текст джерелаTanasković, Slađana, Branka Dražić, and Mirjana Antonijević Nikolić. "Biological activity of new mixed ligand copper(II) complexes." In RAD Conference. RAD Centre, 2022. http://dx.doi.org/10.21175/rad.spr.abstr.book.2022.24.2.
Повний текст джерелаJoshi, S. K., R. K. Katare, and B. D. Shrivastava. "EXAFS Studies of Some Copper(II) Mixed-Ligand Complexes." In X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644675.
Повний текст джерелаGoodrich, Michael, and David Moore. "CARBON DIOXIDE CLUSTERS AND COPPER COMPLEXES FORMED IN ARGON MATRICES." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wg09.
Повний текст джерелаQader, Taiseer Abdul, Hussein Abdel-Jabbar, and Bakr Ismail. "Spectrophotometric estimation of isoniazid using copper complexes for the Schiff base." In 1ST SAMARRA INTERNATIONAL CONFERENCE FOR PURE AND APPLIED SCIENCES (SICPS2021): SICPS2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0121173.
Повний текст джерелаDarwish, Abdalla M., Robert R. Copeland, R. Sliz, Putcha Venkateswarlu, Mohan D. Aggarwal, Alton Williams, Kamala N. Bhat, James M. Thompson, and N. B. Laxmeshwar. "Highly polarizable metallic complexes for nonlinear optics copper(II) and nickel(II) complexes of bis(salicylaldiminato) Schiff base." In SPIE's 1996 International Symposium on Optical Science, Engineering, and Instrumentation. SPIE, 1996. http://dx.doi.org/10.1117/12.256169.
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