Relevant bibliographies by topics / Complexes du platine(II)

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Complexes du platine(II)'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Complexes du platine(II)"

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Carmona-Negrón, José A., Mayra E. Cádiz, Curtis E. Moore, Arnold L. Rheingold, and Enrique Meléndez. "New platinum(II) complexes with benzothiazole ligands." Acta Crystallographica Section E Crystallographic Communications 72, no. 3 (2016): 412–16. http://dx.doi.org/10.1107/s2056989016002826.

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Four new platinum(II) complexes, namely tetraethylammonium tribromido(2-methyl-1,3-benzothiazole-κN)platinate(II), [NEt4][PtBr3(C8H7NS)] (1), tetraethylammonium tribromido(6-methoxy-2-methyl-1,3-benzothiazole-κN)platinate(II), [NEt4][PtBr3(C9H9NOS)] (2), tetraethylammonium tribromido(2,5,6-trimethyl-1,3-benzothiazole-κN)platinate(II), [NEt4][PtBr3(C10H11NS)] (3), and tetraethylammonium tribromido(2-methyl-5-nitro-1,3-benzothiazole-κN)platinate(II), [NEt4][PtBr3(C8H6N2O2S)] (4), have been synthesized and structurally characterized by single-crystal X-ray diffraction techniques. These species ar
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Watanabe, Rogério H., Maurício C. Gois, and Benedito S. Lima-Neto. "Organic additive–copper(II) complexes as plating precursors." Surface and Coatings Technology 204, no. 4 (2009): 497–502. http://dx.doi.org/10.1016/j.surfcoat.2009.08.020.

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de Oliveira, M. B., J. Miller, R. E. Banks, et al. "New Perfluorophtalate Complexes of Platinum(II) With Chemotherapeutic Potential." Metal-Based Drugs 3, no. 3 (1996): 117–22. http://dx.doi.org/10.1155/mbd.1996.117.

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Two new platinum(II) complexes have been synthesized and their anti-tumour and anti-HIV activities have been evaluated.The new complexes are: (i) cis-tetrafluorophthalate-ammine-morpholine-platinum(II) or MMF3 and (ii) cis-tetrafluorophthalate- ammine-piperidine-platinum(II) or MPF4. They were characterized by elemental analysis, IR spectra and H1 and C13 NMR spectra.They were tested against five human ovarian carcinoma cell lines, viz., CH1, CH1cisR, A2780, A2780cisR and SKOV-3. They were less active than cis-platin and showed cross-resistance with cis-platin in the CH1cisR and A2780cisR acqu
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Castetbon, A., M. Corralès, M. Potin-Gauthier, and M. Astruc. "Etude cinétique de la complexation du cuivre en milieu hydrogénocarbonate par électrochimie." Revue des sciences de l'eau 4, no. 2 (2005): 239–52. http://dx.doi.org/10.7202/705098ar.

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La détermination de la capacité complexante des eaux naturelles est généralement effectuée par titrage ampérométrique du cuivre à pH fixé. Beaucoup, sinon tous les tampons classiques utilisés perturbent les études de spéciation du cuivre par formation de complexes peu stables. Dans ce travail nous nous sommes intéressés à la complexation du cuivre par les ions carbonates généralement présents dans les eaux naturelles. Afin de mener à bien notre étude, nous avons mesuré, dans un milieu synthétique de force ionique et pH contrôlés (KNO3 0,02 M + NaHCO3 2,38.10-3 M) toutes les constantes des dive
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Norkus, E., P. Norkus, J. Vaičiūniené, and J. Jačiauskiené. "Determination of Copper(II) in Electroless Copper Plating Solutions Containing Cobalt(II) Complexes as Reducing Agent." Transactions of the IMF 79, no. 2 (2001): 77–78. http://dx.doi.org/10.1080/00202967.2001.11871367.

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Rashidi, Mehdi, Ahmad R. Esmaeilbeig, Nahid Shahabadi, Shahram Tangestaninejad, and Richard J. Puddephatt. "Some mono- and binuclear platinacyclopentane complexes: a comparative kinetic study of reaction of ethyl iodide with platina(II)cyclopentane and dimethylplatinum(II) complexes." Journal of Organometallic Chemistry 568, no. 1-2 (1998): 53–61. http://dx.doi.org/10.1016/s0022-328x(98)00761-x.

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Cavicchioli, M., Filipe Boccato Payolla, and Antonio Carlos Massabni. "Síntese de novos complexos de platina(II) de interesse biológico. Um novo complexo dinuclear de platina(II) com 5-fluorouracil." Eclética Química Journal 40, no. 1 (2015): 180. http://dx.doi.org/10.26850/1678-4618eqj.v40.1.2015.p180-185.

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Many strategies have been used for the treatment of cancer and, following the success of cisplatin and carboplatin, metal complexes have been excelled and showed efficiency on the treatment of many types of cancer. The use of ligands that already have antitumor activity allows an increase on the drugs efficiency. In this work, synthesis of obtained a binuclear compound of platinum and 5-fluorouracil is described. The compound was characterized by elemental analysis and the results show a molar ratio of 2:1 (M:L). The IR spectra shows the complexation of the ligands to the metal by the N atoms
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Werner, Michael, Clemens Bruhn та Dirk Steinborn. "From platina-β-diketones to diacetylplatinum(II) complexes – Synthesis, characterization and structural features". Journal of Organometallic Chemistry 693, № 13 (2008): 2369–76. http://dx.doi.org/10.1016/j.jorganchem.2008.04.016.

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Van Tan, Le, Tran Quang Hieu, and Nguyen Van Cuong. "Spectrophotometric Determination of Cr(III) and Pb(II) Using Their Complexes with 5,11,17,23-Tetra[(2-ethyl acetoethoxyphenyl)(azo)phenyl]calix[4]arene." Journal of Analytical Methods in Chemistry 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/860649.

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New complexes of 5,11,17,23-tetra[(2-ethyl acetoethoxyphenyl)(azo)phenyl]calix[4]arene (TEAC) with Pb(II) and Cr(III) were prepared in basic solution with a mixture of MeOH and H2O as solvent. The ratio of TEAC and metal ion in complexes was found to be 1 : 1 under investigated condition. The complex formation constants (based on Benesi-Hildebrand method) for TEAC-Pb(II) and TEAC-Cr(III) were 4.03 × 104and 1.2 × 104, respectively. Additionally, the molar extinction coefficients were 5 × 104and 1.42 × 104for TEAC-Pb(II) and TEAC-Cr(III), respectively. The H-Point Standard Addition Method (HPSAM
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Steinborn, Dirk, Tobias Hoffmann, Michael Gerisch та ін. "On the Reactivity of Platina-β-diketones - Synthesis and Characterization of Acylplatinum(II) Complexes". Zeitschrift für anorganische und allgemeine Chemie 626, № 3 (2000): 661–66. http://dx.doi.org/10.1002/(sici)1521-3749(200003)626:3<661::aid-zaac661>3.0.co;2-4.

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Dissertations / Theses on the topic "Complexes du platine(II)"

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Blondel, Benoît. "Complexes de platine(II) pour des diodes organiques électroluminescentes (OLEDs) rouges et bistables." Thesis, Toulouse 3, 2017. http://www.theses.fr/2017TOU30173/document.

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Ce travail de thèse décrit l'utilisation de complexes de platine(II) dans les diodes électroluminescentes organiques (OLEDs). Ces complexes ([Pt(II) (tetra-tert-butylSalophen)] et [Pt(II) Salophen]) ont été caractérisés par les méthodes usuelles (1H RMN, spectroscopie UV-visible, électrochimie, diffraction des rayons X pour le [Pt(II) (tetra-tert-butylSalophen)]). Des calculs DFT ont corroboré les données expérimentales qui ont guidé le choix du Tris(8-hydroxyquinolinato) aluminum (Alq3) en tant que matrice. Des dispositifs bistables, susceptibles d'être utilisés en tant que mémoires, ont été
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Soares, Marie C. "Synthèses et études de la réactivité des complexes ferrocénylphosphines du platine(II) et du palladium(II) /." [S.l.] : [s.n.], 1997. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=12178.

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Diring, Stéphane Ziessel Raymond. "Synthèse de complexes luminescents de platine (II) appliquée à la construction d'édifices multichromophoriques." Strasbourg : Université de Strasbourg, 2009. http://eprints-scd-ulp.u-strasbg.fr:8080/1085/01/DIRING_Stephane_2008.pdf.

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Diring, Stéphane. "Synthèse de complexes luminescents de platine (II) appliquée à la construction d’édifices multichromophoriques." Strasbourg, 2009. https://publication-theses.unistra.fr/public/theses_doctorat/2009/DIRING_Stephane_2009.pdf.

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Les travaux réalisés durant cette thèse s’articulent autour de deux grands axes. La première partie des travaux a consisté à étudier des complexes luminescents de platine(II). Une méthodologie de synthèse reposant sur une réaction de Diels-Alder nous a permis d’obtenir une série de ligands de type phényl-bipyridine diversement fonctionnalisés. Nous avons obtenu les complexes de platine(II) correspondants et avons étudié et la variation de leurs propriétés photophysiques, en fonction de la nature des groupes fonctionnels présents sur le ligand ou directement connectés au centre métallique. La s
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Hamel, Matthieu. "Les phénylphosphonates ortho-sulfinylés : nouvelle synthèse asymétrique et préparation de complexes de platine (II)." Caen, 2005. http://www.theses.fr/2005CAEN2036.

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Ce travail a porté sur la synthèse, notamment asymétrique, de composés aromatiques ortho-difonctionnalisés phosphorosulfurés, et de leurs applications dans le domaine thérapeutique, en tant que ligands du cisplatine et en tant qu'inhibiteurs d'enzymes. Une nouvelle méthode de synthèse de sulfinates diastéréoenrichis (précurseurs de sulfoxydes), basée sur l'oxydation asymétrique de sulfénates énantiopurs a été développée. Cette méthode a permis d'accéder à des ortho-sulfinylbenzènephosphonates optiquement actifs avec des excès énantiomériques atteignant 86 %. Le réarrangement sigmatropique [1,3
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Souchard, Jean-Pierre. "Synthèse, propriétés physico-chimiques, et activités pharmacologiques de complexes antitumoraux dérivés du platine (II): relations structure-activité." Toulouse 3, 1990. http://www.theses.fr/1990TOU30128.

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L'auteur a mis au point une methode de synthese rapide et fiable des complexes cis-pta#2(ono#2)#2 (a etant une amine ou une pyridine substituee a partir des complexes cis-pta#2i#2 dissous dans l'acetone. L'etude rmn #1h des complexes cis- et trans-pta#2x#2 (x etant un iodure, un chlorure ou un nitrate) a mis en evidence une constante de couplage j(pt-h) permettant d'identifier sans ambiguite l'isomerie des complexes. Les derives cis-pta#2 (ono#2)#2 s'hydrolysent rapidement en solution aqueuse pour donner les complexes diaquo (cis(pta#2(h#2o)#2#2#+, 2 no#3) qui sont stables pendant au moins deu
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REDON, SOPHIE. "Structures quadruplexes de sequences telomeriques : etudes structurales et pontages a l'aide de complexes du platine(ii)." Paris 11, 2001. http://www.theses.fr/2001PA112200.

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L'adn telomerique simple-brin riche en guanines (g), situe aux extremites des chromosomes, adopte in vitro et en presence de cations monovalents, des structures quadruplexes qui correspondent a des empilements de quartets de g. Ces structures inhibent la telomerase, une enzyme active dans la plupart des cellules cancereuses et responsable de leur immortalisation. Le but etait de figer avec des complexes du platine(ii) des structures quadruplexes de tetrahymena (t 2g 4) 4 et humaines (t 2)ag 3(t 2ag 3) 3 en pontant deux purines. Le complexe monofonctionnel pt(nh 3) 3(h 2o)(no 3) 2 est une sonde
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Soliman, Ahmed M. "Synthèses et propriétés photophysiques de nouveaux complexes hétérométalliques de platine(II)-iridium(III) et leurs polymères." Mémoire, Université de Sherbrooke, 2012. http://hdl.handle.net/11143/5765.

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Platinum(1I) and charged cationic iridium(III) complexes have attracted great interest as luminophores in a myriad of applications. Notably, each class of these complexes has been incorporated into organic light emitting diodes (OLEDs), light-emitting electrochemical cells (LEECs), nonlinear optical materials and photovoltaic devices. This thesis reports the synthesis of hybrid Pt-Ir-containing organometallic complexes and polymers with the goal of obtaining high performance luminophores for electroluminescent devices. As a first step towards the polymer construction, the synthesis of a series
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Fourmy, Kévin. "Complexes d'or(I) et de platine(II) portant des ligands phospholes : synthèse et applications dans l'activation d'alcynes." Toulouse 3, 2013. http://thesesups.ups-tlse.fr/2108/.

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L'activation homogène d'alcynes par des complexes d'or(I) et de platine(II) a connu un important essor ces 10 dernières années. Initialement, les sels métalliques, AuCl ou PtCl2, étaient utilisés. La conception de nouveaux ligands est primordiale afin d'améliorer l'activité, la sélectivité, mais aussi la stabilité des catalyseurs. Historiquement, des ligands phospholes sont utilisés au laboratoire pour développer des nouveaux outils catalytiques. C'est dans ce contexte que nous nous sommes intéressés aux applications des ligands phospholes dans l'activation d'alcyne. Des complexes d'or(I), [Au
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Chantson, Janine. "Platinum (II) complexes of heteroaromatic derivatives." Pretoria : [s.n.], 2002. http://upetd.up.ac.za/thesis/available/etd-08012005-143742/.

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Books on the topic "Complexes du platine(II)"

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Quyoum, Ruhksana. Pentamethylclopentadienyl complexes of platinum(II): Their synthesis and reactivity. University of Salford, 1992.

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Zou, Taotao. Anti-Cancer N-Heterocyclic Carbene Complexes of Gold(III), Gold(I) and Platinum(II). Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-0657-9.

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Campbell, Colm J. Synthesis and study of platinum(II) and platinum(IV) complexes of EDTA derivatives as potential antitumour agents. University College Dublin, 1996.

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Zhao, Zhongwei. Pulse radiolysis of iron (II) complexes. University of Salford, 1989.

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Buchler, J. W., ed. Metal Complexes with Tetrapyrrole Ligands II. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/3-540-52899-7.

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Zhao, Zhongwei. Free radical chemistry of iron (II) complexes. University of Salford, 1992.

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Harris, J. Robin, and Jon Marles-Wright, eds. Macromolecular Protein Complexes II: Structure and Function. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28151-9.

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Fourez, I. G. Reaction of sulphur dioxide with Manganese(II) complexes. UMIST, 1996.

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Peter, Day, Dahl Jens Peder, and SpringerLink (Online service), eds. Molecular Electronic Structures of Transition Metal Complexes II. Springer Berlin Heidelberg, 2012.

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Mingos, David Michael P., Peter Day, and Jens Peder Dahl, eds. Molecular Electronic Structures of Transition Metal Complexes II. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-27378-0.

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Book chapters on the topic "Complexes du platine(II)"

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Yakovlev, K. I., A. I. Stetsenko, G. M. Alekseyeva, A. A. Tulub, L. B. Selderkhanova, and I. Yu Mamelkina. "Platinum (II) Complexes with Aminopyrimidines." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_91.

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Phillips, Julia R., William C. Trogler, Mick Brammer, and Dianne L. Packett. "Chlorohydridobis(Trialkylphosphine)-Platinum(II) Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch46.

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Mann, David J., and Ramon Vilar. "Platinum(II) Complexes, Inhibition of Kinases." In Encyclopedia of Metalloproteins. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-1533-6_535.

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Sperline, Roger P., D. Max Roundhill, A. J. Cartv, and D. K. Johnson. "(Dimethyl Phosphito) Complexes of Platinum(II)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132500.ch20.

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Hill, Geoffrey S., Michael J. Irwin, Christopher J. Levy, et al. "Platinum(II) Complexes of Dimethyl Sulfide." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132630.ch25.

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White, D. A., J. R. Doyle, and H. Lewis. "Cationic Diene Complexes of Palladium(II) and Platinum(II)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch12.

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Hsu, Chao-Yang, Brian T. Leshner, Milton Orchin, and Michel Laurent. "Trans Phosphine Complexes of Platinum(II) Chloride." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132500.ch25.

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Okeya, Seichi, Shinichi Kawaguchi, Erven Kuhlmann, and Milton Orchin. "The bis(β-Diketonato)Platinum(II) Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132517.ch20.

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Lo, Yan-Chung, and Andrew H. J. Wang. "Platinum(II), Terpyridine Complexes, Inhibition of Cysteine Proteases." In Encyclopedia of Metalloproteins. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-1533-6_559.

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Totani, T., K. Aono, Y. Adachi, M. Komura, O. Shiratori, and K. Sato. "Bidentate Hydroxycarboxylic Acid Platinum(II) Complexes with Antitumor Activity." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_87.

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Conference papers on the topic "Complexes du platine(II)"

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Verdejo, Begoña, Javier Pitarch-Jarque, Estefanía Delgado-Pinar, Lorena Magraner-Pardo, Jesus de Julián-Ortiz, and Enrique García-España. "Synthesis and Platinum (II) Complexes of Different Polyazacyclophane Receptors." In MOL2NET, International Conference on Multidisciplinary Sciences. MDPI, 2015. http://dx.doi.org/10.3390/mol2net-1-a014.

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Fillaut, Jean-Luc, Pierre-Henri Lanoe, Veronique Guerchais, Hubert Le Bozec, and J. A. Gareth Williams. "Engineering of cyclometallated platinum(II) complexes incorporating acetylide ligands for chemosensing." In 2009 3rd ICTON Mediterranean Winter Conference (ICTON-MW 2009). IEEE, 2009. http://dx.doi.org/10.1109/ictonmw.2009.5385644.

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Xiang, Hai-Feng, Siu-Chung Chan, Chi-Ming Che, P. T. Lai, and Po C. Chui. "High-efficiency electrophosphorescent organic light-emitting devices based on Schiff base platinum(II) complexes." In Optical Science and Technology, the SPIE 49th Annual Meeting, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2004. http://dx.doi.org/10.1117/12.565320.

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Santos, José V. Dos, Sergio R. de Lazaro, Luis H. S. Lacerda, et al. "Theoretical simulation for the [6-p-cymene)RuCl2(meapy)] complex." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020196.

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Anticarcinogen compounds are extensively investigated in current days. Among the potential alternatives to develop effective drugs for this purpose, stands out the ruthenium (II) complex presents satisfactory anti-tumor activity. In particular, this kind of compounds has been investigated as a possible substitute for Platinum-based drugs. However, Ru (II) complexes need more investigation to understand the ligands' effect on biological environments, such as cytotoxicity, metabolism, accumulation on tumor issues, and others. Therefore, in this work, a robust DFT/B3LYP theoretical investigation
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Antonichen, Magno R., Sergio R. de Lazaro, Luis H. S. Lacerda, et al. "DFT simulations for the [6-p-cymene)RuCl2(apy)] complex." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202097.

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Anticarcinogen compounds are extensively investigated in current days. Among the potential alternatives to develop effective drugs for this purpose, stands out the ruthenium (II) complex presents satisfactory anti-tumor activity. In particular, this kind of compounds has been investigated as a possible substitute for Platinum-based drugs. However, Ru (II) complexes need more investigation to understand the ligands' effect on biological environments, such as cytotoxicity, metabolism, accumulation on tumor issues, and others. Therefore, in this work, a robust DFT/B3LYP theoretical investigation
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Antonijevic, Marko, Jelena Đorovic Jovanovic, Ana Kesic, Dejan Milenkovic та Zoran Markovic. "КOMPLEKSI ZLATA KAO POTENCIJALNI SUPLEMENTI SA ANTIKANCEROGENIM I ANTIVIRUSNIM DELOVANJEM". У XXVI savetovanje o biotehnologiji sa međunarodnim učešćem. University of Kragujevac, Faculty of Agronomy, 2021. http://dx.doi.org/10.46793/sbt26.429a.

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The pharmacologic properties of gold compounds have been known since the end of the 19th century. They have been used for different studies, even though they are usually used for the treatment of arthritis. In the last decade, gold complexes have received increased attention due to the variety of their applications. Primary, they have been investigated as potential anticancer and chemotherapeutic agents. It is well known that gold(III) complexes are very similar to platinum(II) compounds, so they could exhibit prospective anticancer, cytotoxic and antitumor properties. In this paper, were inve
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Nimir, Hassan, Norah Al Mohaideb, Mariem Hamad, et al. "Synthesis, Characterization, Crystal Structures, and in vitro Antitumor Activity of Palladium and Platinum (Ii) Complexes with 2-Acetyl-4-Methylthiazole Thiosemicarbazone and 2-Acetylpyrazine Thiosemicarbazone." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2016. http://dx.doi.org/10.5339/qfarc.2016.hbpp3347.

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El-Maraghy, Salah B., K. A. Salib, and S. L. Stefen. "Palladium (II) Hydrazopyrazolone Complexes." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969594.

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Singh, Puja, and S. Sharma. "Spectroscopic characterization of some Cu(II) complexes." In LIGHT AND ITS INTERACTIONS WITH MATTER. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898270.

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Darwish, Abdalla M., Robert R. Copeland, R. Sliz, et al. "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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Reports on the topic "Complexes du platine(II)"

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Ratilla, E. Platinum(II) complexes as spectroscopic probes for biomolecules. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6491206.

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Zhou, Xia-Ying. Effects of ancillary ligands on selectivity of protein labeling with platinum(II) chloro complexes. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6941351.

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Brown, David Stephen. I. Redox chemistry of bimetallic fulvalene complexes II. Oligocyclopentadienyl complexes. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10165274.

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Kincaid, J. Resonance Raman and photophysical studies of polypyridine complexes of ruthenium (II). Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6816606.

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Shen, Wen-Tang. A polarographic study of Fe(II) and Fe(III) complexes with catechol. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2795.

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Burgeson, I. Mechanism and applicability of hydrolysis of peptides and proteins utilizing Pt(II) complexes. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6812379.

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Wagner, M. R. NMR investigation of dynamic processes in complexes of nickel(II) and zinc(II) with iminodiacetate, n-methyliminodiacetate and n-ethyliminodiacetate. Office of Scientific and Technical Information (OSTI), 1985. http://dx.doi.org/10.2172/5982240.

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Enscore, Susan I., and Martin J. Stupich. HAER Level II Documentation of Launch Complexes 1/2, 3/4, 9/10, 14, and 34 at Cape Canaveral Air Force Station, Florida. Defense Technical Information Center, 2016. http://dx.doi.org/10.21236/ada637019.

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Hammamieh, Rasha. Apoptosis Use Case: In Silico Evaluation of a Library of Small Molecule Pharmacophore Models for Blocking the Formation of SEB-Major Histocompatibility Class II Complexes. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada482295.

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