Bibliografías temáticas / Polynuclear Transition Metal Complexes

Literatura académica sobre el tema "Polynuclear Transition Metal Complexes"

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Publicado: 7 de septiembre de 2023

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Artículos de revistas sobre el tema "Polynuclear Transition Metal Complexes"

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Yam, Vivian Wing-Wah. "Molecular design of luminescent metal-based materials". Pure and Applied Chemistry 73, n.º 3 (1 de enero de 2001): 543–48. http://dx.doi.org/10.1351/pac200173030543.

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A series of soluble di- and polynuclear transition-metal acetylides with rich luminescence behavior have been designed and successfully isolated. The photophysical and photochemical properties have been studied. Luminescent polynuclear metal complexes have also been obtained based on the metal chalcogenide building block. These high-nuclearity transition-metal chalcogenide complexes have been structurally characterized and shown to display rich luminescence behavior. Various approaches and strategies to design and synthesize luminescent polynuclear metal complexes that may find potential applications as chemosensors and luminescence signalling devices will also be described.
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Umakoshi, Keisuke. "Stereocontrol and Metal-metal Interactions of Polynuclear Transition Metal Complexes". Bulletin of Japan Society of Coordination Chemistry 79 (6 de junio de 2022): 58–67. http://dx.doi.org/10.4019/bjscc.79.58.

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Balzani, Vincenzo, Alberto Juris, Margherita Venturi, Sebastiano Campagna y Scolastica Serroni. "Luminescent and Redox-Active Polynuclear Transition Metal Complexes†". Chemical Reviews 96, n.º 2 (enero de 1996): 759–834. http://dx.doi.org/10.1021/cr941154y.

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Siddiqi, K. S., Sadaf Khan, Shahab A. A. Nami y M. M. El-ajaily. "Polynuclear transition metal complexes with thiocarbohydrazide and dithiocarbamates". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 67, n.º 3-4 (julio de 2007): 995–1002. http://dx.doi.org/10.1016/j.saa.2006.09.019.

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Podewitz, Maren, Carmen Herrmann, Astrid Malassa, Matthias Westerhausen y Markus Reiher. "Spin–Spin interactions in polynuclear transition-metal complexes". Chemical Physics Letters 451, n.º 4-6 (enero de 2008): 301–8. http://dx.doi.org/10.1016/j.cplett.2007.12.011.

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Klingele, Julia, Sebastian Dechert y Franc Meyer. "Polynuclear transition metal complexes of metal⋯metal-bridging compartmental pyrazolate ligands". Coordination Chemistry Reviews 253, n.º 21-22 (noviembre de 2009): 2698–741. http://dx.doi.org/10.1016/j.ccr.2009.03.026.

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Satpathy, K. C., A. K. Panda, R. Mishra, A. Mahapatra y A. Patel. "Polynuclear Metal Complexes: Transition Metal Complexes of bis(3-Formyl-Salicylic Acid)-hydrazone". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 22, n.º 2-3 (febrero de 1992): 201–15. http://dx.doi.org/10.1080/00945719208021383.

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Ahmed, Ejaz y Michael Ruck. "Chemistry of polynuclear transition-metal complexes in ionic liquids". Dalton Transactions 40, n.º 37 (2011): 9347. http://dx.doi.org/10.1039/c1dt10829h.

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Provent, Christophe y Alan F. Williams. "ChemInform Abstract: The Chirality of Polynuclear Transition Metal Complexes". ChemInform 31, n.º 42 (17 de octubre de 2000): no. http://dx.doi.org/10.1002/chin.200042291.

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Cirera, Jordi, Yuan Jiang, Lei Qin, Yan-Zhen Zheng, Guanghua Li, Gang Wu y Eliseo Ruiz. "Ferromagnetism in polynuclear systems based on non-linear [MnII2MnIII] building blocks". Inorganic Chemistry Frontiers 3, n.º 10 (2016): 1272–79. http://dx.doi.org/10.1039/c6qi00189k.

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Design of new polynuclear transition metal complexes showing ferromagnetic interactions to achieve high spin values is an important challenge due to the scarcity of bridging ligands that provide such coupling.
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Tesis sobre el tema "Polynuclear Transition Metal Complexes"

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Sun, Ziming. "Polynuclear transition metal complexes and single-molecule magnets /". Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1998. http://wwwlib.umi.com/cr/ucsd/fullcit?p9906469.

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Young, George Hansen. "Reactions of transition-metal propargyl complexes with polynuclear metal carbonyls /". The Ohio State University, 1989. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487672631602474.

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Ahmed, Ejaz y Michael Ruck. "Chemistry of polynuclear transition-metal complexes in ionic liquids". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-138716.

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Transition-metal chemistry in ionic liquids (IL) has achieved intrinsic fascination in the last few years. The use of an IL as environmental friendly solvent, offers many advantages over traditional materials synthesis methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room-temperature IL have been found to be excellent media for stabilising transition-metal clusters in solution and to crystallise homo- and heteronuclear transition-metal complexes and clusters. Furthermore, the use of IL as solvent provides the option to replace high-temperature routes, such as crystallisation from the melt or gas-phase deposition, by convenient room- or low-temperature syntheses. Inorganic IL composed of alkali metal cations and polynuclear transition-metal cluster anions are also known. Each of these areas will be discussed briefly in this contribution
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
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Stephens, Peter M. B. "Polynuclear transition metal complexes of tetraazamacroycles and their derivatives". Thesis, University of Kent, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385273.

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Lacy, O. M. "Synthesis, structure and reactivity of polynuclear transition metal complexes". Thesis, University of Newcastle Upon Tyne, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370145.

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Ahmed, Ejaz y Michael Ruck. "Chemistry of polynuclear transition-metal complexes in ionic liquids". Royal Society of Chemistry, 2011. https://tud.qucosa.de/id/qucosa%3A27774.

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Transition-metal chemistry in ionic liquids (IL) has achieved intrinsic fascination in the last few years. The use of an IL as environmental friendly solvent, offers many advantages over traditional materials synthesis methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room-temperature IL have been found to be excellent media for stabilising transition-metal clusters in solution and to crystallise homo- and heteronuclear transition-metal complexes and clusters. Furthermore, the use of IL as solvent provides the option to replace high-temperature routes, such as crystallisation from the melt or gas-phase deposition, by convenient room- or low-temperature syntheses. Inorganic IL composed of alkali metal cations and polynuclear transition-metal cluster anions are also known. Each of these areas will be discussed briefly in this contribution.
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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Ibrahim, Masooma [Verfasser]. "Polynuclear Transition Metal-Oxo Complexes Stabilized by Heteropolytungstates / Masooma Ibrahim". Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2012. http://d-nb.info/1035217686/34.

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Organtzis, Stefanos. "Polynuclear transition metal complexes containing azido and pyrazolinato bridging ligands". Thesis, University of Manchester, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496513.

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Following the discovery that a single molecule can behave as a magnet, the field of research on magnetism has become of great interest to scientists. A large number of polynuclear compounds have been produced and studied worldwide over the past two decades, in an effort to obtain better single molecule magnets (SMMs). The synthesis of such compounds involves mainly first row transition metals and a wide range of bridging ligands.
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Taylor, Stephanie Merac. "Calixarene supported transition metal clusters". Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/7770.

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This thesis describes a series of calix[n]arene polynuclear transition metal and lanthanide complexes. Calix[4]arenes possess lower-rim polyphenolic pockets that are ideal for the complexation of various transition metal and lanthanide centres. Surprisingly however, with only a few exceptions, the coordination chemistry of p-tBucalix[ 4]arene (TBC[4]), p-tBu-calix[8]arene (TBC[8]) and p-tBuhomotrioxacalix[ 3]arene (TBOC[3]) with paramagnetic transition metal ions for the purpose of making and studying magnetically interesting molecules is unknown. Chapter two describes the reaction of TBC[4] with manganese salts in the presence of an appropriate base (and in some cases co-ligand) resulting in the formation of a family of calixarene-supported [MnIII 2MnII 2] clusters (1-7) that behave as Single-Molecule Magnets (SMMs). These are: [MnIII 2MnII 2(OH)2(TBC[4])2(DMF)6]·2MeOH (1), [MnIII 2MnII 2(OH)2(TBC[4])2(DMF)4(H2O)2]·4MeOH·2DMF (2), [MnIII 2MnII 2(OH)2(TBC[4])2(DMF)6]·2.8MeOH (3), [MnIII 2MnII 2(OH)2(TBC[4])2(DMF)4(EtOH)(H2O)] (4), [MnIII 2MnII 2(OH)2(TBC[4])2(DMSO)6]·2MeOH·2DMSO (5) , [MnIII 2MnII 2(OH)2(TBC[4])2(DMSO)6] (6) and [MnIII 2MnII 2(OH)2(C[4])2(MeOH)6]·4MeOH (7). Variation in the alkyl groups present at the upper-rim of the cone allows for the expression of a degree of control over the self-assembly of these SMM building blocks, whilst retaining the general magnetic properties. The presence of various different ligands around the periphery of the magnetic core has some effect over the extended self-assembly of these SMMs. Chapter three describes how the combination of complementary cluster ligands; sodium phenylphosphinate and the N,O-chelate 2-(hydroxy-methyl)pyridine (hmpH) with TBC[4] results in the formation of two new calixarene-supported clusters. This being an unusual [MnIIIMnII]2 dimer of dimers [MnIIIMnII(O2P(H)Ph)(DMF)2(MeOH)2]2 (8) and a ferromagnetic [Mn5] cage that displays the characteristic bonding modes of each support [MnIII 3MnII 2(OH)2(TBC[4])2(hmp)2(DMF)6](TBC[4]-H)·xDMF ·xH2O (9). Chapter four details how using oxacalix[3]arenes can tune the nature of the metal binding site, by introduction of ≥ 1 ethereal bridge. This results in Mn(II) rather than Mn(III) bonding in the phenolic pocket, and that these components self-assemble with additional Mn(II) and Mn(III) ions to form a [Mn10] supertetrahedron with an unusual oxidation state distribution, [MnII 6MnIII 4O4(TBOC[3])4(Cl)4(DMF)3]∙3.3H2O ∙ 1.5DMF (10). Chapter five introduces a family of lanthanide complexes formed using TBC[8]. Variation in the experimental conditions employed in the reaction of TBC[8] with lanthanide salts (LnX3) provides access to Ln1, Ln2, Ln4, Ln5, Ln6, Ln7 and Ln8 complexes, [Gd(TBC[8]-2H)Cl(DMSO)4]·MeCN·H2O·(DMSO)2·hex (11), [CeIV 4(TBC[8]-6H)2(μ3- O)2(DMF)4]·(DMF)5·hex·MeCN (12), [TbIII 5(TBC[8]-5H)(μ4-O)(μ3- OH)4Cl(DMSO)8(H2O)3]Cl3·(DMSO)2(hex)2 (13), [CeIV 6(TBC[8]-6H)2(μ4-O)2(μ2-OMe)4(μ2- O)2(DMF)4]·(DMF)6·hex (14), [Dy7(TBC[8]-7H)(TBC[8]-6H)(μ4-O)2(μ3-OH)2(μ2- OH)2(DMF)9]·(DMF)3 (15) and [Gd8(TBC[8]-7H)2(μ4-CO3)2(μ5-CO3)2(μ2-HCO2)2(DMF)8] (16), with all polymetallic clusters containing the common bi-nuclear lanthanide fragment. Closer inspection of the structures of the polymetallic clusters reveals that all but one (Ln8) are in fact based on metal octahedra or the building blocks of octahedra.
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Hashiguchi, Ryota. "Studies on Polynuclear Metal Complexes and Low-Dimensional Mixed-Valence Halogen-Bridged Transition Metal Complexes Based on them". 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225426.

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Libros sobre el tema "Polynuclear Transition Metal Complexes"

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1947-, Adams Richard D. y Cotton F. Albert 1930-, eds. Catalysis by di- and polynuclear metal cluster complexes. New York: Wiley-VCH, 1998.

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Nishibayashi, Yoshiaki, ed. Transition Metal-Dinitrogen Complexes. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527344260.

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Kreißl, F. R., ed. Transition Metal Carbyne Complexes. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4.

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Yam, Vivian W. W., ed. Photofunctional Transition Metal Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-36810-6.

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R, Kreissl F. y North Atlantic Treaty Organization. Scientific Affairs Division., eds. Transition metal carbyne complexes. Dordrecht: Kluwer Academic, 1993.

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W, Yam Vivian W. y Balch Alan L, eds. Photofunctional transition metal complexes. Berlin: Springer Verlag, 2007.

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El-Gamati, Ibrahim Mohamed T. Studies of mono- and polynuclear metal carbonyl phosphine complexes. Dublin: University College Dublin, 1997.

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Qiu, Zaozao. Late Transition Metal-Carboryne Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-24361-5.

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Molecular orbitals of transition metal complexes. Oxford: Oxford University Press, 2005.

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Kettle, Sidney. The theory of transition metal complexes. London: Royal Society of Chemistry. Educational Techniques Group Trust, 1994.

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Capítulos de libros sobre el tema "Polynuclear Transition Metal Complexes"

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Provent, Christophe y Alan F. Williams. "The Chirality of Polynuclear Transition Metal Complexes". En Perspectives in Supramolecular Chemistry, 135–91. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470511510.ch4.

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Balzani, Vincenzo, Sebastiano Campagna, Gianfranco Denti y Scolastica Serroni. "Supramolecular Photochemistry: Antenna Effect in Polynuclear Metal Complexes". En Photoprocesses in Transition Metal Complexes, Biosystems and Other Molecules. Experiment and Theory, 233–52. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2698-4_10.

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Case, David A., Louis Noodleman y Jian Li. "Modern Computational Approaches to Modeling Polynuclear Transition Metal Complexes". En Metal-Ligand Interactions in Chemistry, Physics and Biology, 19–47. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4245-8_2.

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Scandola, F., C. A. Bignozzi, C. Chiorboli, M. T. Indelli y M. A. Rampi. "Photophysics of Polynuclear Complexes. Intercomponent Energy and Electron Transfer Processes". En Photoprocesses in Transition Metal Complexes, Biosystems and Other Molecules. Experiment and Theory, 253–69. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2698-4_11.

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Hidai, Masanobu y Yasushi Mizobe. "Toward Novel Organic Synthesis on Multimetallic Centers: Synthesis and Reactivities of Polynuclear Transition-Metal—Sulfur Complexes". En ACS Symposium Series, 310–23. Washington, DC: American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0653.ch019.

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Adams, Richard D. y Burjor Captain. "Chapter 31. Polynuclear Transition Metal Cluster Complexes Containing Tin Ligands: Precursors to New Heterogeneous Nano-Catalysts". En Turning Points in Solid-State, Materials and Surface Science, 534–49. Cambridge: Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847558183-00534.

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Scandola, F., C. A. Bignozzi y M. T. Indelli. "Intramolecular Energy and Electron Transfer in Polynuclear Metal Complexes". En Catalysis by Metal Complexes, 161–216. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-2626-9_6.

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Hendrickson, David N., David M. Adams, Chi-Cheng Wu y Sheila M. J. Aubin. "Bistable Transition Metal Complexes". En Magnetism: A Supramolecular Function, 357–82. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-015-8707-5_19.

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Atwood, David A. "(II) Transition Metal Complexes". En Inorganic Reactions and Methods, 176. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch169.

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Harrod, John F. y Bruce Arndtsen. "Transition Metal Hydride Complexes". En Inorganic Reactions and Methods, 337–41. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch238.

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Actas de conferencias sobre el tema "Polynuclear Transition Metal Complexes"

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Petrović, Biljana. "TRANSITION METAL ION COMPLEXES AS POTENTIAL ANTITUMOR AGENTS". En 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.009p.

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Discovery of the antitumor activity of platinum complex, cisplatin, cis-Pt(NH3)2Cl2, and later carboplatin and oxaliplatin, led to the intensive investigation of the potential antitumor activity of the huge number of platinum complexes. Furthermore, it is well-known that platinum complexes express toxicity, numerous side effects and resistance, so the scientists make a lot of efforts to synthetize, beside Pt(II) and Pt(IV), other non-platinum compounds with potential antitumor activity, such as Pd(II), Ru(II/III) and Au(III) complexes. The goal of this study is to summarize the results of the investigation of the interactions between some mononuclear, homo- and hetero-polynuclear Pt(II), Pd(II), Ru(II/III) and Au(III) complexes with different sulfur- and nitrogen-donor biologically relevant nucleophiles. Among mononuclear complexes, the compounds with aromatic terpy (tepyridine) or bpma (bis-(2- pyridylmethyl)amine) and aliphatic dien (diethylentriamine) nitrogen-containing inert ligands were studied. Different homo- and hetero-polynuclear complexes with pz (pyrazine) or 4,4’-bipy (4,4’- bipyridine) as bridging and mostly en (ethylenediamine), bipy (2,2’-bipyridine) and dach (trans-1,2- diaminocyclohexane) as inert ligands were studied as well. The research was focused on the connection between the structure and the mechanisms of interactions with different biomolecules, such as L- cysteine (L-Cys), L-methionine (L-Met), tripeptide glutathione (GSH), guanosine-5’-monophosphate (5’-GMP), DNA and bovine serum albumin (BSA). Some of these complexes were selected for in vitro studies of the cytotoxicity on different tumor cell lines. Observed results contribute a lot as a guidance for the future design and determination of the structure-activity relationship (SAR) of different transition metal ion complexes.
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Davidenko, N., V. Kokozay, D. Nesterov y D. Shevchenko. "The Photoelectric Properties of Polymeric Composites for Magneto-Optic Applications Containing Hetero Polynuclear Complexes of Transition Metals". En Photorefractive Effects, Materials, and Devices. Washington, D.C.: OSA, 2005. http://dx.doi.org/10.1364/pemd.2005.319.

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Lee, Taewoo, Christian Reich, Christopher M. Laperle, Xiaodi Li, Margaret Grant, Christoph G. Rose-Petruck y Frank Benesch-Lee. "Ultrafast XAFS of transition metal complexes". En International Conference on Ultrafast Phenomena. Washington, D.C.: OSA, 2006. http://dx.doi.org/10.1364/up.2006.wd4.

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Slinker, Jason, Dan Bernards, Samuel Flores-Torres, Stefan Bernhard, Paul L. Houston, Héctor D. Abruña y George G. Malliaras. "Light emitting diodes from transition metal complexes". En Frontiers in Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/fio.2003.wnn2.

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Latouche, Camille, Vincenzo Barone y Julien Bloino. "ANHARMONIC VIBRATIONAL SPECTROSCOPY ON METAL TRANSITION COMPLEXES". En 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.rc08.

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Xu, Wenying, James N. Demas y Benjamin A. DeGraff, Jr. "Highly luminescent transition metal complexes as sensors". En OE/LASE '94, editado por James A. Harrington, David M. Harris, Abraham Katzir y Fred P. Milanovich. SPIE, 1994. http://dx.doi.org/10.1117/12.180739.

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Malliaras, George G. "Light Emitting Devices from Ionic Transition Metal Complexes". En Frontiers in Optics. Washington, D.C.: OSA, 2005. http://dx.doi.org/10.1364/fio.2005.smb3.

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Chi-Chiu, Ko, Han Jingqi, Cheng Shun-Cheung y Ng Chi-On. "SSpectroscopic study on luminescent mechanochromic transition metal complexes". En Asian Spectroscopy Conference 2020. Institute of Advanced Studies, Nanyang Technological University, 2020. http://dx.doi.org/10.32655/asc_8-10_dec2020.13.

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Demas, J. N. y B. A. DeGraff. "Design Of Transition Metal Complexes As Luminescence Probes". En OE/FIBERS '89, editado por Robert A. Lieberman y Marek T. Wlodarczyk. SPIE, 1990. http://dx.doi.org/10.1117/12.963191.

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Pietschnig, Rudolf, Carmen Moser, Stefan Spirk y Sven Schäfer. "Synthesis and Structure of Transition Metal Bisalkinylselenolato Complexes". En The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01518.

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Informes sobre el tema "Polynuclear Transition Metal Complexes"

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White, Carter James. Selenophene transition metal complexes. Office of Scientific and Technical Information (OSTI), julio de 1994. http://dx.doi.org/10.2172/10190649.

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Sharp, P. R. Late transition metal oxo and imido complexes. Office of Scientific and Technical Information (OSTI), diciembre de 1992. http://dx.doi.org/10.2172/7017245.

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Sharp, P. R. Late transition metal. mu. -oxo and. mu. -imido complexes. Office of Scientific and Technical Information (OSTI), enero de 1990. http://dx.doi.org/10.2172/6332549.

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Sharp, P. Late transition metal. mu. -oxo and. mu. -imido complexes. Office of Scientific and Technical Information (OSTI), enero de 1990. http://dx.doi.org/10.2172/7003275.

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Norton, Jack. The Activation of Hydrogen by First-Row Transition-Metal Complexes. Office of Scientific and Technical Information (OSTI), marzo de 2020. http://dx.doi.org/10.2172/1604425.

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Du, Guodong. Group 4 Metalloporphyrin diolato Complexes and Catalytic Application of Metalloporphyrins and Related Transition Metal Complexes. Office of Scientific and Technical Information (OSTI), enero de 2003. http://dx.doi.org/10.2172/835301.

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Krishnan Balasubramanian. Electronic Structure of Transition Metal Clusters, Actinide Complexes and Their Reactivities. Office of Scientific and Technical Information (OSTI), julio de 2009. http://dx.doi.org/10.2172/959347.

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Meyer, T. J. Excited state processes in transition metal complexes: Redox splitting in soluble polymers. Office of Scientific and Technical Information (OSTI), marzo de 1992. http://dx.doi.org/10.2172/5573491.

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Meyer, T. J. y J. M. Papanikolas. Excited State Processes in Transition Metal Complexes, Redox Splitting in Soluble Polymers. Office of Scientific and Technical Information (OSTI), agosto de 2002. http://dx.doi.org/10.2172/830013.

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Schmehl, Russell H. Energy, Electron Transfer and Photocatalytic Reactions of Visible Light Absorbing Transition Metal Complexes. Office of Scientific and Technical Information (OSTI), marzo de 2016. http://dx.doi.org/10.2172/1240023.

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