Relevant bibliographies by topics / Metal complex

Academic literature on the topic 'Metal complex'

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Published: 4 June 2021
Last updated: 9 March 2023

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Journal articles on the topic "Metal complex"

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Mamedova, Shafa Agаеvna. "METAL COMPLEX CATALYSIS." Globus 7, no. 5(62) (August 4, 2021): 31–33. http://dx.doi.org/10.52013/2658-5197-62-5-7.

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Complexes of transition metals with chiral ligands are considered as catalysts. Among metal-containing organic complexes with semiconducting properties, compounds of the porphin series occupy a special place in electrocatalytic studies. The properties of the porphyrin macrocycle, their role in catalysis, and the influence of the nature of the metal on the catalytic properties of the complex are considered.
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Lisichkin, Georgii V., and A. Ya Yuffa. "Metal complex catalysis." Russian Chemical Reviews 59, no. 12 (December 31, 1990): 1117. http://dx.doi.org/10.1070/rc1990v059n12abeh003580.

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Farzaliyev, V. M., M. P. Bayramov, S. Kh Jafarzadeh, P. Sh Mammadova, E. R. Babayev, and I. M. Eyvazova. "METAL COMPLEX COMPOUNDS AS EFFECTIVE ADDITIVES TO CUTTING FLUIDS." Chemical Problems 17, no. 1 (2019): 81–86. http://dx.doi.org/10.32737/2221-8688-2019-1-81-86.

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de Vekki, Dimitriy Andreevich, and Nikolai Konstantinovich Skvortsov. "METAL COMPLEX CATALYZED HYDROSILYLATION OF VINYL- WITH HYDROSILOXANES (A REVIEW)." Bulletin of the Saint Petersburg State Institute of Technology (Technical University) 19, no. 45 (January 2013): 97–114. http://dx.doi.org/10.15217/issn1998984-9.2013.19.97.

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Peni, Peni, Risya Sasri, and Imelda Hotmarisi Silalahi. "Synthesis of Metal–Curcumin Complex Compounds (M = Na⁺, Mg²⁺, Cu²⁺)." Jurnal Kimia Sains dan Aplikasi 23, no. 3 (March 20, 2020): 75–82. http://dx.doi.org/10.14710/jksa.23.3.75-82.

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Curcumin complex compound, MLn (L = curcumin; M = Na+, Mg2+, Cu2+) has been synthesized from the reaction between curcumin and metal precursors (NaCl, MgSO4.7H2O, CuCl2.2H2O) in ethanol under reflux conditions. Synthesis takes place through the reaction between the metal ions Na+, Mg2+, or Cu2+ as the central atom and curcumin as the ligand. Curcumin has been consumed after the reaction lasts for four hours, shown by thin-layer chromatography in which a new spot appears at higher Rf as the spot of curcumin disappears in the reaction mixture. Compared with the spectrum of curcumin, the FTIR spectra of the complexes show changes in the absorption bands and shifts of wave numbers particularly in absorption bands of phenolic –OH and C=O enol groups which strongly indicates the coordination of metal ions with the curcumin ligand which is proposed to be in β–1,3 diketone system. Also, the FTIR spectra of the reaction product showed typical absorption bands for the metal-oxygen group, M–O, at 524 cm–1, 670 cm–1 and 470 cm–1 in Na+–curcumin, Mg2+–curcumin and Cu2+–curcumin, respectively.
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Bogdanović, Borislav, and Gary Sandrock. "Catalyzed Complex Metal Hydrides." MRS Bulletin 27, no. 9 (September 2002): 712–16. http://dx.doi.org/10.1557/mrs2002.227.

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AbstractComplex hydrides are mixed ionic–covalent compounds that can serve as reversible H2 storage media only when they are catalyzed by a transition metal such as Ti. As the prime example, the phenomenology of Ti-catalyzed sodium alanate (NaAlH4) is reviewed from a historical perspective. Dehydriding yields a theoretical 5.6 wt% H2 during two-step decomposition, NaAlH4 → Na3AlH6 → NaH + Al, although 100% recovery of that H2 is not currently possible. H2 can be discharged and recharged at practical rates at 125°C. More work is needed on the alanates, in particular, as well as the identification and optimization of the catalytic mechanism and a broad extension of the concept to other than Na-based alanates. The possibility of an even further extension of the concept to other complex hydrides (e.g., the borohydrides and transition-metal complexes) is discussed.
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Bronger, Welf. "Complex Transition Metal Hydrides." Comments on Inorganic Chemistry 7, no. 3 (June 1988): 159–70. http://dx.doi.org/10.1080/02603598808072305.

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BAUM, RUDY. "Metal-enterobactin complex characterized." Chemical & Engineering News 70, no. 16 (April 20, 1992): 24. http://dx.doi.org/10.1021/cen-v070n016.p024.

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Hang, Tian, Wen Zhang, Heng-Yun Ye, and Ren-Gen Xiong. "Metal–organic complex ferroelectrics." Chemical Society Reviews 40, no. 7 (2011): 3577. http://dx.doi.org/10.1039/c0cs00226g.

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Bronger, Welf. "Complex Transition Metal Hydrides." Angewandte Chemie International Edition in English 30, no. 7 (July 1991): 759–68. http://dx.doi.org/10.1002/anie.199107591.

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Dissertations / Theses on the topic "Metal complex"

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McQuaid, Michael James. "Spectroscopic characterization of metal-based complexes and metal-based complex oxidation processes." Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/30334.

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Sooksawat, Dhassida. "Transition metal complex-based molecular machines." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/10045.

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Inspired by the performance and evolutionarily-optimised natural molecular machines that carry out all the essential tasks contributing to the molecular basis of life, chemists aim towards fabricating synthetic molecular machines that mimic biological nanodevices. The use of rotaxanes as a prototype for molecular machines has emerged as a result of their ability to undergo translational motion between two or more co-conformations. Although biological machines are capable of complex and intricate functions, their inherent stability and operational conditions are restricted to in vivo. Synthetic systems offer a limitless number of building blocks and a range of interactions to be manipulated. Transition metal-ligand interactions are utilised as one strategy to control the directional movement of submolecular components in artificial machines due to their well-defined geometric requirements and significant strength. This thesis presents new externally addressable and switchable molecular elements for transition metal complexed-molecular machines involving an acid-base switch. The proton input that induces changes to cyclometallated platinum complexes can be exploited to control exchange between different coordination modes. The development of the pH-switchable metal-ligand motif for the stimuli-responsive platinum-complexed molecular shuttle has also been explored. The metal-directed self-assembly of tubular complexes were studied in order to develop self-assembled rotaxanes. A series of metal building blocks was explored to extend the scope for a tube self-assembly.
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McCarthy, David Lee. "Creating Complex Hollow Metal Geometries Using Additive Manufacturing and Metal Plating." Thesis, Virginia Tech, 2012. http://hdl.handle.net/10919/43530.

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Additive manufacturing introduces a new design paradigm that allows the fabrication of geometrically complex parts that cannot be produced by traditional manufacturing and assembly methods. Using a cellular heat exchanger as a motivational example, this thesis investigates the creation of a hybrid manufacturing approach that combines selective laser sintering with an electroforming process to produce complex, hollow, metal geometries. The developed process uses electroless nickel plating on laser sintered parts that then undergo a flash burnout procedure to remove the polymer, leaving a complex, hollow, metal part. The resulting geometries cannot be produced directly with other additive manufacturing systems. Copper electroplating and electroless nickel plating are investigated as metal coating methods. Several parametric parts are tested while developing a manufacturing process. Copper electroplating is determined to be too dependent on the geometry of the part, with large changes in plate thickness between the exterior and interior of the tested parts. Even in relatively basic cellular structures, electroplating does not plate the interior of the part. Two phases of electroless nickel plating combined with a flash burnout procedure produce the desired geometry. The tested part has a density of 3.16g/cm3 and withstands pressures up to 25MPa. The cellular part produced has a nickel plate thickness of 800µm and consists of 35% nickel and 65% air (empty space). Detailed procedures are included for the electroplating and electroless plating processes developed.
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Schnepp, Zoé. "Control of morphology in complex metal oxides." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.504239.

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The exceptional electronic, magnetic, optical and catalytic properties demonstrated by many ceramic materials when confined to the nano-scale are well established. However, the synthesis of complex metal oxide nanowires and nanoparticles is notoriously problematic due to the difficulty of controlling homogeneity and achieving the correct stoichiometry. This thesis describes a new paradigm in solid-state synthesis. By organizing precursor metal cations within a gel of the structural biopolymer alginate. initial nucleation of preceramic crystalline phases is restricted to the nano-scale. On further calcination, the decomposition products of the biopolymer prevent sintering of these nanoparticles before the final crystallographic transformation to the ceramic product.
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Yao, Jing Wen. "Systematic structural studies in metal complex chemistry." Thesis, Durham University, 1998. http://etheses.dur.ac.uk/5055/.

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A procedure is presented for detecting geometrical preferences, deformations and interconversion pathways between different geometries for the transition metal coordination sphere ML(_n). A discrepancy index [R(_ang)(x)] was proposed initially to address the problems of dimensionality and permutation complexity in the systematic analysis of coordination sphere geometry with higher coordination numbers (n > 7). But it can also be used generally for the lower coordination numbers. A set of standard geometries for coordination numbers 2-9 are presented and the angles between the center point and each vertex for the polyhedra which are used to describe the coordination sphere geometries for coordination numbers 7-9 are idealised. These angles correspond to the metal-ligand valence angles in the coordination complex and are used as the standard values to measure the deviation of a real coordination sphere in the complex from these standard polyhedra. Geometry of each coordination sphere (ML(_7-9)) from the Cambridge Structural Database (CSD) is identified by the calculations of R(_ang)(x) values. Also the unique enumeration numbers of the ligands corresponding to each geometry can be derived over the n! ligand permutations. The different geometrical clusters and interconversion pathways from one to another are mapped in a designed two-dimensional plot. The symmetry coordinates and principal component analysis are initially applied in these higher coordination number systems. They not only map the clusters represented to those standard geometries in the different symmetric point groups but also provide and confirm the interconversion pathways between the different geometries. The other systematic study involves the analysis and correlation of the metal σ-π bond in the transition metal alkyne and alkene complexes from the CSD. Geometrical features of this specific bond are examined in the view of structure and some useful correlation between the key geometrical parameters are defined. Finally, X-ray crystal structure determinations are briefly described and the crystal structures of ten transition metal compounds in coordination numbers 4-6 are presented.
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Monti, Mauro. "Metal ligand complex syntheses for imaging applications." Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/101041/.

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This thesis describes an investigation into the roles and effects of nitrogen-donor chelating ligands and complexes containing metal centres as tools for molecular imaging. Chapter 1 gives a brief introduction to Positron Emission Tomography (PET) imaging,the radionuclides and metal centres currently available for therapeutic use, and a discussion and comparison between metal and organic-based contrast agents. Chapter 1 also contains an introduction to macrocycles and their role as ligands, with particular focus on azamacrocycles and their applications. Finally, a brief introduction to luminescence spectroscopy and optical imaging is made. Chapter 2 reports the synthetic procedures used, and gives characterisation data for the compounds synthesised and discussed in subsequent chapters. Chapter 3 investigates the role of the triazine core of the azamacrocycles, showing some compounds of biological interest and the synthesis of new ligands and complexes based on a tetraazamacrocycle (DO3A) moiety with a triazine core. One example has been successfully used to study the coordination chemistry and structure of different metal centres, while another has shown promise with a potential application in mimicking dipyridamole compounds. Moreover it has been conducted a study to determinate the empirical formula and the nature of the complexes in solution. Chapter 4 contains an introduction to the benzothiazole group, which has relevance in the study of Alzheimer's disease as it is a biological marker for metal-dependant formation of Aβ plaques. The synthesis of new ligands derived from several macrocycles (including those reported earlier, and those containing an acyclic moiety with a benzothiazole core) are reported, including procedures to produce complexes of lanthanides and PET-active metal centres including copper, vanadium and gallium. Benzothiazole ligands and complexes have been characterised by fluorimetry, allowing discussion of the role of the ligand.
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Yadnum, Sudarat. "Tailoring complex heterogeneous metal-organic framework structures." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0299/document.

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Dans cette thèse, de nouvelles stratégies pour la préparation de matériaux de type Metal-Organic-Frameworks (MOF) ont été étudiés et développés. L’électrodeposition bipolaire indirecte (IBED) a été utilisé pour préparer ZIF-8 et HKUST-1 sur des substrats métalliques de façon simple et avec une sélectivité spatiale. Ce concept devrait pouvoir être généralisée pour la synthèse de nombreux autres composés MOF, permettant ainsi une synthèse pas chère et verte, conduisant à de nouvelles générations de composites de type Janus basés sur des MOFs. En outre, des électrodes avec une structure hiérarchique macro-/ microporeux de HKUST-1 ont été préparées par une technique de dissolution-dépôt électrochimique. L'approche de synthèse mis au point est très pratique en ce qui concerne la durée des expériences, et ouvre diverses applications pour les MOFs. Enfin des nanoparticules de métaux nobles sur un substrat à base de MIL-101 ont été préparées comme la dernière partie de l'étude expérimentale par dépôt colloïdal. Ce concept peut être généralisé pour la synthèse d'autres composites nanoparticules métalliques / MOF, et pourrait améliorer l'activité catalytique des MOFs. En dehors de l'étude expérimentale, afin de comprendre mieux la catalyse de matériaux MOF, le comportement catalytique de Cu (II) dans le MOF-505 a été théoriquement étudié pour la réaction d'aldolisation Mukayiama par la théorie de densité fonctionnelle et comparé à celui d'un autre catalyseur, Cu-ZSM-5. En outre, le comportement catalytique d'amas homo- et hétéro-bimétalliques, qui sont des complexes métalliques qui représentent les agrégats métalliques dans les MOFs, a également été étudié théoriquement pour la réaction de cycloaddition de dioxyde de carbone et des oxydes d'éthylène
In this thesis, new strategies for the preparation of Metal 0rganic Frameworks (MOF) materials with designed structures were studied and developed. Indirect bipolar electrodeposition (IBED) was used to prepare ZIF-8 and HKUST-1 on metal substrates in a straightforward and site-selective way. This concept is expected to be able to be generalized for the synthesis of many other MOF compounds, thus allowing a cheap and green synthesis, leading to new generations of MOF-based Janus-type composites. Furthermore, rationally designed hierarchical macro-/microporous HKUST-1 electrodes were prepared via an electrochemical dissolution-deposition technique. The developed synthesis approach is very practical in terms of the time consumption, and opens up MOFs for various applications. Finally, MIL-101-supported noble metal nanoparticles were prepared as the last part of the experimental studies via a simple colloidal deposition technique. This concept might be generalized for the synthesis of other metal nanoparticle/MOF composites, and might improve the catalytic activity of MOFs. Apart from the experimental study, in order to gain a deeper insight into the catalysis of MOF materials, the catalytic behavior of Cu(II) in the paddle-wheel unit of MOF-505 was theoretically investigated for the Mukaiyama aldol reaction via the density functional theory and compared to that of another catalyst, Cu-ZSM-5 zeolite. Besides, the catalytic behavior of homo-metallic clusters and hetero-bimetallic clusters, that are the metal complexes representing the metal clusters in MOFs, were also theoretically investigated for the cycloaddition reaction of carbon dioxide and ethylene oxides
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Perenlei, Ganchimeg. "Energy band engineering of complex metal oxides." Thesis, Queensland University of Technology, 2015. https://eprints.qut.edu.au/90056/1/Ganchimeg_Perenlei_Thesis.pdf.

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This doctoral studies focused on the development of new materials for efficient use of solar energy for environmental applications. The research investigated the engineering of the band gap of semiconductor materials to design and optimise visible-light-sensitive photocatalysts. Experimental studies have been combined with computational simulation in order to develop predictive tools for a systematic understanding and design on the crystal and energy band structures of multi-component metal oxides.
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Gourdon, André. "Synthèse et étude structurale de clusters de fer contenant un hétéroatome du type carbure, nitrure, phosphure." Paris 6, 1986. http://www.theses.fr/1986PA066404.

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Jones, Michael David. "Trimethylenemethane and oxodimethylenemethane metal complexes." Thesis, University of Leicester, 1986. http://hdl.handle.net/2381/33764.

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Chapter 1 reviews the literature concerning trimethylenemethane and oxodimethylenemethane metal complexes and their r?le in organic synthesis. The preparation and characterisation of ?4-trimethylenemethane metal complexes of iridium, rhodium, osmium and ruthenium are presented in Chapter 2, together with the molecular structure of three of these complexes which establishes the presence of the ?4-trimethylenemethane ligand. The room temperature 1H n.m.r. spectra show the expected features for a static structure and no sign of rotation of the trimethylenemethane ligand was observed at higher temperatures. Preliminary investigation into the reactivity of these trimethylenemethane complexes is detailed in Chapter 3. A series of cationic ?4-trimethylenemethane complexes are prepared by the reaction of [Ir{?4-C(CH2)3}C1 (CO)(PPh3)] with silver hexafluorophosphate in the presence of a donor ligand such as carbon monoxide or ethene. The reactions of these cationic complexes with neutral and anionic nucleophiles are investigated and show that displacement of other donor ligands or attack on co-ordinated carbonyl and ethene ligands occurs, rather than attack at, or displacement of the trimethylenemethane ligand. Chapter 4 describes the reaction of 3-trimethylsilyl-2-(methyl- sulphonyloxymethyl) prop-l-ene with d10-metal complexes of platinum, palladium and nickel. The isolation of ?3-2-trimethylsilylmethylallyl palladium and platinum complexes are of interest since they are postulated intermediates implicated in the generation of the catalytic species [Pd (?3-trimethylenemethane) (PPh3)2]. The d10 -nickel complex [Ni{P(OEt)3}4] catalyses the cycloaddition of trimethylenemethane to electron-deficient alkenes and imines, the latter reaction affords a high yield synthesis of 4-methylenepyrrolidines. The final Chapter describes the reactions of 3-chloro-l-(trimethyl-silyl)propan-2-one and 3-chloro-2-(trimethylsiloxy)prop-l-ene with low-valent metal complexes to afford oxodimethylenemethane complexes of platinum, iridium, and osmium. The molecular structure of two of these complexes establishes the presence of an ?3-oxodimethylenemethane ligand. The silylenol ether, 3-chloro-2-(trimethylsiloxy)prop-l-ene was readily prepared from 3-chloro-l-(trimethylsilyl)propan-2-one, the isomerisation being catalysed by a number of low-valent metal complexes.
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Books on the topic "Metal complex"

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Tomasik, Piotr. Pyridine-metal complexes. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. New York: Wiley, 1985.

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S, Abd-El-Aziz Alaa, ed. Metal-coordination polymers. Hoboken, N.J: Wiley, 2005.

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Sau, Tapan K., and Andrey L. Rogach, eds. Complex-Shaped Metal Nanoparticles. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527652570.

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Hadjiliadis, Nick, and Einar Sletten, eds. Metal Complex–DNA Interactions. Chichester, UK: John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9781444312089.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. New York: Wiley, 1985.

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Tomasik, Piotr. Pyridine-metal complexes. Edited by Ratajewicz Zbigniew, Newkome George R, and Strekowski Lucjan. New York: Wiley, 1985.

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Zbigniew, Ratajewicz, Newkome George R, and Strękowski Lucjan, eds. Pyridine-metal complexes. New York: Wiley, 1985.

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Book chapters on the topic "Metal complex"

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Namba, Kenryo. "Metal Complex Dyes." In Infrared Absorbing Dyes, 57–70. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2046-1_6.

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Chakraborty, J. N. "Dye, Metal Complex." In Encyclopedia of Color Science and Technology, 1–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-27851-8_197-1.

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Chakraborty, J. N. "Dye, Metal Complex." In Encyclopedia of Color Science and Technology, 605–15. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4419-8071-7_197.

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Page, E. M., and D. A. Rice. "Wiih Complex Metal Halides." In Inorganic Reactions and Methods, 232. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch150.

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Jessop, Philip, and Walter Leitner. "Metal-Complex-Catalyzed Reactions." In Chemical Synthesis Using Supercritical Fluids, 351–87. Weinheim, Germany: Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527613687.ch17.

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Kustin, Kenneth, and James Swinehart. "Fast Metal Complex Reactions." In Progress in Inorganic Chemistry, 107–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166147.ch2.

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Hikita, Yasuyuki, and Harold Y. Hwang. "Complex Oxide Schottky Junctions." In Thin Film Metal-Oxides, 169–204. Boston, MA: Springer US, 2009. http://dx.doi.org/10.1007/978-1-4419-0664-9_5.

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Sau, Tapan K., and Andrey L. Rogach. "Colloidal Synthesis of Noble Metal Nanoparticles of Complex Morphologies." In Complex-Shaped Metal Nanoparticles, 7–90. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527652570.ch1.

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Herrmann, Anne-Kristin, Nadja C. Bigall, Lehui Lu, and Alexander Eychmüller. "Ordered and Nonordered Porous Superstructures from Metal Nanoparticles." In Complex-Shaped Metal Nanoparticles, 339–59. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527652570.ch10.

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Noguez, Cecilia, and Ana L. González. "Localized Surface Plasmons of Multifaceted Metal Nanoparticles." In Complex-Shaped Metal Nanoparticles, 361–93. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527652570.ch11.

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Conference papers on the topic "Metal complex"

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KUZIN, Evgenii, Natalya KRUCHININA, Julia AVERINA, Andrey KURBATOV, and Tatyana NOSOVA. "Obtaining complex coagulants from waste OF metallurgical plants." In METAL 2020. TANGER Ltd., 2020. http://dx.doi.org/10.37904/metal.2020.3451.

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Brewer, Karen J., Shawn Swavey, Rodd L. Williams, Zhenglai Fang, and Elizabeth R. Bullock. "Designing mixed-metal supramolecular complexes." In Complex Adaptive Structures, edited by William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446777.

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Šmátralová, Magdalena, Petr Čížek, and Ladislav Kander. "COMPLEX EVALUATION OF STRUCTURE AND MATERIAL PROPERTIES OF SELECTED WELDING JOINTS." In METAL 2020. TANGER Ltd., 2020. http://dx.doi.org/10.37904/metal.2020.3520.

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VORON, Mykhailo, Yuriy KOSTETSKY, and Marina FON PRUSS. "GETTING A COMPLEX MASTER ALLOY FOR ALLOYING HIGH-MANGANESE STEELS AND CAST ALUMINUM ALLOYS." In METAL 2020. TANGER Ltd., 2020. http://dx.doi.org/10.37904/metal.2020.3458.

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ANASIEI, Ioana, Ioana Cristina BADEA, Beatrice Adriana SERBAN, Mihai Tudor OLARU, Denisa VONICA, Lidia LICU, Marian BURADA, and Dumitru MITRICA. "RESEARCHES REGARDING STRUCTURAL CHARACTERISTICS OF A NEW COMPLEX CONCENTRATED ALLOY OBTAINED BY RAPID SOLIDIFICATION." In METAL 2021. TANGER Ltd., 2021. http://dx.doi.org/10.37904/metal.2021.4225.

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Swavey, Shawn, Rodd L. Williams, Zhenglai Fang, Matthew Milkevitch, and Karen J. Brewer. "DNA binding of supramolecular mixed-metal complexes." In Complex Adaptive Structures, edited by William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446779.

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KUZIN, Evgenii, Natalya KRUCHININA, and Tatyana NOSOVA. "COMPLEX TITANIUM-CONTAINING REAGENTS IN THE PROCESSES OF WASTE WATER TREATMENT IN THE METALLURGICAL INDUSTRY." In METAL 2021. TANGER Ltd., 2021. http://dx.doi.org/10.37904/metal.2021.4215.

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KLIMECKA-TATAR, Dorota, and Renata DWORNICKA. "THE ASSEMBLY PROCESS STABILITY ASSESSMENT BASED ON THE STRENGTH PARAMETERS STATISTICAL CONTROL OF COMPLEX METAL PRODUCTS." In METAL 2019. TANGER Ltd., 2019. http://dx.doi.org/10.37904/metal.2019.870.

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ZAMOZDRA, Maxim, Sergey GANIN, and Valery TSEMENKO. "PHYSICAL MODELING OF HOT PLASTIC DEFORMATION PROCESS OF POWDER HIGH-SPEED STEEL ON THE GLEEBLE 3800 COMPLEX." In METAL 2020. TANGER Ltd., 2020. http://dx.doi.org/10.37904/metal.2020.3504.

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Syvänen, T., O. Nyrhilä, J. Kotila, and J.-E. Lind. "Direct metal laser sintering of complex metal structures." In ICALEO® 2001: Proceedings of the Laser Materials Processing Conference and Laser Microfabrication Conference. Laser Institute of America, 2001. http://dx.doi.org/10.2351/1.5059928.

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Reports on the topic "Metal complex"

1

Sharp, Paul. Late transition metal m-or chemistry and D6 metal complex photoeliminations. Office of Scientific and Technical Information (OSTI), July 2015. http://dx.doi.org/10.2172/1313940.

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Davis, Benjamin. REDOX FLOW BATTERY HAVING METAL-LIGAND COMPLEX. Office of Scientific and Technical Information (OSTI), December 2020. http://dx.doi.org/10.2172/1739916.

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Dr. Henry Bass and Dr. J. R. Gladden. Resonant Ultrasound Studies of Complex Transition Metal Oxides. Office of Scientific and Technical Information (OSTI), August 2008. http://dx.doi.org/10.2172/936503.

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Gates, B. C. Characterization of the metal-support interface in supported metal and supported metal complex catalysts. [Final report]. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10191456.

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WALTERS, R. A General Initial Decomposition Reaction for Complex Metal Hydrides. Office of Scientific and Technical Information (OSTI), November 2004. http://dx.doi.org/10.2172/836748.

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White, James Lawrence, Takuji Ohigashi, Keith G. Ray, Yi-Sheng Liu, Vitalie Stavila, Mark D. Allendorf, and Jinghua Guo. Phase Evolution of Complex Metal Hydrides During De/Rehydrogenation. Office of Scientific and Technical Information (OSTI), March 2018. http://dx.doi.org/10.2172/1515146.

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Schmehl, Russell, and Igor Rubtsov. Transition Metal Complex/Polymer Systems as Optical Limiting Materials. Fort Belvoir, VA: Defense Technical Information Center, May 2013. http://dx.doi.org/10.21236/ada584374.

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Chung, Whasun Oh. Titanate-Metal Complex as a Novel Antimicrobial in Dentistry. Science Repository, July 2018. http://dx.doi.org/10.31487/j.dobcr.2018.02.003.

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Talu, Orhan, and Surendra N. Tewari. Sub-Nanostructured Non Transition Metal Complex Grids for Hydrogen Storage. Office of Scientific and Technical Information (OSTI), October 2007. http://dx.doi.org/10.2172/918886.

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Mackenzie L. Gorham and John D. Bess. GROTESQUE: Complex Geometric Arrangement of Unreflected HEU (93.15) Metal Pieces. Office of Scientific and Technical Information (OSTI), September 2011. http://dx.doi.org/10.2172/1042364.

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