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Artykuły w czasopismach na temat "Coordination Chemistry - Non-Transition Metals"

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Salzer, A. "Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)." Pure and Applied Chemistry 71, no. 8 (1999): 1557–85. http://dx.doi.org/10.1351/pac199971081557.

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Organometallic compounds are defined as containing at least one metal-carbon bond between an organic molecule, ion, or radical and a metal. Organometallic nomenclature therefore usually combines the nomenclature of organic chemisty and that of coordination chemistry. Provisional rules outlining nomenclature for such compounds are found both in Nomenclature of Organic Chemistry, 1979 and in Nomenclature of Inorganic Chemistry, 1990This document describes the nomenclature for organometallic compounds of the transition elements, that is compounds with metal-carbon single bonds, metal-carbon multi
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Kostova, Irena. "Anticancer Metallocenes and Metal Complexes of Transition Elements from Groups 4 to 7." Molecules 29, no. 4 (2024): 824. http://dx.doi.org/10.3390/molecules29040824.

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With the progression in the field of bioinorganic chemistry, the role of transition metal complexes as the most widely used therapeutics is becoming a more and more attractive research area. The complexes of transition metals possess a great variety of attractive pharmacological properties, including anticancer, anti-inflammatory, antioxidant, anti-infective, etc., activities. Transition metal complexes have proven to be potential alternatives to biologically active organic compounds, especially as antitumor agents. The performance of metal coordination compounds in living systems is anticipat
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Gallen, Albert, Sílvia Orgué, Guillermo Muller, et al. "Synthesis and coordination chemistry of enantiopure t-BuMeP(O)H." Dalton Transactions 47, no. 15 (2018): 5366–79. http://dx.doi.org/10.1039/c8dt00897c.

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Baumgartner, Judith, and Christoph Marschner. "Coordination of non-stabilized germylenes, stannylenes, and plumbylenes to transition metals." Reviews in Inorganic Chemistry 34, no. 2 (2014): 119–52. http://dx.doi.org/10.1515/revic-2013-0014.

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AbstractComplexes of transition metals with heavy analogs of carbenes (tetrylenes) as ligands have been studied now for some 40 years. The current review attempts to provide an overview about complexes with non-stabilized (having no π-donating substituents) germylenes, stannylenes, and plumbylenes. Complexes are known for groups 4–11. For groups 6–10 not only examples of monodentate tetrylene ligands, but also of bridging ones are known. While this review covers almost 200 complexes, the field in general has been approached only very selectively and real attempts for systematic studies are ver
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Kubas, Gregory J. "Molecular Hydrogen Coordination to Transition Metals." Comments on Inorganic Chemistry 7, no. 1 (1988): 17–40. http://dx.doi.org/10.1080/02603598808072297.

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Bobrov, Sergey V., Andrey A. Karasik, and Oleg G. Sinyashin. "Heterocyclic Phosphorus Ligands in Coordination Chemistry of Transition Metals." Phosphorus, Sulfur, and Silicon and the Related Elements 144, no. 1 (1999): 289–92. http://dx.doi.org/10.1080/10426509908546238.

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Molter, Anja, Julia Kuchar, and Fabian Mohr. "Acylselenoureas, selenosemicarbazones and selenocarbamate esters: Versatile ligands in coordination chemistry." New Journal of Chemistry 46, no. 10 (2022): 4534–49. http://dx.doi.org/10.1039/d2nj00026a.

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M., N. PATEL, and N. JANI B. "Coordination Polymers of some First Row Transition Metals." Journal of Indian Chemical Society Vol. 63, Mar 1986 (1986): 278–80. https://doi.org/10.5281/zenodo.6240907.

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Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388 120 <em>Manuscript received 16 August 1984, revised 3 June 1985, accepted 24 December 1985</em> This paper describes the synthesis and characterisation of some new coordination polymers derived from poly Schiff base (PSB) and first row transition metal ions. Ir study showed that the metal ions are coordinated through oxygen of hydroxy group and nitrogen of adjacent azomethme group. The decomposition temperatures of the polymeric chelates were found to be in the&nbsp;order.&nbsp;Ni&gt;Co&gt;Cu&gt;Mn&nbsp;and the thermal ac
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Fischer, Roland A., and Jurij Weiß. "Coordination Chemistry of Aluminum, Gallium, and Indium at Transition Metals." Angewandte Chemie International Edition 38, no. 19 (1999): 2830–50. http://dx.doi.org/10.1002/(sici)1521-3773(19991004)38:19<2830::aid-anie2830>3.0.co;2-e.

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Holloway, Clive, and Milan Melnik. "Crystallographic and structural characterisation of heterometallic platinum compounds: Part I. Heterobinuclear Pt compounds." Open Chemistry 9, no. 4 (2011): 501–48. http://dx.doi.org/10.2478/s11532-011-0054-2.

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AbstractThis review covers almost 290 heterobinuclear Pt derivatives. When the heterometals (M) are non transition and the binuclear are found both with and without a metal to metal bond. Where M is a transition metal or actinide, only those with a metal-metal bond have been included here. There are thirteen non-transition metals (Sn, Hg, Ge, Sb, Tl, Zn, Pb, Cd, Na, K, Ga, Ca and In). The shortest Pt-M bond distance is 235.2(1) (Pt-Ge). There are eighteen transition metals (Fe, W, Rh, Re, Pd, Ag, Ir, Mo, Mn, Re, Co, Cu, Cr, Au, Ni, Ti, Ta and V). The shortest Pt-M bond distance is 249.5(2) pm
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Rozprawy doktorskie na temat "Coordination Chemistry - Non-Transition Metals"

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Sze-To, Lap, and 司徒立. "The structural chemistry of coordination compounds containing d-block or f-block metals." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B45204470.

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Aucott, Stephen Mark. "Coordination chemistry of aminophosphine ligands." Thesis, Loughborough University, 1999. https://dspace.lboro.ac.uk/2134/34492.

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The reaction of [MCl2(cod)] (M = Pt, Pd) with two equivalents of 2-(diphenylphosphinoamino)pyridine, Ph2PNHpy, in warm acetonitrile led to cationic complexes of the type cis-[MCl(Ph2PNHpy-P,N){Ph2PNHpy-P}][Cl] (M = Pt, Pd) which exhibit broad single 31P{1H} NMR resonances due to their dynamic pyridyl exchange behaviour in solution. A single crystal X-ray diffraction study of the platinum species confirmed the proposed structure and revealed that adjacent complex molecules were held together by hydrogen bonding to the same chloride counter-ion. The bromo- and iodo-cis[MX(Ph2PNHpy-P,N){Ph2PNHpy-
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Chotalia, Rohit. "The synthesis and coordination chemistry of novel oligopyridine ligands." Thesis, University of Cambridge, 1993. https://www.repository.cam.ac.uk/handle/1810/272580.

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Baisya, Siddhartha Sankar. "Coordination chemistry of pteridine ligands with transition and d10 metals." Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/2555.

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Reinhardt, Maxwell James. "Metal complexes containing non-innocent ligands for functional materials." Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/11723.

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The existence of complexes of that display non-innocence has been of interest in the field of coordination chemistry since the investigations of square-planar dithiolene complexes of the late transition metals in the 1960s. The ligands used in these systems are termed “non-innocent” when bound to a number of the late transition metals, because the orbital energy levels are similar to those of the central metal ion. This allows there to be significant electron delocalisation over the complex with the potential for the complexes to exist in a number of electronic states due to the combined elect
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McCart, Mark Kevin. "Some diphosphine chemistry of the transition metals ruthenium, palladium, platinum and nickel." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263849.

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Moneo, Corcuera Andrea. "Bistable molecular materials: triazole-based coordination chemistry of first row transition metals." Doctoral thesis, Universitat Rovira i Virgili, 2019. http://hdl.handle.net/10803/668881.

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En la present tesi doctoral presentem el magnetisme molecular bàsic de compostos de coordinació basats en un lligant di-anionico: (L-2 = 4- (1,2,4-triazole-4-il) etanosulfonato). En particular, vam estudiar el fenomen de transició d'espín d'un trímer de ferro (II) poli-aniònic en diferents escales, des d'una escala macroscòpica ("bulk") fins a nivells moleculars, acabant amb la deposició en superfície. D'una banda, el comportament SCO "macroscòpic" es va modular canviant l'empaquetatge de vidre i la connectivitat entre els trímers amb una estratègia d'intercanvi catiònic. D'altra banda, hem tr
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Jafarpour, Laleh. "New ligands, design and coordination chemistry with the transition metals and lanthanides." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0009/NQ38903.pdf.

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Holmes, Nicholas J. "Synthesis and coordination of stibine and bismuthine ligands with transition metals." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299499.

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Haque, Nadera. "Coordination Chemistry of Barbituric Acid, its Diethyl Derivative and Benzildiimine with Transition Metals." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-115621.

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Książki na temat "Coordination Chemistry - Non-Transition Metals"

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A, Herrmann W., Astruc D, Okuda J, and Zybill Ch, eds. Transition metall [sic] coordination chemistry. Springer-Verlag, 1992.

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1940-, Trautwein Alfred, and Deutsche Forschungsgemeinschaft, eds. Bioinorganic chemistry: Transition metals in biology and their coordination chemistry. Deutsche Forschungsgemeinschaft, 1997.

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Veillard, A., ed. Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9.

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1934-, Veillard A., North Atlantic Treaty Organization. Scientific Affairs Division., and Société de chimie physique. International Meeting, eds. Quantum chemistry: The challenge of transition metals and coordination chemistry. D. Reidel Pub. Co., 1986.

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Yamaguchi, Ryohei. Ligand platforms in homogenous catalytic reactions with metals: Practice and applications for green organic transformations. Wiley, 2015.

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Herrmann, W. A., ed. Transition Metall Coordination Chemistry. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/3-540-54324-4.

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Chi-Ming, Che, and Yam Vivian W. W, eds. Advances in transition metal coordination chemistry. Jai Press, 1996.

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Okuda, J., C. Zybill, Wolfgang A. Herrmann, and D. Astruc. Transition Metal Coordination Chemistry. Springer Berlin / Heidelberg, 2013.

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Housecroft, Catherine E. The Heavier d-Block Metals: Aspects of Inorganic and Coordination Chemistry (Oxford Chemistry Primers, 73). Oxford University Press, USA, 1999.

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(Contributor), D. Astruc, J. Okuda (Contributor), Ch Zybill (Contributor), and W. A. Herrmann (Editor), eds. Transition Metal Coordination Chemistry (Topics in Current Chemistry 160) (Topics in Current Chemistry). Springer, 1992.

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Części książek na temat "Coordination Chemistry - Non-Transition Metals"

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Escudero, Daniel. "Photodeactivation Channels of Transition Metal Complexes: A Computational Chemistry Perspective." In Transition Metals in Coordination Environments. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-11714-6_9.

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Stein, Matthias. "Anisotropic Magnetic Spin Interactions of Transition Metal Complexes and Metalloenzymes from Spectroscopy and Quantum Chemistry." In Transition Metals in Coordination Environments. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-11714-6_2.

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McCleverty, J. A. "Towards Molecular Wires and Switches: Exploiting Coordination Chemistry for Non-Linear Optics and Molecular Electronics." In Transition Metals in Supramolecular Chemistry. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-015-8380-0_14.

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Hirao, Hajime. "Applications of Computational Chemistry to Selected Problems of Transition-Metal Catalysis in Biological and Nonbiological Systems." In Transition Metals in Coordination Environments. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-11714-6_15.

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Hall, Michael B. "Multiple Metal-Metal and Metal-Carbon Bonds." In Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9_28.

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Wedig, Ulrich, Michael Dolg, Hermann Stoll, and Heinzwerner Preuss. "Energy-Adjusted Pseudopotentials for Transition-Metal Elements." In Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9_6.

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Koga, Nobuaki, and Keiji Morokuma. "Transition State for Carbonyl and Olefin Insertion Reactions." In Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9_25.

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Rösch, N., H. Jörg, and B. I. Dunlap. "Applications of the LCGTO-Xα Method to Transition Metal Carbonyls." In Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9_13.

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Walch, Stephen P., and Charles W. Bauschlicher. "The Nature of the Bonding in the Transition Metal Trimers." In Quantum Chemistry: The Challenge of Transition Metals and Coordination Chemistry. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4656-9_9.

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Peruzzini, Maurizio, Isaac De Los Rios, and Antonio Romerosa. "Coordination Chemistry of Transition Metals with Hydrogen Chalcogenide and Hydrochalcogenido Ligands." In Progress in Inorganic Chemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166512.ch3.

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Streszczenia konferencji na temat "Coordination Chemistry - Non-Transition Metals"

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Mudrinić, Tihana, Biljana Pantić, and Predrag Banković. "DEVELOPMENT OF COST-EFFECTIVE ELECTROCATALYST FOR ELECTROCHEMICAL GLUCOSE SENSORS BASED ON ALUMINUM PILLARED CLAY—SUPPORTED COBALT OXIDE." In 17th International Conference on Fundamental and Applied Aspects of Physical Chemistry. Society of Physical Chemists of Serbia, 2024. https://doi.org/10.46793/phys.chem24i.173m.

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There is no doubt that electrochemical glucose sensors have revolutionized the management of diabetes and improved the quality of life of diabetic patients. However, these sensors typically rely on enzymatic-based catalysts, which are thermally and pH unstable or noble metals, which are expensive. Nanostructured non-precious transition metal-based catalysts (NNPTM) are considered promising alternatives. However, NNPTMs also have weaknesses that limit their practical application, such as the agglomeration of nanoparticles and the fact that they can operate only in highly alkaline conditions.
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