Academic literature on the topic 'Transition metal organic compounds'

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Journal articles on the topic "Transition metal organic compounds"

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Frazier, C. C., M. A. Harvey, M. P. Cockerham, H. M. Hand, E. A. Chauchard, and Chi H. Lee. "Second-harmonic generation in transition-metal-organic compounds." Journal of Physical Chemistry 90, no. 22 (October 1986): 5703–6. http://dx.doi.org/10.1021/j100280a046.

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Salzer, A. "Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)." Pure and Applied Chemistry 71, no. 8 (August 30, 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 multiple bonds as well as complexes with unsaturated molecules (metal-p-complexes).Organometallic compounds are considered to be produced by addition reactions and so they are named on an addition principle. The name therefore is built around the central metal atom name. Organic ligand names are derived according to the rules of organic chemistry with appropriate endings to indicate the different bonding modes. To designate the points of attachment of ligands in more complicated structures, the h, k, and m-notations are used. The final section deals with the abbreviated nomenclature for metallocenes and their derivatives.ContentsIntroduction Systems of Nomenclature2.1 Binary type nomenclature 2.2 Substitutive nomenlcature 2.3 Coordination nomenclature Coordination Nomenclature3.1 General definitions of coordination chemistry 3.2 Oxidation numbers and net charges 3.3 Formulae and names for coordination compounds Nomenclature for Organometallic Compounds of Transition Metals 4.1 Valence-electron-numbers and the 18-valence-electron-rule 4.2 Ligand names 4.2.1 Ligands coordinating by one metal-carbon single bond 4.2.2 Ligands coordinating by several metal-carbon single bonds 4.2.3 Ligands coordinating by metal-carbon multiple bonds 4.2.4 Complexes with unsaturated molecules or groups 4.3 Metallocene nomenclature
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Wang, Jianbo. "When diazo compounds meet with organoboron compounds." Pure and Applied Chemistry 90, no. 4 (March 28, 2018): 617–23. http://dx.doi.org/10.1515/pac-2017-0713.

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AbstractTransition-metal free reactions of diazo compounds with organoboron compounds provide some unique approaches for the formation of C–C, C–B and C–Si bonds. WithN-tosylhydrazones as the precursors for non-stabilized diazo compound, this type of reaction becomes practically useful in organic synthesis. Transition-metal-free synthetic methodologies for borylation,gem-diborylation,gem-silylborylation arylation, 2,2,2-trifluoroethylation andgem-difluorovinylation have been successfully developed.
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OGAWA, Akiya, and Noboru SONODA. "Transition Metal-Catalyzed Reactions of Chalcogen Compounds." Journal of Synthetic Organic Chemistry, Japan 51, no. 9 (1993): 815–25. http://dx.doi.org/10.5059/yukigoseikyokaishi.51.815.

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Arisawa, Mieko, and Masahiko Yamaguchi. "Transition-metal-catalyzed synthesis of organosulfur compounds." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 993–1003. http://dx.doi.org/10.1351/pac200880050993.

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Rhodium complexes are efficient catalysts for the synthesis of organosulfur compounds. They catalyze the addition reaction of organosulfur groups to unsaturated compounds, the substitution of C-H with organosulfur groups, and single-bond metathesis reactions. They cleave S-S bonds and transfer the organosulfur groups to various organic and inorganic molecules, including alkynes, allenes, disulfides, sulfur, isonitriles, imines, diphosphines, thiophosphinites, hydrogen, 1-alkylthio-1-alkynes, thioesters, and allyl sulfides.
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Barata-Vallejo, Sebastián, Damian E. Yerien, Beatriz Lantano, and Al Postigo. "Transition Metal-free Photoorganocatalytic Fluoroalkylation Reactions of Organic Compounds." Current Organic Chemistry 20, no. 27 (October 28, 2016): 2838–47. http://dx.doi.org/10.2174/1385272820666160614080432.

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Arisawa, Mieko. "Transition-Metal-Catalyzed Synthesis of Organophosphorus Compounds Involving P–P Bond Cleavage." Synthesis 52, no. 19 (July 7, 2020): 2795–806. http://dx.doi.org/10.1055/s-0040-1707890.

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Organophosphorus compounds are used as drugs, pesticides, detergents, food additives, flame retardants, synthetic reagents, and catalysts, and their efficient synthesis is an important task in organic synthesis. To synthesize novel functional organophosphorus compounds, transition-metal-catalyzed methods have been developed, which were previously considered difficult because of the strong bonding that occurs between transition metals and phosphorus. Addition reactions of triphenylphosphine and sulfonic acids to unsaturated compounds in the presence of a rhodium or palladium catalyst lead to phosphonium salts, in direct contrast to the conventional synthesis involving substitution reactions of organohalogen compounds. Rhodium and palladium complexes catalyze the cleavage of P–P bonds in diphosphines and polyphosphines and can transfer organophosphorus groups to various organic compounds. Subsequent substitution and addition reactions proceed effectively, without using a base, to provide various novel organophosphorus compounds.1 Introduction2 Transition-Metal-Catalyzed Synthesis of Phosphonium Salts by Addition Reactions of Triphenylphosphine and Sulfonic Acids3 Rhodium-Catalyzed P–P Bond Cleavage and Exchange Reactions4 Transition-Metal-Catalyzed Substitution Reactions Using Diphosphines4.1 Reactions Involving Substitution of a Phosphorus Group by P–P Bond Cleavage4.2 Related Substitution Reactions of Organophosphorus Compounds4.3 Substitution Reactions of Acid Fluorides Involving P–P Bond Cleavage of Diphosphines5 Rhodium-Catalyzed P–P Bond Cleavage and Addition Reactions6 Rhodium-Catalyzed P–P Bond Cleavage and Insertion Reactions Using Polyphosphines7 Conclusions
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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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Mhaske, Santosh, and Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes." Synthesis 50, no. 01 (November 22, 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.

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The plethora of transformations attainable by the transition-metal-catalyzed reactions of arynes has found immense contemporary interest in the scientific community. This review highlights the scope and importance of transition-metal-catalyzed aryne reactions in the field of synthetic organic chemistry reported to date. It covers transformations achieved by the combination of arynes and various transition metals, which provide a facile access to a biaryl motif, fused polycyclic aromatic compounds, different novel carbocycles, various heterocycles, and complex natural products.1 Introduction2 Insertion of Arynes3 Annulation of Arynes4 Cycloaddition of Arynes5 Multicomponent Reactions of Arynes6 Miscellaneous Reactions of Arynes7 Total Synthesis of Natural Products Using Arynes8 Conclusion
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Brunner, Henri, Andreas Winter, and Bernhard Nuber. "Optically active transition metal compounds 114." Journal of Organometallic Chemistry 558, no. 1-2 (May 1998): 213–18. http://dx.doi.org/10.1016/s0022-328x(98)00412-4.

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Dissertations / Theses on the topic "Transition metal organic compounds"

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Robertson, A. H. Jean. "Properties of CH bonds in alkyl transition metal compounds." Thesis, University of Aberdeen, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241468.

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This Thesis describes the results of a detailed vibrational study of a representative series of methyl and ethyl derivatives of transition metals. The primary objective of the work was to show that vibrational frequency data can be used to provide information on CH bond lengths, HCH angles and alkyl group geometries with an accuracy and reliability which is not readily attainable by other methods, and that the vibrational technique is generally applicable to a wide variety of organometallic compounds. The work involved the preparation of protonated, partially deuterated and fully deuterated examples of the molecules studied and made particular use of correlations between 'isolated' CH stretching frequencies, v15CH, measured in partially deuterated systems, and CH bond length and HCH angles. In the case of MeM(CO)2Cp (M = Fe,Ru), it is shown that, unlike related molecules of this type, the results show no evidence for a high barrier to internal rotation of the methyl group. The titanium compound MeTiCl2Cp, is shown to be non-agnostic, with the only unusual feature being an unusually low δ5CH3 frequency. In the ethyl series preliminary studies necessitated a careful re-examination of the accepted assignments for ethyl halides, leading to changes in some cases. Following this, detailed assignments are made, wherever possible, for the ethyl metal compounds, with particular emphasis on the CH stretching region. In all of the ethyl metal compounds, the α and β-CH bonds are considerably longer, and weaker, than those in the ethyl halides, and the terminal methyl group invariably contains two dissimilar types of CH bond, differing in the CH stretching frequency by as much as 58cm-1. The longer CH bonds in these ethyl compounds are trans to the metal atoms and are amongst the weakest to have been identified in alkyl metal systems.
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McIntosh, Alan Paton. "Reaction of phosphorus containing compounds with transition metal multiple bonds." Thesis, University of Edinburgh, 1988. http://hdl.handle.net/1842/30483.

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Yu, Yaqin Albrecht-Schmitt Thomas E. "Studies on the structures and properties of bimetallic uranium transition metal and hybrid organic-inorganic compounds." Auburn, Ala, 2009. http://hdl.handle.net/10415/1748.

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Graham, Andrew J. "Studies of the reactions of perfluoroarylborane Lewis acids with transition metal compounds." Thesis, University of Oxford, 1998. https://ora.ox.ac.uk/objects/uuid:1253189a-b593-496d-8fde-e9a994dc9fd1.

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This thesis describes the preparation of strongly electrophilic boranes and their reactivity with transition metal compounds. Chapter One presents an overview of the reactivity of boron-containing Lewis acids as found in the literature focusing primarily on reactions of electrophiles containing a boron-perfluoroaryl bond that are of synthetic rather than catalytic interest. Chapter Two presents studies into the reactivity of boranes of the general formula RB(C6F5)2 [R = (C6F5), Ph, H or Cl] with some metallocene hydrides. The previously synthesised adduct [(η5-C5H5)2Mo(H)(η1-HB(C6F5)3)] has been further investigated and the analogous adduct of HB(C6F5)2 is also reported. The zwitterionic compounds [(η5-C5H4B(C6F5)2R)(η5-C5H5)WH3] {R = (C6F5), Ph, H or Cl*} and [(η5-C5H4B(C6F5)3)(η5-C5H5)ReH2] are described and have been fully characterised (* indicates that an X-ray crystal structure was obtained). Investigations into the reactivity of these compounds towards competing Lewis bases have been undertaken and reveal that the rhenium zwitterion is considerably more stable than the tungsten analogues. Chapter Three presents reactions between B(C6F5)3 and transition metal nitrido complexes. B(C6F5)3 reacts directly with a number of nitrido compounds; [{(C66F5)3BN}Re(PR3)(S2CNR'2)2] (R3 = MePh2 and R' = Et*; R3 = Me2Ph and R' = Me*), [{(C6F5)3BN}ReCl(PMePh2)2(S2CNMe2)], [{(C6F5)3BN}Mo(S2CNR2)3] (R = Me or Et) and [{(C66F5)3BN}Os(1,2-S2C6H4)2][nBu4N] have all been prepared (* indicates that an X-ray crystal structure has been obtained). The reactivity of these adducts towards competing Lewis bases has been probed revealing a range of stabilities over the three metals considered. The adduct of an osmium nitrido compound has also been reacted with competing Lewis acids and the compound [{(C6F5)3BN}Os(1,2- (S)(SMe)C6H4)(1,2-S2C6H4)] has been made and characterised by NMR spectroscopy. Chapter Four describes the synthesis of Lewis acids containing a boronperfluoroaryl bond. Firstly, modified literature preparations of RB(C6F5)2 [R = (C6F5), Cl or H] are reviewed. Attempts to prepare the new Lewis acid BAr'3 [Ar' = (3,5- C6H3(CF3)2)] are described, including the synthesis and characterisation of the new tin reagent nBu3SnAr'. Additionally, the new electrophile B(C6H5)(C6F5)2 has been prepared using either nBu3Sn(C6F5) or [LiC6F5] as the source of (C6F5). Chapter Five contains experimental details for the thesis, characterising data for new compounds are presented in Chapter Six and details of the X-ray crystal structures may be found in the Appendices.
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Grill, Joseph Michael. "The design of new ligands and transition metal compounds for the oxidation of organic compounds." [College Station, Tex. : Texas A&M University, 2006. http://hdl.handle.net/1969.1/ETD-TAMU-1746.

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McMorn, Paul. "Oxidation of selected organic compounds using transition metal containing silicates and aluminophosphates." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266048.

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Thu, Hung-yat. "Catalytic C-H bond functionalization reactions catalyzed by rhodium(III) porphyrin, palladium(II) and platinum(II) acetate complexes." View the Table of Contents & Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B38027872.

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Park, Jaena [Verfasser], and Rüdiger [Akademischer Betreuer] Klingeler. "High-field Electron Spin Resonance study on Correlated Transition Metal Compounds and Metal-Organic Compounds / Jaena Park ; Betreuer: Rüdiger Klingeler." Heidelberg : Universitätsbibliothek Heidelberg, 2015. http://d-nb.info/1180608984/34.

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Carson, Cantwell G. "Noble and transition metal aromatic frameworks synthesis, properties, and stability /." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29657.

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Thesis (Ph. D.)--Materials Science and Engineering, Georgia Institute of Technology, 2009.
Committee Chair: Rina Tannenbaum; Committee Co-Chair: Rosario A. Gerhardt; Committee Member: E. Kent Barefield; Committee Member: Karl I. Jacob; Committee Member: Preet Singh; Committee Member: R. Bruce King. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Gegham, Galstyan [Verfasser]. "Computation of Protonation Patterns for Organic Compounds and Transition Metal Complexes / Galstyan Gegham." Berlin : Freie Universität Berlin, 2014. http://d-nb.info/1060368153/34.

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Books on the topic "Transition metal organic compounds"

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McQuillin, F. J. Transition metal organometallics for organic synthesis. Cambridge: Cambridge University Press, 1991.

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Brandsma, L. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1998.

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1940-, Vasilevsky S. F., and Verkruijsse H. D, eds. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1999.

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Jongh, L. J. Magnetic Properties of Layered Transition Metal Compounds. Dordrecht: Springer Netherlands, 1990.

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Brandsma, Lambert. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1998.

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Transition metals in the synthesis of complex organic molecules. Mill Valley, Calif: University Science Books, 1994.

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G, Söderberg Björn C., ed. Transition metals in the synthesis of complex organic molecules. 3rd ed. Sausalito, Calif: University Science Books, 2009.

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Transition metals in the synthesis of complex organic molecules. 2nd ed. Sausalito, Calif: University Science Books, 1999.

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Petrus Adrianus Johannes Marinus Angevaare. Surface chemistry of oxygen containing organic compounds on oxides. Gravenhage: Pasmans Offsetdrukkerij BV, 1991.

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Kazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2012.

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Book chapters on the topic "Transition metal organic compounds"

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Brunner, Henri. "Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts and Transition Metal Compounds." In Organometallics in Organic Synthesis 2, 277–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74269-9_15.

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Kotz, John C. "The Electrochemistry of Transition Metal Organometallic Compounds." In Topics in Organic Electrochemistry, 81–176. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4899-2034-8_3.

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Shimada, Shigeru, and Maddali L. N. Rao. "Transition-Metal Catalyzed C–C Bond Formation Using Organobismuth Compounds." In Bismuth-Mediated Organic Reactions, 199–228. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_202.

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Brandsma, L., H. D. Verkruijsse, and S. F. Vasilevsky. "Procedures for the Preparation of Halogen Compounds." In Application of Transition Metal Catalysts in Organic Synthesis, 19–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0_2.

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Iwasawa, Nobuharu, and Koichi Narasaka. "Transition Metal Promoted Ring Expansion of Alkynyl- and Propadienylcyclopropanes." In Small Ring Compounds in Organic Synthesis VI, 69–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48255-5_2.

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Tolman, Chadwick A., and Norman Herron. "The Oxidation of Organic Compounds by Metal Complexes in Zeolites." In Oxygen Complexes and Oxygen Activation by Transition Metals, 293–303. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0955-0_21.

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Suginome, Michinori, and Toshimichi Ohmura. "Transition Metal-Catalyzed Element-Boryl Additions to Unsaturated Organic Compounds." In Boronic Acids, 171–212. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639328.ch3.

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Gray, Gary M., and Christopher M. Lawson. "Structure-Property Relationships in Transition Metal-Organic Third-Order Nonlinear Optical Materials." In Optoelectronic Properties of Inorganic Compounds, 1–27. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4757-6101-6_1.

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Caneschi, A., D. Gatteschi, J. Laugier, P. Rey, R. Sessoli, and C. Zanchini. "Synthetic Pathways to Low-Dimensional Compounds Containing Transition Metal Ions and Nitroxide Radicals." In Organic and Inorganic Low-Dimensional Crystalline Materials, 381–84. New York, NY: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-2091-1_41.

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Brunner, Henri. "Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts in Substoichiometric Quantities." In Topics in Stereochemistry, 129–247. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147276.ch3.

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Conference papers on the topic "Transition metal organic compounds"

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Lekishvili, N., Kh Barbakadze, W. Brostow, T. Datashvili, A. Fainleib, and O. Grigorieva. "Inorganic-organic hybrid antibiocorrosive covers based on polyurethanes and coordination compounds of some transition metals." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738469.

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Stoyanova, A., C. de Graaf, R. Broer, Theodore E. Simos, and George Maroulis. "Many-Electron Bands in Transition Metal Compounds." In COMPUTATIONAL METHODS IN SCIENCE AND ENGINEERING: Theory and Computation: Old Problems and New Challenges. Lectures Presented at the International Conference on Computational Methods in Science and Engineering 2007 (ICCMSE 2007): VOLUME 1. AIP, 2007. http://dx.doi.org/10.1063/1.2836029.

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REDDY, B. V. "MAGNETISM OF TRANSITION METAL CLUSTERS AND THEIR COMPOUNDS." In Proceedings of the International Symposium. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812793805_0017.

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Soni, Shubhangi, Netram Kaurav, A. Jain, S. Shah, and K. K. Choudhary. "Pressure induced structural phase transition in IB transition metal nitrides compounds." In NANOFORUM 2014. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4917593.

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Obukhova, Tetiana, Mykhailo Dusheiko, Oleksiy Tymoshenko, and Yurii Chubenko. "Volatile Organic Compounds Detection by Metal-Assisted Etched Structures." In 2019 IEEE 39th International Conference on Electronics and Nanotechnology (ELNANO). IEEE, 2019. http://dx.doi.org/10.1109/elnano.2019.8783261.

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de Groot, Frank. "X-ray absorption and dichroism of transition metal compounds." In X-RAY AND INNER-SHELL PROCESSES. ASCE, 1997. http://dx.doi.org/10.1063/1.52258.

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Burzo, E. "Induced transition metal moments in rare-earth (yttrium) compounds." In SIXTH INTERNATIONAL CONFERENCE OF THE BALKAN PHYSICAL UNION. AIP, 2007. http://dx.doi.org/10.1063/1.2733125.

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Wang, Jun, Ningning Dong, Saifeng Zhang, and Yuanxin Li. "Two-photon absorption in layered transition metal dichalcogenides." In Organic Photonic Materials and Devices XX, edited by Christopher E. Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2018. http://dx.doi.org/10.1117/12.2288365.

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Jiménez-Mier, J., P. Olalde-Velasco, G. Carabalí-Sandoval, G. Herrera-Pérez, E. Chavira, W. L. Yang, and J. Denlinger. "X-ray absorption to determine the metal oxidation state of transition metal compounds." In RADIATION PHYSICS: IX International Symposium on Radiation Physics. AIP, 2013. http://dx.doi.org/10.1063/1.4813463.

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Burzo, Emil. "Exchange enhanced paramagnetism of rare-earth (yttrium)-transition metal compounds." In TIM14 PHYSICS CONFERENCE - PHYSICS WITHOUT FRONTIERS. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4937245.

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Reports on the topic "Transition metal organic compounds"

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Adams, R. The transformation of organic amines by transition metal cluster compounds. Office of Scientific and Technical Information (OSTI), February 1990. http://dx.doi.org/10.2172/7108222.

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Adams, R. D. The transformation of organic amines by transition metal cluster compounds: Progress report. Office of Scientific and Technical Information (OSTI), November 1994. http://dx.doi.org/10.2172/10105409.

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Adams, R. D. The transformation of organic amines by transition metal cluster compounds. Progress report, 1992--1993. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/10150203.

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Adams, R. D. The transformation of organic amines by transition metal cluster compounds. Progress report, 1993--1994. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/10175474.

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Vasbinder, Michael John. Oxidations of Organic and Inorganic Substrates by Superoxo-, hydroperoxo-, and oxo-compounds of the transition metals. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/897378.

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Ogut, Serdar. Manipulating Light with Transition Metal Clusters, Organic Dyes, and Metal Organic Frameworks. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1389151.

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Jimenez, J., D. L. Ederer, and T. Shu. Raman scattering in transition metal compounds: Titanium and compounds of titanium. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/603585.

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Rothwell, I. P. Catalytic arene hydrogenation using early transition metal hydride compounds. Office of Scientific and Technical Information (OSTI), March 1993. http://dx.doi.org/10.2172/6443562.

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Dunkerton, L., C. Hinckley, J. Tyrrell, and P. Robinson. Interactions of sulfur-containing compounds with transition metal clusters and metal surfaces III. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/7019171.

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Doerrer, Linda H. Development of Earth-Abundant Transition Metal Compounds for Water Oxidation. Office of Scientific and Technical Information (OSTI), January 2019. http://dx.doi.org/10.2172/1489778.

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