Synthesis and Chemistry of Cationic D Sup 0 Metal Alkyl Complexes PDF Download
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Languages : en
Pages : 2
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The long term goals of this project are to design and synthesize highly unsaturated, electrophilic metal complexes and to explore their use as catalysts, reagents, and/or model systems for olefin polymerization and C-H activation chemistry. During the 1990 budget year we have focused our attention on (i) the ligand C-H activation chemistry of Cp2Zr(CH3)(THF) and related cationic, d{sup o} Zr alkyl complexes, and (ii) the synthesis of new classes of group 4 metal alkyl complexes with non-Cp2M ligand environments.
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Languages : en
Pages : 2
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Book Description
The long term goals of this project are to design and synthesize highly unsaturated, electrophilic metal complexes and to explore their use as catalysts, reagents, and/or model systems for olefin polymerization and C-H activation chemistry. During the 1990 budget year we have focused our attention on (i) the ligand C-H activation chemistry of Cp2Zr(CH3)(THF) and related cationic, d{sup o} Zr alkyl complexes, and (ii) the synthesis of new classes of group 4 metal alkyl complexes with non-Cp2M ligand environments.
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Languages : en
Pages : 29
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The objective of this project is to develop new types of electrophilic metal alkyl complexes for catalytic C-H activation and olefin polymerization chemistry, and associated fundamental mechanistic studies. We have focused our efforts on four classes of early metal alkyl complexes: (1) cationic group 4 Cp2M(R) complexes (1) which are active species in Cp2MX2-based Ziegler-Natta olefin polymerization catalyst systems and which catalyze productive C-H activation reactions of heterocycles, (2) neutral (dicarbollide)(Cp*)M(R) complexes (2) which are structurally are electronically very similar to 1, (3) half-sandwich complexes CpM(R)2(L){sub n} which are highly coordinatively and electronically unsaturated, and (4) new group 5 (dicarbollide)(Cp)MR2 and (dicarbollide)2 MR complexes which are more unsaturated than group 5 Cp2M systems due to incorporation of the dicarbollide ligand.
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Category : Aeronautics
Languages : en
Pages : 312
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Author: Stefan Arndt
Publisher:
ISBN: 9783861304043
Category : Polymerization
Languages : en
Pages : 174
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Author: Andrew James Jaggar
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Category :
Languages : en
Pages :
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Category : Government reports announcements & index
Languages : en
Pages : 1396
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Author: Gerhard Erker
Publisher: Springer
ISBN: 3642377599
Category : Science
Languages : en
Pages : 321
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Frustrated Lewis Pairs: From Dihydrogen Activation to Asymmetric Catalysis, by Dianjun Chen, Jürgen Klankermayer Coexistence of Lewis Acid and Base Functions: A Generalized View of the Frustrated Lewis Pair Concept with Novel Implications for Reactivity, by Heinz Berke, Yanfeng Jiang, Xianghua Yang, Chunfang Jiang, Subrata Chakraborty, Anne Landwehr New Organoboranes in "Frustrated Lewis Pair" Chemistry, by Zhenpin Lu, Hongyan Ye, Huadong Wang Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry, by Lutz Greb, Jan Paradies Novel Al-Based FLP Systems, by Werner Uhl, Ernst-Ulrich Würthwein N-Heterocyclic Carbenes in FLP Chemistry, by Eugene L. Kolychev, Eileen Theuergarten, Matthias Tamm Carbon-Based Frustrated Lewis Pairs, by Shabana Khan, Manuel Alcarazo Selective C-H Activations Using Frustrated Lewis Pairs. Applications in Organic Synthesis, by Paul Knochel, Konstantin Karaghiosoff, Sophia Manolikakes FLP-Mediated Activations and Reductions of CO2 and CO, by Andrew E. Ashley, Dermot O’Hare Radical Frustrated Lewis Pairs, by Timothy H. Warren and Gerhard Erker Polymerization by Classical and Frustrated Lewis Pairs, by Eugene Y.-X. Chen Frustrated Lewis Pairs Beyond the Main Group: Transition Metal-Containing Systems, by D. Wass Reactions of Phosphine-Boranes and Related Frustrated Lewis Pairs with Transition Metal Complexes, by Abderrahmane Amgoune, Ghenwa Bouhadir, Didier Bourissou
Author: Waldemar Mond
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ISBN:
Category :
Languages : en
Pages : 165
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Author: David Armstrong
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Category :
Languages : en
Pages :
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In the first section of this thesis, the synthesis and reactivity of the first reported palladium(IV) aryldiazenido complex is explored, as well as its relevance toward the potential for catalytic coupling cycles based on the Pd(II)/Pd(IV) redox pair. The synthesis was achieved by two-electron oxidation of the anionic palladium(II) complex KPd(Tp*)Me2 (Tp*- = hydridotris(3,5-dimethylpyrazolyl)borate) by an aryldiazonium cation. The resulting Pd(IV) complex could be cleanly isolated in good yields, is stable for weeks as a solid when kept cold, and decays in solution over a period of days at room temperature. The decomposition was studied in great depth by both NMR and EPR spectroscopy and it was determined that one-electron pathways were involved. From the synthesis of the Pd(IV) aryldiazenido complex, side reactions were observed whereby free Tp*- ligand could be modified via hydride abstraction by an aryldiazonium cation to form the elusive tris(pyrazolyl)borane which could be trapped and isolated as its acetone adduct in a Frustrated Lewis-pair type reaction. The resulting compound can act as a bidentate N-donor ligand with unusual axial steric bulk. Addition of a second equivalent of aryldiazonium cation further abstracts a 3,5-dimethylpyrazolide group to form a cationic intermediate which can again be trapped by acetone to form a C2-chiral cation. In the later chapters of this thesis, extensive work towards the synthesis of 1- and 2- adamantyl anion equivalents was explored, as well as their utility in the synthesis of transition metal adamantyl complexes. The development of new reliable synthetic methods to produce adamantyl magnesium and zinc compounds (including the unknown diadamantylzincs) was achieved, producing clean and shelf stable compounds. The applications of these adamantyl anions toward organometallic chemistry was investigated. It was observed that the diadamantylzinc compounds were particularly potent in transmetallation reactions, cleanly producing several new transition metal and main group adamantyl complexes. While compounds containing mercury, gold, bismuth, tungsten, and platinum have now been synthesized, those of particular interest have the potential for C-H bond activation chemistry and could open access to new compound classes of facially trifunctionalized adamantanes.
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Publisher: Academic Press
ISBN: 0080580335
Category : Science
Languages : en
Pages : 415
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Advances in Organometallic Chemistry
