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Synthesis Structures Bonding And Reactivity Of Group 4 Metal Alkyl Complexes Incorporating 8 Quinolinolato Ligands
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Book Synopsis Synthesis, Structures, Bonding, and Reactivity of Group 4 Metal Alkyl Complexes Incorporating 8-quinolinolato Ligands by : Xiaohong Bei
Download or read book Synthesis, Structures, Bonding, and Reactivity of Group 4 Metal Alkyl Complexes Incorporating 8-quinolinolato Ligands written by Xiaohong Bei and published by . This book was released on 1997 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Stereoselective Polymerization with Single-Site Catalysts by : Lisa S. Baugh
Download or read book Stereoselective Polymerization with Single-Site Catalysts written by Lisa S. Baugh and published by CRC Press. This book was released on 2007-11-29 with total page 698 pages. Available in PDF, EPUB and Kindle. Book excerpt: New synthetic techniques allow chemists to modify polymer microstructures more precisely than ever, making it possible to design materials that meet increasingly demanding performance requirements. Written and edited by experts in the field, Stereoselective Polymerization with Single-Site Catalysts reviews how the relative stereochemistry of
Book Synopsis Synthesis of Group 4 Metal -diketimine Complexes by : William James Scanlon
Download or read book Synthesis of Group 4 Metal -diketimine Complexes written by William James Scanlon and published by . This book was released on 1998 with total page 190 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Group 4 Complexes Bearing Tridentate Aryloxide-Based Ancillary Ligands by : Ka-Ho Tam
Download or read book Group 4 Complexes Bearing Tridentate Aryloxide-Based Ancillary Ligands written by Ka-Ho Tam and published by Open Dissertation Press. This book was released on 2017-01-27 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation, "Group 4 Complexes Bearing Tridentate Aryloxide-based Ancillary Ligands: Synthesis, Characterization and Application as Olefin Polymerization Catalysts" by Ka-ho, Tam, 譚家豪, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. Abstract: Abstract of thesis entitled GROUP 4 COMPLEXES BEARING TRIDENTATE ARYLOXIDE- BASED ANCILLARY LIGANDS: SYNTHESIS, CHARACTERIZATION AND APPLICATION AS OLEFIN POLYMERIZATION CATALYSTS Submitted by Tam Ka Ho for the degree of Doctor of Philosophy at The University of Hong Kong in 2006 The preparation, characterization, crystal structures and olefin polymerization behavior of a class of Group 4 complexes, and in particular the Zr(IV) derivatives 1 1 [Zr(L )Cl (D)] [H L = 2,6-di(3-tert-butyl-5-methylphen-2-ol)pyridine; D = ethers, 2 2 ketones and Cl(HPR )], have been undertaken. These [O, N, O] catalysts exhibit excellent activities with MAO for ethylene polymerization. Studies to assess the impact of the donor group during catalysis suggest that the same active species is generated and the donor does not play an active role. Superior activities were observed with the Bu Al/Ph CB(C F ) cocatalyst in ethylene polymerization and - 3 3 6 5 4 -1 -1 propylene copolymerization (36,590 and 15,700 g mmol h respectively). Insight into the behavior of the catalytic system with MAO has been derived from gel permeation chromatography and NMR analyses of the polymers prepared under 1 13 different reaction conditions. H and C NMR end-group analyses reveal resonances for saturated methyl chain-end groups only, and undetectable levels of unsaturated vinyl chain ends. This indicates that for the polymerization chain-transfer mechanism, the conventional β-H transfer reactions are insignificant and the unusual chain transfer to Al pathway is vastly dominant. Group 4 complexes supported by unsymmetric tridentate [O, N, O] ligands bearing different substituents on the two aryloxide rings have been prepared, in order to develop new catalytic systems capable of stereospecific α-olefin polymerization. Their activities for ethylene polymerization with MAO are significantly lower than the symmetric [O, N, O] analogues. A number of group 4 bis(benzyl) complexes supported by tridentate pyridine-2- phenolate-6-aryl [O, N, C] ligands, with alkyl and halogen substituents at the R position ortho to the metal, have been prepared. This enabled direct comparison with the CF -substituted [O, N, C] analogues, which were recently reported to exhibit novel C-H---F-C contacts in solution with potential applications for attractive ligand---polymer interactions. The molecular structure of the Zr derivative bearing an ortho-Cl group was determined, revealing the benzyl moieties in an unusual 'anti, anti' configuration. Saliently, this polyethylene catalyst in conjunction with Bu Al/Ph CB(C F ) displayed the best activity thus far observed for [O, N, C] 3 3 6 5 4 -1 -1 catalysts (8630 g mmol h ). A series of group 4 bis(benzyl) complexes supported by newly designed [O, C, N] ligands bearing R substituents ortho to the metal has been prepared, such that the σ- aryl moiety resides trans to the alkyl/polymer chain, and catalyst decomposition pathways such as olefin insertion into the M-C(sp ) bond are impeded. The crystal structure of the CF -substituted hafnium(IV) complex features weak intramolecular 31 C-H---F-C (CF ---methylene) interactions. The H NMR spectra of [M(O, C, N- CF )(CH Ph) ] analogues revealed coupling (assigned to J [via M---F] for Hf and
Download or read book Chemical Abstracts written by and published by . This book was released on 2002 with total page 2364 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Synthesis, Structure, and Reactivity of Group 13 Diketiminate Complexes by : Baixin Qian
Download or read book Synthesis, Structure, and Reactivity of Group 13 Diketiminate Complexes written by Baixin Qian and published by . This book was released on 1999 with total page 362 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis American Doctoral Dissertations by :
Download or read book American Doctoral Dissertations written by and published by . This book was released on 1996 with total page 872 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Synthesis and Chemistry of Cationic D Sup 0 Metal Alkyl Complexes by :
Download or read book Synthesis and Chemistry of Cationic D Sup 0 Metal Alkyl Complexes written by and published by . This book was released on 1990 with total page 2 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Book Synopsis Synthesis and Reactivity Studies of Square Pyramidal Complexes on Group 5 and 6 Metals for Nitrogen and Small Molecule Fixation by : Richard S. Morris
Download or read book Synthesis and Reactivity Studies of Square Pyramidal Complexes on Group 5 and 6 Metals for Nitrogen and Small Molecule Fixation written by Richard S. Morris and published by . This book was released on 2015 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Dissertation Abstracts International by :
Download or read book Dissertation Abstracts International written by and published by . This book was released on 1997 with total page 824 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Design, Synthesis, and Reactivity of Bimetallic Complexes of Dimethylplatinum(II) Containing Ditopic Ligands by : Matthew S. McCready
Download or read book Design, Synthesis, and Reactivity of Bimetallic Complexes of Dimethylplatinum(II) Containing Ditopic Ligands written by Matthew S. McCready and published by . This book was released on 2015 with total page 658 pages. Available in PDF, EPUB and Kindle. Book excerpt: This thesis describes a study of monometallic and bimetallic dimethylplatinum(II) complexes containing ditopic nitrogen donor ligands. This work details the design and synthesis of side-to-side and cofacial arranged ligands and their respective coordination chemistry. The study of the synthesis, characterization and reaction mechanisms of the various dimethylplatinum(II) complexes is outlined in detail with special emphasis focused on the reactivity of the complexes towards oxidative addition. The ditopic ligand 6-dppd, 1,4-di(2-pyridyl)-5,6,7,8,9,10- hexahydrocycloocta[d]pyridazine, was observed to coordinate only a single equivalent of a platinum(II) center. The inability to coordinate a second equivalent, even through an assisted bridging atom, is presumed to be due to a steric clash between the free pyridyl group and the cyclooctyl backbone. In attempts to make heterobimetallic complexes of 6-dppd, the complex [PtMe2(6-dppd)] was observed to react preferentially with mercuric halides by oxidative addition rather than coordination of the mercuric salt in the second coordination site giving complexes [PtXMe2(HgX)(6-dppd)] where X = Br, Cl, OAc. This indicates that the platinum center is actually a better nucleophile than the free pyridyl nitrogen atom. The oxidative addition of solvent dichloromethane was also observed showing the enhancedreactivity of [PtMe2(6-dppd)]. Finally, [PtMe2(6-dppd)] was treated with DCl at low temperature to give the deuteridoplatinum(IV) complex. The deuteridoplatinum(IV) complex reductively eliminates methane in solution and extensive H/D exchange occurs into the CH4 product at low temperature indicating very easy reversibility of the exchange between hydridomethylplatinum(IV) and methaneplatinum(II) complexes. The abstraction of a chloride ligand from [PtClMe(6-dppd)] led to the formation of a complex dimer structure endo, endo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2. This process allowed for the formation of a bimetallic platinum(II) complex which retained the initial stereochemistry. The protonolysis of [PtMe2(6-dppd)] with one equivalent of HOTf led to the generation of methane gas and the concomitant formation of both endo, endo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2 and exo, exo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2. The structures of the exo isomeric clamshell dimers appeared much less sterically hindered in the solid state and were observed experimentally and computationally to be the thermodynamically preferred isomers. The mechanism, selectivity and reversibility of this isomerism process was explored in detail. The reactions of [PtMe2(6-dppd)] with alkyl bromides RCH2Br, which possess hydrogen bonding functionality, result in the formation of stable organoplatinum(IV) complexes capable of forming supramolecular structure via hydrogen bonding. Both intra and inter molecular hydrogen bonding is observed in the formation of supramolecular architectures which self-assemble in the solid state through additional?-stacking and weak secondary interactions. The new anthracene derived ditopic ligands, bpad = N1,N8-bis(pyridin-2- ylmethylene)anthracene-1,8-diamine and adpa = (N, N)-4,4'-(anthracene-1,8-diylbis(ethyne- 2,1-diyl))-bis(N-(pyridin-2-ylmethylene)aniline) were prepared, characterized and used to coordinate dimethylplatinum(II) centers giving cofacial bimetallic complexes of dimethylplatinum(II). [Pt2Me4(bpad)] was shown to degrade over time in solution through a proposed metalation event involving the anthracene backbone. The oxidative addition of a variety of substrates was performed using [Pt2Me4(adpa)] giving stable diplatinum(IV) complexes as characterized by 1H NMR spectroscopy. The new xanthene derived ditopic ligands, ppxda = 2,7-di-tert-butyl-9,9-dimethyl-N4,N5-bis(4-(pyridin-2- ylmethyleneamino)phenyl)-xanthene-4,5-dicarboxamide and pmxda = 2,7-di-tert-butyl-9,9- dimethyl-bis(pyridine-2-ylmethylene)-9H-xanthene-4,5-diamine were prepared characterized and used to ligate two equivalents of a dimethylplatinum(II) center. Diplatinum complexes of both ligands were shown to easily undergo oxidative addition to give the corresponding diplatinum(IV) complexes which adopt the anti orientation. The syn alignment of metal centers was accessible through the abstraction of halides ligands and incorporation of bridging groups as is the case for the pyrazine bridged bimetallic platinum complex [Pt2Me6(C4H4N2)(pmxda)][OSO2CF3]2.
Book Synopsis Structure, Bonding and Reactivity of Metal-alkyl Complexes by : Emanuel Gullo
Download or read book Structure, Bonding and Reactivity of Metal-alkyl Complexes written by Emanuel Gullo and published by . This book was released on 2002 with total page 296 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Synthesis, Reactivity, and Catalysis of Group 3 and Lanthanide Alkyl Complexes by : Daniel Steven Levine
Download or read book Synthesis, Reactivity, and Catalysis of Group 3 and Lanthanide Alkyl Complexes written by Daniel Steven Levine and published by . This book was released on 2016 with total page 160 pages. Available in PDF, EPUB and Kindle. Book excerpt: Group 3 and lanthanide alkyl complexes supported by PNP-pincer ligands were prepared to investigate the sigma-bond metathesis reaction. These complexes were found to effectively carry out this reaction. Alkylidene complexes were prepared by sigma-bond metathesis with gamma-hydrogens of neopentyl groups to generate metallacyclobutanes which undergo a retro-[2+2] reaction. These complexes were also competent hydrogenation, semihydrogenation, hydrosilation, semihydosilation, and cross-dehydocoupling (amines and silanes) catalysts. The mechanisms of these catalytic reactions as well as the sigma-bond metathesis reaction in general were thoroughly studied by computational techniques. The sigma-bond metathesis reaction was probed by energy decomposition analysis to reveal that polarizability of the metal complex is key to promoting efficient metathesis. A new energy decomposition analysis was developed to treat these bonds in unbiased ways. Work towards the preparation of 1,3-dilithiopropane, a useful molecule for possible preparation of alkylidene complexes, was reported.
Book Synopsis Mass Spectrometry in Medicinal Chemistry by : Klaus Wanner
Download or read book Mass Spectrometry in Medicinal Chemistry written by Klaus Wanner and published by John Wiley & Sons. This book was released on 2007-06-27 with total page 460 pages. Available in PDF, EPUB and Kindle. Book excerpt: This first overview of mass spectrometry-based pharmaceutical analysis is the key to improved high-throughput drug screening, rational drug design and analysis of multiple ligand-target interactions. The ready reference opens with a general introduction to the use of mass spectrometry in pharmaceutical screening, followed by a detailed description of recently developed analytical systems for use in the pharmaceutical laboratory. Applications range from simple binding assays to complex screens of biological activity and systems containing multiple targets or ligands -- all highly relevant techniques in the early stages in drug discovery, from target characterization to hit and lead finding.
Book Synopsis Directory of Graduate Research by : American Chemical Society. Committee on Professional Training
Download or read book Directory of Graduate Research written by American Chemical Society. Committee on Professional Training and published by . This book was released on 1977 with total page 920 pages. Available in PDF, EPUB and Kindle. Book excerpt: Faculties, publications and doctoral theses in departments or divisions of chemistry, chemical engineering, biochemistry and pharmaceutical and/or medicinal chemistry at universities in the United States and Canada.
Book Synopsis Modern Oxidation Methods by : Jan-Erling Bäckvall
Download or read book Modern Oxidation Methods written by Jan-Erling Bäckvall and published by John Wiley & Sons. This book was released on 2006-03-06 with total page 350 pages. Available in PDF, EPUB and Kindle. Book excerpt: At the very latest, with the award of the 2001 Nobel Prize for work on asymmetric oxidation, there has been a need for a comprehensive book on such methods. Edited by J.-E. Backvall, one of the world's leaders in the field, this book fills that gap by covering the topic, from classical to green chemistry methods. He has put together a plethora of well-established authors from all over the world who cover every important aspect in high-quality contributions -- whether aerobic oxidation or transition metal-catalyzed epoxidation of alkenes. By providing an overview of this huge topic, this book represents an unparalleled aid for any chemist working in the field. Chapters include: Recent Developments in the Osmium-Catalyzed Dihydroxylation of Olefins Transition Metal-Catalyzed Epoxidation of Alkenes Organocatalytic Oxidation - Ketone-Catalyzed Asymmetric Epoxidation of Olefins Modern Oxidation of Alcohols using environmentally Benign Oxidants Aerobic Oxidations and Related Reactions Catalyzed by N-Hydroxyphthalimide Ruthenium-Catalyzed Oxidation of Alkenes, Alcohols, Amines, Amides, b-Lactams, Phenols, and Hydrocarbons Selective Oxidations of Sulfides and Amines Liquid Phase Oxidation Reactions Catalyzed by Polyoxometalates Oxidation of Carbonyl Compounds Mn-catalysed Oxidation with Hydrogen Peroxide
Download or read book Sulfur Chemistry written by Xuefeng Jiang and published by Springer Nature. This book was released on 2019-08-28 with total page 475 pages. Available in PDF, EPUB and Kindle. Book excerpt: The series Topics in Current Chemistry Collections presents critical reviews from the journal Topics in Current Chemistry organized in topical volumes. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience. Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.
