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Author: Stephen Vijay Tarlton
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Stephen Vijay Tarlton
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Allan J. Canty
Publisher: Springer
ISBN: 3642174299
Category : Science
Languages : en
Pages : 195
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Book Description
Kyle A. Grice, Margaret L. Scheuermann and Karen I. Goldberg: Five-Coordinate Platinum(IV) Complexes.- Jay A. Labinger and John E. Bercaw: The Role of Higher Oxidation State Species in Platinum-Mediated C-H Bond Activation and Functionalization.- Joy M. Racowski and Melanie S. Sanford: Carbon-Heteroatom Bond-Forming Reductive Elimination from Palladium(IV) Complexes.- Helena C. Malinakova: Palladium(IV) Complexes as Intermediates in Catalytic and Stoichiometric Cascade Sequences Providing Complex Carbocycles and Heterocycles.- Allan J. Canty and Manab Sharma: h1-Alkynyl Chemistry for the Higher Oxidation States of Palladium and Platinum.- David C. Powers and Tobias Ritter: Palladium(III) in Synthesis and Catalysis.- Marc-Etienne Moret: Organometallic Platinum(II) and Palladium(II) Complexes as Donor Ligands for Lewis-Acidic d10 and s2 Centers.
Author: F. R. Hartley
Publisher:
ISBN:
Category : Science
Languages : en
Pages : 570
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Author: Richard J. Puddephatt
Publisher: Elsevier
ISBN: 9780080423166
Category : Organometallic chemistry
Languages : en
Pages : 670
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Author: William P. Griffith
Publisher: Springer Science & Business Media
ISBN: 3662091887
Category : Science
Languages : en
Pages : 371
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Book Description
With platinum and rhodium, palladium is one of the most important members of the platinum metal group. The last Gmelin treatment of it was in 1942, and knowledge of its properties and chemistry has made enormous strides since then. This volume is primarily concerned with binary compounds and with the coordination complexes derived from them. Although it is a member of the nickel-palladium-platinum triad, it more closely resernblas platinum in its binary and coordination chemistry, though being a second-row transition element it displays less tendency than does platinum to assume higher oxidation states. ln heterogeneous and homogeneous catalysis, referred to at appropriate points, palladium and its complexes are of great importance in bulk and fine chemieals production, effecting a wide variety of organic transformations. The arrangement of material in this volume follows the traditional Gmelin arrangement. Within each category of compounds or complexes the material is arranged, as usual, in order of ascending metal oxidation states (e. g., palladium(ll) precedes palladium(IV)). The chemistry of the palladium-hydrogen system is so large that it merits a separate volume, so this book starts with the binary oxides and oxopalladates followed by hydroxides, hydroxo complexes and aquo complexes. Then nitrides and nitrates are treated. They are followed by the large chapters on halides and their complexes (172 pages). The largest single chapter in this volume (11 0 pages) deals with chlorides, chloropalladates and other chloro complexes.
Author: M. E. Vol'pin
Publisher: Taylor & Francis
ISBN: 9783718604098
Category : Science
Languages : en
Pages : 542
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Book Description
First published in 1987. Routledge is an imprint of Taylor & Francis, an informa company.
Author: F.R. Hartley
Publisher: Elsevier
ISBN: 0080933955
Category : Science
Languages : en
Pages : 645
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Book Description
The chemistry of platinum group metals is a rapidly expanding commercially important field. It is dominated by the catalytic properties of the metals. They are useful in petrochemical and general chemical plants and are becoming increasingly important as autocatalysts for pollution control. The book covers recent developments in the chemistry of the six platinum group metals, namely, platinum, palladium, rhodium, iridium, ruthenium and osmium. The material falls into three broad areas. Firstly, the occurrence, extraction and use of the metals, especially in catalysis, electrochemistry, energy and electronics. Secondly, organometallic and homogeneous catalytic chemistry and last but not least coordination chemistry including biochemistry and cancer therapy. The work is aimed at scientists in universities and in industry using any of the six platinum group metals in research. It will be useful for those studying the compounds of the metals themselves, and those considering to use either the metals or their complexes and catalysts in their experimental work.
Author: Charlene Tsay
Publisher:
ISBN:
Category :
Languages : en
Pages : 266
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Book Description
Chapter 1 A general introduction to the concepts and background of several types of transition metal complexes that motivate and inform the research described herein. These include a-complexes and molecular adducts of dinitrogen, dihydrogen, and carbon dioxide. Chapter 2 Trigonal bipyramidal platinum(II) complexes of the monoanionic, tetradentate, triphosphine [SiPR3 ([SiP3R]- = [(2-R2PC6H4)3Si]-; R = Ph, iPr) ligand are prepared and shown to provide access to cationic species with divergent behavior. The less electron-rich phenyl-substituted ligand renders the platinum center extremely electrophilic, leading to structurally characterized examples of weakly-donating ligands bound in the fifth, apical coordination site. Of particular interest is the structure of the toluene adduct, which suggests a possible interaction between the platinum center and an aryl C-H bond. When the ligand phosphines are instead substituted by the more electron-rich isopropyl groups, the electrophilicity of the cationic platinum is shown to be mitigated, allowing access to a four-coordinate, trigonal pyramidal platinum center. The crystallographically characterized geometry for this divalent platinum is in contrast to the canonical square planar configuration for d8, 16-electron transition metal complexes. The palladium analogue is also synthesized and shown to possess the same coordination. Chapter 3 Cationic nickel complexes of the [SiPR3] ligand are synthesized and, in contrast to their platinum and palladium congeners, facilitate the surprising binding of molecular dinitrogen to electrophilic nickel(II) centers. The extremely high stretching frequencies of these bound N2 moieties attest to their minimal activation, and the stability of these complexes is shown to arise from increased adonation from the N2 to the cationic nickel center, which compensates for the relative lack of it back-bonding that stabilizes N2 adducts in less electrophilic systems. These cationic nickel species are additionally shown to form thermally stable adducts of molecular dihydrogen. The relative binding strengths of N2 and H2 to these nickel centers are explored and shown to be modulated by the ligand phosphine substituents. Furthermore, evidence of linear binding of carbon dioxide is presented, representing an electrophilic approach to carbon dioxide activation that is in contrast to the low-valent, nucleophilic metal paradigm. Chapter 4 The four-coordinate neutral nickel boratrane (TPiPrB = (2-iPr2PC6H4)3B) reported in the literature represents an isostructural counterpart to the cationic {[SiiPr3]Ni}+ species presented in Chapter 3. Though these two compounds are formally separated by two oxidation states of nickel, the Lewis-acidic nature of the Z-type borane ligand in (TP'PrB)Ni renders it valence-isoelectronic with {[SiiPr3]Ni}+. The reactivity toward N2 and H2 of (TPiPr'B)Ni, as well as that of the new compound (TPPhB)Ni, is explored and discussed in context of what is observed for the {[SiPR3]Ni}+ system. The neutral (TPiPr'B)Ni, while presumably a better [pi] back-bonder than cationic {I[SiPip' 3]Ni}T, is demonstrated not to bind N2, though a very weak, fluxional interaction with H2 at low temperature is hypothesized. The more electrophilic (TP PhB)Ni exhibits room temperature interactions with both N2 and H2, though the nature of these interactions has yet to be confirmed. These results thus underline the importance of [sigma]-donation in stabilizing N2 and H2 adducts of poorly 7r back-bonding metal centers. Chapter 5 Cobalt(I) complexes of [SiPR3] provide an additional isostructural, isoelectronic point of comparison to the cationic nickel species presented in Chapter 3. The dinitrogen adducts [SiP'i' 3]Co(N2) and [SiPPh3]Co(N2), previously reported from our laboratory, feature strongly bound N2 ligands that are not labile to vacuum. The corresponding dihydrogen adducts are generated slowly under an H2 atmosphere. The intact nature of both dihydrogen ligands, which also are not labile to vacuum, is reflected in their NMR spectroscopic parameters. The thermal stability of these compounds enabled crystallization of [SiPi'' 3]Co(H2) which, along with the related (TP'i'B)Co(H2) complex also developed in our laboratory, represent the first structurally characterized dihydrogen adducts of cobalt. Additional comparisons are made between the relative N2 and H2 binding strengths of this system and those of the structurally and electronically related family of [SiPR3] and (TpRB) metal complexes. Appendix A The asymmetric dinucleating ligand [NOPPh], designed to contain both a hard, N-donor binding site and a soft-P-donor binding site, is synthesized and shown to form a diiron complex that features asymmetric bonding to the bridging acetates. The corresponding symmetric, allphosphine dinucleating ligand [POPPh], proves to be more conducive to further study, and provides access to the symmetric diiron, di-([mu]-bromide) starting material {[POPPh ]Fe 2Br2} {BArF4 }. Addition of hydrazine generates the asymmetric, unbridged N2H4 adduct, which features localized diamagnetic and paramagnetic iron centers. The conformation of this species additionally demonstrates the flexibility of this ligand framework. Reduction of the diiron(II) starting material in the presence of PMe3 results in formation of a putative asymmetric iron(O)/iron(I) dimetallic complex, in which an N2 molecule is bound to the diamagnetic iron center, while the PMe3 is ligated to the high-spin iron center and rendered NMR silent. The N2 ligand is shown to be reversibly displaced by H2 , suggesting the formation of a dihydrogen adduct, as well as by CO2, which is postulated to bind as a bent, [eta]2(C,O) ligand.
Author: N. N. Greenwood
Publisher: Elsevier
ISBN: 0080501095
Category : Science
Languages : en
Pages : 1365
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Book Description
When this innovative textbook first appeared in 1984 it rapidly became a great success throughout the world and has already been translated into several European and Asian languages. Now the authors have completely revised and updated the text, including more than 2000 new literature references to work published since the first edition. No page has been left unaltered but the novel features which proved so attractive have been retained. The book presents a balanced, coherent and comprehensive account of the chemistry of the elements for both undergraduate and postgraduate students. This crucial central area of chemistry is full of ingenious experiments, intriguing compounds and exciting new discoveries. The authors specifically avoid the term `inorganic chemistry' since this evokes an outmoded view of chemistry which is no longer appropriate in the final decade of the 20th century. Accordingly, the book covers not only the 'inorganic' chemistry of the elements, but also analytical, theoretical, industrial, organometallic, bio-inorganic and other cognate areas of chemistry. The authors have broken with recent tradition in the teaching of their subject and adopted a new and highly successful approach based on descriptive chemistry. The chemistry of the elements is still discussed within the context of an underlying theoretical framework, giving cohesion and structure to the text, but at all times the chemical facts are emphasized. Students are invited to enter the exciting world of chemical phenomena with a sound knowledge and understanding of the subject, to approach experimentation with an open mind, and to assess observations reliably. This is a book that students will not only value during their formal education, but will keep and refer to throughout their careers as chemists. Completely revised and updated Unique approach to the subject More comprehensive than competing titles
Author: R.A. Mackay
Publisher: CRC Press
ISBN: 148226840X
Category : Science
Languages : en
Pages : 625
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Book Description
This popular and comprehensive textbook provides all the basic information on inorganic chemistry that undergraduates need to know. For this sixth edition, the contents have undergone a complete revision to reflect progress in areas of research, new and modified techniques and their applications, and use of software packages. Introduction to Modern Inorganic Chemistry begins by explaining the electronic structure and properties of atoms, then describes the principles of bonding in diatomic and polyatomic covalent molecules, the solid state, and solution chemistry. Further on in the book, the general properties of the periodic table are studied along with specific elements and groups such as hydrogen, the 's' elements, the lanthanides, the actinides, the transition metals, and the "p" block. Simple and advanced examples are mixed throughout to increase the depth of students' understanding. This edition has a completely new layout including revised artwork, case study boxes, technical notes, and examples. All of the problems have been revised and extended and include notes to assist with approaches and solutions. It is an excellent tool to help students see how inorganic chemistry applies to medicine, the environment, and biological topics.
