The Molecular Structure and Characterization of Some First Row Transition Metal Complexes with Monodentate Ligands PDF Download
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Author: William John Rozell
Publisher:
ISBN:
Category : Complex compounds
Languages : en
Pages : 340
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Author: William John Rozell
Publisher:
ISBN:
Category : Complex compounds
Languages : en
Pages : 340
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Book Description
Author: David Michael P. Mingos
Publisher: Springer Science & Business Media
ISBN: 3642273696
Category : Science
Languages : en
Pages : 227
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Book Description
J.P. Dahl: Carl Johan Ballhausen (1926–2010).- J.R. Winkler and H.B. Gray: Electronic Structures of Oxo-Metal Ions.- C.D. Flint: Early Days in Kemisk Laboratorium IV and Later Studies.- J.H. Palmer: Transition Metal Corrole Coordination Chemistry. A Review Focusing on Electronic Structural Studies.- W.C. Trogler: Chemical Sensing with Semiconducting Metal Phthalocyanines.- K.M. Lancaster: Biological Outer-Sphere Coordination.- R.K. Hocking and E.I. Solomon: Ligand Field and Molecular Orbital Theories of Transition Metal X-ray Absorption Edge Transitions.- K.B. Møller and N.E. Henriksen: Time-resolved X-ray diffraction: The dynamics of the chemical bond.
Author: Dr. Manas Layek
Publisher: Laxmi Book Publication
ISBN: 1304220567
Category : Art
Languages : en
Pages : 136
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Book Description
Now a days, coordination chemistry of metal ion complexes with various types of ligands has been a major area of research among the scientists working in the fields of inorganic chemistry. Due to the applicability of such complexes in a diverse range of areas such as industry, research, medical science and numerous other fields, the focus on the designing, synthesize and characterization of coordination complexes is continuously increasing. A special feature of these complexes is that they play vital roles in living and other systems. This is corroborated by the fact that many chemical compounds that are essential components of important substances in living systems (such as enzymes, chlorophylls, haemoglobin) are metal complexes. In fact bioinorganic chemistry has become a bridge between Biological Sciences and Chemical Sciences. This inter relation is proven by the fact that one third of all enzymes have metal ions as constituents
Author: Sarah Ouanounou
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Benjamin Mogesa
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Author: Maria Paula Juanico
Publisher: Cuvillier Verlag
ISBN: 3865370306
Category :
Languages : en
Pages : 151
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Book Description
Author: B.I. Kharisov
Publisher: Elsevier
ISBN: 0128110627
Category : Science
Languages : en
Pages : 470
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Book Description
Direct Synthesis of Metal Complexes provides in-depth coverage of the direct synthesis of coordination and organometallic compounds. The work is primarily organized by methods, but also covers highly relevant complexes, such as metal-polymer coordination compounds. This updated reference discusses recent developments in cryosynthesis, electrosynthesis, and tribosynthesis (popular as it doesn’t require organic solvents), with special attention paid to ‘greener’ methodologies and approaches. Additionally, the book describes physical methods of zero-valent metal interaction with organic matter, including sputtering, ultrasonic treatment and synthesis in ionic liquids. The book presents completely new content as a follow-up to the 1999 Elsevier Science publication Direct Synthesis of Coordination and Organometallic Compounds that was edited by Dr. Garnovskii and Dr. Kharisov. Covers current methods and techniques of metal interactions with organic media leading to metal chelates, adducts, di- and polymetallic complexes, metal-containing macrocycles, supported coordination compounds (i.e., metal complexes on carbon nanotubes), and more Describes reactivities of distinct forms of elemental metals (powders, sheets, nanoparticles (including a host of less-common metal nanostructures) with organic phase (liquid, solid and gaseous) and water Includes experimental procedures, with examples of direct synthesis, at the end of each chapter
Author: Justin C. Biffinger
Publisher:
ISBN:
Category : Complex compounds
Languages : en
Pages : 152
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Book Description
Describes the synthesis and structure of mononuclear M(III) complexes and what factors control the stereochemistry.
Author:
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 818
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Book Description
Vols. for 1973- include the following subject areas: Biological sciences, Agriculture, Chemistry, Environmental sciences, Health sciences, Engineering, Mathematics and statistics, Earth sciences, Physics, Education, Psychology, Sociology, Anthropology, History, Law & political science, Business & economics, Geography & regional planning, Language & literature, Fine arts, Library & information science, Mass communications, Music, Philosophy and Religion.
Author: Jessica Nicole Boynton
Publisher:
ISBN: 9781321210804
Category :
Languages : en
Pages :
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Book Description
The research in this dissertation is focused on the synthesis, structural, and magnetic characterization of two-coordinate open shell (d1-d4) transition metal complexes. Background information on this field of endeavor is provided in Chapter 1. In Chapter 2 I describe the synthesis and characterization of the mononuclear chromium (II) terphenyl substituted primary amido complexes and a Lewis base adduct. These studies suggest that the two-coordinate chromium complexes have significant spin-orbit coupling effects which lead to moments lower than the spin only value of 4.90 [mu]B owing to the fact that [lambda] (the spin orbit coupling parameter) is positive. The three-coordinated complex 2.3 had a magnetic moment of 3.77 [mu]B. The synthesis and characterization of the first stable two-coordinate vanadium complexes are described in Chapter 3. The values suggest a significant spin orbital angular momentum contribution that leads to a magnetic moment that is lower than their spin only value of 3.87 [mu]B. DFT calculations showed that the major absorptions in their UV-Vis spectra were due to ligand to metal charge transfer transitions. The titanium synthesis and characterization of the bisamido complex along with its three-coordinate titanium(III) precursor are described in Chapter 4. Compound 4.1 was obtained via the stoichiometric reaction of LiN(H)AriPr 6 with the Ti(III) complex TiCl3 *2NMe3 in trimethylamine. The precursor 4.1 has trigonal pyramidal coordination at the titanium atom, with bonding to two amido nitrogens and a chlorine as well as a secondary interaction to a flanking aryl ring of a terphenyl substituent. Compound 4.2 displays a very distorted four-coordinate metal environment in which the titanium atom is bound to two amido nitrogens and to two carbons from a terphenyl aryl ring. This structure is in sharp contrast to the two-coordinate linear structure that was observed in its first row metal (V-Ni) analogs. The synthesis and characterization of mononuclear chromium(II) terphenyl primary substituted thiolate complexes are described in Chapter 5. Reaction of the terphenyl primary thiolate lithium derivatives LiSAriPr4 and LiSArMe6 with CrCl2THF2 in a 2:1 ratio afforded complexes 5.1 and 5.2, which are the very rare examples of chromium(II) thiolates with quasi-two-coordination at the metal center. Both deviate from linearity and have S-Cr-S angles of 111.02(3)° and 107.86(3)° with secondary Cr-C(aryl ring) interactions of ca. 2.115 Å and 1.971 Å respectively. The initial work on titanium and vanadium terphenyl thiolates is described in Appendix I and II. In Chapter 6 I show that the reaction of K2COT (COT= 1,3,5,7-cyclooctatetraene, C8H8) with an aryl chromium(II) halide gave (CrAriPr4)2([mu]2-n3:n4-COT) (6.1) in which a non-planar COT ring is complexed between two CrAriPr4 moieties -- a configuration previously unknown for chromium complexes of COT. OneCr2+ ion is bonded primarily to three COT carbons (Cr--C= 2.22-2.30 Å ) as well as an ipso carbon (Cr-C= ca. 2.47 Å) from a flanking aryl ring of its terphenyl substituent. The other Cr2+ ion bonds to an ipso carbon (Cr-C= ca. 2.53 Å) from its terphenyl substituent as well as four COT carbons (Cr--C= 2.24-2.32 Å). The COT carbon-carbon distances display an alternating pattern, consistent with the non-planarity and non-aromatic character of the ring. The magnetic properties of 6.1 indicate that the Cr2+ ions have a high-spin d4 configuration with S = 2. The temperature dependence of the magnetism indicates that their behavior is due to zero-field splitting of the S = 2 state. Attempts to prepare 6.1 by the direct reaction of quintuple-bonded (CrAriPr4)2 with COT were unsuccessful. (Abstract shortened by UMI.) --Proquest.
