High Oxidation State Molybdenum and Tungsten Imido Alkylidene and Metallacycle Chemistry PDF Download
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Author: W. C. Peter Tsang
Publisher:
ISBN:
Category :
Languages : en
Pages : 526
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(Cont.) unsubstituted tungstacyclobutane complexes (82), ethylene complexes (84), tungstacyclopentane complexes (86), and a heterochiral methylene dimer (85a). The tungstacyclopentane complexes catalyzed slow dimerization of ethylene to 1-butene. The observation of the methylene dimer provides the first direct evidence of a bimolecular decomposition pathway for methylene complexes. Chapter 3 Racemic and enantiomerically pure molybdenum alkylimido alkylidene complexes, Mo(NAd)(CHCMe2Ph)(Biphen) (19d, Ad = 1-adamantyl) and Mo(NAd)(CHCMe2Ph)[Trip]-(THF) (20d) were prepared and structurally characterized. Complex 19d was observed almost exclusively as a syn alkylidene isomer, in contrast with 20d which was observed almost exclusively as an anti-THF adduct. Complexes 19d and 20d are the only reported chiral alkylimido alkylidene complexes for enantioselective olefin metathesis reactions. Complex 19d is the first crystallographically characterized four-coordinate adamantylimido alkylidene complex in its base-free form. It offers unique reactivity and selectivity profiles in tandem AROM/RCM and AROM/CM reactions. Complex 19d is compatible with a variety of common functional groups, including boron-containing reagents. Van't Hoff analyses suggest that the bias toward syn-19d isomer is entropy-driven. Chapter 4: Solvent- and base-free molybdenum methylene complexes, Mo(NAr)(Biphen)(CH2) (114a, Ar = 2,6-i-Pr2C6H3) and Mo(NAd)(Biphen)(CH2) (114d, Ad = 1-adamantyl) ...
Author: W. C. Peter Tsang
Publisher:
ISBN:
Category :
Languages : en
Pages : 526
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Book Description
(Cont.) unsubstituted tungstacyclobutane complexes (82), ethylene complexes (84), tungstacyclopentane complexes (86), and a heterochiral methylene dimer (85a). The tungstacyclopentane complexes catalyzed slow dimerization of ethylene to 1-butene. The observation of the methylene dimer provides the first direct evidence of a bimolecular decomposition pathway for methylene complexes. Chapter 3 Racemic and enantiomerically pure molybdenum alkylimido alkylidene complexes, Mo(NAd)(CHCMe2Ph)(Biphen) (19d, Ad = 1-adamantyl) and Mo(NAd)(CHCMe2Ph)[Trip]-(THF) (20d) were prepared and structurally characterized. Complex 19d was observed almost exclusively as a syn alkylidene isomer, in contrast with 20d which was observed almost exclusively as an anti-THF adduct. Complexes 19d and 20d are the only reported chiral alkylimido alkylidene complexes for enantioselective olefin metathesis reactions. Complex 19d is the first crystallographically characterized four-coordinate adamantylimido alkylidene complex in its base-free form. It offers unique reactivity and selectivity profiles in tandem AROM/RCM and AROM/CM reactions. Complex 19d is compatible with a variety of common functional groups, including boron-containing reagents. Van't Hoff analyses suggest that the bias toward syn-19d isomer is entropy-driven. Chapter 4: Solvent- and base-free molybdenum methylene complexes, Mo(NAr)(Biphen)(CH2) (114a, Ar = 2,6-i-Pr2C6H3) and Mo(NAd)(Biphen)(CH2) (114d, Ad = 1-adamantyl) ...
Author: Jonathan Clayton Axtell
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Chapter 1 details the synthesis of tungsten imidoalkylidene compounds bearing strongly electron-withdrawing imido ligands. An alternative synthesis involving the treatment of WCl6 with 4 equivalents of N-trimethylsilyl-substituted anilines and subsequent workup with 1,2-dimethoxyethane (DME) has been employed to form complexes of the type W(NAr)2C12(dme); syntheses employing WO2C 2(dme) as the tungsten precursor were unsuccessful. Alkylation with neopentylmagnesium chloride (ClMgNp) and subsequent treatment with trifluoromethanesulfonic acid (HOTf) affords imidoalkylidene species W(NAr)(CHCMe 3)(OTf)2(dme) (OTf = trifluoromethanesulfonate); analogous neophylidene ([W]CHCMe 2Ph) species could not be made under these conditions. Treatment of these compounds with two equivalents of LiO(2,6-(CHCPh 2)C6H3)-Et2O affords the bisaryloxide complexes of the type W(NAr)(CHCMe3)(OR)2. Ring-Opening Metathesis Polymerization (ROMP) studies using a series of these bisaryloxides show that rates of ROMP increase as the electron-withdrawing power of the substituents on the imido ligand increase if steric bulk about the metal center is held constant. A similar trend between two bisaryloxides is observed for anti-to-syn alkylidene rotation rates at 50*C in toluene-d8 . Difficulties synthesizing bis-pyrrolide complexes of the type W(NAr)(CHCMe3)(pyr)2 precluded their use as catalyst precursors; some MAP species containing the more sterically encumbering 2,5-dimethylpyrrolide ligand are presented and the metathesis activity of MAP species bearing the 2,5-dimethylpyrrolide ligand is discussed. Chapter 2 introduces Mo and W complexes bearing the current extreme in sterically bulky imido ligands, the NHIPT (HIPT = 2,6-(2,4,6-iPr 3CH2)CH3) ligand, in an effort to generate all anti alkylidene species. A non-traditional synthetic route is employed in order to install this ligand first as an anilide, and after subsequent proton transfer, as an imido ligand to form a mixed imido species of the type M(NHIPT)(N'Bu)(NH'Bu)Cl. Addition of one equivalent of 2,6-lutidinium chloride, followed by alkylation affords dialkyl species M(NHIPT)(N'Bu)Np 2, and treatment with three equivalents of pyridinium chloride yields all anti imidoalkylidene dichloride species as mono-pyridine adducts, M(NHIPT)(CHCMe 3)C 2(py) (M = Mo, W). General reactivity, including strategies for removal of the pyridine adduct as well as substitution and metathesis chemistry, are discussed. ROMP of MPCP (MPCP = 3-methyl-3-phenylcyclopropene) by a Mo-based MAP species bearing the NHIPT ligand yields predominantly cis,syndiotactic poly(MPCP) and in the homo-metathesis of 1 -octene yields ~81% cis-7-tetradecene. The possible source of trans olefinic product is addressed. Chapter 3 presents the synthesis of the first (1-adamantyl)imido species of tungsten. The functional equivalent of common bisimido precursors for other Mo/W alkylidene species, [W(NAd) 2C 2(AdNH2)1 2, is shown to be a dimer stabilized by hydrogen-bonding interactions between adamantylamine protons and adjacent chlorides bound to the second metal of the dimer. Subsequent alkylation with ClMgNp affords the expected dialkyl species, and treatment with three equivalents of 3,5-lutidinium chloride affords imidoalkylidene complex W(NAd)(CHCMe 3)(C) 2(lut)2 (lut = 3,5-dimethylpyridine). The most desirable synthetic route toward monoalkoxide pyrrolide (MAP) species proceeds through a monoaryloxide monochloride intermediate W(NAd)(CHCMe 3)(Cl)(OAr)(lut) (Ar = 2,6-(2,4,6-Me 3)C6H3, 2,6-(2,4,6-'Pr 3)C6H3). Removal of lutidine with B(C6 F5 )3 and subsequent treatment with lithium pyrrolide affords W(NAd)(CHCMe3)(pyr)(OAr) (pyr = pyrrolide); 2,5-dimethylpyrrolide analogues (W(NAd)(CHCMe3)(Me2pyr)(OAr) can be accessed via protonolysis by HOAr from W(NAd)(CHCMe3)(Me2pyr)2(lut).
Author: Kapil Shyam Lokare
Publisher:
ISBN:
Category : Alkenes
Languages : en
Pages : 308
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Author: Richard Michael Kolodziej
Publisher:
ISBN:
Category :
Languages : en
Pages : 308
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Author: Andy Hen Liu
Publisher:
ISBN:
Category :
Languages : en
Pages : 446
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Author: Russ Hille
Publisher: Royal Society of Chemistry
ISBN: 1782628789
Category : Science
Languages : en
Pages : 340
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Book Description
There has been enormous progress in our understanding of molybdenum and tungsten enzymes and relevant inorganic complexes of molybdenum and tungsten over the past twenty years. This set of three books provides a timely and comprehensive overview of the field and documents the latest research. Building on the first and second volumes that focussed on biochemistry and bioinorganic chemistry aspects, the third volume focusses on spectroscopic and computational methods that have been applied to both enzymes and model compounds. A particular emphasis is placed on how these important studies have been used to reveal critical components of enzyme mechanisms.This text will be a valuable reference to workers both inside and outside the field, including graduate students and young investigators interested in developing new research programs in this area.
Author:
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ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 692
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Author: W. T. Elwell
Publisher: Elsevier
ISBN: 1483280616
Category : Science
Languages : en
Pages : 290
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International Series of Monographs in Analytical Chemistry, Volume 47: Analytical Chemistry of Molybdenum and Tungsten describes the chemical and instrumental methods of analysis of molybdenum and tungsten. This book is composed of 15 chapters that particularly consider detailed methods for determining these metals in typical samples and their alloys by both classical and modern techniques. The opening chapters discuss the history, occurrence, physico-chemical properties, and applications of molybdenum and tungsten. The succeeding chapters deal with the metals’ sampling, decomposition, separation, and qualitative detection. Considerable chapters are devoted to various chemical and instrumental methods for their analysis, including gravimetry, titrimetry, colorimetry, polarography, amperometry, coulometry, emission and atomic absorption spectroscopy, X-ray spectrophotometry, mass spectrometry, and radiochemical methods. The concluding chapter examines the determination of impurities and alloying elements. This book will prove useful to analytical and inorganic chemists, as well as analytical and inorganic chemistry students.
Author: Robin Riddle Kucharczyk
Publisher:
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Category :
Languages : en
Pages :
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Author: Carola Schulzke
Publisher:
ISBN: 9781616687502
Category : Coenzymes
Languages : en
Pages : 0
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Book Description
Molybdenum is crucially important for almost all organisms ranging from ancient single cell micro-organisms to modern human beings. The reactions catalyzed by molybdenum and tungsten co-factors involve two electron oxidation or reduction usually accompanied by an oxygen atom transfer from water to substrate or vice versa as part of the carbon, nitrogen and sulphur metabolism. This book deals with the advances of molybdenum and tungsten co-factor model chemistry including a brief survey of the earlier stages of even older inorganic dithiolene chemistry.
