EBookClubs

Read Books & Download eBooks Full Online

EBookClubs

Read Books & Download eBooks Full Online

Book Synthesis and Investigation of Some New Complexes of Molybdenum  II  and Tungsten  II  Containing Sulphur Donor Ligands

Download or read book Synthesis and Investigation of Some New Complexes of Molybdenum II and Tungsten II Containing Sulphur Donor Ligands written by Sharman Donna Harris and published by . This book was released on 1995 with total page 444 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Characterisation of Some New Complexes of Molybdenum II  and Tungsten II  Containing Anionic and Neutral Sulphur Donor Ligands

Download or read book Synthesis and Characterisation of Some New Complexes of Molybdenum II and Tungsten II Containing Anionic and Neutral Sulphur Donor Ligands written by Alec Ian Clark and published by . This book was released on 1997 with total page 338 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Characterisation of Some New Complexes of Molybdenum II  and Tungsten II  Containing Anionic and Neutrual Sulphur Donor Ligands

Download or read book Synthesis and Characterisation of Some New Complexes of Molybdenum II and Tungsten II Containing Anionic and Neutrual Sulphur Donor Ligands written by Alec Ian Clark and published by . This book was released on 1997 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Complexes of Molybdenum and Tungsten with Sulphur donor Ligands

Download or read book Complexes of Molybdenum and Tungsten with Sulphur donor Ligands written by Charles Graham Young and published by . This book was released on 1982 with total page 217 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Studies of Mo and W Complexes for 2N Reduction

Download or read book Synthesis and Studies of Mo and W Complexes for 2N Reduction written by Jia Min Chin and published by . This book was released on 2010 with total page 188 pages. Available in PDF, EPUB and Kindle. Book excerpt: A series of monopyrroletriamine ligands [Arpyr(Ar')2]H3 of the form ArC4H2NHCH2N(CH2CH2NHAr')2 (Ar = 2,4,6-mesityl (Mes), 2,4,6-triisopropylphenyl (TRIP); Ar' = C6F5, 2-tolyl (o-tol), naphthyl, 3,5-(2,4,6-triisopropylphenyl)phenyl (HIPT), 3,5- dimethylphenyl, 3,5-di-tert-butylphenyl were synthesized. [Mespyr(C6F5)2]MoCl, ([Mespyr(C6F5)2]Mo = MesitylC4H2NCH2N(CH2CH2NC6F5)2) was prepared by reaction of [Mespyr(C6F5)2]H3 with MoCl4(THF)2 and base and [Mespyr(3,5-t-Bu)2]MoCl and [Mespyr(3,5- Me)2]MoCl (3,5-t-Bu=3,5-di-tert-butylphenyl, Me = 3,5-dimethylphenyl) were synthesized likewise. All three monochlorides are paramagnetic. [Mespyr(C6F5)2]MoNMe2, [[Mespyr(otol) 2]MoNMe2, [Mespyr(3,5-t-Bu)2]MoNMe2, [Mespyr(3,5-Me)2]MoNMe2 were synthesized by reaction of the ligands with Mo(NMe2)4. The resulting compounds are diamagnetic and range in color from teal blue to emerald green. These low spin monodimethylamide complexes exist in rapid equilibria with their high spin forms. [Mespyr(C6F5)2]MoN and [Mespyr(3,5-t-Bu)2]MoN were synthesized by reaction of their respective monochlorides with NaN3 and are yellow diamagnetic species. Reaction of [Mespyr(3,5-t-Bu)2]MoN with Et3OBF4 leads to {[Mespyr(3,5- t-Bu)2]MoNEt}BF4, also a diamagnetic yellow species. [Mespyr(C6F5)2]MoOTf is synthesized by the reaction of [Mespyr(C6F5)2]MoCl with AgOTf. Reduction of [Mespyr(3,5-t-Bu)2]MoCl with Na under N2 led to [Mespyr(3,5-t-Bu)2]MoNNNa(THF)x, several species with varying numbers of THF coordination, x. A single species can be obtained when [Mespyr(3,5-t- Bu)2]MoNNNa(THF)x is reacted with either NBu4Cl or 15-crown-5 ether to yield purple green 4 {[Mespyr(3,5-t-Bu)2]MoNN}NBu4 or [Mespyr(3,5-t-Bu)2]MoNNNa(15-c-5). All the diazenide species are diamagnetic. Oxidation of the diazenide with AgOTf yields [Mespyr(3,5-t- Bu)2]Mo(N2). [Mespyr(3,5-t-Bu)2]Mo(CO) is synthesized by exposure of [Mespyr(3,5-t- Bu)2]Mo(N2) to CO. Reaction of [Mespyr(3,5-t-Bu)2]MoCl with NaBPh4 and NH3 yields {[Mespyr(3,5-t-Bu)2]Mo(NH3)}BPh4. Catalytic runs employing [Mespyr(3,5-t-Bu)2]MoN as the catalyst yielded one equivalent of NH3. A triamidoamine ligand [(HIPTNCH2CH2CH2)3N]3- was synthesized and metalated with MoCl4(THF)2 to produce [(HIPTNCH2CH2CH2)3N]MoCl ([HIPTtrpn]MoCl). Reduction of [HIPTtrpn]MoCl by KC8 under an atmosphere of dinitrogen leads to the green species [HIPTtrpn]MoNNK which can be oxidized by ZnCl2(dioxane) to produce [HIPTtrpn]Mo(N2). Other complexes synthesized include {[HIPTtrpn]Mo(NH3)}+ salts and [HIPTtrpn]Mo(CO). Xray studies were carried out on [HIPTtrpn]MoN and {[HIPTtrpn]Mo(NH3)}BAr'4. This system is not catalytic for the reduction of dinitrogen to ammonia and studies were carried out to elucidate the reasons. Oxidation studies were carried out on [HIPTN3N]Mo(N2) and [HIPTN3N]W(N2) ([HIPTN3N] = [(HIPTNCH2CH2)3N]3- ). The rate of conversion of [HIPTN3N]Mo(NH3) to [HIPTN3N]Mo(N2) was studied and found to be increased in the presence of BPh3. [HIPTN3N]Mo(N2) conversion to [HIPTN3N]Mo(CO) was found to be dependent on CO pressure. Protonation studies of [HIPTN3N]Mo(N2) were also carried out. Studies of [HIPTN3N]MoNNH decomposition showed that decomposition is not base-catalyzed. [HIPTN3N]W(CO) was synthesized by exposure of [HIPTN3N]W(N2) to CO. It is a green, paramagnetic compound and its use as a standard (for determining relative concentrations of other compounds in the IR sample) in IR spectroscopic studies appears to be promising. [HIPTN3N]MoCNH2 was synthesized by addition of acid and reducing agent to [HIPTN3N]MoCN and is a yellow, diamagnetic compound. Two triamidophosphine ligands, triHIPTamine and tri-n-Buamine were synthesized. Metalation of Zr(NMe2)4 with these ligands leads to formation of pn3HIPTZrNMe2 and pn3-n- BuZrNMe2, both diamagnetic, pale yellow complexes.

Book Some New Seven coordinate Tungsten II  and Molybdenum II  Carbonyl Complexes Containing Mono  and Bidentate N  S Donor Ligands

Download or read book Some New Seven coordinate Tungsten II and Molybdenum II Carbonyl Complexes Containing Mono and Bidentate N S Donor Ligands written by S. Hughes and published by . This book was released on 1994 with total page 109 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Physical and Preparative Studies of Molybdenum and Tungsten Complexes

Download or read book Physical and Preparative Studies of Molybdenum and Tungsten Complexes written by Ronald D. Archer and published by . This book was released on 1966 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Several new molybdenum complexes containing chelated 8-hydroxy-quinolinato ligands, including (MoCl(C5H5N) (C9H6NO)2) and (MoCl2(C5H5N)2(C9H6NO) and three oxomolybdenum(V) derivatives were prepared and studied. A cationic molybdenum(III) species containing chelated ethylenediamine and a cationic tungsten(IV) species containing chelated 2,2(1)-bipyridine were also synthesized. Other preparative studies included photochemical investigations with tungsten(IV). The complex formerly designated as K2MoCl5H2O by other workers was shown to have less than enough potassium for such a formula, the spectra of K3MoCl6 as currently in the literature has been shown to be incorrect, and the apparent discrepancy in the literature concerning the tetrazole complex Fe(C2F3N4)2.2H2O was explained. (Author).

Book New Organometallic Complexes of Molybdenum II  and Tungsten II  Containing 3 hexyne And or Tripodal Triphos  MeC CH2PPh2 3  Ligands

Download or read book New Organometallic Complexes of Molybdenum II and Tungsten II Containing 3 hexyne And or Tripodal Triphos MeC CH2PPh2 3 Ligands written by M Al-jahdali and published by . This book was released on 1999 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book The Preparation and Properties of Some Molybdenum Complexes with Sulphur donor Ligands

Download or read book The Preparation and Properties of Some Molybdenum Complexes with Sulphur donor Ligands written by Adrian Butcher and published by . This book was released on 1968 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Reactivity of High Oxidation State Tungsten and Molybdenum Olefin Metathesis Catalysts Bearing New Imido Ligands

Download or read book Synthesis and Reactivity of High Oxidation State Tungsten and Molybdenum Olefin Metathesis Catalysts Bearing New Imido Ligands written by Jonathan Clayton Axtell and published by . This book was released on 2015 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: 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).

Book Index to Theses with Abstracts Accepted for Higher Degrees by the Universities of Great Britain and Ireland and the Council for National Academic Awards

Download or read book Index to Theses with Abstracts Accepted for Higher Degrees by the Universities of Great Britain and Ireland and the Council for National Academic Awards written by and published by . This book was released on 2005 with total page 998 pages. Available in PDF, EPUB and Kindle. Book excerpt: Theses on any subject submitted by the academic libraries in the UK and Ireland.

Book Synthesis  Characterization  and Some Novel Reactions of Seven Coordinate Complexes of Molybdenum  II  and Tungsten  II

Download or read book Synthesis Characterization and Some Novel Reactions of Seven Coordinate Complexes of Molybdenum II and Tungsten II written by Christen Michael Giandomenico and published by . This book was released on 1981 with total page 406 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book The Synthesis and Reactions of Molybdenum II  and Tungsten II  Alkyne Complexes

Download or read book The Synthesis and Reactions of Molybdenum II and Tungsten II Alkyne Complexes written by Elaine M. Armstrong and published by . This book was released on 1989 with total page 710 pages. Available in PDF, EPUB and Kindle. Book excerpt: