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Book Mono  and Dinuclear Late Transition Metal Complexes Based on Phosphorus and Nitrogen Ligands

Download or read book Mono and Dinuclear Late Transition Metal Complexes Based on Phosphorus and Nitrogen Ligands written by Esther Karoline van den Beuken and published by . This book was released on 1997 with total page 130 pages. Available in PDF, EPUB and Kindle. Book excerpt: Zsfassung in niederländ. Sprache.

Book Mono  and Dinuclear Transition Metal Complexes Based on Phosphorus and Nitrogen Ligands

Download or read book Mono and Dinuclear Transition Metal Complexes Based on Phosphorus and Nitrogen Ligands written by Esther van den Beuken and published by . This book was released on 1997 with total page 130 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis  Structure and Reactivity of the Later Transition Metal Complexes Containing a Multidentate Phosphorus nitrogen Hybrid Ligand

Download or read book Synthesis Structure and Reactivity of the Later Transition Metal Complexes Containing a Multidentate Phosphorus nitrogen Hybrid Ligand written by Steven Michael Fornara Kennedy and published by . This book was released on 2000 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Transition Metal Complexes of Phosphorus  Arsenic and Antimony Ligands

Download or read book Transition Metal Complexes of Phosphorus Arsenic and Antimony Ligands written by Charles Andrew McAuliffe and published by John Wiley & Sons. This book was released on 1973 with total page 458 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Transition Metal Complexes of Phosphorus  Arsenic and Antimony Ligands

Download or read book Transition Metal Complexes of Phosphorus Arsenic and Antimony Ligands written by Charles Andrew McAuliffe and published by . This book was released on 1973 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Transition Metal Complexes with Multidentate Phosphorous nitrogen Ligands  Synthesis  Characterization and Reactivity

Download or read book Transition Metal Complexes with Multidentate Phosphorous nitrogen Ligands Synthesis Characterization and Reactivity written by Sergio Santiago Rozenel and published by . This book was released on 2011 with total page 256 pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract Transition metal complexes with multidentate phosphorous/nitrogen ligands. Synthesis, characterization and reactivity. By Sergio Santiago Rozenel Doctor in Philosophy in Chemistry University of California, Berkeley Professor John Arnold, Chair Chapter 1: Chromium complexes supported by the multidentate monoanionic ligand [N2P2] {H[N2P2] = tBuN(H)SiMe2N(CH2CH2PiPr2)2} are presented, and the activity of these complexes towards ethylene oligomerization/polymerization is examined. The complexes [N2P2]CrCl2 (1) and [N2P2]CrCl (2) polymerized ethylene after activation with MAO. Derivatives of 1 and 2 were synthesized in order to gain insights about the active species in the ethylene oligomerization/polymerization processes. The alkyl complexes [N2P2]CrMe (3), [N2P2]CrCH2SiMe3 (4) and [N2P2]Cr(Cl)CH2SiMe3 (5), the cationic species {[N2P2]CrCl}BF4 (7), {[N2P2]CrCl}BPh4 (8) and {[N2P2]CrCH2SiMe3}BF4 (9), and the Cr(II) complex [N2P2]CrOSO2CF3 (11) were not active ethylene oligomerization/polymerization catalysts in absence of an activator. Reaction of 1 with two equivalents of MeLi led to reduction to 3. However, with one equivalent of MeLi the stable mixed alkyl-halide derivative [N2P2]Cr(Cl)Me (6) was obtained. Reaction of 2 with Red-Al® produced the hydride ([N2P2]Cr)2(ì-H)2 (10), which reacted with CO to produce the Cr(I) complex [N2P2]Cr(CO)2 (12). Reduction of 2 with KC8 in the presence of p-tolyl azide produced the dimeric cis μ-imido ([N2P2]Cr)2(ì-NC7H7)2 (13). A similar reduction in the presence of ethylene resulted in the isolation of the Cr(III) metallacyclohexane compound [N2P2]CrC4H8 (14). Chapter 2: A series of Co, Ni and Cu complexes with the ligand HN(CH2CH2PiPr2)2 (HPNP) has been isolated and their electrochemical behavior investigated by cyclic voltammetry. The nickel complexes [(HPNP¬)NiOTf]OTf and [(HPNP)NiNCCH3](BF4)2 display reversible reductions, as does the related amide derivative (NP2)NiBr. Related copper(I) and cobalt(II) derivatives were isolated and characterized. Addition of piperidine to [(HNP2)NiNCCH3](BF4)2 led to the formation of the new species [(HPNP)Ni(N(H)C(CH3)NC5H10)](BF4)2. Nucleophilic addition of piperidine to acetonitrile to produce HN=C(CH3)NC5H10 was catalyzed by [(HPNP)NiNCCH3](BF4)2. Chapter 3: A series of bimetallic ruthenium complexes [HPNPRu(N2)]2(μ-Cl)2](BF4)2 (2), [(HPNPRu(H2)Cl)2(μ-Cl)2](BF4)2 (3), [(HPNPRu)2(μ-H2NNH2)(μ-Cl)2](BF4)2 (4), [(HPNPRu)2(μ-Cl)2(μ-HNNPh)](BF4)2 (5), [HPNPRu(NH3)(ç2-N2H4)](BF4)Cl (6), [(HNP2Ru)2(μ-Cl)2(μ2-OSO2CF3)]OSO2CF3 (7), [HPNPRu]2(μ-Cl)3]BPh4 (8) and [HPNPRu]2(μ-Cl)3]BF4 (9) were isolated and characterized in the course of reactions aimed at studying the reduction of N2 and hydrazine. Complex 4 produces ammonia catalytically from hydrazine, and complex 2 generates ammonia upon reaction with Cp2Co/HLuBF4. DFT calculations support the idea that the diazene complex formed is more stable than the expected Chatt-type intermediate. Chapter 4: The reduction chemistry of cobalt complexes with the PNP ligand was explored. Reaction of (HPNP)CoCl2 (1) with n-BuLi generated the deprotonated Co(II) product (PNP)CoCl (2), and the Co(I) reduced species (HPNP)CoCl (3). The reaction of complex 2 with KC8 was investigated, where it was found that the products obtained depended upon the inert gas used to carry out the reaction: (PNP)CoN2 (4) under N2, bimetallic complex [(PNP)Co]2 (5) under Ar, and (HPNP)Co(H)3 (8) under H2. Complex 5 reacted with H2 to generate the bimetallic complex [(PNP)CoH]2 (6). With H2, H3SiPh and AgBPh4 complex 3 generated the species (HPNP)CoCl(H)2 (9), (HPNP)CoCl(H)SiH2Ph (10) and [(HPNP)CoCl]BPh4 (11) respectively. DFT calculations were performed to gain insights about the transformations observed.

Book Synthesis  Structure and Catalytic Property of Transition Metal Complexes with Phosphorus nitrogen and Sulfur nitrogen Ligands

Download or read book Synthesis Structure and Catalytic Property of Transition Metal Complexes with Phosphorus nitrogen and Sulfur nitrogen Ligands written by Xiaoping Chen and published by . This book was released on 2002 with total page 530 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Late Transition Metal Complexes of Bulky Mono  and Bi nucleaeting Ligands

Download or read book Late Transition Metal Complexes of Bulky Mono and Bi nucleaeting Ligands written by Yohan D. M. Champouret and published by . This book was released on 2006 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Low Valent  Late Transition Metal Complexes with Sulfoxide and Nitrogen Ligands

Download or read book Low Valent Late Transition Metal Complexes with Sulfoxide and Nitrogen Ligands written by Reto Dorta and published by . This book was released on 2002 with total page 123 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Structural Characterization of Mono  and Dinuclear Transition Metal Complexes Containing the Tetraaza  14  Annulene Ligand

Download or read book Synthesis and Structural Characterization of Mono and Dinuclear Transition Metal Complexes Containing the Tetraaza 14 Annulene Ligand written by Joanna Czuchajowska-Wiesinger and published by . This book was released on 1991 with total page 362 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Late Transition metal Complexes Supported by Pincer Ligands

Download or read book Late Transition metal Complexes Supported by Pincer Ligands written by Wilson D. Bailey and published by . This book was released on 2016 with total page 181 pages. Available in PDF, EPUB and Kindle. Book excerpt: Late transition-metal pincer complexes of primarily palladium(II) and platinum(II) have been investigated for their application as catalysts in partial oxidation reactions. The epoxidation of higher olefins using molecular oxygen as the oxidant has been targeted, and the individual reaction steps needed to accomplish this overall transformation are described herein, including: (1) hydrogenolysis of a metal hydroxide (M-OH) species to yield a metal hydride (M-H), (2) insertion of O2 into the M-H bond to form a metal hydroperoxide (M-OOH), and (3) O-atom transfer from the M-OOH to epoxides, yielding a M-OH and completing the catalytic cycle. Previous results from our group on these individual transformations using (tBuPCP)Pd and (tBuPCO)Pd fragments are also reviewed. The requirements for O2 insertion into PdII and PtII hydrides are discussed. An array of cationic, neutral, and anionic Pd-H and Pt-H complexes supported by a tBuPNP backbone were synthesized and evaluated for O2 insertion (tBuPNP = 2,6-bis-(di-tbutylphosphinomethyl)pyridine). Metal-ligand cooperation was observed in the activation of H2 to form neutral hydride complexes. The effect of ligand protonation/deprotonation on the trans influence experienced by the hydride ligand was investigated. No reaction with O2 was observed with the cationic hydrides, while the neutral and anionic forms reacted with O2 at the tBuPNP backbone. The synthesis and characterization of mono- and dinuclear Pd-OH complexes supported by a PCNR pincer ligand (PCNR = (1-(3-((di-tert-butylphosphino)methyl)phenyl)-1H-5-R-pyrazole), R = H, Me) is presented. When R = H, ligand pyrazole "rollover" C-H activation was observed, forming a mixed ligand (PCNH)Pd(μ-OH)Pd(PCC) dinuclear structure. This "rollover" was investigated using DFT computations. The mono- and dinuclear hydroxide species were evaluated for hydrogenolysis. The dinuclear compounds {[(PCNR)Pd]2(μ-OH)}[OTf] reacted under an H2 atmosphere to yield the corresponding dinuclear hydrides {[(PCNR)Pd]2(μ-H)}[OTf]. A mechanistic study on the hydrogenolysis of the μ-bridged hydroxide {[(PCNMe)Pd]2(μ-OH)}[OTf] revealed first order kinetics in both [Pd] and [H2]. Terminal hydrides were not detected, and reduction of the mononuclear hydroxide complexes (PCNR)Pd-OH to Pd0 was observed under H2. The reduction was proposed to proceed through displacement of the pyrazole arm, and was examined by DFT computations. Lastly, a new strategy to promote O-atom transfer from M-OOH to epoxides, the final step in the targeted catalytic cycle, is proposed. Preliminary studies on NNNPyz, NNNEt, and NNMe ligated PdII and PtII are discussed (NNNPyz = 2,6-bis(5-tbutyl-1H-pyrazol-3-yl)pyridine; NNNEt = 2-(5-tbutyl-1H-pyrazol-3-yl)-6-(diethylaminomethyl)pyridine; NNMe = 2-(5-tBu-1H-pyrazol-3-yl)-6-methylpyridine). The NNNPyz ligand, containing two acidic sites in proximity to the fourth site in the square plane, was found to protonate M-O2 complexes, chelate to the metal center and oxidize phosphine substrates. Similar reactivity was observed with NNNEt and NNMe, however hemilability of these ligands resulted in undesired coordination modes.

Book Transition Metal Complexes of Phosphorus Ligands

Download or read book Transition Metal Complexes of Phosphorus Ligands written by O. Stelzer and published by . This book was released on 1977 with total page 229 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Comprehensive Coordination Chemistry II

Download or read book Comprehensive Coordination Chemistry II written by J. A. McCleverty and published by Newnes. This book was released on 2003-12-03 with total page 11845 pages. Available in PDF, EPUB and Kindle. Book excerpt: Comprehensive Coordination Chemistry II (CCC II) is the sequel to what has become a classic in the field, Comprehensive Coordination Chemistry, published in 1987. CCC II builds on the first and surveys new developments authoritatively in over 200 newly comissioned chapters, with an emphasis on current trends in biology, materials science and other areas of contemporary scientific interest.

Book Transition metal Complexes Containing Nitrogen  Phosphorus  Or Sulfur

Download or read book Transition metal Complexes Containing Nitrogen Phosphorus Or Sulfur written by R. B. King and published by . This book was released on 1967 with total page 36 pages. Available in PDF, EPUB and Kindle. Book excerpt: The results of four years' work are outlined. Major advances were achieved in the following areas: (1) New arylazo derivatives of molybdenum, (2) new cyclopentadienyl metal nitrosyl derivatives of molybdenum and manganese, (3) new isonitrile derivatives of chromium, molybdenum, and tungsten, (4) trisacetonitrilemetal tricarbonyls of chromium, molybdenum and tungsten as preparative reagents, (5) novel complexes from trifluoroacetonitrile, (6) cyclic acyl derivatives with organonitrogen and organosulfur ligands, (7) metal carbonyl complexes of unsaturated phosphines, (8) new pi-CH3SCH2 derivatives, (9) new complexes with terminal and with bridging methylthio groups, (10) new complexes obtained from bis(trifluoromethyl)dithietene and disodium cis-ethylenedithiolate, (11) new chemistry of the metal carbonyl anions, (12) preparation and reactions of cyclopentadienyl-diiodocarbonylcobalt, (13) new pi-pentamethylcyclopentadienyl derivatives of various metals, and (14) new polynuclear cyclopentadienylmetal carbonyls of iron and cobalt. (Author).

Book Transition Metal Complexes with Two New Series of Tetradentate Ligands

Download or read book Transition Metal Complexes with Two New Series of Tetradentate Ligands written by Devon W. Meek and published by . This book was released on 1966 with total page 11 pages. Available in PDF, EPUB and Kindle. Book excerpt: An investigation was undertaken of the coordinating properties of flexible tetradentate phosphorus, arsenic, and nitrogen ligands of the type D(CH2CH2CH2D')3, (where D does not = D'). A series of nickel (II) complexes with the five coordinate (Ni(ligand)X)(+) cations was isolated and studied extensively. A number of Pd(II) and Co(II) complexes were also examined. A second series of studies involved the nature of bonding in boron-transition metal complexes having groups of the type B(OCH2CH2NR2). Also, the synthesis of a number of tetradentate compounds with boron-carbon bonds was undertaken (e.g., B(Ph-AsO2)3).