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Metal Compounds (metal + compound)

Distribution by Scientific Domains

Chemistry	59%
Polymers and Materials Science	25%
Physics and Astronomy	6%
2 Other Domains	10%

Kinds of Metal Compounds

transition metal compound

Selected Abstracts

Formation of Nanostructures in Multi Component Systems Based on Organic Polymer and Coordination Metal Compound

MACROMOLECULAR SYMPOSIA, Issue 1 2006
Nataly Kozak
Abstract Structuring of polyurethane (PU) networks is analyzed under influence of transition metal coordination compounds: mono-ionic ,-diketonates and polyheteronuclear metal-organic complexes. Formed in situ nanostructures both organic and inorganic were found in organic polymer modified with coordination metal compound. Influence of coordination junction point spatial symmetry and content of metal ion in modifier on structure and dielectric characteristics of modified PUs is analyzed using X-ray, EPR, SEM and transmission optical microscopy, DRS and DSC methods. [source]

A General Process for the Fabrication of Air-Stable Metallic Particles (Cd, Zn and Al) by the Decomposition of Alkyl,Metal Compounds

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 15 2008
Aharon Gedanken
Abstract The thermolysis of alkyl,metal compounds under autogenic pressure, with the three metals Cd, Zn, and Al as examples, suggest that this might become a general method for preparing a composite where the metal is the core and carbon the shell. The air-stability of these composites is also demonstrated. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

Reductive Activation of tripod Metal Compounds: Identification of Intermediates and Preparative Application,

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 9 2008
Jürgen Mautz
Abstract [tripodCoCl2] {tripod = CH3C(CH2PPh2)3} when treated with KC8 in THF solution under an argon atmosphere produces a reactive species ["tripodCo0"] (A) which undergoes oxidative additions with stannanes, [tripodCo(H)2(SnBu3)] (4), formed, for example, by addition of Bu3SnH. Silanes, R3SiH, undergo the same type of reaction producing [tripodCo(H)2(SiR3)] (R = Et: 5a; R = Ph: 5b). The solid-state structures of all the compounds [tripodCo(H)2(ER3)] (E = Si, R = Ph; E = Sn, R = Ph, Bu) are rather similar. While they contain six-coordinate cobalt with the formal oxidation state of cobalt being +III the coordination geometry is not octahedral: the heteroelement E deviates from the position which it would have in octahedral coordination by around 40° while the other five ligands, three phosphorus and two hydrogen, have the expected interligand angles of around 90° and 180°, respectively. The deviation of the heteroelement E is such that it approaches the metal bonded hydrogen atoms leading to short H···E contacts of only about 190 pm (E = Si) and 230 pm (E = Sn), respectively. The generation of a reactive species ["tripodCo0"] (A) was transferred to the synthesis of a reactive tripodnickel(0) species by treating a THF solution of [(DME)NiBr2] with KC8 in the presence of tripod. This species reacts with two electron donor ligands L to produce the pseudo tetrahedral compounds [tripodNi(L)] {L = PPh3 (6), AsPh3 (7), cHexNC (8), tBuNC (9), C2H4 (10)}. The identity of the reactive nickel(0) species as unequivocally deduced from NMR experiments is [tripod4Ni3] (12). All compounds were characterised by the usual analytic techniques including X-ray analysis where applicable.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

Configuration of Octahedral Metal Compounds , Equilibrium, Crystal and Molecular Structure of Nickel(II) Complexes of Linear N2O4, N4S2 or N6 Donors Set Atoms Ligands

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2004
Aminou Mohamadou
Abstract Two new nickel(II) complexes of symmetric hexadentate mixed-ligand N,O [1,12-bis(2-pyridyl)-5,8-dioxa-2,11-diazadodecane (pydado)] and N,S [1,12-bis(2-pyridyl)-5,8-dithia-2,11-diazadodecane (pydadt)] donor atoms have been synthesised as perchlorate salts and characterised by X-ray crystallography and ligand-field spectroscopy. In both complexes the Ni2+ ion is hexacoordinate. The cation [Ni(pydado)]2+ is pseudo-octahedral with the two pyridyl groups in trans position; all Ni,N and Ni,O bond lengths are practically equivalent. In [Ni(pydadt)]2+ complex, however, the size of the thioether sulfur atoms imposes a C2v symmetry; the pyridyl groups and the sulfur atoms are in trans positions and all Ni,N bond lengths are equivalent. The comparison of these structures with those of octahedral cobalt, copper and zinc complexes with the same ligands shows that their configurations depend not only on the nature of the two central donor atoms of the ligand, but also on the nature of the metallic ion. In aqueous solution, the stability constants of the NiII chelates with these two ligands, determined by potentiometry, show the formation of [Ni(LH)]3+ and [NiL]2+ species in all cases. The chelating power of the pydadt ligand is slightly greater than that of pydado. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source]

Catalytic Cyclopropanation of Alkenes via (2-Furyl)carbene Complexes from 1-Benzoyl-cis-1-buten-3-yne with Transition Metal Compounds.

CHEMINFORM, Issue 29 2004
Koji Miki
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

Catalysis of intumescent flame retardancy of polypropylene by metallic compounds,

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 1 2003
Menachem Lewin
Abstract Divalent and multivalent metallic compounds catalyze the flame retardancy performance of intumescent systems based on ammonium polyphosphate (APP) and pentaerythritol (petol) in poly(propylene) (PP). The catalytic effect is shown by increases in the oxygen index (OI) and UL-94 ratings. The effect is exerted by small concentrations of the metallic compounds in the range of 0.1,2.5 wt% of the compositions. The effect increases with the concentration of the catalyst until a maximum is reached. At higher concentrations of the catalyst a decrease in the flame retardancy parameters is observed, accompanied in several cases by a degradation and discoloration of the composition. The catalyst replaces melamine in intumescent systems. Catalytic effectiveness is defined and calculated for a number of compounds. Thermogravimetric parameters, such as initial decomposition temperature, temperature of the transition point and residue-after-transitions (RAT) change in parallel with the catalytic effect of the metal compound concentration. Metal compounds investigated include oxides, acetates, acetyl acetonates, borates and sulfates of Mn, Zn, Mg, Al, Ca, Ba,,V, Co, Ni, Cu, Mo, Zr, and Cr. Mechanistic considerations on the activity of the catalysts are presented. Copyright © 2003 John Wiley & Sons, Ltd. [source]

Formation of Nanostructures in Multi Component Systems Based on Organic Polymer and Coordination Metal Compound

Modelling the influence of reactive elements on the work of adhesion between a thermally grown oxide and a bond coat alloy

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 3 2006
I. J. Bennett
Abstract The durability of thermal barrier coating systems is primarily determined by the degree of adhesion between the thermally grown oxide (TGO) and the bond coat. Failure of the TBC is often the result of delamination at this interface. Adhesion can be improved by the addition of reactive elements (RE) to the bond coat alloy. REs include oxide forming elements such as Y, Zr and Hf. The so-called reactive element effect has been attributed to a direct improvement of the bonding between the TGO and the bond coat. A macroscopic atom model has been developed to allow the work of adhesion between two compounds (e.g. an oxide and a metal compound) to be estimated. By calculating the work of adhesion across a number of different interfaces, the influence of reactive elements and impurities present in the substrate can be assessed. It has been found that the REs have a limited direct influence on the work of adhesion and can even result in a weaker interface. A large reduction in the work of adhesion is calculated when S and C are present at the interface. REs have a high affinity for both S and C. This indicates that the RE effect is primarily that of impurity scavenging, preventing diffusion of impurities to the interface. A number of experiments are reported, which demonstrate the RE effect and support the modelling results. [source]

Electromagnetic interference shielding by using conductive polypyrrole and metal compound coated on fabrics

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 8 2002
C. Y. Lee
Abstract Electromagnetic interference (EMI) shielding materials of complex type of conductive polypyrrole (PPy) as an intrinsically conducting polymer and silver-palladium (AgPd) metal compound coated on woven or non-woven fabrics are synthesized. From dc conductivity and SEM photographs of PPy/fabric complexes, we discuss charge transport mechanism and the homogeneity of coating on the fabrics. The EMI shielding efficiency of PPy/fabric and AgPd/fabric complexes is in the range of 8,,,80 dB depending on the conductivity and the additional Ag vacuum evaporation. The highest EMI shielding efficiency of PPy/fabric complexes vacuum-evaporated by Ag is ,80 dB, indicating potential materials for military uses. We propose that PPy/fabrics are excellent RF and microwave absorber because of the relatively high absorbance and low reflectance of the materials. Copyright © 2002 John Wiley & Sons, Ltd. [source]

Synthesis, crystal structure and characterization of new transition metal compounds of bromophenols: Bis(2,4,6-tribromophenolato) di(N-methylimidazole)M(II) (M=Co, Cu)

CRYSTAL RESEARCH AND TECHNOLOGY, Issue 3 2005
P. Camurlu
Abstract Bis(2,4,6-tribromophenolato)di(N-methyl imidazole)M(II), where M stands for cobalt and copper metals, was synthesized via reaction of the corresponding metal sulphate and 2,4,6-tribromophenolate in aqueous media in the presence of N-methyl imidazole and sodium hydroxide. Although various crystallization procedures were applied only cobalt complex was obtained as single crystals. The Co(II) ion has a distorted octahedral enviroment involving two O atoms and two N atoms of the Bis(2,4,6-tribromophenolato)di(N-methyl imidazole) ligand. Powder x-ray diffraction pattern of copper compound was used for cooper complex. For characterizations of complexes carbon, hydrogen and nitrogen elemental analysis, FTIR and UV spectroscopy, DSC thermal analysis and magnetic susceptibility measurements at room temperature were performed. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]

Relative sensitivity distribution of aquatic invertebrates to organic and metal compounds

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 1 2004
Peter Carsten von der Ohe
Abstract In the field, a multitude of species can be exposed to numerous toxicants; thus, the sensitivity of individual species to particular toxicants must be known to predict effects and to analyze changes in species composition. For most species, no information about their toxicant sensitivity is available. To address this limitation, we have grouped the available information to assign sensitivities to aquatic invertebrate taxa relative to Daphnia magna. With respect to organic compounds, most taxa of the orders Anisoptera, Basommatophora, Coleoptera, Decapoda, Diptera, Ephemeroptera, Eulamellibranchiata, Heteroptera, Hirudinea, Isopoda, Oligochaeta, Prosobranchia, Trichoptera, Tricladida, and Zygoptera are less sensitive than D. magna. Some taxa of the Amphipoda, Plecoptera, and Cladocera (other than D. magna) are significantly more sensitive. For organic compounds, approximately 22% of the investigated taxa were more sensitive than D. magna. Most taxa of the orders Amphipoda, Basommatophora, Diptera, Ephemeroptera, Eulamellibranchiata, Heteroptera, Isopoda, Oligochaeta, and Tricladida are significantly less sensitive than D. magna to metal compounds. The taxa belonging to the Crustacea, with the exception of the order Isopoda, are much more sensitive. For metal compounds, approximately 30% of the investigated taxa were more sensitive than D. magna. Hence, D. magna is among the most sensitive taxa regarding both groups of toxicants. The sensitivities for several taxa are listed, and use of the relative sensitivity distribution to link toxicant effects in mesocosm studies and field investigations is discussed. [source]

A General Process for the Fabrication of Air-Stable Metallic Particles (Cd, Zn and Al) by the Decomposition of Alkyl,Metal Compounds

Synthesis of (1,2,4-Oxadiazole)palladium(II) Complexes by [2 + 3] Cycloaddition of Nitrile Oxides to Organonitriles in the Presence of PdCl2

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 5 2005
Nadezhda A. Bokach
Abstract The reaction between the nitrile oxides 2,4,6-R3C6H2CNO (R = Me, OMe) and trans -[PdCl2(RCN)2], or RCN (R = Me, Et, CH2CN, NMe2, Ph) in the presence of PdCl2, proceeded smoothly under mild conditions and allowed the isolation of the 1,2,4-oxadiazole complexes trans -[PdCl2{Na=C(R)-ON=Cb(C6H2R3)(Na,Cb)}2] (1,8) in 40,85,% yields. In CH2Cl2, the reaction between 2,4,6-R3C6H2CNO and [PdCl2(MeCN)2] furnishes [PdCl2(ONCC6H2R3)2] (9 and 10), which are the first representatives of metal compounds where nitrile oxides act as ligands. The 1,2,4-oxadiazole complexes 1,8 were characterized by elemental analysis, FAB mass spectrometry, and IR, 1H and 13C{1H} NMR spectroscopy, while 2, 3, 7, and 8 were additionally characterized by X-ray crystallography. The liberation of the heterocyclic species from 1,8 was successfully performed by substitution reaction either with 1,2-bis(diphenylphosphanyl)ethane or with an excess amount of Na2S·7H2O in MeOH; the liberated 1,2,4-oxadiazoles (11,18) were characterized by positive-ion FAB mass spectrometry and 1H and 13C{1H} NMR spectroscopy. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source]

Metal Chalcogenide Clusters on the Border between Molecules and Materials,

ADVANCED MATERIALS, Issue 18 2009
John F. Corrigan
Abstract The preparative and materials chemistry of high nuclearity transition metal chalcogenide nanoclusters has been in the focus of our research for many years. These polynuclear metal compounds possess rich photophysical properties and can be understood as intermediates between mononuclear complexes and binary bulk phases. Based on our previous results we discuss herein recent advances in three different areas of cluster research. In the field of copper selenide clusters we present the synthesis of monodisperse, nanostructured , -Cu2Se via the thermolysis of well-defined cluster compounds as well as our approaches in the synthesis of functionalized clusters. In case of silver chalcogenides we established a strategy to synthesis cluster compounds containing several hundreds of silver atoms with the nanoclusters arranging in a closely packed crystal lattice. Finally the presented chalcogenide clusters of the group 12 metals (Zn, Cd, Hg) can be taken as model compounds for corresponding nanoparticles as even the smallest of frameworks display a clear structural relationship to the bulk materials. [source]

Improved third-order Møller,Plesset perturbation theory

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 13 2003
Stefan Grimme
Abstract Based on a partitioning of the total correlation energy into contributions from parallel- and antiparallel-spin pairs of electrons, a modified third-order Møller,Plesset (MP) perturbation theory is developed. The method, termed SCS,MP3 (SCS for spin-component-scaled) continues previous work on an improved version of MP2 (S. Grimme, J Chem Phys 2003, 118, 9095). A benchmark set of 32 isogyric reaction energies, 11 atomization energies, and 11 stretched geometries is used to assess to performance of the model in comparison to the standard quantum chemical approaches MP2, MP3, and QCISD(T). It is found, that the new method performs significantly better than usual MP2/MP3 and even outperforms the more costly QCISD method. Opposite to the usual MP series, the SCS third-order correction uniformly improves the results. Dramatic enhancements are especially observed for the more difficult atomization energies, some of the stretched geometries, and reaction and ionization energies involving transition metal compounds where the method seems to be competitive or even superior to the widely used density functional approaches. Further tests performed for other complex systems (biradicals, C20 isomers, transition states) demonstrate that the SCS,MP3 model yields often results of QCISD(T) accuracy. The uniformity with which the new approach improves for very different correlation problems indicates significant robustness, and suggests it as a valuable quantum chemical method of general use. © 2003 Wiley Periodicals, Inc. J Comput Chem 24: 1529,1537, 2003 [source]

Density functional theory studies on the dissociation energies of metallic salts: relationship between lattice and dissociation energies

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 8 2001
Chang Kon Kim
Abstract The formation and physicochemical properties of polymer electrolytes strongly depend on the lattice energy of metal salts. An indirect but efficient way to estimate the lattice energy through the relationship between the heterolytic bond dissociation and lattice energies is proposed in this work. The heterolytic bond dissociation energies for alkali metal compounds were calculated theoretically using the Density Functional Theory (DFT) of B3LYP level with 6-311+G(d,p) and 6-311+G(2df,p) basis sets. For transition metal compounds, the same method was employed except for using the effective core potential (ECP) of LANL2DZ and SDD on transition metals for 6-311+G(d,p) and 6-311+G(2df,p) calculations, respectively. The dissociation energies calculated by 6-311+G(2df,p) basis set combined with SDD basis set were better correlated with the experimental values with average error of ca. ±1.0% than those by 6-311+G* combined with the LANL2DZ basis set. The relationship between dissociation and lattice energies was found to be fairly linear (r>0.98). Thus, this method can be used to estimate the lattice energy of an unknown ionic compound with reasonably high accuracy. We also found that the dissociation energies of transition metal salts were relatively larger than those of alkaline metal salts for comparable ionic radii. © 2001 John Wiley & Sons, Inc. J Comput Chem 22: 827,834, 2001 [source]

Prediction of a conducting hard ductile cubic IrC

PHYSICA STATUS SOLIDI - RAPID RESEARCH LETTERS, Issue 8-9 2010
Zhisheng Zhao
Abstract Nine IrC structures were investigated using ab initio calculations based on the structures of known transition metal compounds. The calculations indicated that zinc blende structured IrC (ZB,IrC) is not only the most energetically stable, but also mechanically and dynamically stable at the ground state. Further studies showed that ZB,IrC is a conducting hard ductile material that is expected to be experimentally synthesized like cubic PtC and RuC. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]

Lung cancer risk associated with occupational exposure to nickel, chromium VI, and cadmium in two population-based case,control studies in Montreal

AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, Issue 5 2010
Rachelle Beveridge MSc
Abstract Background Nickel, chromium VI, and cadmium have been identified as lung carcinogens in highly exposed cohorts. The purpose of this study was to examine the etiological link between lung cancer and these metals in occupations, that usually entail lower levels of exposure than those seen in historical cohorts. Methods Two population-based case,control studies were conducted in Montreal, from 1979 to 1986 and from 1996 to 2001, comprising 1,598 cases and 1,965 controls. A detailed job history was obtained to evaluate lifetime occupational exposure to many agents, including nickel, chromium VI, and cadmium compounds. Results Lung cancer odds ratios were increased only among former or non-smokers: 2.5 (95% CI: 1.3,4.7) for nickel exposure, 2.4 (95% CI: 1.2,4.8) for chromium VI, and 4.7 (95% CI: 1.5,14.3) for cadmium. The metals did not increase risk among smokers. Conclusions While excess risks due to these metal compounds were barely discernable among smokers, carcinogenic effects were seen among non-smokers. Am. J. Ind. Med. 53:476,485, 2010. © 2010 Wiley-Liss, Inc. [source]

Polymerization of styrene with a simple rare earth metal initiator

POLYMER INTERNATIONAL, Issue 11 2001
Toshiyuki Hayakawa
Abstract The catalytic activity in the polymerization of styrene has been examined using commercially available simple rare earth metal compounds such as Sm(OiPr)3, Sm(acac)3, Sm(OCOMe)3, SmI2(THF)2 or SmCl3 coupled with Et3Al or methylaluminoxane (MAO). Among these compounds, the Sm(OiPr)3/AlEt3 system shows the highest catalytic activity, especially in the presence of a minor amount of toluene at 60,°C. The random copolymerization of styrene with methyl methacrylate suggests that the present polymerization proceeds with a radical polymerization mechanism. (C5Me5)SmCl3Na(THF) and (C5Me5)SmCl3Li(THF) systems exhibit relatively low catalytic activity, even in the presence of AlEt3. © 2001 Society of Chemical Industry [source]

Bond catastrophes in rhodium complexes: experimental charge-density studies of [Rh(C7H8)(PtBu3)Cl] and [Rh(C7H8)(PCy3)Cl]

ACTA CRYSTALLOGRAPHICA SECTION B, Issue 5 2010
Hazel A. Sparkes
Rhodium complexes have potential uses in both catalysis and promoting the cleavage of C,C bonds. In order to further our understanding of these species and their potential applications, it is vital to obtain insight into the bonding within the species, particularly the Rh,C interactions, and to this end experimental charge-density studies have been undertaken on the title complexes. High-resolution single-crystal datasets to sin,,/, = 1.06,Å,1 were obtained at 100,K and analysed using Bader's `Atoms in Molecules' (AIM) approach. The results of the studies have provided unique insights into the bonding involving rhodium and highlight the importance of undertaking such investigations for transition metal compounds. [source]

Inverse bilayer structure of mononuclear CoII and NiII complexes of the type M(H2O)3(SO4)(4-CNpy)2

ACTA CRYSTALLOGRAPHICA SECTION B, Issue 4 2009
Birinchi K. Das
Two new metal compounds of the formula [M(H2O)3(SO4)(4-CNpy)2]·H2O [M = Ni (1) and Co (2), 4-CNpy = 4-cyanopyridine] have been prepared and studied by X-ray diffraction. In both of these compounds the 4-CNpy ligands are coordinated via pyridyl-N atoms to the metal ions in a cis fashion. The neutral complexes along with the uncoordinated H2O molecules are glued together preferentially into inverse bilayers by non-covalent interactions, including unique interlayer ,,, interactions between antiparallel nitrile groups. Hartree,Fock and density-functional theory (DFT) calculations indicate that the ,,, interactions are energetically significant. The unit-cell similarity index (,) of 0.0046 for the compounds suggests their isostructurality, which is also supported by their X-ray powder diffraction patterns that can be almost superimposed. [source]

Carbonyl group-containing organometallic intramolecular-coordination five-membered ring compounds

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 5 2010
Iwao Omae
Abstract Carbonyl group-containing organometallic intramolecular-coordination five-membered ring compounds are easily synthesized by the following five reaction methods: (1) cyclometalation, especially, orthometalation reactions; (2) the reactions of the moieties of an unsaturated carboncarbon bond attached to a carbonyl group (CCCO, CCCO); (3) the reactions of an unsaturated carboncarbon bond with carbon monoxide (CC and CO, CC and CO); (4) carbonylative ring expansion reactions; and (5) others. These compounds are very easily and regio-specifically synthesized with many kinds of metal compounds, including both transition metals and main group metals. Many of such the reactions are easily applied to organic syntheses. Copyright © 2010 John Wiley & Sons, Ltd. [source]

Silane reduction of onium salts

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 3 2010
James V. Crivello
Abstract Novel redox initiators for cationic polymerizations were developed consisting of an onium salt together with a SiH functional silane or siloxane. The reduction of the onium salt by the silane is catalyzed by noble metal complexes or certain transition metal compounds and takes place spontaneously at room temperature. The redox reaction of the onium salt with the silane results in the liberation of a strong Brønsted acid that can be subsequently used to initiate cationic polymerizations. Typical onium salts that have been employed in these redox initiator systems are diaryliodonium salts, triarylsulfonium salts and S,S -dialkyl- S -phenacylsulfonium salts. Studies of the effects of variations in the structures of the onium salt, the silane and the type of noble metal catalyst were carried out. In principle, the redox initiator systems are applicable to all types of cationically polymerizable monomers and oligomers, including the ring-opening polymerizations of such heterocyclic monomers as epoxides and oxetanes and, in addition, the polymerization of vinyl monomers such as vinyl ethers, N -vinylcarbazole and styrenic monomers. The use of these novel initiator systems for carrying out commercially attractive crosslinking polymerizations for coatings, composites and encapsulations is discussed. Copyright © 2009 John Wiley & Sons, Ltd. [source]

Characteristic reactions of group 9 transition metal compounds in organic synthesis

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 3 2009
Iwao Omae
Abstract Group 9 metal compounds in organic synthesis have two characteristic reactions. The first occurs because the group 9 metals have a high affinity to carbon,carbon or carbon,nitrogen ,-bonds. The first type of characteristic reactions in these group 9 metal compounds includes Pauson,Khand reactions, the Pauson,Khand-type reactions ([2 + 2 + 1] cyclization), the other cyclizations and coupling reactions. The second occurs because the group 9 metals have a high affinity to carbonyl groups. The second type of characteristic reactions includes carbonylations such as hydroformylations, the carbonylations of methanol, amidocarbonylations and other carbonylations. The first characteristic reactions are applied for the synthesis of fine chemicals such as pharmaceuticals and agrochemicals. However, the second characteristic reactions are utilized not only for fine chemicals but also for important bulk commodity chemicals such as aldehydes, carboxylic acids and alcohols. Copyright © 2009 John Wiley & Sons, Ltd. [source]

Three characteristic reactions of alkynes with metal compounds in organic synthesis

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 3 2008
Iwao Omae
Abstract Alkynes have two sets of mutually orthogonal ,-bonds that are different from the ,-bonds of alkenes. These ,-bonds are able to bond with transition metal compounds. Alkynes easily bond with the various kinds of compounds having a ,-bond such as carbon monoxide, alkenes, other alkynes and nitriles in the presence of the transition metal compounds. The most representative reaction of alkynes is called the Pauson,Khand reaction. The Pauson,Khand reactions include the cyclization of alkynes with alkenes and carbon monoxide in the presence of cobalt carbonyls. Similar Pauson,Khand reactions also proceed in the presence of other transition metal compounds. These reactions are the first type of characteristic reaction of alkynes. Other various kinds of cyclizations with alkynes also proceed in the presence of the transition metal compounds. These reactions are the second type of characteristic reaction of alkynes. These include cyclooligomerizations and cycloadditions. The cyclooligomerizations include mainly cyclotrimerizations and cyclotetramerizations, and the cycloadditions are [2 + 2], [2 + 2 + 1], [2 + 2 + 2], [3 + 2], [4 + 2], etc., type cycloadditions. Alkynes are fairly reactive because of the high s character of their ,-bonds. Therefore, simple coupling reactions with alkynes also proceed besides the cyclizations. The coupling reactions are the third type of characteristic reactions of alkynes in the presence of, mainly, the transition metal compounds. These reactions include carbonylations, dioxycarbonylations, Sonogashira reactions, coupling reactions with aldehydes, ketones, alkynes, alkenes and allyl compounds. Copyright © 2008 John Wiley & Sons, Ltd. [source]

Editorial: main group metal compounds

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 1 2003
Peter Craig
No abstract is available for this article. [source]

Metal-free MIRAS phasing: structure of apo-S100A3

ACTA CRYSTALLOGRAPHICA SECTION D, Issue 8 2002
Peer R. E. Mittl
S100 proteins are involved in metal-dependent intracellular signalling. Metal-free S100A3, a cysteine-rich Ca2+ - and Zn2+ -binding protein, has been crystallized by vapour diffusion under the strict exclusion of oxygen and in the absence of divalent metal ions. Metal binding induces large conformational changes, rendering the apo-S100A3 crystals very sensitive to various metal compounds. Therefore, the structure was solved by MIRAS phasing using potassium iodide and xenon derivatives. Iodide replaces a water molecule at the surface of the S100A3 protein, whereas xenon binds in a hydrophobic cavity at the dimer interface. Despite significant non-isomorphism, the combination of both derivatives was sufficient for structure determination. The overall apo-S100A3 structure resembles the structures of metal-free S100B and S100A6 solution structures. In contrast to the NMR structures, the EF-hand loops are well ordered in the apo-S100A3 crystal structure. In the N-terminal pseudo-EF-hand loop a water molecule occupies the position of the Ca2+ ion. The C-terminal canonical EF-hand loop shows an extended conformation and a different helix arrangement to other S100/metal complex crystal structures. [source]

Speciation of Rare-Earth Metal Complexes in Ionic Liquids: A Multiple-Technique Approach

CHEMISTRY - A EUROPEAN JOURNAL, Issue 6 2009
Peter Nockemann Dr.
Abstract The dissolution process of metal complexes in ionic liquids was investigated by a multiple-technique approach to reveal the solvate species of the metal in solution. The task-specific ionic liquid betainium bis(trifluoromethylsulfonyl)imide ([Hbet][Tf2N]) is able to dissolve stoichiometric amounts of the oxides of the rare-earth elements. The crystal structures of the compounds [Eu2(bet)8(H2O)4][Tf2N]6, [Eu2(bet)8(H2O)2][Tf2N]6,2H2O, and [Y2(bet)6(H2O)4][Tf2N]6 were found to consist of dimers. These rare-earth complexes are well soluble in the ionic liquids [Hbet][Tf2N] and [C4mim][Tf2N] (C4mim=1-butyl-3-methylimidazolium). The speciation of the metal complexes after dissolution in these ionic liquids was investigated by luminescence spectroscopy, 1H, 13C, and 89Y,NMR spectroscopy, and by the synchrotron techniques EXAFS (extended X-ray absorption fine structure) and HEXS (high-energy X-ray scattering). The combination of these complementary analytical techniques reveals that the cationic dimers decompose into monomers after dissolution of the complexes in the ionic liquids. Deeper insight into the solution processes of metal compounds is desirable for applications of ionic liquids in the field of electrochemistry, catalysis, and materials chemistry. [source]