Abstract: A precursor is made by mixing a metal alkoxycarboxylate-containing liquid with a 2-ethylhexanoic acid in an effective amount for shelf-stabilizing said liquid by substituting 2-ethylhexanoate ligands for alkoxide ligands, thereby forming a mixture, and heating said mixture to substitute said carboxylate ligands for said alkoxide ligands. Specficially, a barium strontium titanate precursor and a strontium bismuth tantalate precursor are made by combining polyoxyalkylated metal moieties to form a liquid solution in which the metal atoms bond with an oxygen atom in a ligand selected from a ligand group consisting of alkoxides and carboxylates, then then heating the liquid solution.

Abstract: A catalyst precursor is provided which is useful, when combined with a cocatalyst, in the manufacture of polyolefins. The catalyst precursor is of the formula: ##STR1## where M is a transition metal, preferably Zr or Hf; L is a substituted or unsubstituted, .pi. bonded ligand coordinated to M, preferably a cyclopentadienyl-type ligand; Q can be the same or different and is independently selected from the group consisting of --O, --NR, --CR.sub.2 and --S; Y is either C or S; Z is selected from the group consisting of --OR, --NR.sub.2, --CR.sub.3, --SR, --SiR.sub.3, --PR.sub.

Abstract: A synthetic nickel (or cobalt) containing hydrotalcite-like material having a sheet-like morphology and a sheet broadness to thickness ratio of at least 50 and a formula M.sub.1-x Al.sub.x (OH).sub.2 .multidot.xA.multidot.mH.sub.2 O where M is Ni or Co, A is a mono carboxylic anion of the form RCOO.sup.- where R is C.sub.n H.sub.2n+1 and n=0-5, and x and m are numbers satisfying the following conditions:0.2<=x<=0.40.0<=m<=4It is made by starting with a synthesis mixture having Ni or Co (divalent cation) to aluminum (trivalent cation) molar ratio between 1:1 and 10:1, mono carboxylic anion to aluminum (trivalent cation) molar ratio between 0.1:1 to 1.2:1 and optionally added other anions. The process comprises of reacting a mixture comprising nickel (or cobalt) and aluminum cations and mono carboxylic anions in an aqueous slurry at a temperature of at least 40.degree. C. and a pH of at least 7.

Abstract: A first metal, an alcohol, and a carboxylic acid are reacted to form a metal alkoxycarboxylate which is then reacted with an alkoxide and/or a carboxylate of a second metal to form a precursor. Alternatively, a metal carboxylate and a metal alkoxide are combined and heated to form a precursor. In either alternative, the precursor includes all or most of the metal-oxygen-metal bonds of a desired metal oxide and a carboxylate ligand. The precursor is applied to a substrate, dried and annealed to form the metal oxide, such as BST. The metal-oxygen-metal bonds in the precursor permit the desired metal oxide to be formed from the precursor in one step, providing excellent thin films suitable for integrated circuits. The carboxylate ligand provides stability to the precursor allowing it to be stored for periods common in large scale manufacturing.

Abstract: An imaging contrast medium comprising a physiologically tolerable multinuclear complex (as defined in claim 1) is disclosed. The multinuclear complex contains at least two, but preferably three or more contrast enhancing atoms. For X-ray or ultrasound imaging techniques heavy metal atoms are used to enhance contrast, whereas in Magnetic Resonance Imaging paramagnetic metal atoms are contrast enhancing. Molybdenum and tungsten are preferred contrast enhancing atoms. The medium may also be used therapeutically.

Abstract: Novel compounds obtainable by reacting together an imido-reagent such as diphenylphosphonimidotriphenylphosphorane) with a chelate of a transition or lanthanide or actinide metal, such as tris(dibenzoylmethide) europium III, has the property of fluorescing in UV radiation. The invention includes solid polymer bodies containing such compounds, or chelates of transition or lanthanide or actinide metals generally, the bodies having the property of emitting light by virtue of internally generated, e.g. by tritium ionising radiation. The body is preferably of polystyrene formed by polymerising the monomer in the presence of the compound or metal chelate.

Abstract: A synthetic hydrotalcite-like material having a sheet-like morphology and a sheet broadness to thickness ratio of at least 50 and a formula Mg.sub.1-x Al.sub.x (OH).sub.2.xA.mH.sub.2 O where A is a mono carboxylic anion of the form RCOO.sup.- where R is C.sub.n H.sub.2n+1 and n=0-5, and x and m are numbers satisfying the following conditions:0.2<=x<=0.40.0<=m<=4It is made by starting with a synthesis mixture having magnesium (divalent cation) to aluminum (trivalent cation) molar ratio between 1:1 and 10:1, mono carboxylic anion to aluminum (trivalent cation) molar ratio between 0.1:1 to 1.2:1 and optionally added other anions. The process comprises of reacting a mixture comprising magnesium and aluminum cations and mono carboxylic anions in an aqueous slurry at a temperature of at least 40.degree. C. and a pH of at least 7.

Abstract: Novel hydrophobicized double-layer hydroxide compounds, processes for their production by reaction of double-layer hydroxides with aliphatic mono- and/or dicarboxylic acids, and their uses as alkoxylation catalysts for compounds containing active H atoms or for fatty acid esters.The hydrophobicized double-layer hydroxide compounds correspond to formula (I)(M(II).sub.1-x M(III).sub.x (OH).sub.2)A.sub.a B.sub.b * z H.sub.2 O (I)in whichM(II) is a divalent metal cation selected from the group consisting of magnesium, zinc, calcium, iron, cobalt, copper, cadmium, nickel and manganese;M(III) is a trivalent metal cation selected from the group consisting of aluminum, iron, chromium, manganese, bismuth and cerium;A is an equivalent of a monoanion of an aliphatic C.sub.2-34 monocarboxylic acid or an equivalent of a dianion of an aliphatic C.sub.

Abstract: Metal organic compounds comprising three atoms of cobalt, nickel or bismuth each linked through oxygen atoms to boron or phosphorus and comprising a combination of aliphatic and aromatic carboxylic acid residues are useful as adhesion promoters to promote the adhesion of brass-coated steel to vulcanised rubber.

Abstract: The disclosure is of the use of chrome humate derivatives to reduce the viscosity of and/or to prevent fluid loss in water-based drilling fluids. The composition is much more effective as a drilling mud thinner, and as a fluid loss control agent than the commercially available ferrochrome lignosulfonate, chrome lignite or humate compositions.

Abstract: The peroxides which include the O.sup.17 isotope, especially the hydrogen peroxides and peroxides and hydroperoxides prepared therefrom, are well adapted as nonradioactive labeled compounds for use in the medicinal and biological arts.

Abstract: The present invention is predicated on the discovery that Mo(III) containing compounds will react with salts of a 1,1-dithioacid to form Mo.sub.4 S.sub.4 L.sub.6. Accordingly, there is provided a method for preparing compounds of the formula Mo.sub.4 S.sub.4 L.sub.6 wherein L is a 1,1-dithioacid ligand comprising:contacting a Mo(III) containing compound with the salt of a 1,1-dithioacid at temperatures and for a time sufficient to form the Mo.sub.4 S.sub.4 L.sub.6 compound. Preferably, the Mo(III) containing compound is dissolved in an organic solvent and the solution is heated at temperatures above about 25.degree. C. up to the boiling point of the solvent and, preferably, at temperatures in the range of about 25.degree. C. to about 250.degree. C.

Abstract: The invention relates to a catalytic process for the synthesis of an alcohol by reaction of an epoxide with a nucleophilic compound containing a labile hydrogen, such as an alcohol, a phenol, a primary amine or a carboxylic acid.The catalyst is a metal complex of general formula (I)[M[Co(CO).sub.4 ].sub.2 ].sub.x in which x is equal to 1 or 2 and M denotes tin, lead and cadmium.The reaction preferably takes place in the presence of carbon monoxide.This process makes it possible to increase the yield and the selectivity of the reaction and the stereoselectivity for alcohol in the case of which the hydroxyl formed is attached to the least hindered carbon atom of the epoxide.The invention also relates to the new complexes of formula (I) in which x equals 2.It also relates to a process for the electrosynthesis of these new compounds by electroreduction of Co.sub.2 (CO).sub.

Abstract: A process for preparing single enantiomers of chiral sulphoxides is provided. The process involves (a) reacting an achiral sulphur-containing compound, e.g. a disulphide, with a single enantiomer of a chiral template having the formula T-(CO)-CH.sub.2 R.sup.1, wherein T is suitably (eta.sup.5 -C.sub.5 H.sub.5)Fe(CO)(PPh.sub.3)- (Ph=phenyl) and (b) thereafter stereospecifically oxidizing the sulphur atom with an oxidizing agent. A single enantiomer of the chiral sulphoxide can then be generated by reacting the oxidized product with a carbanion. In a preferred embodiment the reaction mixture is thereafter treated with further achiral sulphide to provide a process which is catalytic on the chiral template.

Abstract: An aluminum- and titanium-containing oligomer is prepared by a controlled hydrolysis reaction between a chelated aluminum compound and an organotitanium compound. The oligomer is heated to 800.degree. C. in an oxygen-containing atmosphere to produce .beta.-aluminum titanate.

Abstract: The present invention constitutes a class of organometallic complexes which reversibly react with hydrogen to form dihydrides and processes by which these compounds can be utilized. The class includes bimetallic complexes in which two cyclopentadienyl rings are bridged together and also separately .pi.-bonded to two transition metal atoms. The transition metals are believed to bond with the hydrogen in forming the dihydride. Transition metals such as Fe, Mn or Co may be employed in the complexes although Cr constitutes the preferred metal. A multiple number of ancilliary ligands such as CO are bonded to the metal atoms in the complexes. Alkyl groups and the like may be substituted on the cyclopentadienyl rings. These organometallic compounds may be used in absorption/desorption systems and in facilitated transport membrane systems for storing and separating out H.sub.2 from mixed gas streams such as the produce gas from coal gasification processes.

Abstract: Titanocenes with .pi.-cyclopentadienyl ligands, in which one or two carbocyclic or heterocyclic aromatic rings are bonded to the metal, the aromatic rings being substituted in at least one of the two ortho-positions relative to the metal-carbon bonds by CF.sub.2 Z (Z=F or substituted or unsubstituted alkyl), are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds. They are distinguished by a high radiation sensitivity, stability to air and thermal effects, and high effectiveness in the range from UV light to visible light.

Abstract: Broadly stated, the present invention encompasses tetranuclear sulfide-bridged complexes of Cr(III) having bridging organo-carboxylate ligands. Indeed, in one embodiment, the present invention is directed toward a novel composition of matter having a complex cation of the general formula Cr.sub.4 S(RCO.sub.2).sub.8 (L).sub.4.sup.2+, wherein R represents alkyl groups having from 1 to 12 carbon atoms, L represents a ligand or ligands containing a donor atom selected from oxygen, nitrogen, carbon, and sulfur. In the complex of the present invention, the four Cr(III) atoms are bound to a central tetrahedral sulfur atom. The chromium atoms also are octahedrally coordinated with bridging carboxylates and the ligand molecule. Also, the bridging carboxylates, RCO.sub.2 of the above formula, are the same or different carboxylates.

Abstract: A solid material useful for producing hexagonal ferrites comprises a homogeneous mixture of the cations of the composition (I) and one or more anions comprising one or more thermally decomposable anions.

Abstract: The disclosed particulate composition of simple or mixed oxalate of ferromagnetic metals is characterized in that it is provided in the form of needle-shaped particles having a length comprised between 0.05 and 0.5 micrometer, with a proportion higher than 60% of particles having a length equal to the average length .+-.0.1 .mu.m. and an acicular ratio higher than 3, said average length being comprised between 0.15 and 0.35 .mu.m; its preparation and its application are also disclosed.

Abstract: This invention relates to heterometallic thiocubane compositions containing the M.sub.2.sup.1 M.sub.2.sup.2 S.sub.4 cluster core and methods of making them wherein M.sup.1 is Re, V, Mo or W and M.sup.2 is Co, Cr, Cu, Ni or Fe but preferably Co. More particularly, the invention relates to compositions of the formula M.sub.2.sup.2 M.sub.2.sup.2 S.sub.4 L.sub.2.sup.1 L.sub.2.sup.2 L.sub.2.sup.3 wherein M.sup.1 and M.sup.2 are as above, L.sup.1 is a bidentate sulfur or nitrogen bearing ligand (most preferably a dialkyldithiocarbamate), L.sup.2 is optional but may be an O, N, P or S-containing monodentate donor ligand, and L.sup.3 may be CO, a monodentate anion ligand such as a halide (preferably C1), mercaptide or alkoxide, or another O, N, P, or S containing monodentate donor ligand. The compositions are suitable for making active hydrotreating catalysts.

Abstract: Described are novel bimetallic complexes particularly useful as homogeneous catalysts for the metathesis of alkynes and metathesizable functionally substituted alkynes, and methods for the preparation of such complexes. The complexes are formed from (i) a Group VI-B metal compound having (a) quadruple metal to metal bonds between a pair of Group VI-B metal atoms at least one of which has an atomic number above 24, and (b) four monovalent anions with a k.sub.A greater than 10.sup.-14, and (ii) a Group III-A phenoxide, a Group III-A alkoxide or a Group IV-B metal alkoxide. Displacement of two of the anions appears to occur during formation of the complex. Usually the complexes can be produced very easily and quickly. All that is required is to establish intimate contact between components (i) and (ii), preferably in an innocuous liquid organic solvent. Addition of a small amount of a nitrile gives a faster and cleaner reaction. In some cases use of slightly elevated temperatures is desirable.

Abstract: The present invention is directed to high-coordination transition metal complexes, i.e., those of coordination number seven and above, and the use thereof in the room temperature/atmospheric pressure formation of carbon-carbon bonds via reductive coupling of linear carbon-containing ligands, and methods for the isolation and recovery of the newly formed C.sub.2 containing species.

Abstract: A hydroformylation catalyst of the formulaL.sub.a CuCo(CO).sub.b L'cwherein L is a monodentate phosphine, a bidentate phosphine or a bidentate amine, a is 1-3, b is 3 or 4, c is 0 or 1; provided that, where b=4, c=0 and L' is CO, phosphine or phosphite. Where the catalysts have the formulaL.sub.a CuCo(CO).sub.4the compounds are novel.