Abstract: Organometallic complex having the formula (IAP)M(X)n which can be used for die formation of catalytic systems wherein: M is a metal selected from transition metals and lanthanides, in oxidation state “s” positive and different from zero; each X is independently a group of an anionic nature bound to the metal as an anion in an ionic couple or with a convalent bond of the “&sgr;” type; “n” expresses the number of X groups sufficient for neutralizing the formal “+s” charge of the metal M, and (IAP) represents a neutral bond consisting of a mono-imine of 2,6-diacylpyridine. Said complex is prepared with relatively simple methods and can be used, combined with a suitable co-catalyst, such as for example, an aluminoxane, as a catalyst in normal (co)polymerization processes of &agr;-olefins, and especially ethylene.

Abstract: A catalyst composition for living free radical polymerization. The catalyst composition includes a transition metal complex MXp and a ligand, wherein M is a transition metal; X is halogen, —NO2, —NCS, —NCO, —SCN, —CN, —N3, —SO4, carboxylate group, or —PF6; p is the valence of the transition metal, the ligand is represented by formula (I): wherein R1 can be the same or different and is C1-20 alkyl, C6-20 aryl, C7-20 alkylaryl, C7-20 arylalkyl, or heterocyclic groups; R2 can be the same or different and is H, C1-20 alkyl, C6-20 aryl, C7-20 alkylaryl, C7-20 arylalkyl, heterocyclic groups, alkyl sulfide groups, nitrile groups, alkylsilyl, or ester groups; n is an integer of 0 to 6; and A is deleted or an S or O atom, wherein the molar ratio of the transition metal complex MXp and the ligand is 1 to 4.

Abstract: A compound useful as a cocatalyst or cocatalyst component, especially for use as an addition polymerization catalyst compound, corresponding to the formula: (A*+a)b(Z*J*j)−cd, wherein:

Abstract: Rational combinatorial computational methods use accurate quantum mechanical and molecular modeling techniques to identify optimum polymerization catalysts for polar olefins. Using mechanistic information to model the polymerization reaction, the methods systematically vary components of a catalyst template to calculate a potential energy surface for a number of catalyst candidates. The potential energy surfaces are compared to identify a catalyst for the catalytic polymerization reaction. Internal Lewis acid single site polar olefin polymerization catalyst compositions and compounds for polymerizing polar olefins are also described.

Abstract: Compounds of the formula (I) and (Ia) in the form of racemates, mixtures of diastereomers or in essentially enantiomerically pure form, (I), (Ia), where R is hydrogen, C1-C8alkyl, C5-C12cycloakyl, phenyl or phenyl substituted by from 1 to 3 C1-C4alky or C1-C4alkoxy groups; n is 0 or an integer from 1 to 4 and R1 are identical or different substituents selected from the group consisting of C1-C4alkyl, C1-C4fluoroalkyl and C1-C4alkoxy; X1 and X2 are each, independently of one another, secondary phosphino; T is C6-C20arylene or C3-C16heteroarylene; and X2 is bound in the ortho position relative to the T-cyclopentadienyl bond.

Abstract: Certain complexes containing ligands having a phosphino group, amino group or an imino group, and a second functional group such as amide, ester or ketone, when complexed to transition metals, catalyze the (co)polymerization of olefinic compounds such as ethylene, &agr;-olefins and/or acrylates. A newly recognized class of ligands for making copolymer containing polar monomers using late transition metal complexes is described.

Abstract: A catalyst system useful for polymerizing olefins is disclosed. The catalyst system comprises an activator and a bimetallic complex that incorporates two Group 3 to 10 transition metal atoms, which may be the same or different, and a neutral or anionic indigoid ligand. By proper selection of the indigoid skeleton and by modifying its substituents and transition metal centers, polyolefin makers can fine-tune the bimetallic complexes to control activity, enhance comonomer incorporation, and optimize polymer properties.

Abstract: The invention discloses a solid catalytic component comprising a metallocene, at least one first ligand of which comprises a cyclopentadienyl group chemically bonded via a methyl group to a support composed of a porous inorganic compound. It also discloses a process for the preparation of such a solid catalytic component.

Abstract: Copolymerization of Ni(II) phenol imine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: A composition suitable for use as a catalyst for the reaction of an isocyanate compound or prepolymer thereof with an alcohol to form a polyurethane comprises a mixture of (a)an organometallic compound selected from: (i) a compound of formula M(RO)4, where M is titanium, zirconium, hafnium, aluminium, cobalt or iron or a mixture of these metals and OR is the residue of an alcohol ROH in which R comprises an (optionally substituted) C1-30 cyclic, branched or linear, alkyl, alkenyl, aryl or alkyl-aryl group or a mixture thereof, or; (ii) a complex of titanium, zirconium and/or hafnium and an acetoacetate ester and (b) a coordinating compound selected from a ketone, aldhehyde, carboxylic acid, sulphonic acid, nitride or an imine. An isocyanate composition containing a catalyst of the claimed composition is also described.

Abstract: The present invention is directed to a process for the production of monoalkylin trihalides of the formula RSnX3 wherein R-alkyl or cycloalkyl and X—Cl, Br or I involving a redistribution reaction between tetraorganotins, triorganotin halides or diorganotin halides and tin tetrahalides, said process comprising contacting tetra-(R4Sn), tri-(R3SnX) or diorganotin halides (R2SnX2) with SnX4 to afford said monoorganotin trihalides in the presence of at least one transition metal complex, said complex comprising at least one transition metal M, selected from Group VIII of the periodic Table of elements, at least one monodentate ligand or bidentate ligand, L, L′, or L″, and optionally one or more anions, X, of an organic or inorganic acid, as a catalyst or catalyst precursor.

Abstract: Polyolefins, preferably polyethylene, having a density of about 0.86 to about 0.93 g/mL, and having methyl branches and at least branches of two other different lengths of six carbon atoms or less, form heat seals at exceptionally low temperatures, thereby allowing good seals to be formed rapidly. This is advantageous when heat sealing these polyolefins, for example in the form of single or multilayer films.

Abstract: Bridged catalyst component in which a bridge spans two cylcopentadienyl or aromatic groups. The Cp or aromatic groups are attached to the same or different heteroatoms of the bridge, which heteroatoms are also bonded to a metal. A catalyst system can be made by contacting the bridged component with a cocatalyst. Polymerization of olefins can be catalyzed by the system.

Abstract: A series of novel late transition metal catalysts for olefin oligomerization have been invented. The catalysts demonstrate high activity and selectivity for linear &agr;-olefins.

Abstract: Novel nitrogen containing transition metal complexes have general formula (I): wherein M is Fe[II], Fe[III], Ni[II], Co[I], Co[II], Co[III], V[III], Mn[I], Mn[II], Mn[III], Mn[IV], Ru[II], Ru[III] or Ru[IV]; Pd[II], V[III], V[IV] or V[V]. X represents an atom or group covalently or ionically bonded to the transition metal M; R is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl; Z is a bridging group comprising a donor atom of N, P or S or alternatively is a neutral group comprising a C1-C4 alkylene group, a silyl or germyl group, and n= an integer to satisfy the valency of M.

Abstract: In one aspect, the invention includes a method of forming a roughened layer of platinum, comprising: a) providing a substrate within a reaction chamber; b) flowing an oxidizing gas into the reaction chamber; c) flowing a platinum precursor into the reaction chamber and depositing platinum from the platinum precursor over the substrate in the presence of the oxidizing gas; and d) maintaining a temperature within the reaction chamber at from about 0° C. to less than 300° C. during the depositing. In another aspect, the invention includes a platinum-containing material, comprising: a) a substrate; and b) a roughened platinum layer over the substrate, the roughened platinum layer having a continuous surface characterized by columnar pedestals having heights greater than or equal to about one-third of a total thickness of the platinum layer.

Abstract: Disclosed is a novel bidentate pyridine transition metal catalyst having the general formula where each R is independently hydrogen, C1-6 alkyl, or C6-14 aryl; where each R′ is independently R, C1-6 alkoxy, C7-20 alkaryl, C7-20 aralkyl, halogen, or CF3; where M is a Group 3 to 10 metal; where each X is independently halogen, C1-6 alkyl, C6-14 aryl, C7-20 alkaryl, C7-20 aralkyl, C1-6 alkoxy, or  L is X, cyclopentadienyl, C1-16 alkyl-substituted cyclopentadienyl, fluorenyl, indenyl, or  where n is an integer from 1 to 4; a is an integer from 1 to 3; b is an integer from 0 to 2; the sum of a+b≦3; c is an integer from 1 to 6; and the sum a+b+c equals the oxidation state of M.

Abstract: The present invention relates to novel hexacoordinated metathesis catalysts and to methods for making and using the same. The inventive catalysts are of the formula wherein: M is ruthenium or osmium; X and X1 are the same or different and are each independently an anionic ligand; L, L1′ and L2 are the same or different and are each independently a neutral electron donor ligand, wherein at least one L, L1′ and L2 is an N-heterocyclic carbene ligand; and, R and R1 are each independently hydrogen or a substituent selected from the group consisting of C1-C20 alkyl, C2-C20 alkenyl, C2-C20 alkynyl, aryl, C1-C20 carboxylate, C1-C20 alkoxy, C2-C20 alkenyloxy, C2-C20 alkynyloxy, aryloxy, C2-C20 alkoxycarbonyl, C1-C20 alkylthio, C1-C20 alkylsulfonyl and C1-C20 alkylsulfinyl.

Abstract: A catalyst system is provided. In one aspect, the catalyst system includes one or more polymerization catalysts and at least one activator.

Abstract: In metallocene complexes of a metal of transition group IV, V or VI of the Periodic Table, at least one substituted or unsubstituted cyclopentadienyl radical is bound to an element of group III of the Periodic Table which is in turn a constituent of a bridge between this cyclopentadienyl radical and the metal atom and bears an organonitrogen, organophosphorus or organosulfur group as sole further substituent.

Abstract: This invention is directed to a catalyst and an associated process for polymerizing olefins or olefin-containing compounds, to corresponding olefin polymers, to derivatives of the olefin polymers, and to lubricant and fuel compositions that include the olefin polymers or their derivatives. The polymerization catalyst is a metal complex and optional cocatalyst where the metal complex is formed from a bidentate ligand having a nitrogen coordinating group and a second coordinating group selected from oxygen, sulfur, selenium and tellurium groups and a metal compound where the metal is a transition metal, boron, aluminum, germanium or tin. Highly branched and reactive ethylene polymers are formed from the catalyst and process of the present invention. The ethylene polymers and their derivatives are useful in various applications including as performance additives in lubricants and fuels.

Abstract: Disclosed is a novel class of modified ruthenium catalysts useful in the one step synthesis of 1,3-PDO comprising (a) a cobalt component comprising one or more non-ligated cobalt compounds; and (b) a ruthenium component comprising in major part a ruthenium carbonyl compound ligated with a phospholanoalkane ligand, solubilized in an ether solvent, that provides potential improvements in cost and performance in one step hydroformylation/hydrogenation. For example, cobalt-ruthenium-bidentate, bis(phospholano)alkane catalyst precursors in ether solvents provide good yields of 1,3-PDO in a one step synthesis.

Abstract: Organolead compounds such as tetraethyllead are useful in catalyst compositions for the oxidative carbonylation of hydroxyaromatic compounds to diaryl carbonates. They are employed in combination with a Group 8, 9, or 10 metal such as palladium, or a compound thereof, and a bromide or chloride such as tetraethylammonium bromide.

Abstract: Functional polymers containing hydroxyl groups as supports for use with catalysts can increase the activity of these catalysts which results in improved ethylene polymerization. The present invention seeks to provide catalysts with improved activity by incorporating 2-hydroxyethyl methacrylate (HEMA) into the support of the catalyst.

Abstract: Zwitterionic compositions of matter comprising cations [Ct]+ and anions connected together with substantially rigid fluorinated linking groups are described. These zwitterionic compositions serve as cocatalysts. They activate olefin polymerization catalysts, and can dissolve in aliphatic solvents. Synthesis and polymerization are illustrated.

Abstract: An olefin polymerization pre-catalyst, an activated catalyst and a process for preparing the catalysts are described herein.

Abstract: Olefins, such as ethylene, are polymerized using as a polymerization catalyst a complex of a selected transition metal with an anionic ligand that has at least three atoms that may coordinate to the transition metal. Also disclosed are the above selected transition metal complexes, and intermediates thereto.

Abstract: A catalyst for olefin polymerization having the following structural formula (I): wherein R1 is selected from the group consisting of hydrogen, C1-C12 alkyl, C1-C12 alkoxy, or C6-C12 aryl, R2 and R2′ are respectively selected from hydrogen and C1-C4 alkyl, R3 is selected from the group consisting of hydrogen, C1-C12 alkyl, C1-C12 alkoxy and C6-C12 aryl, and M is selected from Ti, Zr, and Hf The catalyst is suitable for olefin polymerization to yield polymerized products with high molecular weight and high insertion rate of comonomers.

Abstract: Catalyst systems useful for olefin polymerization are disclosed. The catalysts include a bimetallic complex that incorporates two linked indenoindolyl groups, each of which is pi-bonded through its cyclopentadienyl ring to one of the metals Compared with conventional indenoindolyl complexes, the bimetallic complexes of the invention have enhanced ability to give polyolefins with desirably low melt indices. Certain bimetallic indenoindolyl complexes also provide a way to broaden polymer molecular weight distribution and thereby improve processability simply by regulating the amounts of comonomer and activator used in the polymerization.

Abstract: The invention relates to phosphacyclohexanes of general formulae I and II, wherein the following designations, among others, apply: R can represent hydrogen, C1-100-alkyl, C7-20-aralkyl, C7-20-alkaryl, and C6-12-aryl: R1 to R10 can independently represent hydrogen, C1-20-alkyl, C7-20-aralkyl, C7-20-alkaryl, and C6-12-aryl: W, W′ can independently represent single bonds or bridges comprising 1 to 20 carbon atoms, which can form part of a cyclic or aromatic group and can be interrupted by heteroatoms. Said phosphacyclohexanes are used as ligands in transition metal complexes of transition metals belonging to groups VIII to X of the periodic table.

Abstract: Bridged metallocene catalyst component in which a bridge spans two cyclopentadienyl groups, which Cp groups are attached to same or different heteroatoms of the bridge, which heteroatoms are also bonded to the metal. A catalyst systems is made by contacting the bridged component with a cocatalyst. Polymerization of olefins in catalyzed by the system.

Abstract: Processes of producing fluorided catalyst compounds and process of producing polyolefins using these catalyst compounds are disclosed. An embodiment of the process includes contacting a nitrogenous metallocene compound with a fluoriding agent, which preferably includes a fluorided anhydrous acid, for a time sufficient to form a fluorided metallocene catalyst compound.

Abstract: Alpha-olefins are manufactured in high yield and with very high selectivity by contacting ethylene with an iron complex of a selected 2,6-pyridinedicarboxaldehyde bisimine or a selected 2,6-diacylpyridine bisimine, and in some cases a selected activator compound such as an alkyl aluminum compound. Novel bisimines and their iron complexes are also disclosed. The &agr;-olefins are useful as monomers and chemical intermediates.

Abstract: The present invention relates to a process for the polymerization of monomers utilizing a bulky ligand hafnium transition metal metallocene-type catalyst compound, to the catalyst compound itself and to the catalyst compound in combination with an activator. The invention is also directed to an ethylene copolymer composition produced by using the bulky ligand hafnium metallocene-type catalyst of the invention, in particular a single reactor polymerization process.

Abstract: A compound is provided including an organometallic complex represented by the formula I: [CpM(CO)2(NHC)Lk]+A−  I wherein M is an atom of molybdenum or tangsten, Cp is substituted or unsubstituted cyclopentadienyl radical represented by the formula [C5Q1Q2Q3Q4Q5], wherein Q1 to Q5 are independently selected from the group consisting of H radical, C1-20 hydrocarbyl radical, substituted hydrocarbyl radical, halogen radical, halogen-substituted hydrocarbyl radical, —OR, —C(O)R′, —CO2R′, —SiR′3 and —NR′R″, wherein R′ and R″ are independently selected from the group consisting of H radical, C1-20 hydrocarbyl radical, halogen radical, and halogen-substituted hydrocarbyl radical, wherein said Q1 to Q5 radicals are optionally linked to each other to form a stable bridging group, NHC is any N-heterocyclic carbene ligand, L is either any neutral electron donor ligand, wherein k is a number from 0 to 1 or L

Abstract: Phosphine compounds represented by the following formula (1): 1

Abstract: The present invention provides a method of synthesizing fluorided metallocene catalyst components comprising contacting at least one fluoriding agent comprising fluorine with one or more alkylated metallocene catalyst components comprising one or more non-halogen leaving groups to produce a fluorided catalyst component; wherein from less than 3 equivalents of fluorine are contacted for every equivalent of leaving group.

Abstract: A supported catalyst for olefin polymerization comprises a combination of a sulfated metal oxide support, an aluminoxane and an organometallic complex of a group 4 metal. The sulfated metal oxide may be quickly and conveniently prepared by, for example, contacting the precursor metal oxide with a sulfuric acid. The supported catalyst of this invention is highly active for olefin polymerization in comparison to conventional catalysts which are prepared with non-sulfated supports.

Abstract: A process for producing substantially amorphous propylene (co)polymers, comprising contacting propylene optionally in the presence of one or more olefins under polymerization conditions with a catalyst system comprising: A) a half sandwich titanium complex wherein the cyclopentadienyl is substituted with one or two heterocyclic rings, according to formula (I): cf formula (I) in claim 1: wherein X is N or P; Z is C, Si or Ge; Y1 is an atom selected from the group consisting of NR7, O, PR7 or S; Y2 is selected from the group consisting of CR8 or Y1 and m is 0 or 1 and B) an activating cocatalyst. The above titanium complex and the ligand useful as intermediates in their synthesis are also described.

Abstract: A supported catalyst for olefin polymerization comprises a combination of a novel metal oxide support and an activator which is an aluminoxane or a boron activator. The novel metal oxide support of this invention is a conventional particulate metal oxide support material (such as silica or alumina) which has been treated with a halosulfonic acid. A catalyst system which contains this novel catalyst support and a transition metal catalyst is highly active for olefin polymerization (in comparison to prior art catalyst systems which use a conventional metal oxide support).

Abstract: The inventions disclosed herein are catalyst systems comprising a complex having one of the formulas LMX1X2 and LML′ and an activating cocatalyst, and use of the catalyst system in polymerizing olefinic monomers. In either of the foregoing formulas, L is a chelating ligand containing sulfur donors; M is a transition metal selected from either copper, silver, gold, manganese, iron, cobalt, palladium or nickel; X1 and X2 are independently selected from either halides, hydride, triflate, acetate, borate, alkyl, alkoxyl, cycloalkyl, cycloalkoxyl, aryl, thiolate, carbon monoxide, cyanate or olefins; and L′ is a bidentate ligand selected from either dithiolene, dithiolate, diphosphine, bisimine, bispyridine, phenanthroline, oxolate, catecholate, thiolatoamide, thiolatoimine or thiolatophosphine.

Abstract: Useful as a catalyst component for polymerizing olefin is the transition metal compound of the present invention represented by Formula (I): wherein M represents a transition metal compound of the fourth group in the periodic table; X represents a &sgr; bonding ligand; Y represents a Lewis base; T represents a group containing a &sgr; bonding atom; E is a specific group containing an atom which can coordinate with M via a lone pair; q is 1 or 2 and represents [(valency of M)−2]; r represents an integer of 0 to 3; R1 to R4 represent a hydrogen atom, a halogen atom, a hydrocarbon group, a halogen-containing hydrocarbon group, a silicon-containing group or a hetero atom-containing group.

Abstract: Storage stability of one-component elastomers prepared from constituents having alkoxysilyl end groups is enhanced by employing bin compounds having a coordination number of 5 or 6 in which tin is coordinately bonded to a P═O group as at least one condensation catalyst.

Abstract: Chiral phosphine ligands derived from chiral natural products including D-mannitol and tartaric acid. The ligands contain one or more 5-membered phospholane rings with multiple chiral centers, and provide high stereoselectivity in asymmetric reactions.

Abstract: A compound useful as a cocatalyst or cocatalyst component, especially for use as an addition polymerization catalyst compound, corresponding to the formula: (A*hu +a)b(Z*J*j)−cd, wherein: A* is a proton or a cation of from 1 to 80 atoms, preferably 1 to 60 atoms, not counting hydrogen atoms, said A* having a charge +a; Z* is an anion group of from 1 to 50 atoms, preferably 1 to 30 atoms, not counting hydrogen atoms, further containing two or more Lewis base sites, said Z* being the conjugate base of an inorganic Bronsted acid or a carbonyl- or non-cyclic, imino-group containing organic Bronsted acid; J* independently each occurrence is a Lewis acid of from 1 to 80 atoms, preferably 1 to 60 atoms, not counting hydrogen atoms, coordinated to at least one Lewis base site of Z*, and optionally two or more such J* groups may be joined together in a moiety having multiple Lewis acidic functionality; j is a number from 1 to 12; and a, b, c, and d are integers from 1 to 3, with the proviso that a

Abstract: There are provided (asymmetric) complex catalysts comprising metal complexes and Lewis acids as components, the metal complex being of formula (1): 1

Abstract: Process for making a non-pourable ultra-low molecular weight ethylene polymer composition and blends thereof. Such polymer compositions tend to have longer lamella and a greater degree of crystalline organization than corresponding higher molecular weight materials at an equivalent density.

Abstract: A catalyst composition for the polymerization of olefins is provided which comprises a catalyst compound and a co-catalyst or a support material or both a co-catalyst and a support material, wherein the catalyst compound comprises a transition metal of Group 4, 5 or 6, an organic compound containing at least one lone pair of electrons, a divalent radical and a Lewis basic group having the following formula: —C(R7)=Z1R8,  (i) wherein R7 and R8 are each independently selected from the group consisting of hydrogen and C1-C8 hydrocarbyl groups, and wherein R7 and R8 are not linked or are linked to form a saturated or unsaturated ring; and Z1 is a nitrogen atom or a phosphorus atom, which bonds to M; or  wherein: Z2 is an oxygen atom, a sulphur atom or a selenium atom, which bonds to the transition metal compound; and R9, R10 and R11 are each independently selected from the group consisting of hydrogen and C1-C8 hydrocarbyl groups, wherein no pair or one pair of su

Abstract: The present invention relates to organometallic compounds of transition metals with an indenyl ligand bonded in the 2-position and substituted in the 1,3-position, a process for their production, and their use as catalysts for the (co)polymerization of olefinic and/or diolefinic monomers.

Abstract: Chiral phospholanes having biaryl chirality for applications in asymmetric catalysis are provided. A series of new chiral mono- or bidentate phosphorus ligands were efficiently prepared through a key intermediate (S)-4-chloro-4,5-dihydro-3H-4-phospha-cyclohepta[2,1-a;3,4-a′]binaphthalene and its derivatives. These ligands were complexed with transition metals to prepare catalysts, which were used in asymmetric catalytic reactions, such as, asymmetric hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution or [m+n] cycloaddition wherein m=3 to 6 and n=2.