Novel, lubricious coatings for medical devices are disclosed. The coatings provide improved lubricity and durability, and are readily applied in coating processes. The present invention is also directed to a novel platinum catalyst for use in such coatings. The catalyst provides for rapid curing, while inhibiting cross-linking at ambient temperatures, thereby improving the production pot life of the coatings.

Disclosed herein are dialkyl cobalt complexes containing pyridine di-imine ligands and their use as catalysts for hydrosilylation, dehydrogenative silylation, and/or crosslinking processes.

A process for the selective partial hydrogenation of conjugated diene compounds includes at least one, preferably terminal, diene function and at least one additional carbon-carbon double bond, the process including reacting the conjugated diene compounds with hydrogen in the presence of a nickel-NHC based catalyst. The disclosure also relates to a reaction mixture that can be obtained at the end of the process and to a catalyst that can be used in the process. The disclosure also relates to the use of the reaction mixture.

A mononuclear iron bivalent complex having iron-silicon bonds, which is represented by formula (1), can exhibit an excellent catalytic activity in at least one reaction selected from three reactions, i.e., a hydrosilylation reaction, a hydrogenation reaction and a reaction for reducing a carbonyl compound.

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(In the formula, R.sup.1 to R.sup.6 independently represent a hydrogen atom, an alkyl group which may be substituted by X, or the like; X represents a halogen atom, or the like; L.sup.1 represents at least one two-electron ligand selected from an isonitrile ligand, an amine ligand, an imine ligand, a nitrogenated heterocyclic ring, a phosphine ligand, a phosphite ligand and a sulfide ligand, wherein, when multiple L.sup.1's are present, two L.sup.1's may be bonded to each other; L.sup.2 represents a two-electron ligand that is different from a CO ligand or the above-mentioned L.sup.1, wherein, when multiple L.sup.2's are present, two L.sup.2's may be bonded to each other; and m.sup.1 represents an integer of 1 to 4 and m.sup.2 represents an integer of 0 to 3, wherein the sum total of m.sup.1 and m.sup.2 (i.e., m.sup.1+m.sup.2) satisfies 3 or 4.)

A ligand component is formed according to formula (1):R.sup.1.sub.2PXNC(R.sup.2)Y, wherein R.sup.1 is Ph or Cyc or a C.sub.1-C.sub.20 substituted or unsubstituted ailkyl group; each Ph is a substituted or unsubstituted phenyl group; each Cyc is a substituted or unsubstituted cycloalkyl group; X is an unsubstituted arylene or a C.sub.2-C.sub.3 substituted or unsubstituted alkylene; R.sup.2 is H, methyl or Ph; and Y N is pyridyl, 6-phenylpyridyl or 6-methylpyridyl; with the proviso that when X is a C.sub.2 substituted or unsubstituted alkylene and Y is pyridyl, R.sup.2 is methyl or Ph. A reaction product including the ligand component and a metal precursor is prepared by combining the ligand component with the metal precursor. An activated reaction product is formed by activating the reaction product as a hydrosilylation catalyst.

The present invention is directed to a process for producing a solid olefin polymerization catalyst component from an emulsion wherein the particle size of the solid catalyst or the droplet size of the emulsion is controlled. The actual size of the droplets or the solid catalyst particles is measured, or alternatively, both are measured. Then a difference between the actual size and the set point is calculated and the process is controlled based on the difference.

The invention relates to a process for preparing polyalpha-olefins using a catalyst composition comprising a reaction product of an organometallic complex and a co-catalyst, wherein the comprising an organometallic complex is represented by the general formula: LMXn wherein: (i) L is an organic ligand; (ii) M is a transition metal having a valency of p, wherein the metal M is selected from Ti, Zr, and Hf; (iii) X is an anionic ligand to the metal M, and wherein X is selected from the group consisting of halogens, alkyls, aralkyls, alkoxides, amides, and combinations thereof; (iv) n is the number of X groups and equals p-2.

Disclosed herein are dual catalyst compositions containing an unbridged metallocene compound, a bridged metallocene compound, a chemically-treated solid oxide, and an optional co-catalyst. These catalyst compositions can be used for the oligomerization of propylene to produce an oligomer product. For example, a heavy propylene oligomer can be recovered from the oligomer product, and the heavy propylene oligomer can be characterized by a high flash point and viscosity index, and a low pour point.

The present invention provides an organic metal complex catalyst for an olefin metathesis reaction, which enables the achievement of a higher yield of a desired substance in an olefin metathesis reaction than the conventional catalysts. The organic metal complex catalyst according to the present invention has a structure represented by formula (1) and is used for an olefin metathesis reaction. In formula (1), M represents a coordination center and is an Ru atom or an ion thereof; R1, R2 and R3 may be the same as or different from each other and independently represent a substituent such as a hydrogen atom; R4, R5, R6 and R7 may be the same as or different from one another and independently represent a substituent such as a hydrogen atom; X represents a halogen atom; and R8 represents a substituent having 3 to 20 carbon atoms and having a bond.

The present invention relates to a catalyst system for olefin oligomerization and a method for olefin oligomerization, and more specifically, a catalyst system for olefin oligomerization and a method for olefin oligomerization that have more improved supporting efficiency due to a ligand compound capable of functioning as a tether to a support, and thus, exhibit high activity in the olefin oligomerization even with smaller amounts of catalyst composition and cocatalyst, thus enabling more efficient preparation of alpha-olefins.