Abstract: Supported catalyst systems and methods of forming the same are described herein. In one specific embodiment, the methods generally include providing an inorganic support material and contacting the inorganic support material with an aluminum fluoride compound represented by the formula AlFpX3-pBq to form an aluminum fluoride impregnated support, wherein X is selected from Cl, Br and OH?, B is H2O, p is selected from 1 to 3 and q is selected from 0 to 6. The method further includes contacting the aluminum fluoride impregnated support with a transition metal compound to form a supported catalyst system, wherein the transition metal compound is represented by the formula [L]mM[A]n; wherein L is a bulky ligand, A is a leaving group, M is a transition metal and m and n are such that a total ligand valency corresponds to the transition metal valency.

Abstract: Olefin polymerization processes are described herein. In one embodiment, the process generally includes introducing propylene monomer to a reaction zone, disposing an isospecific metallocene catalyst within the reaction zone, wherein the isospecific metallocene catalyst has the formula: (SiRA2)(CpRB4)(FluRC8)MAn wherein Si is silicon and is a structural bridge between Cp and Flu, Cp is a cyclopentadienyl group, Flu is a fluorenyl group, M is a transition metal, A is a leaving group, n is an integer equal to the valence of M minus 2, RA is independently selected from hydrogen, alkyls, aromatics and combinations thereof, RB is independently selected from hydrogen, alkyls and combinations thereof and RC is independently selected from hydrogen, alkyls, aromatics and combinations thereof, contacting the propylene monomer with the isospecific metallocene catalyst to form isotactic polypropylene and recovering the isotactic polypropylene from the reaction zone.

Abstract: Bidentate catalyst systems and the methods or forming such are described herein. The catalyst systems generally are compounds having the general formula: where R, R1, R2 and R3 are optional and independently selected from hydrogen, C1 to C20 alkyl groups or C6 to C20 aryl groups, A? and A? are independently selected from coordination groups, M is a Group 4 or 5 transition metal, X is selected from halogens, alkyl groups, aromatic groups or combinations thereof and n is less than 4.

Abstract: Supported catalyst systems, methods of forming polyolefins and the formed polymers are generally described herein. The methods generally include identifying desired polymer properties, providing a transition metal compound and selecting a support material capable of producing the desired polymer properties, wherein the support material includes a bonding sequence selected from Si—O—Al—F, F—Si—O—Al, F—Si—O—Al—F and combinations thereof.

Abstract: Catalyst systems, polymers and methods of forming the same are described herein. The catalyst systems generally include an inorganic support material having a bonding sequence selected from Si—O—Al—F, F—Si—O—Al, F—Si—O—Al—F and combinations thereof, wherein the inorganic support material has an acid strength (pKa) of less than about 4.8 and a transition metal compound, wherein the transition metal compound is represented by the formula [L]mM[A]n; wherein L is a bulky ligand, A is a leaving group, M is a transition metal and m and n are such that a total ligand valency corresponds to a transition metal valency.

Abstract: Supported catalyst systems and methods of forming polyolefins are generally described herein. The polymerization methods generally include introducing an inorganic support material to a reaction zone, wherein the inorganic support material includes a bonding sequence selected from Si—O—Al—F, F—Si—O—Al, F—Si—O—Al—F and combinations thereof, introducing a transition metal compound to the reaction zone and contacting the transition metal compound with the inorganic support material for in situ activation/heterogenization of the transition metal compound to form a catalyst system. The method further includes introducing an olefin monomer to the reaction zone and contacting the catalyst system with the olefin monomer to form a polyolefin.

Abstract: Catalyst systems and methods of forming the same are described herein. The catalyst system may be formed by contacting an alumina-silica support composition with ammonium bifluoride in the presence of water to form a first fluorinated support composition. The method then includes heating the first fluorinated support composition in an oxygen containing atmosphere to a temperature of from about 200° C. to about 600° C. to form a second fluorinated support composition, wherein the second fluorinated support composition includes a bonding sequence selected from Si—O—Al—F, F—Si—O—Al, F—Si—O—Al—F and combinations thereof and then contacting the second fluorinated support composition with a transition metal compound to form a supported catalyst system, wherein the transition metal compound is represented by the formula [L]mM[A]n; wherein L is a bulky ligand, A is a leaving group, M is a transition metal and m and n are such that a total ligand valency corresponds to the transition metal valency.

Abstract: Copolymers and methods of forming copolymers are described herein. The methods generally include providing a transition metal compound represented by the formula [L]mM[A]n, wherein L is a bulky ligand including bis-indenyl, A is a leaving group, M is a transition metal and m and n are such that the total ligand valency corresponds to the transition metal valency and providing a support material having a bonding sequence selected from Si—O—Al—F, F—Si—O—Al, F—Si—O—Al—F and combinations thereof. The methods further include contacting the transition metal compound with the support material to form an active supported catalyst system, wherein the contact of the transition metal compound with the support material occurs in proximity to contact with monomer and contacting the active supported catalyst system with a plurality of monomers to form an olefin copolymer.

Abstract: A process for the preparation of a pyridinyl-linked bis-amino ligand that comprises, (a) reacting 2,6-dibromophenyl amine with an arylboronic acid component which is substituted or unsubstituted to produce a 2,6-diarylphenyl amine which is substituted or unsubstituted; (b) reacting the 2,6-diarylphenyl amine with a 2,6-dialkanoic pyridine characterized by the formula: wherein R? and R? are each independently a C1–C20 hydrocarbyl group; to produce a mono-imine ligand characterized by the formula: wherein TRP is a terphenyl group which is substituted or unsubstituted; and (c) reacting the mono-imine ligand with an aniline which may be substituted or unsubstituted to produce a bis-amine ligand characterized by the structure: wherein: TRP is a substituted or unsubstituted terphenyl group; and AR is a substituted or unsubstituted aryl group.