Abstract: Elastomeric polyolefin-based ionomers and methods for making same. The ionomers can include a copolymer comprising: C2-C60 ?-olefin monomer units; optional C2-C60 ?-olefin comonomer units different than the monomer units; optional diene units; and about 0.1 wt % to about 20 wt % metal alkenyl units, based on the weight of the copolymer, wherein the metal alkenyl units have the formula —R(A?)—, wherein R is an alkyl group containing 2 to 10 carbon atoms, and A? is an anionic group. The copolymer can further include one or more metal cations derived from the group consisting of alkali metals, alkaline earth metals, group 3-12 metals, group 13-16 metals, and combination(s) thereof. The ionomer has a glass transition temperature of ?60° C. to 5° C., and a weight average (Mw) of 50 to 5,000 kg/mol.

Abstract: This invention relates to mono cyclopentadienyl pyridyl hydroxyl amine catalyst compounds represented by Formula I(a) or I(b): wherein: M is a group 3-12 metal; R1 is a hydrocarbyl group or a silyl group; R2, R3, R4, R5, R6, R7, R8, R9, and R10 are independently selected from the group consisting of hydrogen, hydrocarbyl, alkoxy, silyl, amino, aryloxy, halogen and phosphino, wherein any two adjacent R groups may be joined to form a saturated or unsaturated single or multicyclic hydrocarbyl ring or heterocyclic ring; and each X1 and X2 is independently an anionic leaving group or X1 and X2 may be joined together to form a dianionic group.

Abstract: A method for producing a higher alcohol from a waste plastic feedstock is disclosed, comprising: (a) providing a hydrocarbon feed stream comprising a pyrolysis oil feed obtained from pyrolysis of plastic waste, wherein the pyrolysis oil comprises at least 20 wt % higher olefins with a carbon number in the range C5-C20, based on its total hydrocarbon content; (b) contacting the hydrocarbon feed stream with synthesis gas under hydroformylation conditions in the presence of a hydroformylation catalyst and recovering a hydroformylation product; (c) subjecting the hydroformylation product to hydrogenation and/or a distillation to recover a higher alcohol product.

Abstract: The present disclosure provides pyridyl hydroxyl amine catalyst compounds and systems containing the compounds. The present disclosure is also directed to polymerization processes to produce polyolefin polymers from catalyst systems including one or more olefin polymerization catalysts, at least one activator, and an optional support.

Abstract: The present disclosure relates to iron-containing compounds including a 2,6-diimino(heteroaryl) ligand useful for producing substituted-cyclo-alkanes, such as vinyl cyclobutanes. The present disclosure provides new and improved iron-containing catalysts with enhanced solubility in hydrophobic (nonpolar) solvents.

Abstract: This invention relates to a composition comprising a compound having a formula of M2(CO)m(PF3)n, wherein M is a group 9 metal (such as cobalt), m is 1, 2, 3, 4, 5, 6, or 7, n is 1, 2, 3, 4, 5, 6, or 7, and the sum of m and n is 8, that may be used as a hydroformylation pre¬catalyst for converting (such as hydroformylating) olefinic feeds, especially complex feeds comprising internal olefins and high degrees of branching.

Abstract: Compositions comprising one or more amphiphilic compounds formed from vinylidene olefins may comprise: a reaction product of one or more vinylidene olefins, in which the reaction product comprises a hydrophobic portion and a hydrophilic portion comprising a polar head group bonded to the hydrophobic portion. The one or more vinylidene olefins each comprise a vinylidene group that undergoes a reaction to become saturated and to produce at least part of the hydrophobic portion.

Abstract: Vinylidene olefins may undergo hydroformylation in the presence of an unmodified cobalt catalyst to form compositions comprising a mixture of alcohol molecules having a specified amount of branching. In particular, the compositions may feature a mixture comprising reduced hydroformylated reaction products of a vinylidene olefin comprising alcohol molecules represented by at least one of Structures 3-5. The mixture has an average of about 1.2 to about 2.1 branches per alcohol molecule. Ra and Rb may be the same or different and comprise a branched or unbranched alkyl group having about 6 to about 14 carbon atoms, excluding branches. Variable m is an integer ranging from 0 to a number of carbon atoms in Rb. Rb is a branched or unbranched alkyl group having m+1 carbon atoms less than Rb.

Abstract: This invention relates to polymers comprising: one or more that include 1) at least 11 wt % 4 substituted 1,4 hexadiene and less than 20 wt % 5-methyl-1,4-hexadiene, based upon the weight of the polymer, and 2) optionally, one or more olefins; and processes to produces such polymers using metallocene or post-metallocene catalyst compounds.

Abstract: Catalysts, catalysts systems and methods of polymerizing olefins are provided. The catalyst system may contain two catalysts. Polyolefin polymers are also provided.

Abstract: Methods for the hydroalkenylation of conjugated, 1,3-dienes using a diimine catalyst. The method comprises mixing a diene having at least five carbon atoms and an iron diimine complex at a temperature of about ?60° C. to about 23° C. to provide a catalyst solution; and introducing one or more alpha olefins at a pressure of at least 300 psig to obtain a product comprising the substituted diene monomer.

Abstract: The present disclosure provides borate or aluminate activators comprising cations having linear alkyl groups, catalyst systems comprising, and methods for polymerizing olefins using such activators. Specifically, the present disclosure provides activator compounds represented by Formula: [R1R2R3EH]d+[Mk+Qn]d?, wherein: E is nitrogen or phosphorous; d is 1, 2 or 3; k is 1, 2, or 3; n is 1, 2, 3, 4, 5, or 6; n?k=d; R1 is C1-C20 linear alkyl group; each of R2 and R3 is a C1-C40 linear alkyl group, a meta- and/or para-substituted phenyl group, an alkoxy group, a silyl group, a halogen, or a halogen containing group, wherein R1+R2+R3?15 carbon atoms; M is an element selected from group 13, typically B or Al; and each Q is independently a hydride, bridged or unbridged dialkylamido, halide, alkoxide, aryloxide, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, or halosubstituted-hydrocarbyl radical, provided that when Q is a fluorophenyl group, then R2 is not a C1-C40 linear alkyl group.

Abstract: This invention relates to mono cyclopentadienyl pyridyl hydroxyl amine catalyst compounds represented by Formula I(a) or I(b): wherein: M is a group 3-12 metal; R1 is a hydrocarbyl group or a silyl group; R2, R3, R4, R5, R6, R7, R8, R9, and R10 are independently selected from the group consisting of hydrogen, hydrocarbyl, alkoxy, silyl, amino, aryloxy, halogen and phosphino, wherein any two adjacent R groups may be joined to form a saturated or unsaturated single or multicyclic hydrocarbyl ring or heterocyclic ring; and each X1 and X2 is independently an anionic leaving group or X1 and X2 may be joined together to form a dianionic group.

Abstract: The present disclosure provides pyridyl hydroxyl amine catalyst compounds and systems containing the compounds. The present disclosure is also directed to polymerization processes to produce polyolefin polymers from catalyst systems including one or more olefin polymerization catalysts, at least one activator, and an optional support.

Abstract: This invention relates to transition metal complexes of a dianionic, tridentate ligand that features a central neutral heterocyclic Lewis base and two phenolate donors, where the tridentate ligand coordinates to the metal center to form two eight-membered rings. Preferably the bis(phenolate) complexes are represented by Formula (I): where M, L, X, m, n, E, E?, Q, R1, R2, R3, R4, R1?, R2?, R3?, R4?, A1, A1?, are as defined herein, where A1QA1? are part of a heterocyclic Lewis base containing 4 to 40 non-hydrogen atoms that links A2 to A2? via a 3-atom bridge with Q being the central atom of the 3-atom bridge.

Abstract: This invention relates to a polymerization catalyst system comprising group 8 or 9 containing non-coordinating anion activator, a polymerization catalyst compound, optional support, and optional scavenger. Preferably, the activator comprises a compound represented by the formula: Hs(L)mM where M is a group 8 or 9 metal, s is 0 or 1, m 1, 2, 3, or 4, each L ligand is independently C?O, NR3, PR3, where each R, independently is halogen, haloalkyl, or haloaryl) or optionally two or more L ligands may together form a multiply-valent ligand complex. Further, this invention relates to anon-coordinating anion activator represented by the formula: [Zd]+[HsLmM]d?, where M, s, m, L, are as defined above, d is 1, 2, or 3 and Z is (L?-H) or a reducible Lewis acid; L? is a neutral Lewis base; H is hydrogen, and (L?-H) is a Bronsted acid.

Abstract: The present disclosure relates to amido-benzoquinone transition metal complexes, catalyst systems including amido-benzoquinone transition metal complexes, and polymerization processes to produce polyolefin polymers such as polyethylene-based polymers and polypropylene-based polymers.

Abstract: Catalysts, catalysts systems and methods of polymerizing olefins are provided. The catalyst system may contain two catalysts. Polyolefin polymers are also provided.

Abstract: The present disclosure relates to amido-benzoquinone transition metal complexes, catalyst systems including amido-benzoquinone transition metal complexes, and polymerization processes to produce polyolefin polymers such as polyethylene-based polymers and polypropylene-based polymers.

Abstract: This invention relates to transition metal complexes of a dianionic, tridentate ligand that features a central neutral heterocyclic Lewis base and two phenolate donors, where the tridentate ligand coordinates to the metal center to form two eight-membered rings. Preferably the bis(phenolate) complexes are represented by Formula (I): where M, L, X, m, n, E, E?, Q, R1, R2, R3, R4, R1?, R2?, R3?, R4?, A1, A1?, are as defined herein, where A1QA1? are part of a heterocyclic Lewis base containing 4 to 40 non-hydrogen atoms that links A2 to A2? via a 3-atom bridge with Q being the central atom of the 3-atom bridge.