Abstract: Embodiments are directed to a metal-ligand complex of formula (I). In addition, a polymerization process includes polymerizing at least one olefin in the presence of a catalyst system comprising the metal-ligand complex and at least one activator to produce an olefinic polymer.

Abstract: An olefin polymerization catalyst system includes a procatalyst component chosen from metal-ligand complexes of Formula (I): In Formula (I), each X is independently a monodentate or polydentate ligand that is neutral, monoanionic, or dianionic; the metal-ligand complex of Formula (I) is overall neutral; each Y1-Y4 and Y7-Y10 independently is selected from C or N such that six membered diaza (N2) or triaza (N3) rings are formed; wherein each R1 and R10 independently are chosen from (C1-C40) hydrocarbyl, substituted (C1-C40) hydrocarbyl, (C1-C40) heterohydrocarbyl, and substituted (C1-C40) heterohydrocarbyl or is absent; each R2, R3, R4, R7, R8, and R9 is chosen from hydrogen; (C1-C40) hydrocarbyl; substituted (C1-C40) hydrocarbyl; (C1-C40) heterohydrocarbyl; substituted (C1-C40) heterohydrocarbyl; halogen, nitro (NO2) or is absent; each R5 and R6 independently is chosen from (C1-C40) hydrocarbyl, substituted (C1-C40) hydrocarbyl, (C1-C40) heterohydrocarbyl, and substituted (C1-C40) heterohydrocarbyl.

Abstract: An olefin polymerization catalyst system includes a procatalyst component chosen from metal-ligand complexes of Formula (I): In Formula (I), each X is independently a monodentate or polydentate ligand that is neutral, monoanionic, or dianionic; the metal-ligand complex of Formula (I) is overall neutral; each Y1-Y4 and Y7-Y10 independently is selected from C or N such that six membered diaza (N2) or triaza (N3) rings are formed; wherein each R1 and R10 independently are chosen from (C1-C40) hydrocarbyl, substituted (C1-C40) hydrocarbyl, (C1-C40) heterohydrocarbyl, and substituted (C1-C40) heterohydrocarbyl or is absent; each R2, R3, R4, R7, R8, and R9 is chosen from hydrogen; (C1-C40) hydrocarbyl; substituted (C1-C40) hydrocarbyl; (C1-C40) heterohydrocarbyl; substituted (C1-C40) heterohydrocarbyl; halogen, nitro (NO2) or is absent; each R5 and R6 independently is chosen from (C1-C40) hydrocarbyl, substituted (C1-C40) hydrocarbyl, (C1-C40) heterohydrocarbyl, and substituted (C1-C40) heterohydrocarbyl.

Abstract: Provided herein are methods for producing cyclic and acyclic ketones from trimerization and dimerization of alkyl ketones, including for example methyl ketones. Such cyclic and acyclic ketones may be suitable for use as fuel and lubricant precursors, and may be hydrodeoxygenated to form their corresponding cycloalkanes and alkanes. Such cycloalkanes and alkanes may be suitable for use as fuels, including jet fuels, and lubricants.

Abstract: Provided herein are methods for producing cyclic and acyclic ketones from trimerization and dimerization of alkyl ketones, including for example methyl ketones. Such cyclic and acyclic ketones may be suitable for use as fuel and lubricant precursors, and may be hydrodeoxygenated to form their corresponding cycloalkanes and alkanes. Such cycloalkanes and alkanes may be suitable for use as fuels, including jet fuels, and lubricants.

Abstract: Provided herein are methods for producing cyclic and acyclic ketones from trimerization and dimerization of alkyl ketones, including for example methyl ketones. Such cyclic and acyclic ketones may be suitable for use as fuel and lubricant precursors, and may be hydrodeoxygenated to form their corresponding cycloalkanes and alkanes. Such cycloalkanes and alkanes may be suitable for use as fuels, including jet fuels, and lubricants.

Abstract: Provided herein are methods for producing ?,?-unsaturated ketones from the condensation of methyl ketones in the presence of an amine catalyst. Such amine catalysts may be supported, for example, on a silica-alumina support. Such amine catalysts may be used in the presence of an additional acid. The ?,?-unsaturated ketones may be produced by dimerization and/or timerization of the methyl ketones. Such ?,?-unsaturated ketones may be suitable for use in producing fuels, gasoline additives, and/or lubricants, or precursors thereof. The methyl ketones may be obtained from renewable sources, such as by the fermentation of biomass.

Abstract: Provided herein are methods for producing ketone(s) from the condensation of methyl ketone(s) and alcohol(s) in the presence of an amine catalyst and a metal catalyst. Such amine catalysts may be supported, for example, on a silica-alumina support. Such ketones may be suitable for use in producing fuels, gasoline additives, and/or lubricants, or precursors thereof. The methyl ketone(s) and/or alcohol(s) may be obtained from renewable sources, such as by fermentation of biomass.

Abstract: Provided herein are methods for producing cyclic and acyclic ketones from trimerization and dimerization of alkyl ketones, including for example methyl ketones. Such cyclic and acyclic ketones may be suitable for use as fuel and lubricant precursors, and may be hydrodeoxygenated to form their corresponding cycloalkanes and alkanes. Such cycloalkanes and alkanes may be suitable for use as fuels, including jet fuels, and lubricants.

Abstract: The present disclosure provides methods to produce ketones suitable for use as fuels and lubricants by catalytic conversion of an acetone-butanol-ethanol (ABE) fermentation product mixture that can be derived from biomass.

Abstract: Provided herein are methods for producing ketone(s) from the condensation of methyl ketone(s) and alcohol(s) in the presence of an amine catalyst and a metal catalyst. Such amine catalysts may be supported, for example, on a silica-alumina support. Such ketones may be suitable for use in producing fuels, gasoline additives, and/or lubricants, or precursors thereof. The methyl ketone(s) and/or alcohol(s) may be obtained from renewable sources, such as by fermentation of biomass.

Abstract: Provided herein are methods for producing ?,?-unsaturated ketones from the condensation of methyl ketones in the presence of an amine catalyst. Such amine catalysts may be supported, for example, on a silica-alumina support. Such amine catalysts may be used in the presence of an additional acid. The ?,?-unsaturated ketones may be produced by dimerization and/or timerization of the methyl ketones. Such ?,?-unsaturated ketones may be suitable for use in producing fuels, gasoline additives, and/or lubricants, or precursors thereof. The methyl ketones may be obtained from renewable sources, such as by the fermentation of biomass.

Abstract: The present disclosure generally relates to the catalytic conversion of alcohols into hydrocarbon ketones suitable for use as fuels. More specifically, the present disclosure relates to the catalytic conversion of a mixture of isopropanol-butanol-ethanol (IBE) or acetone-butanol-ethanol (ABE), into ketones suitable for use as fuels. The ABE or IBE mixtures may be obtained from the fermentation of biomass or sugars.

Abstract: The present disclosure generally relates to the production of fuels, gasoline additives, and/or lubricants, and precursors thereof. The compounds used to produce the fuels, gasoline additives, and/or lubricants, and precursors thereof may be derived from biomass. The fuels, gasoline additives, and/or lubricants, and precursors thereof may be produced by a combination of intermolecular and/or intramolecular aldol condensation reactions, Guerbet reactions, hydrogenation reactions, and/or oligomerization reactions.

Abstract: The present disclosure generally relates to the catalytic conversion of alcohols into hydrocarbon ketones suitable for use as fuels. More specifically, the present disclosure relates to the catalytic conversion of a mixture of isopropanol-butanol-ethanol (IBE) or acetone-butanol-ethanol (ABE), into ketones suitable for use as fuels. The ABE or IBE mixtures may be obtained from the fermentation of biomass or sugars.

Abstract: The present disclosure generally relates to the production of fuels, gasoline additives, and/or lubricants, and precursors thereof. The compounds used to produce the fuels, gasoline additives, and/or lubricants, and precursors thereof may be derived from biomass. The fuels, gasoline additives, and/or lubricants, and precursors thereof may be produced by a combination of intermolecular and/or intramolecular aldol condensation reactions, Guerbet reactions, hydrogenation reactions, and/or oligomerization reactions.

Abstract: The present disclosure provides methods to produce ketones suitable for use as fuels and lubricants by catalytic conversion of an acetone-butanol-ethanol (ABE) fermentation product mixture that can be derived from biomass.