Methods and catalysts for oxidizing ammonia to nitrogen are described. Specifically, diruthenium complexes that spontaneously catalyze this reaction are disclosed. Accordingly, the disclosed methods and catalysts can be used in various electrochemical cell-based energy storage and energy production applications that could form the basis for a potential nitrogen economy.

Catalyst systems for tetramerizing ethylene to form 1-octene may include a catalyst which may include a chromium compound coordinated with a ligand and a co-catalyst which may include an organoaluminum compound. The ligand may have a chemical structure according to Chemical Structure (I), wherein R.sub.5, R.sub.6, and R.sub.7 are each independently chosen from a (C.sub.1-C.sub.50) hydrocarbyl group or a (C.sub.1-C.sub.50) heterohydrocarbyl group, and wherein the (C.sub.1-C.sub.50) hydrocarbyl or (C.sub.1-C.sub.50) heterohydrocarbyl groups of R.sub.5, R.sub.6, and R.sub.7 have greater than 10 carbon atoms combined and R.sub.A, R.sub.B, R.sub.C, and R.sub.D and R.sub.1, R.sub.2, R.sub.3, and R.sub.4, are independently chosen from a hydrogen atom or a (C.sub.1-C.sub.50) hydrocarbyl group.

The present invention provides a novel ligand compound, a transition metal compound and a catalyst composition including the same.

A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

The present invention relates to a novel method for photocatalytic oxidation of allylic C—H bonds present in alkenes containing at least three carbon atoms. In this newly disclosed method, such alkenes, when reacted with carbon dioxide (CO.sub.2) in an organic solvent containing a catalyst comprising of a supported molecular complex of transition metal ions under conditions of ambient temperature and pressure using a readily available household LED lamp, yield oxygenated products. The developed method represents a unique way to use CO.sub.2 as an oxygen transfer agent to unsaturated organic compounds along with the formation of CO as a co-product using light as an energy source.

The invention describes metal catalysts such as Pt single-site centers on metal oxide supports, e.g., powdered supports, such as MgO, Al.sub.2O.sub.3, CeO.sub.2 or mixtures thereof with phenyl or biphenyl ligands substituted with two or more carboxylic acid groups.

The present invention relates an alkanolamine/amine-grafted metal-organic framework-based carbon dioxide adsorbent and, more specifically, to an alkanolamine/amine-grafted metal-organic framework-based carbon dioxide adsorbent that can effectively reduce renewable energy generated in the process of adsorption and desorption of carbon dioxide, and maintain structural stability against moisture present in exhaust gas, thereby being capable of effectively capturing carbon dioxide in an actual fluidized bed. According to the present invention, it is possible to provide a carbon dioxide adsorbent capable of maintaining structural stability against changes in adsorption/desorption temperatures and moisture.

Catalyst systems for tetramerizing ethylene to form 1-octene may include a catalyst which may include a chromium compound coordinated with a ligand and a co-catalyst which may include an organoaluminum compound. The ligand may have a chemical structure according to Chemical Structure (I), wherein R.sub.5 is a (C.sub.1-C.sub.15) alkyl group, a (C.sub.3-C.sub.15) cyclohydrocarbyl group, a (C.sub.3-C.sub.15) cycloheterohydrocarbyl group, or a (C.sub.1-C.sub.15) aryl group, and R.sub.A, R.sub.B, R.sub.C, R.sub.D, R.sub.E, R.sub.F, R.sub.G, R.sub.H, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.6, R.sub.7, R.sub.8, and R.sub.9 are independently chosen from a hydrogen atom, a (C.sub.1-C.sub.50) hydrocarbyl group, or a (C.sub.1-C.sub.50) heterohydrocarbyl group.

The present disclosure relates to a ligand compound, a catalyst system for oligomerization, and a method for olefin oligomerization using the same. The catalyst system for oligomerization using the ligand compound according to the present disclosure has excellent catalytic activity, exhibits high selectivity to 1-hexene and 1-octene, and greatly reduces the production of the by-products, thereby enabling efficient preparation of alpha-olefin.

The present invention discloses a homogeneous, single site catalyst of formula (I) and a process for preparation thereof using a ligand. The present invention further discloses a process for preparation of linear polyethylene of high molecular weight and degree of crystallinity by using the homogeneous, single site catalyst of formula I.

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