B01J31/2226

Targeted Near-Infrared Imaging by Metal-Organic Frameworks
20210311041 · 2021-10-07 ·

Metal-organic frameworks (MOFs) comprising amines on the organic linker can be used for cell targeting. In particular, primary amine groups represent one of the most versatile chemical moieties for conjugation to biologically relevant molecules, including antibodies and enzymes. Different chemical conjugation schemes can be used to conjugate biological molecules to the amino functionality on the organic linker. For example, carbodiimide chemistry can be used to link a primary amine to available carboxyl groups on the protein. For example, sulfhydryl crosslinking chemistry can be used via Traut's reagent scheme. As a demonstration of the invention, the ability of EpCAM antibody-targeted MOFs to bind to a human epithelial cell line (A549), a common target for imaging studies, was confirmed with confocal microscopy.

CATALYSTS AND METHODS FOR FORMING ALKENYL AND ALKYL SUBSTITUTED ARENES

Embodiments of the present disclosure provide for Rh(I) catalysts, methods of making alkenyl substituted arenes (e.g., allyl arene, vinyl arene, and the like), methods of making alkyl substituted arenes, and the like.

METATHESIS CATALYSTS

This invention relates generally to olefin metathesis catalysts, to the preparation of such compounds, compositions comprising such compounds, methods of using such compounds, and the use of such compounds in the metathesis of olefins and in the synthesis of related olefin metathesis catalysts. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and in industrial applications such as oil and gas, fine chemicals and pharmaceuticals.

USE OF CATALYSTS FOR THE METATHESIS OF NITRILE RUBBER
20210260568 · 2021-08-26 ·

The present invention relates to the use of specific catalysts for the metathesis degradation of nitrile rubber (NBR).

The invention further relates to a method for preparing nitrile rubber with reduced molecular weight using specific catalysts.

CHIRAL N-SUBSTITUTED ALLYLIC AMINE COMPOUNDS
20210238200 · 2021-08-05 ·

The method relates to the field of asymmetric allylic amination and comprises preparing a chiral N-substituted allylic amine compound from the corresponding allylic substrates and substituted hydroxylamines, in the presence of a catalyst, said catalyst comprising copper compounds and a chiral ligand. Examples of chiral amine compounds which can be made using the method include Vigabatrin, Ezetimibe Terbinafine, Naftifine 3-methylmorphine, Sertraline, Cinacalcet, Mefloquine hydrochloride, and Rivastigmine. There are over 20,000 known bioactive molecules with chiral N-substituted allylic amine substructure. The method may also be used to produce non-natural chiral β-aminoacid esters, a sub-class of chiral N-substituted allylic amine compounds. Examples of β-aminoacid ester which can be produced by the disclosed method, include, but are not limited to, N-(2-methylpent-1-en-3-yl)benzenamine and Ethyl 2-methylene-3-(phenylamino)butanoate. Further, the products of the method described herein can be used to produce chiral heterocycles and bioactive molecules or materials. A novel chiral copper-BINAM nitrosoarene complex is also set forth.

Synthesis of a MoVNbTe catalyst having a reduced niobium and tellurium content and higher activity for the oxidative dehydrogenation of ethane

A novel mixed oxide material is disclosed which contains molybdenum, vanadium, tellurium and niobium and the use of the molybdenum mixed oxide material as catalyst for the oxidative dehydrogenation of ethane to ethene or the oxidation of propane to acrylic acid and a process for producing the mixed oxide material.

COMPOSITE CATALYST FOR CARBON DIOXIDE REDUCTION AND METHOD OF FABRICATING OF THE SAME

Provided is a carbon dioxide reduction composite catalyst, comprising an organic-inorganic porous body, and a molecular reduction catalyst combined with the organic-inorganic porous body, wherein the organic-inorganic porous body includes metal oxide clusters, and a light-condensing organic material as linkers between the metal oxide clusters, and the linkers absorb visible light to form excitons, and move the excitons through energy transfer between the linkers to transfer the electrons of the excitons to the molecular reduction catalyst.

Single threaded composite fibers and yarns for the degradation of and protection against toxic chemicals and biological agents

The present invention relates to single thread composite fibers comprising at least one binder and at least one active catalyst for the capture and degradation of chemical threats such as chemical warfare agents (CWA), biological warfare agents, and toxic industrial chemicals (TIC) and a method for producing the same. The invention fibers are applicable to the fields of protective garments, filtration materials, and decontamination materials.

CATALYST FOR CONTAMINANT REDUCTION AND METHODS OF USE THEREOF
20210252492 · 2021-08-19 ·

Described herein are heterogeneous catalysts for removing impurities, such as halogen oxyanions (e.g., ClO.sub.4.sup.− and ClO.sub.3.sup.−), from a fluid, the catalyst can comprise: an oxygen atom transfer (OAT) transition metal, a Group VIII metal, and a support, where the transition metal, and the Group VIII metal can be in physical communication with the support either directly or indirectly through each other, whereby the catalyst can chemically remove impurities from the fluid. Certain embodiments provide catalysts that further comprise nitrogen donor ligand(s). Accordingly, such catalysts that comprise the OAT transition metal in the form of a complex with one or more nitrogen donor ligands have enhanced efficiency in reducing halogen oxyanion (e.g., ClO.sub.4.sup.−) to Cl.sup.−. Also described are methods or kits for making the catalysts and methods or reactor for the treatment of a fluid utilizing the catalyst.

Low Molecular Weight Sterically Encumbered Oligomers

Low molecular weight, high Tg resins, with applications including tire additives and adhesives. An oligomer is obtained by ring opening metathesis polymerization (ROMP) of a sterically encumbered cyclic monomer with an olefinic chain transfer agent. The sterically encumbered cyclic monomer and the olefinic chain transfer agent are present in the polymerization at a molar ratio of from 2:1 to about 40:1. Also, methods for making the oligomer by ROMP.