The present disclosure provides a method for purifying nanostructured material comprising carbon nanotubes, metal impurities and amorphous carbon impurities. The method generally includes oxidizing the unpurified nanostructured material to remove the amorphous carbon and thereby exposing the metal impurities and subsequently contacting the nanostructured material with carbon monoxide to volatilize the metal impurities and thereby substantially remove them from the nanostructured material.

The present disclosure provides a method for purifying nanostructured material comprising carbon nanotubes, metal impurities and amorphous carbon impurities. The method generally includes oxidizing the unpurified nanostructured material to remove the amorphous carbon and thereby exposing the metal impurities and subsequently contacting the nanostructured material with carbon monoxide to volatilize the metal impurities and thereby substantially remove them from the nanostructured material.

Mixture of bisphosphites having an open and a closed outer unit and the use thereof as a catalyst mixture in hydroformylation.

The present disclosure provides methods, compositions, devices, systems and uses that pertain to the electrochemical reduction of CO.sub.2 to CO. The application presents a class of electrodes, incorporating molecular catalysts in nanostructures, for robust and efficient electrochemical systems, specifically, selective and robust hybrid electrodes, by incorporating a rhenium (Re) catalyst into the structure of highly porous heterogeneous materials. These electrodes can be scaled up to desired manufacturing dimensions due to their robust nature and methods of preparation.

Nanoparticles that can be used as hydrosilylation and dehydrogenative silylation catalysts. The nanoparticles have at least one transition metal with an oxidation state of 0, chosen from the metals of columns 8, 9 and 10 of the periodic table, and at least one carbonyl ligand, preferably a silicide.

Nanoparticles that can be used as hydrosilylation and dehydrogenative silylation catalysts. The nanoparticles have at least one transition metal with an oxidation state of 0, chosen from the metals of columns 8, 9 and 10 of the periodic table, and at least one carbonyl ligand, preferably a silicide.

Described herein is a hydroformylation catalyst system and method useful for producing aldehydes from olefin substrates, without using carbon monoxide gas. The hydroformylation catalyst system includes a hydroformylation catalyst complex including a Group 9 metal complexed with a phosphine-based ligand; a syngas surrogate including formic acid and an anhydride compound, which forms carbon monoxide in situ; and hydrogen, which may derive from the syngas surrogate or not derived from the syngas surrogate. The method involves reacting the olefin substrate with a syngas surrogate in the presence of a hydroformylation catalyst complex, wherein the syngas surrogate forms carbon monoxide, and optionally hydrogen, in situ, and then isolating the aldehyde compound from a reaction mixture.

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.

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.

A cyclopropanation method includes reacting an alcohol, an ester, or an aldehyde with a sulfone in an organic solvent containing a base providing a counter cation to form a cyclopropane; and isolating the cyclopropane. When using the alcohol or ester, the organic solvent further contains a catalyst having an alcohol dehydrogenation activity.