C07F7/10

Method of making an organoaminosilane

A method of making an aminosilane, the method comprising: forming a reaction mixture comprising a hydridosilane, an amine and a dehydrogenative coupling catalyst in a reactor; subjecting the reaction mixture to conditions sufficient to cause a dehydrogenative coupling reaction between the hydridosilane and the amine to form the aminosilane and hydrogen gas; and venting the hydrogen gas; wherein the forming of the reaction mixture comprising the hydridosilane, the amine and the dehydrogenative coupling catalyst comprises continuously feeding the hydridosilane to the reactor containing the amine and the dehydrogenative coupling catalyst.

Method of making an organoaminosilane

A method of making an aminosilane, the method comprising: forming a reaction mixture comprising a hydridosilane, an amine and a dehydrogenative coupling catalyst in a reactor; subjecting the reaction mixture to conditions sufficient to cause a dehydrogenative coupling reaction between the hydridosilane and the amine to form the aminosilane and hydrogen gas; and venting the hydrogen gas; wherein the forming of the reaction mixture comprising the hydridosilane, the amine and the dehydrogenative coupling catalyst comprises continuously feeding the hydridosilane to the reactor containing the amine and the dehydrogenative coupling catalyst.

METHOD FOR SYNTHESIZING C-NUCLEOSIDE COMPOUND

Disclosed is a method for preparing a C-nucleoside compound represented by Formula (III) or salt thereof. The present method has a high reaction yield, is simple to operate, uses a single metal reagent, has stable reaction temperature conditions, does not require frequent changes to the reaction system during the operation process, is suitable for scale-up synthesis, is suitable for large-scale production of Remdesivir, and has low costs.

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METHOD FOR SYNTHESIZING C-NUCLEOSIDE COMPOUND

Disclosed is a method for preparing a C-nucleoside compound represented by Formula (III) or salt thereof. The present method has a high reaction yield, is simple to operate, uses a single metal reagent, has stable reaction temperature conditions, does not require frequent changes to the reaction system during the operation process, is suitable for scale-up synthesis, is suitable for large-scale production of Remdesivir, and has low costs.

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Electrolyte for secondary battery and secondary battery comprising same

Disclosed is an electrolyte for a secondary battery, and a secondary battery comprising the same, and in particular, to an electrolyte for a secondary battery including an electrolyte salt, an organic solvent and an additive, wherein the additive includes at least one compound selected from the group consisting of a compound having an N—Si-based bond and a compound having an O—Si-based bond.

Nitric oxide-releasing particles for nitric oxide therapeutics and biomedical applications

The presently disclosed subject matter relates to nitric oxide-releasing particles for delivering nitric oxide, and their use in biomedical and pharmaceutical applications.

Nitric oxide-releasing particles for nitric oxide therapeutics and biomedical applications

The presently disclosed subject matter relates to nitric oxide-releasing particles for delivering nitric oxide, and their use in biomedical and pharmaceutical applications.

1,1,1-tris(organoamino)disilane compounds and method of preparing same

A 1,1,1-tris(organoamino)disilane compound and a method of preparing the 1,1,1-tris(organoamino)disilane compound are disclosed. The method comprises aminating a 1,1,1-trihalodisilane with an aminating agent comprising an organoamine compound to give a reaction product comprising the 1,1,1-tris(organoamino)disilane compound, thereby preparing the 1,1,1-tris(organoamino)disilane compound. A film-forming composition is also disclosed. The film-forming composition comprises the 1,1,1-tris(organoamino)disilane compound. A film formed with the film-forming composition, and a method of forming the film, are also disclosed. The method of forming the film comprises subjecting the film-forming composition comprising the 1,1,1-tris(organoamino)disilane compound to a deposition condition in the presence of a substrate, thereby forming the film on the substrate.

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES
20230002417 · 2023-01-05 · ·

Provided are a family of chromophores including naphthyl or naphthyl-like carbocyclic or heterocyclic rings as luminescent dyes that can be useful as emitters in OLEDs. These compounds have Formula I,

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Also provided are formulations including these inventive compounds. Further provided are OLEDs and related consumer products that utilize these inventive compounds.

Organic compound and manufacturing method thereof, and organic light emitting diode electroluminescent device

An organic compound and a manufacturing method thereof, and an organic light emitting diode electroluminescent device are provided. The organic compound has a suitable HOMO energy level and a high hole mobility. Compared with traditional hole transport materials, when the organic compound is applied in a hole transport layer of the organic light emitting diode electroluminescent device, the organic light emitting diode electroluminescent device has enhanced maximum current efficiency, maximum external quantum efficiency, and service lifespans.