C07F9/53

POLYCYCLIC AROMATIC DERIVATIVE COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE USING SAME

A polycyclic aromatic derivative compound according to the present invention is employed in an organic layer in a device, thus being able to implement a high-efficiency organic light-emitting device, and thus can be industrially and effectively used in various display devices such as flexible displays, and illumination apparatuses such as monochromatic or white flat illumination and monochromatic or white flexible illumination.

Crystalline form of phenyl bis (2,4,6-trimethylbenzoyl) phosphine oxide with large particle size and crystallization method for making same

A crystalline form of phenyl bis (2,4,6-trimethylbenzoyl) phosphine oxide, with a large particle size, which belongs to a triclinic crystal system and space group P-1. A crystallization method for making the crystalline form of phenyl bis (2,4,6-trimethylbenzoyl) phosphine oxide, comprising adding a solid of phenyl bis (2,4,6-trimethylbenzoyl) phosphine oxide to a solvent and mixing; followed by heating to 50 to 70° C. to achieve complete dissolution; cooling the solution to room temperature; and adding an anti-solvent to the resulting solution to cause precipitation of crystals. The crystals are allowed to grow at a constant temperature for 10 to 60 minutes, so as to give a slurry containing the crystals. Said slurry is subjected to filtration and then drying to obtain the crystalline form of phenyl bis (2,4,6-trimethylbenzoyl) phosphine oxide.

INHIBITORS OF MEK KINASE
20230279033 · 2023-09-07 ·

Provided herein are inhibitors of MEK kinase, pharmaceutical compositions comprising said inhibitory compounds, and methods for using said MEK kinase inhibitory compounds for the treatment of disease.

Phosphorus-containing silane compound, method of making the same, resin composition and article made therefrom

A phosphorus-containing silane compound has a structure of SiR.sub.1(R.sub.2).sub.n(R.sub.3).sub.3-n, wherein R.sub.1 is a phenyl group, R.sub.2 is a vinyl group, R.sub.3 each independently is a structure of Formula (I) or Formula (II), and n is 1 or 2. Moreover, a method of making the phosphorus-containing silane compound, a resin composition including the phosphorus-containing silane compound and a resin additive and an article made from the resin composition are described. The article includes a prepreg, a resin film, a laminate or a printed circuit board, wherein one or more properties including Z-axis ratio of thermal expansion, copper foil peeling strength, inner resin flow, branch-like pattern, dielectric constant, dissipation factor and flame retardancy may be improved. ##STR00001##

POLYMERIC TANDEM DYES WITH LINKER GROUPS
20230012304 · 2023-01-12 ·

Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I):

##STR00001##

or a stereoisomer, tautomer or salt thereof, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, L.sup.1, L.sup.2, L.sup.3, L.sup.4, M.sup.1, M.sup.2, m and n are as defined herein. Methods associated with preparation and use of such compounds is also provided.

POLYMERIC TANDEM DYES WITH LINKER GROUPS
20230012304 · 2023-01-12 ·

Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I):

##STR00001##

or a stereoisomer, tautomer or salt thereof, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, L.sup.1, L.sup.2, L.sup.3, L.sup.4, M.sup.1, M.sup.2, m and n are as defined herein. Methods associated with preparation and use of such compounds is also provided.

Synthesis strategy for gap protecting group
11827660 · 2023-11-28 · ·

The present invention relates to a novel synthesis method to form particular molecules. These molecules have multiple uses, most notably in the field of protecting groups used throughout organic and synthetic chemistry. The disclosed method is safer, more cost- and time-effective, and more amenable to large scale production than those currently known in the art. The protecting groups synthesized are useful in GAP peptide synthesis.

A METHOD OF EXTRACTING CARBONIC ACID, ALIPHATIC ACIDS, ESTERS AND ALCOHOLS FROM AN AQUEOUS MEDIUM
20220289773 · 2022-09-15 · ·

The present invention relates to a method of extracting at least one selected from carbonic acid, aliphatic acid, aliphatic acid ester and aliphatic alcohol from an aqueous medium, the method comprising the steps: (a) contacting the carbonic acid, aliphatic acid, aliphatic acid ester and/or aliphatic alcohol in the aqueous medium with an extracting medium containing at least one alkyl-phosphine oxide for a time sufficient to extract the carbonic acid, aliphatic acid, aliphatic acid ester and/or aliphatic alcohol from the aqueous medium into the extracting medium, and (b) separating the extracting medium with the extracted carbonic acid, aliphatic acid, aliphatic acid ester and/or aliphatic alcohol from the aqueous medium, characterized in, that the at least one alkyl-phosphine oxide contains at least two different alkyl radicals per alkyl-phosphine oxide molecule and the aqueous medium in (a) contains a microorganism, preferably a living microorganism, producing the carbonic acid, aliphatic acid, aliphatic acid ester and/or aliphatic alcohol.

EXTRACTION OF ALIPHATIC ALCOHOLS
20220281789 · 2022-09-08 · ·

The present invention relates to a method of extracting an aliphatic alcohol, preferably containing 5 to 16 carbon atoms, from an aqueous medium, the method comprising: (a) contacting the aliphatic alcohol in the aqueous medium with at least one extracting medium for a time sufficient to extract the aliphatic alcohol from the aqueous medium into the extracting medium, (b) separating the extracting medium with the extracted aliphatic alcohol from the aqueous medium wherein the extracting medium comprises: at least one trialkyl-phosphine-oxide, preferably trioctyl-phosphine-oxide, and optionally at least one alkane, and wherein the aliphatic alcohol is produced from a carbon source by contacting the carbon source with at least one microorganism capable of converting the carbon source to the aliphatic alcohol.

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE COMPRISING SAME

The present specification relates to a heterocyclic compound represented by Chemical Formula 1, and an organic light emitting device including the same.