C08F28/06

POLYMER, ELECTROLUMINESCENCE MATERIAL, ELECTROLUMINESCENCE DEVICE, AND ELECTRONIC DEVICE

A polymer including a structural unit represented by Chemical Formula 1, an electroluminescence device material including the polymer, an electroluminescence device including the polymer or the electroluminescence device material, and an electronic device including the electroluminescence device are provided:

##STR00001##

In Chemical Formula 1, the definition of each substituent is the same as described in the specification.

POLYMER, ELECTROLUMINESCENCE MATERIAL, ELECTROLUMINESCENCE DEVICE, AND ELECTRONIC DEVICE

A polymer including a structural unit represented by Chemical Formula 1, an electroluminescence device material including the polymer, an electroluminescence device including the polymer or the electroluminescence device material, and an electronic device including the electroluminescence device are provided:

##STR00001##

In Chemical Formula 1, the definition of each substituent is the same as described in the specification.

POLYMERS FOR PHOTOVOLTAIC APPLICATIONS

A polymer comprising

##STR00001## wherein m+n=1.

POLYMERS FOR PHOTOVOLTAIC APPLICATIONS

A polymer comprising

##STR00001## wherein m+n=1.

Preparation and application of 4-methyl-5-vinylthiazolyl polymeric ionic liquid

Disclosed are a preparation method and application of a 4-methyl-5-vinylthiazolyl polymerized spherical ionic liquid catalyst. The method comprises: preparing a functional ionic liquid monomer successfully by taking 4-methyl-5-vinylthiazole as the matrix, and preparing the polymerized spherical ionic liquid from the monomer. The catalyst combines the advantages of both ionic liquid and the polymer, and has the characteristics of large specific surface area, high catalytic activity, high mass transfer rate, good selectivity, high stability, easy recycling and separating, environmental friendliness, wide industrial application prospect, etc. The spherical ionic liquid is made into a novel catalytic packing and then put into a reactive distillation column for continuous reactive distillation of esterification and transesterification to realize the organic combination of the ionic liquid and the reactive distillation technology, achieving good catalytic activity, high product yield, environmental friendliness, and low corrosivity, which has great significance in realizing an environment-friendly process.

Preparation and application of 4-methyl-5-vinylthiazolyl polymeric ionic liquid

Disclosed are a preparation method and application of a 4-methyl-5-vinylthiazolyl polymerized spherical ionic liquid catalyst. The method comprises: preparing a functional ionic liquid monomer successfully by taking 4-methyl-5-vinylthiazole as the matrix, and preparing the polymerized spherical ionic liquid from the monomer. The catalyst combines the advantages of both ionic liquid and the polymer, and has the characteristics of large specific surface area, high catalytic activity, high mass transfer rate, good selectivity, high stability, easy recycling and separating, environmental friendliness, wide industrial application prospect, etc. The spherical ionic liquid is made into a novel catalytic packing and then put into a reactive distillation column for continuous reactive distillation of esterification and transesterification to realize the organic combination of the ionic liquid and the reactive distillation technology, achieving good catalytic activity, high product yield, environmental friendliness, and low corrosivity, which has great significance in realizing an environment-friendly process.

FORMING ESTER-SUBSTITUTED POLYMERS FOR ORGANIC PHOTOVOLTAICS

A method comprised of combining

##STR00001## form a solution containing a polymer

##STR00002##

In this polymer R, R′, and R″ are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups; and X is selected from aryl groups.

FORMING ESTER-SUBSTITUTED POLYMERS FOR ORGANIC PHOTOVOLTAICS

A method comprised of combining

##STR00001## form a solution containing a polymer

##STR00002##

In this polymer R, R′, and R″ are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups; and X is selected from aryl groups.

SYNTHESIS OF FUNCTIONALIZABLE OR FUNCTIONALIZED POLY(3,4-ETHYLENEDIOXYTHIPHENE)-BASED POLYMERS AND MONOMERS THEREFOR
20230132381 · 2023-04-27 ·

A method of forming a compound having the formula:

##STR00001##

includes the reaction:

##STR00002##

n the presence of a base comprising teat-butyl lithium, lithium diisopropylamide, sodium hydroxide, potassium hydroxide, lithium hydroxide, a potassium alkoxide or a sodium alkoxide to achieve a yield of at least 90%, wherein X is a halo atom selected from the group consisting of Cl, Br and I.

SYNTHESIS OF FUNCTIONALIZABLE OR FUNCTIONALIZED POLY(3,4-ETHYLENEDIOXYTHIPHENE)-BASED POLYMERS AND MONOMERS THEREFOR
20230132381 · 2023-04-27 ·

A method of forming a compound having the formula:

##STR00001##

includes the reaction:

##STR00002##

n the presence of a base comprising teat-butyl lithium, lithium diisopropylamide, sodium hydroxide, potassium hydroxide, lithium hydroxide, a potassium alkoxide or a sodium alkoxide to achieve a yield of at least 90%, wherein X is a halo atom selected from the group consisting of Cl, Br and I.