Patent classifications
C09B1/00
Charge transport material, organic electroluminescent element, and illumination device, display device, or light-emitting device characterized by using said element
[This] charge transport material which comprises a compound expressed by the following formula has a high efficiency and drive durability after high-temperature storage and resists the occurrence of dark spots (X.sup.101 represents a sulfur atom or an oxygen atom; R.sup.101 and R.sup.102 represent each independently an alkyl group, an aryl group, a heteroaryl group, a fluorine atom, or a silyl group, and may further be substituted with these groups; n101 represents an integer from 0 to 11; n102 represents an integer from 0 to 7; a plurality of R.sup.101 and R.sup.102 [groups] may be the same or different; and L.sup.101 represents a single bond or a divalent linking group; however, one of R.sup.101, L.sup.101, and R.sup.102 includes a fluorine atom, a fluoroalkyl group, a cycloalkyl group, a cycloalkylene group, a silyl group, an alkylsilyl group, an arylsilyl group, or a silicon atom linking group.) ##STR00001##
Charge transport material, organic electroluminescent element, and illumination device, display device, or light-emitting device characterized by using said element
[This] charge transport material which comprises a compound expressed by the following formula has a high efficiency and drive durability after high-temperature storage and resists the occurrence of dark spots (X.sup.101 represents a sulfur atom or an oxygen atom; R.sup.101 and R.sup.102 represent each independently an alkyl group, an aryl group, a heteroaryl group, a fluorine atom, or a silyl group, and may further be substituted with these groups; n101 represents an integer from 0 to 11; n102 represents an integer from 0 to 7; a plurality of R.sup.101 and R.sup.102 [groups] may be the same or different; and L.sup.101 represents a single bond or a divalent linking group; however, one of R.sup.101, L.sup.101, and R.sup.102 includes a fluorine atom, a fluoroalkyl group, a cycloalkyl group, a cycloalkylene group, a silyl group, an alkylsilyl group, an arylsilyl group, or a silicon atom linking group.) ##STR00001##
Compounds and organic electronic device using the same
The present specification relates to an organic electronic device in which a novel compound that may improve a life-span, efficiency, a driving voltage drop, and stability of the organic electronic device is contained in an organic material layer.
Compounds and organic electronic device using the same
The present specification relates to an organic electronic device in which a novel compound that may improve a life-span, efficiency, a driving voltage drop, and stability of the organic electronic device is contained in an organic material layer.
Organic light-emitting device
An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; an emission layer (EML) between the first electrode and the second electrode; a hole transport region between the first electrode and the EML; an electron transport layer (ETL) between the EML and the second electrode, and including a first electron transport material; a first buffer layer between the EML and the ETL, and including a first buffer material; and a second buffer layer between the first buffer layer and the ETL, and including a second buffer material and a second electron transport material, wherein the first buffer material and the second buffer material are each independently selected from compounds represented by Formula 1 below, and the first buffer layer does not include an electron transport material: ##STR00001##
Organic light-emitting device
An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; an emission layer (EML) between the first electrode and the second electrode; a hole transport region between the first electrode and the EML; an electron transport layer (ETL) between the EML and the second electrode, and including a first electron transport material; a first buffer layer between the EML and the ETL, and including a first buffer material; and a second buffer layer between the first buffer layer and the ETL, and including a second buffer material and a second electron transport material, wherein the first buffer material and the second buffer material are each independently selected from compounds represented by Formula 1 below, and the first buffer layer does not include an electron transport material: ##STR00001##
Near-IR glucose sensors
The present disclosure provides polymerizable luminescent dyes useful for incorporation into polymers. The dyes and the polymers can be used in sensing and imaging applications, for example, to provide accurate and optionally long term measurements of glucose in vivo. The present disclosure also provides sensors including the polymers described herein. The sensors can be implanted into a tissue of a subject and used for long-term or short-term continuous and semi-continuous collection of data of various biochemical analytes, optionally without the use of implantable hardware of any type and/or enzymatic and electrochemical detection methods.
ORGANIC LIGHT-EMITTING ELEMENT
The present specification relates to an organic light emitting device having high light emission efficiency.
WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE
Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I):
##STR00001##
including stereoisomers, salts and tautomers thereof, wherein R.sup.1, R.sup.2, R.sup.3, L.sup.1, L.sup.2, L.sup.3, L.sup.4, L.sup.5, L.sup.6, M.sup.1, M.sup.2, A, q, w and n are as defined herein. Methods associated with preparation and use of such compounds are also provided.
WATER SOLUBLE FLUORESCENT OR COLORED DYES AND METHODS FOR THEIR USE
Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I):
##STR00001##
including stereoisomers, salts and tautomers thereof, wherein R.sup.1, R.sup.2, R.sup.3, L.sup.1, L.sup.2, L.sup.3, L.sup.4, L.sup.5, L.sup.6, M.sup.1, M.sup.2, A, q, w and n are as defined herein. Methods associated with preparation and use of such compounds are also provided.