Compound, material for organic electroluminescent elements, organic electroluminescent element, and electronic device

US12543494B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12543494-B2
Application numberUS-202217859480-A
CountryUS
Kind codeB2
Filing dateJul 7, 2022
Priority dateJul 12, 2021
Publication dateFeb 3, 2026
Grant dateFeb 3, 2026

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A compound represented by the following formula (1A) or (1B): (the symbols in the formulae (1A) and (1B) have the same meaning as defined in the specification), an organic electroluminescent device containing the compound, and an electronic device including the organic electroluminescent device.

First claim

Opening claim text (preview).

What is claimed is: 1 . A compound represented by the following formula (1A) or (1B): wherein at least one selected from R 1 to R 16 and at least one selected from R 21 to R 36 are represented by the following formula (2A), (2B), (2C) or (2D): where * represents a bonding position to a carbon atom in the formula (1A) at which R 1 to R 16 are bonded or a bonding position to a carbon atom in the formula (1B) at which R 21 to R 36 are bonded, L 1 to L 6 each independently represent a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms, or a substituted or unsubstituted divalent heterocyclic group having 5 to 50 ring atoms, a, b, c, d, e and f each independently represent 0, 1, 2 or 3, and (L 1 ) 0 , (L 2 ) 0 , (L 3 ) 0 , (L 4 ) 0 , (L 5 ) 0 and (L 6 ) 0 each independently represent a single bond, when two or more L 1 s are present, they may be the same or different, when two or more L 2 s are present, they may be the same or different, when two or more L 3 s are present, they may be the same or different, when two or more L 4 s are present, they may be the same or different, when two or more L 5 s are present, they may be the same or different, and when two or more L 6 s are present, they may be the same or different, HET represents a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, X 1 and X 2 each independently represent a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, Ar represents a substituted or unsubstituted aryl group having 10 to 50 ring carbon atoms, Y represents a group selected from the following formulae (i) to (viii): where ** represents a bonding position at which Y is bonded to L 6 in the formula (2D), R A and R B each independently represent a hydrogen atom or a substituent Z 1 , R C , R D and R E each independently represent a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, the substituent Z 1 is a halogen atom, a nitro group, a cyano group, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 50 carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted haloalkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted haloalkoxy group having 1 to 50 carbon atoms, a group represented by —Si(R 901 ) (R 902 ) (R 903 ), a group represented by —O—(R 904 ), a group represented by —S—(R 905 ), or a group represented by —N(R 906 ) (R 907 ), R 901 to R 907 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, when two or more R 901 's are present, the R 901 's may be the same or different, when two or more R 902 's are present, the R 902 's may be the same or different, when two or more R 903 's are present, the R 903 's may be the same or different, when two or more R 904 's are present, the R 904 's may be the same or different, when two or more R 905 's are present, the R 905 's may be the same or different, when two or more R 906 's are present, the R 906 's may be the same or different, when two or more R 907 's are present, the R 907 's may be the same or different, when R 1 , R 2 , R 9 and R 10 in the formula (1A) are all represented by the formula (2A), at least one selected from R 1 , R 2 , R 9 and R 10 is the formula (2A) in which HET contains a nitrogen atom, when two or more selected from R 1 to R 16 in the formula (1A) are represented by the formula (2A), they may be the same or different, when two or more selected from R 1 to R 16 are represented by the formula (2B), they may be the same or different, when two or more selected from R 1 to R 16 are represented by the formula (2C), they may be the same or different, and when two or more selected from R 1 to R 16 are represented by the formula (2D), they may be the same or different, and R 1 to R 16 are not bonded to each other, when two or more selected from R 21 to R 36 in the formula (1B) are represented by the formula (2A), they may be the same or different, when two or more selected from R 21 to R 36 are represented by the formula (2B), they may be the same or different, when two or more selected from R 21 to R 36 are represented by the formula (2C), they may be the same or different, and when two or more selected from R 21 to R 36 are represented by the formula (2D), they may be the same or different, and R 21 to R 36 are not bonded to each other, in the formulae (1A) and (1B), R 1 to R 16 and R 21 to R 36 which are not represented by the formula (2A), (2B), (2C) or (2D) each independently represent a hydrogen atom or a substituent Z 2 , the substituent Z 2 is a halogen atom, a nitro group, a cyano group, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted phenyl group, a substituted or unsubstituted aralkyl group having 7 to 50 carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted haloalkoxy group having 1 to 50 carbon atoms, a group represented by —Si(R 901 )(R 902 )(R 903 ), a group represented by —S—(R 905 ), or a group represented by —N(R 906 )(R 907 ), R 901 to R 907 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, when two or more R 901 's are present, the R 901 's may be the same or different, when two or more R 902 's are present, the R 902 's may be the same or different, when two or more R 903 's are present, the R 903 's may be the same or different, when two or more R 905 's are present, the R 905 's may be the same or different, when two or more R 906 's are present, the R 906 's may be the same or different, when two or more R 907 's are present, the R 907 's may be the sam

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What does patent US12543494B2 cover?
A compound represented by the following formula (1A) or (1B): (the symbols in the formulae (1A) and (1B) have the same meaning as defined in the specification), an organic electroluminescent device containing the compound, and an electronic device including the organic electroluminescent device.
Who is the assignee on this patent?
Idemitsu Kosan Co, National Univ Corporation Tokai National Higher Education And Research System
What technology area does this patent fall under?
Primary CPC classification C07D251/24. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 03 2026 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).