Organic light-emitting device

US2016190475A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016190475-A1
Application numberUS-201514741622-A
CountryUS
Kind codeA1
Filing dateJun 17, 2015
Priority dateDec 26, 2014
Publication dateJun 30, 2016
Grant date

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

An organic light-emitting device includes a first electrode, a second electrode facing the first electrode, and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer. The organic layer includes a first compound represented by one of Formulae 1-1 to 1-3 below and a second compound represented by Formula 2 below: where A 1 to A 5 , B 1 to B 5 , D 1 to D 5 , R 1 to R 5 , R 12 , R 13 , R 41 to R 44 , L 11 , L 2 , L 3 , and ba to bi are as defined in the specification.

First claim

Opening claim text (preview).

What is claimed is: 1 . An organic light-emitting device, comprising a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes a first compound represented by one of Formulae 1-1 to 1-3 below and a second compound represented by Formula 2 below: wherein in Formulae 1-1 to 1-3 and 2, ring A 1 , ring A 2 , and ring A 3 are condensed together, ring B 1 , ring B 2 , and ring B 3 are condensed together, and ring D 1 , ring D 2 , and ring D 3 are condensed together, ring A 2 , ring B 2 , and ring C 2 are each independently represented by the following Formula 3: in Formula 3, Y 1 is O, S, or N-(L 1 ) aa -(R 11 ) ab , ring A 1 , rings A 3 , to A 5 , ring B 1 , rings B 3 to B 5 , ring D 1 , and rings D 3 to D 5 are each independently a substituted or unsubstituted benzene ring or a substituted or unsubstituted naphthalene ring, R 1 to R 6 are each independently selected from a hydrogen, a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid or a salt thereof, a sulfonic acid or a salt thereof, a phosphoric acid or a salt thereof, a substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, wherein each of R 1 and R 2 , R 3 and R 4 , and R 5 and R 6 is a non-ring forming substituent which are not linked to each other and do not form a ring, L 1 to L 3 and L 1 are each independently selected from a substituted or unsubstituted C 3 -C 10 cycloalkylene group, a substituted or unsubstituted C 1 -C 10 heterocycloalkylene group, a substituted or unsubstituted C 3 -C 10 cycloalkenylene group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenylene group, a substituted or unsubstituted C 6 -C 60 arylene group, a substituted or unsubstituted C 1 -C 60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed heteropolycyclic group, aa and ba to be are each independently selected from 0, 1, 2, and 3, and, when aa and ba to be are 0, *-(L 1 ) aa -*′, *-(L 11 ) ba -*′, *-(L 2 ) bb -*′, and *-(L 3 ) bc -*′ represent a single bond, and when aa and ba to bc are 2 or more, 2 or more L 1 s, 2 or more L 11 s, 2 or more L 2 s, and 2 or more L 3 s are identical to or different from each other, R 11 to R 13 and R 41 to R 44 are each independently selected from a hydrogen, a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid or a salt thereof, a sulfonic acid or a salt thereof, a phosphoric acid or a salt thereof, a substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), —B(Q 4 )(Q 5 ), and N(Q 6 )(Q 7 ), ab, bd and be are each independently 1 selected from 1, 2, and 3, and when ab, bd, and be are 2 or more, 2 or more R 11 s, 2 or more R 12 s, and 2 or more R 13 s are identical to or different from each other, bf and bi are each independently 0 selected from 0, 1, 2, 3, and 4, and when bf and bi are 2 or more, 2 or more R 41 s and 2 or more R 44 s are identical to or different from each other, respectively, bg and bh are each independently selected from 0, 1, 2, and 3, and when bg and bh are 2 or more, 2 or more R 42 s and 2 or more R 43 s are identical to or different from each other, respectively, at least one of substituents of the substituted benzene ring, the substituted naphthalene ring, the substituted C 3 -C 10 cycloalkylene group, the substituted C 1 -C 10 heterocycloalkylene group, the substituted C 3 -C 10 cycloalkenylene group, the substituted C 1 -C 10 heterocycloalkenylene group, the substituted C 6 -C 60 arylene group, the substituted C 1 -C 60 heteroarylene group, the substituted divalent non-aromatic condensed polycyclic group, the substituted divalent non-aromatic condensed heteropolycyclic group, the substituted C 1 -C 60 alkyl group, the substituted C 2 -C 60 alkenyl group, the substituted C 2 -C 60 alkynyl group, the substituted C 1 -C 60 alkoxy group, the substituted C 3 -C 10 cycloalkyl group, the substituted C 1 -C 10 heterocycloalkyl group, the substituted C 3 -C 10 cycloalkenyl group, the substituted C 1 -C 10 heterocycloalkenyl group, the substituted C 6 -C 60 aryl group, the substituted C 6 -C 60 aryloxy group, the substituted C 6 -C 60 arylthio group, the substituted C 1 -C 60 heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group is selected from: a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid or a salt thereof, a sulfonic acid or a salt thereof, a phosphoric acid or a salt thereof, a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, and a C 1 -C 60 alkoxy group; a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, a C 2 -C 60 alkynyl group, and a C 1 -C 60 alkoxy group, each substituted with at least one of a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid or a salt thereof, a sulfonic acid or a salt thereof, a phosphoric acid or a salt thereof, a C 3 -C 10 cycloalkyl group, a C 1 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 1 -C 10 heterocycloalkenyl group, a C 6 -C 60 aryl group, a C 6 -C 60 aryloxy group, C 6 -C 60 arylthio group, C 1 -C 60 heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 11 )(Q 12 )

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What does patent US2016190475A1 cover?
An organic light-emitting device includes a first electrode, a second electrode facing the first electrode, and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer. The organic layer includes a first compound represented by one of Formulae 1-1 to 1-3 below and a second compound represented by Formula 2 below: …
Who is the assignee on this patent?
Samsung Display Co Ltd
What technology area does this patent fall under?
Primary CPC classification H01L51/0072. Mapped technology areas include Electricity.
When was this patent published?
Publication date Thu Jun 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).