Fluorescent organic light emitting elements having high efficiency

US9853224B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9853224-B2
Application numberUS-201515301863-A
CountryUS
Kind codeB2
Filing dateMar 30, 2015
Priority dateApr 4, 2014
Publication dateDec 26, 2017
Grant dateDec 26, 2017

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention relates to organic light emitting elements, comprising thermally activated delayed fluorescence (TADF) emitters and/or hosts on basis of benzotriazoles, which have a sufficiently small energy gap between S 1 and T 1 (ΔE ST ) to enable up-conversion of the triplet exciton from T 1 to S 1 . The organic light emitting elements show high electroluminescent efficiency.

First claim

Opening claim text (preview).

The invention claimed is: 1. An organic light-emitting element, comprising a light-emitting layer comprising i) a compound of formula  as guest and a host material; or ii) a compound of formula  as host and a fluorescent guest material, wherein R 1 , R 2 , R 3 and R 4 are independently of each other H, D, F, Cl, a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group, a C 6 -C 10 aryloxy group, or a donor group of formula R 5 , R 6 , R 7 , R 8 and R 9 are independently of each other H, D, F, Cl, a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group, a C 6 -C 10 aryloxy group, a group of formula  (Xa), (Xb), or (Xd); R 1′ , R 2′ , R 3′ and R 4′ are independently of each other H, D, F, Cl, a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group, or a C 6 -C 10 aryloxy group; or R 1 and R 2 together form a group of formula R 1′ and R 2′ together form a group of formula R 3 and R 4 together form a group of formula R 3′ and R 4′ together form a group of formula R 5 and R 6 together form a group of formula  and/or R 8 and R 9 together form a group of formula A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 and A 8 are independently of each other H, D, F, Cl, a C 1 -C 25 alkyl group, or a donor group of formula (Xa), (Xb), or (Xd); A 9 , A 10 , A 11 , A 12 , A 13 , A 14 , A 15 and A 16 are independently of each other H, D, F, Cl, a C 1 -C 25 alkyl group, or a donor group of formula (Xa), (Xb), or (Xd); X 1 and X 2 are independently of each other a single bond, O, S, N(R 15 ), C(═O), C(R 16 )(R 17 ), B(R 18 ), or Si(R 19 )(R 20 ) and R 10 , R 11 , R 12 , R 21 and R 21′ are independently of each other H, D, F, Cl, or a C 1 -C 25 alkyl group; R 15 , R 16 , R 17 , R 18 , R 19 and R 20 are independently of each other H, D, a C 1 -C 25 alkyl group, or a C 6 -C 14 aryl group, which can optionally be substituted by one, or more groups selected from a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group and a C 6 -C 10 aryloxy group; with the proviso that at least one donor group of formula (Xa), (Xb), or (Xd) is present in the compound of formula (I); characterized in that it emits delayed fluorescence. 2. The organic light-emitting element according to claim 1 , wherein R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 and R 9 are independently of each other H, a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group, a C 6 -C 10 aryloxy group, a donor group of formula  or R 1 and R 2 together form a group of formula  and/or R 8 and R 9 together form a group of formula R 5 is H, a C 1 -C 25 alkyl group, a group of formula  or a donor group of formula (Xa), (Xb), or (Xd); X 1 and X 2 are independently of each other a single bond, O, S, C(O), N(R 15 ), or C(R 16 )(R 17 ); and R 10 , R 11 , R 12 , R 21 and R 21′ are independently of each other H, or a C 1 -C 25 alkyl group; R 15 is a group of formula R 16 and R 17 are independently of each other H, a C 1 -C 25 alkyl group; R 22 and R 23 are independently of each other H, a C 1 -C 25 alkyl group, a C 1 -C 25 alkoxy group, or a C 6 -C 10 aryloxy group; with the proviso that at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 is a donor group of formula (Xa), (Xb), or (Xd). 3. The organic light-emitting element according to claim 1 , wherein the compound of formula (I) is a compound of formula wherein R 1 and R 2 are independently of each other H, or a C 1 -C 25 alkyl group, or R 1 and R 2 together form a group of formula R 3 , R 7 and R 8 are independently of each other H, a C 1 -C 25 alkyl group, or a donor group of formula R 5 is H, a C 1 -C 25 alkyl group, a group of formula  or a donor group of formula (Xa), (Xb), or (Xd); R 9 is H, or R 8 and R 9 together form a group of formula X 1 and X 2 are independently of each other a single bond, O, S, N(R 15 ), or C(R 16 )(R 17 ); R 10 , R 11 , R 12 , R 21 and R 21′ are independently of each other H, or a C 1 -C 25 alkyl group; R 15 is a group of formula R 16 and R 17 are independently of each other H, a C 1 -C 25 alkyl group; R 22 and R 23 are independently of each other H, or a C 1 -C 25 alkyl group; with the proviso that at least one of R 3 , R 5 and R 7 is a donor group of formula (Xa), (Xb), or (Xd). 4. The organic light-emitting element according to claim 3 , wherein the compound of formula (I) is a compound of formula wherein R 1 and R 2 are independently of each other H, or a C 1 -C 25 alkyl group, or R 1 and R 2 together form a group of formula R 3 is H, a C 1 -C 25 alkyl group, or a donor group of formula R 7 is H, a C 1 -C 25 alkyl group, or a donor group of formula (Xa), (Xb), or (Xd); R 8 and R 9 are H, or R 8 and R 9 together form a group of formula X 1 and X 2 are independently of each other a single bond, O, S, N(R 15 ), or C(R 16 )(R 17 ); R 10 , R 11 , R 12 , R 21 and R 21′

Assignees

Inventors

Classifications

  • Use of particular materials as binders, particle coatings or suspension media therefor · CPC title

  • C09K11/06Primary

    containing organic luminescent materials · CPC title

  • containing three or more hetero rings · CPC title

  • non-luminescent particle coatings or suspension media · CPC title

  • Electricity · mapped topic

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What does patent US9853224B2 cover?
The present invention relates to organic light emitting elements, comprising thermally activated delayed fluorescence (TADF) emitters and/or hosts on basis of benzotriazoles, which have a sufficiently small energy gap between S 1 and T 1 (ΔE ST ) to enable up-conversion of the triplet exciton from T 1 to S 1 . The organic light emitting elements show high electroluminescent efficiency.
Who is the assignee on this patent?
Udc Ireland Ltd
What technology area does this patent fall under?
Primary CPC classification C09K11/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 26 2017 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).