Materials for organic electroluminescent devices

US9978957B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9978957-B2
Application numberUS-201615281480-A
CountryUS
Kind codeB2
Filing dateSep 30, 2016
Priority dateOct 20, 2011
Publication dateMay 22, 2018
Grant dateMay 22, 2018

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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.

Triphenylene derivatives, in particular for use as triplet matrix materials in organic electroluminescent devices, one of example of which is represented by formula I. The invention furthermore relates to a process for the preparation of the triphenylene derivatives and to electronic devices comprising the triphenylene derivatives.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of formula (1) where Y is C if a group X 2 is bonded to this group Y, or is identically or differently on each occurrence CR if no group X 2 is bonded to this group Y; E is a single bond X 1 is N(R 1 ) and X 2 is C(R 1 ) 2 ; R, R 1 are identically or differently on each occurrence H, D, F, Cl, Br, I, N(R 2 ) 2 , N(Ar) 2 , C(═O)Ar, P(═O)Ar 2 , S(═O)Ar, S(═O) 2 Ar, CR 2 ═CR 2 Ar, CN, NO 2 , Si(R 2 ) 3 , B(OR 2 ) 2 , OSO 2 R 2 , a straight-chain alkyl, alkoxy, or thioalkoxy group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which is optionally substituted by one or more radicals R 2 , where one or more non-adjacent CH 2 groups are optionally replaced y R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , C═O, C═NR 2 , P(═O)(R 2 ), SO, SO 2 , NR 2 , O, S, or CONR 2 , and where one or more H atoms are optionally replaced by D, F, Cl, Br, I, CN, or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 2 , or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 2 , or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 2 , or a combination of these systems; Ar is identically or differently on each occurrence an aromatic or heteroaromatic ring system, optionally substituted by one or more radicals R 3 ; R 2 is identically or differently on each occurrence H, D, F, Cl, Br, I, N(R 3 ) 2 , N(Ar) 2 , C(═O)Ar, P(═O)Ar 2 , S(═O)Ar, S(═O) 2 Ar, CR 3 ═CR 3 Ar, CN, NO 2 , Si(R 3 ) 3 , B(OR 3 ) 2 , OSO 2 R 3 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which is optionally substituted by one or more radicals R 3 , where one or more non-adjacent CH 2 groups are optionally replaced by R 3 C═CR 3 , C≡C, Si(R 3 ) 2 , C═O, C═NR 3 , P(═O)(R 3 ), SO, SO 2 , NR 3 , O, S or CONR 3 , and where one or more H atoms are optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 3 , or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 3 , or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 3 , or a combination of these systems; R 3 is identically or differently on each occurrence H, D, an aliphatic hydrocarbon radical having 1 to 20 C atoms, an aryl or heteroaryl group having 5 to 40 ring atoms, or a combination of these groups; n, m are identically or differently on each occurrence 0 or 1, with the proviso that n+m=1; wherein at least one group R and/or R 1 is present and is a group of formula (5), and the dashed bond indicates the linking of the group of the formula (5), R 2 has the meanings given above, and: X is C if the group Ar 1 or the remainder of the molecule is bonded to this X, and is otherwise identically or differently on each occurrence CR 2 or N; Ar 1 is a divalent aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 2 ; p is identically or differently on each occurrence 0 or 1; q, r is identically or differently on each occurrence 0, 1, or 2. 2. The compound of claim 1 , wherein X is CR 2 , except where X is C if the group Ar 1 or the remainder of the molecule is bonded to this X. 3. The compound of claim 1 , wherein the group of the formula (5) is a group of formula (5a), 4. The compound of claim 1 , wherein the group of the formula (5) represents a group of formula (5b) or (5c), 5. A mixture comprising at least one compound of claim 1 and at least one further compound. 6. A formulation comprising at least one compound of claim 1 and one or more solvents. 7. An electronic device comprising the compound of claim 1 . 8. The electronic device of claim 7 , wherein said electronic device is selected from the group consisting of organic electroluminescent devices, organic integrated circuits, organic field-effect transistors, organic thin-film transistors, organic light-emitting transistors, organic solar cells, organic dye-sensitised solar cells, organic optical detectors, organic photoreceptors, organic field-quench devices, light-emitting electrochemical cells, organic laser diodes, and organic plasmon emitting devices. 9. The electronic device of claim 8 , wherein said electronic device is an organic electroluminescent device and the compound is employed as matrix material for fluorescent or phosphorescent emitters and/or in a hole-blocking layer and/or in an electron-transport layer and/or in an electron-blocking or exciton-blocking layer and/or in a hole-transport layer.

Assignees

Inventors

Classifications

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • Ortho-condensed systems · CPC title

  • the oxygen-containing ring being five-membered · CPC title

  • containing three or more hetero rings · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

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What does patent US9978957B2 cover?
Triphenylene derivatives, in particular for use as triplet matrix materials in organic electroluminescent devices, one of example of which is represented by formula I. The invention furthermore relates to a process for the preparation of the triphenylene derivatives and to electronic devices comprising the triphenylene derivatives.
Who is the assignee on this patent?
Merck Patent Gmbh
What technology area does this patent fall under?
Primary CPC classification C07D209/94. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 22 2018 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).