Compound for organic electric element, organic electric element comprising the same and electronic device thereof
US-2015380661-A1 · Dec 31, 2015 · US
US9978957B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9978957-B2 |
| Application number | US-201615281480-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 30, 2016 |
| Priority date | Oct 20, 2011 |
| Publication date | May 22, 2018 |
| Grant date | May 22, 2018 |
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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.
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.
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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