Compound, organic electroluminescent device material, organic electroluminescent device, and electronic equipment

US2017005274A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017005274-A1
Application numberUS-201515107300-A
CountryUS
Kind codeA1
Filing dateAug 14, 2015
Priority dateAug 15, 2014
Publication dateJan 5, 2017
Grant date

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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.

Disclosed are a compound having, as a main skeleton, a polycyclic structure represented by the following general formula (1), a material for organic electroluminescence devices including the compound, an organic electroluminescence device using the compound, and electronic equipment having the organic electroluminescence device mounted thereon. A compound capable of realizing an organic EL device with high emission efficiency, a material for organic electroluminescence devices including the compound, an organic electroluminescence device using the compound, and electronic equipment having the organic electroluminescence device mounted thereon, are provided. In the formula (1), A, L, X 1 to X 16 , R, R A , and R B are those defined in the specification.

First claim

Opening claim text (preview).

1 . A compound represented by the following general formula (1): wherein, in the general formula (1), A is a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 3 to 50 ring atoms; L is a single bond, a substituted or unsubstituted arylene group having 6 to 60 ring carbon atoms, or a substituted or unsubstituted heteroarylene group having 3 to 50 ring atoms; two selected from X 1 to X 4 are a carbon atom bonding to * 1 or * 2 , respectively, and the other two of X 1 to X 4 are each independently C(R) or a nitrogen atom; two selected from X 9 to X 12 are a carbon atom bonding to *3 or *4, respectively, and the other two of X 9 to X 12 are each independently C(R) or a nitrogen atom; X 5 to X 8 and X 13 to X 16 are each independently C(R) or a nitrogen atom, Rs are each independently a hydrogen atom or a substituent, plural Rs may be the same as or different from every other R, and two selected from plural Rs may be bonded to each other to form a ring; and R A and R B are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 ring atoms, a halogen atom, a mono-substituted, di-substituted, or tri-substituted silyl group having a substituent selected from an alkyl group having 1 to 50 carbon atoms and an aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 20 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, or a cyano group, R A and R B may be the same as or different from each other, and R A and R B may be bonded to each other to form a ring. 2 . The compound according to claim 1 , which is represented by the following general formula (2): wherein, in the general formula (2), A, L, R A , and R B are the same as those described regarding the general formula (1) of claim 1 , two groups selected from R 1 to R 4 split off, the carbon atoms bonded to the subject groups bond to * 11 or * 12 , and the other two of R 1 to R 4 are each independently a hydrogen atom or a substituent; two groups selected from R 9 to R 12 split off, the carbon atoms bonded to the subject groups bond to * 13 or * 14 , and the other two of R 9 to R 12 are each independently a hydrogen atom or a substituent; and R 5 to R 8 and R 13 to R 16 are each independently a hydrogen atom or a substituent and may be the same as or different from each other, provided that two selected from R 1 to R 16 which do not take part in the bonding to * 11 to * 14 may be bonded to each other to form a ring. 3 . The compound according to claim 1 , which is represented by the following general formula (3): wherein, in the general formula (3), A, L, R A , and R B are the same as those described regarding the general formula (1) of claim 1 , two groups selected from R 1 to R 4 split off, the carbon atoms bonded to the subject groups bond to * 11 or * 12 , and the other two of R 1 to R 4 are a hydrogen atom; and two groups selected from R 9 to R 12 split off, the carbon atoms bonded to the subject groups bond to * 13 or * 14 , and the other two of R 9 to R 12 are a hydrogen atom. 4 . The compound according to claim 2 , wherein in the general formula (2) or (3), two groups selected from R 1 and R 2 , R 2 and R 3 , and R 3 and R 4 split off, the carbon atoms bonded to the subject groups bond to * 11 or * 12 ; and that two groups selected from R 9 and R 10 , R 10 and R 11 , and R 11 and R 12 split off, the carbon atom bonded to the subject groups bond to * 13 or * 14 . 5 . The compound according to claim 2 , which is represented by any one of the following general formulae (2-1) to (2-36): wherein, in the general formulae (2-1) to (2-36), A, L, R A , and R B are the same as those described regarding the general formula (2) of claim 2 ; and R 1 to R 16 and * 11 to * 14 are the same as those described regarding the general formula (2) of claim 2 . 6 . The compound according to claim 5 , which is represented by any one of the general formulae (2-2), (2-3), (2-4), (2-6), (2-7), (2-8), (2-9), (2-10), (2-11), (2-12), (2-13), (2-14), (2-15), (2-16), (2-17), (2-18), (2-19), (2-21), (2-23), (2-24), (2-25), (2-26), (2-27), (2-28), (2-29), (2-30), (2-31), (2-32), (2-33), (2-34), (2-35), and (2-36). 7 . The compound according to claim 5 , which is represented by any one of the general formulae (2-7), (2-9), (2-11), (2-12), (2-14), (2-15), (2-16), (2-18), (2-26), (2-27), (2-28), (2-30), (2-31), (2-33), (2-35), and (2-36). 8 . The compound according to claim 1 , wherein A is a substituted or unsubstituted aryl group having 6 to 24 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 3 to 24 ring atoms and containing a nitrogen atom, an oxygen atom, or a sulfur atom. 9 . The compound according to claim 1 , wherein A is a substituted or unsubstituted fused aryl group. 10 . The compound according to claim 9 , wherein the fused aryl group is a monovalent residual group of a compound represented by any one of the following general formulae (a1-1) to (a1-6): wherein, in the general formulae (a1-1) to (a1-5), each of Ar 1 to Ar 7 independently forms a ring structure having 6 to 18 ring carbon atoms together with two carbon atoms expressed by a and b, or c and d, in each of the formulae; and in the general formula (a1-6), Ar 8 forms a ring structure having 6 to 18 ring carbon atoms together with three carbon atoms expressed by a, b, and c in the formula, and Ar 9 forms a ring structure having 6 to 18 ring carbon atoms together with four carbon atoms expressed by b, c, d, and e in the formula, provided that the carbon atoms bonding to the hydrogen atoms in the structures in the general formula (a1-1) to (a1-6) may be substituted with the aforementioned substituents in place of the hydrogen atoms. 11 . The compound according to claim 1 , wherein A is a monovalent residual group of a compound represented by the following general formula (a2):

Assignees

Inventors

Classifications

  • containing one nitrogen atom as the heteroatom · CPC title

  • containing organic luminescent materials · CPC title

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

  • of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd · CPC title

  • Non-condensed systems · CPC title

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What does patent US2017005274A1 cover?
Disclosed are a compound having, as a main skeleton, a polycyclic structure represented by the following general formula (1), a material for organic electroluminescence devices including the compound, an organic electroluminescence device using the compound, and electronic equipment having the organic electroluminescence device mounted thereon. A compound capable of realizing an organic EL devi…
Who is the assignee on this patent?
Idemitsu Kosan Co
What technology area does this patent fall under?
Primary CPC classification C07D491/048. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 05 2017 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).