IP Library Granted Patent US 10,497,877
Granted Patent B2
US 10,497,877 · App. 15/650,363 · Granted Dec 3, 2019

Compounds and organic electronic devices

Inventors: Teresa Mujica-Fernaud (Darmstadt, DE); Elvira Montenegro (Weinheim, DE); Amir Hossain Parham (Frankfurt am Main, DE); Arne Buesing (Frankfurt am Main, DE); Frank Voges (Bad Duerkheim, DE)
Assignee: Merck Patent GmbH
H01L51/006C07C211/61C07D307/91C09K11/06H01L51/0039H01L51/0052H01L51/0059H01L51/0061H05B33/20C07C2603/18C09K2211/1011C09K2211/1014C09K2211/1029C09K2211/1088C09K2211/1433C09K2211/185H01L51/0058H01L51/0073H01L51/5012H01L51/5056H01L51/5088H01L51/5096Y02E10/549
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,497,877
App. No.
15/650,363
Granted
Dec 3, 2019
Kind
B2
Abstract

The present invention relates to certain fluorenes, to the use of the compounds in an electronic device, and to an electronic device comprising at least one of these compounds. The present invention furthermore relates to a process for the preparation of the compounds and to a formulation and composition comprising one or more of the compounds.

Claims (85)

1. An electroluminescent device comprising at least one compound of the general formula (1)

where the following applies to the symbols and indices occurring:

Ar 1 and Ar 2

are on each occurrence, identically or differently, an aromatic or heteroaromatic group having two or more aromatic or heteroaromatic rings and having 10 to 60 ring atoms in said aromatic or heteroaromatic group, which is optionally substituted by one or more radicals R 4 , which are identical to or different from one another, wherein either Ar 1 or Ar 2 comprises at least one heteroaromatic group having 6 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 4 , which are identical to or different from one another;

wherein at least one Ar 1 or Ar 2 is selected from the group consisting of radicals having the formulae (43)-(54) and (55):

wherein the radicals having the formulas (43) to (55) may be substituted, by one or more radicals R 4 , which are identical to or different from one another;

R 1

is on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 5 , CN, Si(R 5 ) 3 , NO 2 , P(═O)(R 5 ) 2 , S(═O)R 5 , S(═O) 2 R 5 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 5 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 5 C═CR 5 —, —C≡C—, Si(R 5 ) 2 , C═O, C═S, C═NR 5 , —C(═O)O—, —C(═O)NR 5 —, P(═O)(R 5 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , or a condensed ring system having 9 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where, in the case of aromatic or heteroaromatic condensed rings, not more than 10 ring atoms is optionally present; the two radicals R 1 may also form a ring closure with one another, so that a spiro compound forms, where no aromatic or heteroaromatic rings are condensed onto the ring formed by the two radicals R 1 ;

R 2 , R 3 and R 4

are on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 5 , CN, Si(R 5 ) 3 , NO 2 , P(═O)(R 5 ) 2 , S(═O)R 5 , S(═O) 2 R 5 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 5 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 5 C═CR 5 —, —C≡C—, Si(R 5 ) 2 , C═O, C═S, C═NR 5 , —C(═O)O—, —C(═O)NR 5 —, P(═O)(R 5 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 ;

R 5

is on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 6 , CN, Si(R 6 ) 3 , NO 2 , P(═O)(R 6 ) 2 , S(═O)R 6 , S(═O) 2 R 6 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 6 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 6 C═CR 6 —, —C≡C—, Si(R 6 ) 2 , C═O, C═S, C═NR 6 , —C(═O)O—, —C(═O)NR 6 —, P(═O)(R 6 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 6 , or an aryloxy or heteroaryloxy group having 5 to 30 aromatic ring atoms, which is optionally substituted by one or more radicals R 6 ;

R 6

is on each occurrence, identically or differently, H, D, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms is optionally replaced by D or F;

n is 0, 1, 2, 3 or 4;

m is 0, 1, 2 or 3;

with the proviso that the compound of the formula (1), besides the one fluorene group and besides the possible condensed or polycyclic groups in position 9 of the fluorene, contains no further polycyclic or condensed groups or

the compound of formula (1) is selected from the group consisting of formula (94)-(96), (138)-(140) and (201)-(203):

2. The device according to claim 1 , wherein the two radicals R 1 in the compound of the formula (1) are identical.

3. The device according to claim 1 , wherein m is equal to 1 and n is equal to 0, 1 or 2.

4. The device according to claim 1 , wherein it comprises at least one compound of the general formula (2)

where the definitions from claim 1 apply to the symbols.

5. The device according to claim 1 , wherein R 3 is equal to H.

6. The device according to claim 1 , wherein Ar 1 and Ar 2 are identical or different and are selected from a biphenyl, terphenyl or quaterphenyl group, each of which is optionally substituted by one or more radicals R 4 .

7. The device according to claim 1 , wherein the two radicals R 1 are identical and are selected from an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , or a condensed ring system having 9 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where, in the case of aromatic or heteroaromatic condensed rings, not more than 10 ring atoms is optionally present and where R 2 is equal to H.

8. The device according to claim 1 , wherein the two radicals R 1 are identical and are selected from a straight-chain alkyl group having 1 to 20 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, where the groups may each be substituted by one or more radicals R 5 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 and where R 2 is an aromatic or heteroaromatic ring system having 6 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 .

9. The device according to claim 1 , wherein it is an organic light-emitting transistor (OLET), an organic field-quench device (OFQD), an organic light-emitting electrochemical cell (OLEC, LEC or LEEC), an organic laser diode (O-laser) or an organic light-emitting diode (OLED).

10. The device according to claim 1 , wherein the device is an organic light-emitting diode (OLED), wherein the compound is employed in one of the following functions: as hole-transport material in a hole-transport or hole-injection layer, as matrix material in an emitting layer, as electron-blocking material or as exciton-blocking material.

11. A compound of the general formula (167)

where the following applies to the symbols used in formula (167):

Ar 3 and Ar 4

are on each occurrence, identically or differently, an aromatic or heteroaromatic group having two or more aromatic or heteroaromatic rings and having 10 to 60 ring atoms in said aromatic or heteroaromatic group, which is optionally substituted by one or more radicals R 5 , which are identical to or different from one another, wherein either Ar 3 or Ar 4 comprises at least one heteroaromatic group having 6 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 5 , which are identical to or different from one another;

wherein at least one Ar 3 or Ar 4 is selected from the group consisting of radicals having the formulae (43)-(54) and (55):

wherein the radicals having the formulas (43) to (55) may be substituted, by one or more radicals R 4 , which are identical to or different from one another;

R 7

is identical on each occurrence and is selected from the group consisting of a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 5 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, CN or NO 2 , or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above, or a condensed ring system having 9 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where, in the case of aromatic or heteroaromatic condensed rings, not more than 10 ring atoms is optionally present in the condensed ring system; the two radicals R 7 may also form a ring closure with one another, so that a spiro compound forms, where no aromatic or heteroaromatic rings are condensed onto the ring formed by the two radicals R 7 ,

and where, if R 7 is a straight-chain or branched alkyl group, R 8 is an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , and where R 5 is defined as indicated above;

R 8

is H, D or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above and where, if R 8 is equal to H, R 7 is an aromatic or heteroaromatic ring system having 6 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above;

a

is either 1, 2, 3 or 4;

with the proviso that the compound of the formula (167), besides the one fluorene group and besides the possible condensed or polycyclic groups in position 9 of the fluorene, contains no further polycyclic or condensed groups

and with the proviso that the compound contains no halogens

the compound of formula (167) is selected from the group consisting of formula (94)-(96), (138)-(140) and (201)-(203):

12. The compound according to claim 11 , wherein the compound has the general formula (168)

where, for the symbols used,

Ar 3 and Ar 4

are identical or different on each occurrence and are selected from a biphenyl, terphenyl or quaterphenyl group, which is optionally substituted by one or more radicals R 5 ;

wherein at least one Ar 3 or Ar 4 is selected from the group consisting of radicals having the formulae (43)-(54) and (55):

wherein the radicals having the formulas (43) to (55) may be substituted, by one or more radicals R, which are identical to or different from one another;

R 7

is identical on each occurrence and is selected from an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above, or a condensed ring system having 9 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 ,

where, in the case of aromatic or heteroaromatic condensed rings, not more than 10 ring atoms is optionally present in the condensed ring system or

the compound of formula (168) is selected from the group consisting of formula (94)-(96), (138)-(140) and (201)-(203):

13. The compound according to claim 11 , wherein the compound has the general formula (169)

where, for the symbols used,

X

is, identically or differently on each occurrence, N or CR 5 , preferably X is equal to CR 5 ;

Ar 3 and Ar 4

are identical or different on each occurrence and are selected from a biphenyl, terphenyl and quaterphenyl group, each of which is optionally substituted by one or more radicals R 5 ; and

wherein at least one Ar 3 or Ar 4 is selected from the group consisting of radicals having the formulae (43)-(54) and (55)

wherein the radicals having the formulas (43) to (55) may be substituted, by one or more radicals R 4 , which are identical to or different from one another;

R 5

is on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 6 , CN, Si(R 6 ) 3 , NO 2 , P(═O)(R 6 ) 2 , S(═O)R 6 , S(═O) 2 R 6 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 6 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 6 C═CR 6 —, —C≡C—, Si(R′) 2 , C═O, C═S, C═NR 6 , —C(═O)O—, —C(═O)NR 6 —, P(═O)(R 6 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 6 , or an aryloxy or heteroaryloxy group having 5 to 30 aromatic ring atoms, which is optionally substituted by one or more radicals R 6 ;

R 6

is on each occurrence, identically or differently, H, D, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms is optionally replaced by D or F or

the compound of formula (169) is selected from the group consisting of formula (94)-(96), (138)-(140) and (201)-(203):

14. A process for the preparation of the compound according to claim 11 by means of one-step Buchwald coupling by reacting a fluorene derivative containing a leaving group with Ar 3 —NH—Ar 4 .

15. A process for the preparation of the compound according to claim 11 by means of two-step Buchwald coupling by stepwise reacting a phenanthrene derivative containing a leaving group with (1) Ar 3 —NH 2 and (2) NH 2 —Ar 4 .

16. An oligomer, polymer or dendrimer containing one or more compounds of the general formula (167)

where the following applies to the symbols used in formula (167):

Ar 3 and Ar 4 are on each occurrence, identically or differently, an aromatic or heteroaromatic group having two or more aromatic or heteroaromatic rings and having 10 to 60 ring atoms in said aromatic or heteroaromatic group, which is optionally substituted by one or more radicals R 5 , which are identical to or different from one another, wherein either Ar 3 or Ar 4 comprises at least one heteroaromatic group having 6 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 5 , which are identical to or different from one another;

R 7 is identical on each occurrence and is selected from the group consisting of a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 5 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, CN or NO 2 , or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above, or a condensed ring system having 9 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where, in the case of aromatic or heteroaromatic condensed rings, not more than 10 ring atoms is optionally present in the condensed ring system; the two radicals R 7 may also form a ring closure with one another, so that a spiro compound forms, where no aromatic or heteroaromatic rings are condensed onto the ring formed by the two radicals R 7 ,

and where, if R 7 is a straight-chain or branched alkyl group, R 8 is an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , and where R 5 is defined as indicated above;

R 8 is H, D or an aromatic or heteroaromatic ring system having 6 to 30 ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above and where, if R 8 is equal to H, R 7 is an aromatic or heteroaromatic ring system having 6 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 , where R 5 is defined as indicated above;

a is either 1, 2, 3 or 4;

with the proviso that the compound of the formula (167), besides the one fluorene group and besides the possible condensed or polycyclic groups in position 9 of the fluorene, contains no further polycyclic or condensed groups

and with the proviso that the compound contains no halogens,

where the bond(s) to the polymer, oligomer or dendrimer is optionally localised at any positions.

17. A composition comprising one or more compounds according to claim 11 and at least one further organically functional material selected from the group consisting of fluorescent emitters, phosphorescent emitters, host materials, matrix materials, electron-transport materials, electron-injection materials, hole-conductor materials, hole-injection materials, electron-blocking materials and hole-blocking materials.

18. A formulation comprising at least one compound according to claim 11 and at least one solvent.

19. An electronic device comprising at least one compound according to claim 11 .

20. The electronic device according to claim 19 , wherein the device is selected from the group consisting of organic integrated circuits (O-ICs), organic field-effect transistors (O-FETs), organic thin-film transistors (O-TFTs), organic light-emitting transistors (O-LETs), organic solar cells (O-SCs), organic optical detectors, organic photoreceptors, organic field-quench devices (O-FQDs), light-emitting electrochemical cells (LECs), organic laser diodes (O-lasers) and organic electroluminescent devices (OLEDs).

21. An organic electroluminescent device which comprises the compound according to claim 11 is employed in one or more of the following functions: as hole-transport material in a hole-transport or hole-injection layer, as matrix material in an emitting layer, as electron-blocking material or as exciton-blocking material.

22. The device according to claim 1 , wherein at least one Ar 1 or Ar 2 is selected from the group consisting of radicals having the formulae (43)-(53) and (54):

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2017
From: MUJICA-FERNAUD, TERESA; MONTENEGRO, ELVIRA; PARHAM, AMIR HOSSAIN; BUESING, ARNE; VOGES, FRANK
To: MERCK PATENT GMBH
Reel/Frame 043062/0016 →
Priority Claims (1)
EP 12005370 · Jul 23, 2012 · regional
Continuity (2)
Continuation 14416863
Related Publication 20170317285A1 · Nov 2, 2017
Cited By (1)
US 12,490,647