IP Library › Granted Patent US 10,868,255
Granted Patent B2
US 10,868,255 · App. 16/067,640 · Granted Dec 15, 2020

Compound for photoactive organic electronic components and photoactive organic electronic component containing the compound

Inventors: Dirk Hildebrandt (Ulm, DE); Olga Gerdes (Ulm, DE); Roland Fitzner (Ulm, DE); Daniel D'Souza (Dresden, DE); Gunter Mattersteig (Ulm, DE); Andre Weiss (Dresden, DE)
Assignee: HELIATEK GMBH
H01L51/0065C07D407/10C07D409/14C07D493/04C07D495/04H01L51/005H01L51/0068H01L51/0071H01L51/0072H01L51/0073H01L51/42Y02E10/549
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Quick Facts
Patent No.
US 10,868,255
App. No.
16/067,640
Granted
Dec 15, 2020
Kind
B2
Abstract

A compound and method of producing the compound of formula (I) that has high absorption in the short wavelength spectral region of visible light and is capable of being used for an organic electronic component.

Claims (92)

1. A compound of the formula (I):

with Y, Y′, Z and Z′ each independently selected from: N or CR a ,

with X selected from: O, S, Se, Si(R b R c ), P(R b ), P(0)R b ,

wherein the R a to R c radicals are each independently selected from the group of the following radicals: H, halogen, CN, NR d R c where R d and R c are each independently selected from the group of the radicals: H, and cyclic or open-chain C 1 -C 20 -alkyl, where individual carbon atoms may be replaced by heteroatoms and where hydrogen atoms in the alkyl radical may be substituted,

cyclic or open-chain C 1 -C 20 -alkyl, where individual carbon atoms may be replaced by heteroatoms,

cyclic or open-chain C 1 -C 20 —O-alkyl,

cyclic or open-chain C 1 -C 20 —S-alkyl,

cyclic or open-chain C 2 -C 20 -alkenyl,

cyclic or open-chain C 2 -C 20 —O-alkenyl,

cyclic or open-chain C 2 -C 20 —S-alkenyl,

cyclic or open-chain C 2 -C 20 -alkynyl,

aryl,

heteroaryl,

wherein hydrogen atoms in the alkyl, O-alkyl, S-alkyl, alkenyl, O-alkenyl, S-alkenyl, alkynyl, aryl and heteroaryl radicals may each independently be substituted; and

wherein A 1 is an electron-withdrawing radical having at least one C═C double bond selected from the group of the following radicals:

wherein, in each of these three radicals for A 1 , either the E isomer or the Z isomer may each independently be present for each C═C double bond in each case, and

wherein A 2 is an electron-withdrawing radical having at least two conjugated C═C double bonds selected from the group of the following radicals:

wherein, in each of these three radicals for A 2 , either the E isomer or the Z isomer may each independently be present for each C═C double bond in each case,

wherein m, 1 and n are each independently 0 or 1,

wherein R 1 to R 10 and R 5 * and R 6 * for the A 1 and A 2 groups are each independently selected from the group of the following radicals: H, halogen, CN, cyclic or open-chain C 1 -C 20 -alkyl, cyclic or open-chain C 2 -C 20 -alkenyl, cyclic or open-chain C 1 -C 20 —O-alkyl, aryl, heteroaryl, where hydrogen atoms in the alkyl, alkenyl, O-alkyl, aryl and heteroaryl radicals may each independently be substituted; and

wherein it is possible in each case independently for a ring to be formed by the following pairs of radicals together: R 1 and R 3 , R 2 and R 4 , R 4 and R 5 , R 3 and R 5 *, R 7 and R 9 , R 6 and R 8 , R 8 and R 10 , R 6 * and R 7 ;

with the proviso that, for A 1 , exactly one of the R 5 *, R 5 , R 4 , R 3 , R 2 and R 1 represents a linkage by means of which A 1 is bonded to the structural element

in the compound of the formula (I), and with the proviso that, for A 2 , exactly one of the R 6 *, R 6 , R 7 , R 8 , R 9 and R 10 radicals represents a linkage by means of which A 2 is bonded to the structural element

of the compound of the formula (I);

wherein R 11 and R 12 for the A 1 and A 2 groups are each independently selected from the group of the radicals: H, CN, COOR f where R f is selected from the group of the radicals: H and cyclic or open-chain C 1 -C 20 -alkyl, where hydrogen atoms in the alkyl may be replaced by fluorine atoms, with the proviso that R 11 and R 12 cannot both be H,

wherein the R 13 and R 14 radicals are independently selected from the same group of radicals as R d and R c , and

wherein U 1 , U 2 , and T 1 to T 4 are each independently selected from the group consisting of: 0, S and C(CN) 2 , and

wherein Q 1 and Q 2 are each independently selected from the group consisting of: O and S, and

wherein the conjugated D 1 , D 2 and D 3 blocks are each independently selected from the group of the following structural units:

wherein the coefficients o and q each independently assume the values of 0 and 1 and the coefficient p assumes the values of 0, 1, 2, 3, 4 and 5, with the proviso that at least one of the coefficients o, p and q is not 0,

Y″ is selected from: N or CR g ;

Z″ is selected from: N or CR h ;

X″ is selected from: O, S, Se, Si(R i R j ), P(R i ), P(O)R i ;

V is selected from: O, S, Se or NR k ;

V′ is selected from: O, S, Se or NR k ; preferably NR k ,

X 1 is selected from: NR l , CR l R m ;

W 1 to W 4 are independently selected from: N, CR n ;

wherein the R g to R n radicals and the W 15 to R 34 radicals are each independently selected from the group of the radicals as R a to R c ; and

wherein the R g and R h radicals may be joined to one another in the form of a ring structure and where an aryl radical may be fused onto the ring structure, where any aryl radical fused to the ring structure may be substituted.

2. The compound as claimed in claim 1 , wherein exactly one of the three coefficients o, p and q is 1, while the two other coefficients are 0.

3. The compound as claimed in claim 1 , wherein, for A 1 , the R 5 * radical represents the linkage by means of which A 1 is bonded to the structural element

of the compound of the formula (I), such that A 1 is selected from the group of the following radicals:

wherein, in each of these three radicals for A 1 , either the E isomer or the Z isomer may each independently be present for each C═C double bond in each case, and

wherein, for A 2 , the R 6 * radical represents the linkage by means of which A 2 is bonded to the structural element

of the compound of the formula (I), such that A 2 is selected from the group of the following radicals:

wherein, in each of these three radicals for A 2 , either the E isomer or the Z isomer may each independently be present for each C═C double bond in each case.

4. The compound as claimed in claim 1 , wherein the R 11 and R 12 radicals are each CN.

5. The compound as claimed in claim 1 , wherein the R 1 to R 10 and R 5 * and R 6 * radicals are each independently selected from the group of the following radicals: H, F, linear or branched C 1 -C 5 -alkyl, and wherein hydrogens in the alkyl may each independently be replaced by fluorine atoms.

6. The compound as claimed in claim 1 , wherein A 1 is selected from the group of the following radicals:

7. The compound as claimed in claim 1 , wherein A 2 is selected from the group of the following radicals:

8. The compound as claimed in claim 1 with X=oxygen.

9. The compound as claimed in claim 1 with X=oxygen, with m=n=0, with o=q=0 and with p selected from: 1, 2, 3, 4 and 5, having the formula:

10. The compound as claimed in claim 1 ,

wherein Y, Y′, Z and Z′ are each independently selected from: N or CR a , and

wherein R a is selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, C 1 -C 5 -alkenyl, C 1 -C 5 —S-Alkyl, C 2 -C 5 —O-alkenyl, C 2 -C 5 —S-alkenyl, C 2 - C 5 -alkynyl, C 2 -C 5 -Alkynyl, phenyl, wherein hydrogen atoms in the alkyl, O-alkyl, S-alkyl, alkenyl, O-alkenyl, S-alkenyl, alkynyl and phenyl radicals may each independently be substituted.

11. The compound as claimed in claim 1 , wherein Y, Y′, Z, Z′ are each independently selected from: N, CH, C—F, C—CH 3 , C—CF 3 , C—C 2 H 5 , C—C 3 H 8 , C—OCH 3 , C—OC 2 H 5 , C—SCH 3 , C—SC 2 H 5 .

12. The compound as claimed in claim 1 , wherein Y, Y′, Z, Z′ are each CH.

13. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

14. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

wherein the R g and R h radicals are independently selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, where individual carbon atoms may be replaced by heteroatoms, C 1 -C 5 —O-alkyl, C 1 -C 5 —S-alkyl, where hydrogen atoms in the alkyl, O-alkyl and S-alkyl radicals may each independently be substituted by fluorine, and

wherein the R g and R h radicals may be joined to one another in the form of a ring structure and where an aryl radical may be fused to the ring structure.

15. The compound as claimed in claim 1 , wherein X″=S.

16. The compound as claimed in claim 1 having the following formula:

17. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

wherein R 17 and R 18 are each independently selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, C 1 -C 5 —O-alkyl, C 1 -C 5 —S-alkyl, where hydrogen atoms in the alkyl, O-alkyl and S-alkyl radicals may each independently be replaced by fluorine atoms.

18. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

wherein X 1 is selected from: NR 1 , CR 1 R m ,

wherein R 1 and R m are each independently selected from the group of the radicals: H, open-chain C 1 -C 5 -alkyl, C 5 -C 12 -aryl, C 5 -C 12 -heteroaryl, where hydrogen atoms in the open-chain C 1 -C 5 -alkyl may at least partly be replaced by fluorine atoms and where hydrogen atoms in the C 5 -C 12 -aryl and the C 5 -C 12 -heteroaryl may at least partly be substituted, and

wherein R 27 to R 32 are each independently selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, C 1 -C 5 —O-alkyl, C 1 -C 5 —S-alkyl, where hydrogen atoms in the alkyl, O-alkyl and S-alkyl radicals may each independently be replaced by fluorine atoms.

19. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

wherein W 1 to W 4 are independently selected from: N and CR n , and

wherein R n is selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, C 1 -C 5 —O-alkyl, C 1 -C 5 —S-alkyl, wherein hydrogen atoms in the alkyl, O-alkyl and S-alkyl radicals may each independently be replaced by fluorine atoms.

20. The compound as claimed in claim 1 , wherein at least one of the conjugated D 1 to D 3 blocks is present in the compound and has the formula

wherein R 33 to R 34 are each independently selected from the group of the following radicals: H, F, C 1 -C 5 -alkyl, C 1 -C 5 —O-alkyl, C 1 -C 5 —S-alkyl, where hydrogen atoms in the alkyl, O-alkyl and S-alkyl radicals may each independently be replaced by fluorine atoms and

with Y″ selected from: N or;

with Z″ selected from: N or CR h ;

with V′ selected from: 0, S, Se or NR k ;

wherein R g and R h selected as one of the R a to R c radicals, and

wherein R k is selected from the group of radicals: H, open-chain C 1 -C 5 -alkyl, C 5 -C 12 -aryl, C 5 -C 12 -heteroaryl, where hydrogen atoms in the open-chain C 1 -C 5 -alkyl may at least partly be replaced by fluorine atoms and where hydrogen atoms in the C 5 -C 12 -aryl and the C 5 -C 12 -heteroaryl may at least partly be substituted.

21. The compound as claimed in claim 1 , wherein the conjugated D 1 to D 3 blocks are independently selected from the group of the following structural units:

22. A method of using one or more of the compound as claimed in claim 1 in a photoactive organic electronic component.

23. The method of use as claimed in claim 22 , wherein the component is an organic solar cell.

24. A photoactive organic electronic component comprising the compound as claimed in claim 1 .

25. The compound as claimed in claim 1 prepared from a compound having the following formula

wherein Y, Z and A 2 are as defined in claim 1 and where M is selected from one of the following functional groups:

—SnR* 3 ,—B(OR*) 2 ,—Zn-Hal*,—Mg-Hal*,

wherein R* is a C l -C 10 -alkyl and where the Hal* group is a halogen.

26. A process for preparing the compound as claimed in claim 1 , comprising, as a process step, a coupling reaction,

wherein either the compound reacts with a further compound of the following formula

wherein A 1 , Y′, Z′, X, D 1 to D 3 and o, p and q are defined as defined in claim 1 , and where the Hal group is a halogen, or

two equivalents of the compound are reacted with a second further compound of the following formula

wherein D 1 to D 3 , o, p and q are as defined in claim 1 , and wherein the Hal group is a halogen.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2020
From: HILDEBRANDT, DIRK; GERDES, OLGA; FITZNER, ROLAND; D'SOUZA, DANIEL; MATTERSTEIG, GUNTER; WEISS, ANDRE
To: HELIATEK GMBH
Reel/Frame 053276/0107 →
Priority Claims (1)
DE 10 2015 123 005 · Dec 30, 2015 · national
Continuity (1)
Related Publication 20190019957A1 · Jan 17, 2019