IP Library Granted Patent US 10,177,313
Granted Patent B2
US 10,177,313 · App. 15/264,183 · Granted Jan 8, 2019

Diketopyrrolopyrrole polymers for use in organic semiconductor devices

Inventors: Pascal Hayoz (Hofstetten, CH); Olivier Aebischer (Dudingen, CH); Mathias Duggeli (Thürnen, CH); Hans Jurg Kirner (Basel, CH); Marta Fonrodona Turon (Blanes, ES)
Assignee: BASF SE
H01L51/0036C07D487/04C07D519/00C08G61/124C08G61/126C09B57/004C09B69/109H01B1/127H01L51/0035H01L51/0043C08G2261/124C08G2261/1412C08G2261/18C08G2261/228C08G2261/3223C08G2261/3241C08G2261/3243C08G2261/334C08G2261/598C08G2261/91C08G2261/92C08G2261/94C08G2261/95H01L51/0003H01L51/0053H01L51/0558H01L51/42Y02E10/549
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Quick Facts
Patent No.
US 10,177,313
App. No.
15/264,183
Granted
Jan 8, 2019
Kind
B2
Abstract

The present invention relates to polymers comprising one or more (repeating) unit(s) of the formula (I) which are characterized in that Ar 1 and Ar 1′ are independently of each other are an annulated (aromatic) heterocyclic ring system, containing at least one thiophene ring, which may be optionally substituted by one, or more groups, and their use as organic semiconductor in organic devices, especially in organic photovoltaics (solar cells) and photodiodes, or in a device containing a diode and/or an organic field effect transistor. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high efficiency of energy conversion, excellent field-effect mobility, good on/off current ratios and/or excellent stability can be observed, when the polymers according to the invention are used in organic field effect transistors, organic photovoltaics (solar cells) and photodiodes.

Claims (46)

1. An organic semiconductor material, layer or component, comprising a polymer comprising one or more (repeating) unit(s) of the formula

wherein a is 1, 2, or 3, a′ is 0, 1, 2, or 3; b is 0, 1, 2, or 3; b′ is 0, 1, 2, or 3; c is 0, 1, 2, or 3; c′ is 0, 1, 2, or 3; d is 0, 1, 2, or 3; d′ is 0, 1, 2, or 3; with the proviso that b′ is not 0, if a′ is 0;

R 1 and R 2 may be the same or different and are selected from hydrogen, a C 1 -C 100 alkyl group, —COOR 103 , a C 1 -C 100 alkyl group which is substituted by one or more halogen atoms, hydroxyl groups, nitro groups, —CN, or C 6 -C 18 aryl groups and/or interrupted by —O—, —COO—, —OCO—, or —S—; a C 7 -C 100 arylalkyl group, which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy; a carbamoyl group, C 5 -C 12 cycloalkyl, which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy; a C 6 -C 24 aryl group, which can be substituted one to three times with C 1 -C 8 alkyl, C 1 -C 8 thioalkoxy, and/or C 1 -C 8 alkoxy, or pentafluorophenyl, Ar 1 and Ar 1′ are independently of each other an annulated (aromatic) heterocyclic ring system, containing at least one thiophene ring, which may be optionally substituted by one, or more groups,

Ar 2 , Ar 2′ , Ar 3 , Ar 3′ , Ar 4 and Ar 4′ have the meaning of Ar 1 , or are independently of each other

wherein one of X 3 and X 4 is N and the other is CR 99 ,

R 99 , R 104 and R 104′ are independently of each other hydrogen, halogen, or a C 1 -C 25 alkyl group, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 arylalkyl, or a C 1 -C 25 alkoxy group, R 105 , R 105′ , R 106 and R 106′ are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms;

C 7 -C 25 arylalkyl, or C 1 -C 18 alkoxy,

R 107 is C 7 -C 25 arylalkyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 perfluoroalkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; C 1 -C 18 alkyl which is interrupted by —O—, or —S—; or —COOR 103 ; R 103 is C 1 -C 50 alkyl;

R 108 and R 109 are independently of each other H, C 1 -C 25 alkyl, C 1 -C 25 alkyl which is substituted by E and/or interrupted by D, C 7 -C 25 arylalkyl, C 6 -C 24 aryl, C 6 -C 24 aryl which is substituted by G, C 2 -C 20 heteroaryl, C 2 -C 20 heteroaryl which is substituted by G, C 2 -C 18 alkenyl, C 2 -C 18 alkynyl, C 1 -C 18 alkoxy, C 1 -C 18 alkoxy which is substituted by E and/or interrupted by D, or C 7 -C 25 aralkyl, or

R 108 and R 109 together form a group of formula ═CR 110 R 111 , wherein

R 110 and R 111 are independently of each other H, C 1 -C 18 alkyl, C 1 -C 18 alkyl which is substituted by E and/or interrupted by D, C 6 -C 24 aryl, C 6 -C 24 aryl which is substituted by G, or C 2 -C 20 heteroaryl, or C 2 -C 20 heteroaryl which is substituted by G, or R 108 and R 109 together form a five or six membered ring, which optionally can be substituted by C 1 -C 18 alkyl, C 1 -C 18 alkyl which is substituted by E and/or interrupted by D,

C 6 -C 24 aryl, C 6 -C 24 aryl which is substituted by G, C 2 -C 20 heteroaryl, C 2 -C 20 heteroaryl which is substituted by G, C 2 -C 18 alkenyl, C 2 -C 18 alkynyl, C 1 -C 18 alkoxy, C 1 -C 18 alkoxy which is substituted by E and/or interrupted by D, or C 7 -C 25 aralkyl,

D is —CO—, —COO—, —S—, —O—, or —NR 112 —,

E is C 1 -C 8 thioalkoxy, C 1 -C 8 alkoxy, CN, —NR 112 R 113 , —CONR 112 R 113 , or halogen,

G is E, or C 1 -C 18 alkyl, and

R 112 and R 113 are independently of each other H; C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—.

2. The organic semiconductor material, layer or component comprising a polymer according to claim 1 , wherein the polymer comprises one or more (repeating) unit(s) of the formula

wherein

R 1 is a C 8 -C 36 alkyl group,

R 3 is hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy;

R 4 , R 4′ , R 5 , R 5′ and R 6 are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy;

R 7 , R 7′ , R 9 and R 9′ are independently of each other hydrogen, C 1 -C 25 alkyl, which may optionally be interrupted by one, or more oxygen, or sulphur atoms, or C 7 -C 25 aralkyl,

R 8 is C 7 -C 25 aralkyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; or C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, and

R 12 and R 12′ are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one, or more oxygen, or sulphur atoms, C 1 -C 25 alkoxy, or

wherein R 13 is C 1 -C 10 alkyl group, or a tri(C 1 -C 8 alkyl)silyl group.

3. The organic semiconductor material, layer or component according to claim 1 , wherein the polymer comprises (repeating) unit(s) of the formula

wherein

A is a repeating unit of formula (I), and

COM 1 - is a repeating unit, which is selected from a group of formula Ar 1 , such as, for example,

wherein

one of X 5 and X 6 is N and the other is CR 14

R 14 , R 14′ , R 17 and R 17′ are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy;

R 18 and R 18′ independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy;

R 19 is hydrogen, C 7 -C 25 aralkyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; or C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms;

R 20 and R 20′ are independently of each other hydrogen, C 7 -C 25 aralkyl, C 1 -C 25 alkyl, which may optionally be interrupted by one, or more oxygen, or sulphur atoms, and Ar 1 is as defined in claim 1 .

4. The organic semiconductor material, layer or component according to claim 3 , wherein A is a repeating unit of formula (Ia), (Ib), (Ic), (Id), (Ie), (If), (Ig), (Ih), (Ii), (Ij), (Ik), (H), (Im), (In), (Io), (Ip), (Iq), (Ir), (Is), (It), (Iu) or (Iv) as defined in claim 2 .

5. The organic semiconductor material, layer or component according to claim 3 , wherein the polymer comprises one or more (repeating) unit(s) of the formula

R 1 is a C 8 -C 36 alkyl group,

R 3 is hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy; R 4 , R 4′ and R 5 are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms, C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy;

R 7 , R 7′ , R 9 and R 9′ are independently of each other hydrogen, C 1 -C 25 alkyl, which may optionally be interrupted by one, or more oxygen, or sulphur atoms; or C 7 -C 25 aralkyl,

R 8 is C 7 -C 25 aralkyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; or C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms;

R 19 is C 7 -C 25 aralkyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; or C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms,

one of X 5 and X 6 is N and the other is CR 14 ,

R 14 , R 14′ , R 17 and R 17′ are independently of each other hydrogen, halogen, C 1 -C 25 alkyl, C 1 -C 25 alkoxy, which may optionally be interrupted by one or more oxygen or sulphur atoms; or C 7 -C 25 aralkyl,

R 18 and R 18′ independently of each other hydrogen, halogen, C 1 -C 25 alkyl, which may optionally be interrupted by one or more oxygen or sulphur atoms;

C 7 -C 25 aralkyl, or C 1 -C 25 alkoxy.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2020
From: BASF SE
To: CLAP CO., LTD.
Reel/Frame 052459/0201 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2018
From: BASF SCHWEIZ AG
To: BASF SE
Reel/Frame 044894/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2017
From: HAYOZ, PASCAL; AEBISCHER, OLIVIER; DUGGELI, MATHIAS; KIRNER, HANS JURG; TURON, MARTA FONRODONA
To: BASF SCHWEIZ AG
Reel/Frame 044037/0679 →
Priority Claims (1)
EP 09155919 · Mar 23, 2009 · regional
Continuity (3)
Continuation 14308766 · Jun 19, 2014
Division 13256943
Related Publication 20170005270A1 · Jan 5, 2017