IP Library Granted Patent US 7,501,076
Granted Patent B2
US 7,501,076 · App. 10/551,976 · Granted Mar 10, 2009

Fluorescent diketopyrrolopyrroles

Assignee: Ciba Specialty Chemicals Corporation
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Quick Facts
Patent No.
US 7,501,076
App. No.
10/551,976
Granted
Mar 10, 2009
Kind
B2
Abstract

The present invention relates to fluorescent diketopyrrolopyrrole of the formula (I), a process for their preparation and their use for the preparation of inks, colorants, pigmented plastics for coatings, non-impact-printing material, color filters, cosmetics, polymeric ink particles, toners, as fluorescent tracers, in color changing media, in solid dye lasers and electroluminescent devices. A luminescent device comprising a composition according to the present invention is high in the efficiency of electrical energy utilisation and high in luminance.

Claims (36)

1. A fluorescent diketopyrrolopyrrole of formula I

wherein

R 1 and R 2 may be the same or different and are a C 1 -C 25 alkyl group, which can be substituted by fluorine, chlorine or bromine, an allyl group, which can be substituted one to three times with C 1 -C 4 alkyl, 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, C 5 -C 12 cycloalkyl condensed one or two times by phenyl which can be substituted one to three times with C 1 -C 4 -alkyl, halogen, nitro or cyano, an alkenyl group, a cycloalkenyl group, an alkynyl group, a haloalkyl group, a haloalkenyl group, a haloalkynyl group, an aldehyde group, an ester group, a carbamoyl group, a ketone group, a silyl group, a siloxanyl group, A 3 or —CR 3 R 4 —(CH 2 ) m -A 3 wherein

R 3 and R 4 independently from each other stand for hydrogen or C 1 -C 4 alkyl, or phenyl which can be substituted one to three times with C 1 -C 4 alkyl,

A 3 stands for aryl or heteroaryl, which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, and m stands for 0, 1, 2, 3 or 4,

A 1 and A 2 are independently of each other a group

wherein

R 5 is a group NR 8 R 9 ,

wherein R 8 is a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, a heteroaryl group, a heterocyclic group, an aralkyl group,

R 9 is an aryl group or a heteroaryl group,

or R 8 and R 9 together with the nitrogen atom to which they are bonded form a five or six membered heterocyclic ring condensed by one or two optionally substituted phenyl groups,

wherein

R 6 and R 7 may be the same or different and are a hydrogen atom, a C 1 -C 25 alkyl group, a cycloalkyl group, an aralkyl group, an alkenyl group, a cycloalkenyl group, an alkynyl group, a hydroxyl group, a mercapto group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, an aryl group, a heterocyclic group, a halogen atom, a haloalkyl group, a haloalkenyl group, a haloalkynyl group, a cyano group, an aldehyde group, a carboxyl group, an ester group, a carbamoyl group, a nitro group, a silyl group, a siloxanyl group, a substituted or unsubstituted vinyl group, a group NR 8 R 9 , wherein R 8 and R 9 independently of each other stand for a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, a heteroaryl group, a heterocyclic group, an aralkyl group, or R 8 and R 9 together with the nitrogen atom to which they are bonded form a five or six membered heterocyclic ring, which can be condensed by one or two optionally substituted phenyl groups.

2. A fluorescent diketopyrrolopyrrole according to claim 1 , wherein R 1 and R 2 independently from each other are C 1 -C 8 alkyl, C 5 -C 12 -cycloalkyl, C 5 -C 12 -cycloalkyl substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, C 5 -C 12 cycloalkyl, condensed one or two times by phenyl which can be substituted one to three times with C 1 -C 4 -alkyl, halogen, nitro or cyano, phenyl or 1- or 2-naphthyl which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, or —CR 3 R 4 —(CH 2 ) m -A 3 wherein R 3 and R 4 stand for hydrogen, A 3 stands for phenyl or 1- or 2-naphthyl, which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, and m stands for 0 or 1.

3. A fluorescent diketopyrrolopyrrole according to claim 1 , wherein A 1 and A 2 are independently of each other

wherein R 5 is a group —NR 8 R 9 ,

wherein R 8 and R 9 independently from each other stand for

or R 8 and R 9 together with the nitrogen atom to which they are bonded form a five or six membered heterocyclic ring condensed by one or two optionally substituted phenyl groups, wherein R 15 , R 16 and R 17 independently from each other stands for hydrogen, C 1 -C 8 -alkyl, C 1 -C 8 -alkoxy, or phenyl.

4. A fluorescent diketopyrrolopyrrole according to claim 3 , which is

wherein

R 1 and R 2 are independently of each other a C 1 -C 12 alkyl group, a C 5 -C 7 cycloalkyl group, a C 5 -C 7 cycloalkyl group substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, or a C 7 -C 14 aralkyl group, which optionally can be substituted by one to three C 1 -C 8 -alkyl or C 1 -C 8 -alkoxy groups, and R 15 and R 16 stands for hydrogen, C 1 -C 8 -alkyl, C 1 -C 8 -alkoxy, or phenyl.

5. A fluorescent diketopyrrolopyrrole according to claim 4 , which is

6. A composition comprising a guest chromophore and a host chromophore, wherein the absorption spectrum of the guest chromophore overlaps with the fluorescence emission spectrum of the host chromophore, wherein the host chromophore is a diketopyrrolopyrrole having a photoluminescence emission peak at 500 to 720 nm and wherein the host choromophore and/or the guest chromophore is a diketopyrrolopyrrole of formula I according to claim 1 .

7. A composition comprising a guest chromophore and a host chromophore, wherein the absorption spectrum of the guest chromophore overlaps with the fluorescence emission spectrum of the host chromophore, wherein the host chromophore is a diketopyrrolopyrrole having a photoluminescence emission peak at 500 to 720 nm and wherein the the guest chromophore is a diketopyrrolopyrrole of formula I according to claim 1 .

8. A composition comprising a guest chromophore and a host chromophore, wherein the absorption spectrum of the guest chromophore overlaps with the fluorescence emission spectrum of the host chromophore, wherein the host chromophore is a diketopyrrolopyrrole having a photoluminescence emission peak at 500 to 720 nm and wherein the guest chromophore is a diketopyrrolopyrrole of formula I according to claim 4 .

9. A composition according to claim 7 , wherein the host chromophore is a diketopyrrolopyrrole (“DPP”) represented by formula II

wherein R 13 and R 14 independently from each other stand for C 1 -C 25 -alkyl, which can be substituted by fluorine, chlorine or bromine, C 5 -C 12 -cycloalkyl or C 5 -C 12 -cycloalkyl, which can be condensed one or two times by phenyl which can be substituted one to three times with C 1 -C 4 -alkyl, halogen, nitro or cyano, silyl, A 6 or —CR 11 R 12 —(CH 2 ) m -A 6 , wherein R 11 and R 12 independently from each other stand for hydrogen, fluorine, chlorine, bromine, cyano or C 1 -C 4 alkyl, which can be substituted by fluorine, chlorine or bromine, or phenyl which can be substituted one to three times with C 1 -C 4 alkyl, A 6 stands for phenyl or 1- or 2-naphthyl which can be substituted one to three times with C 1 -C 8 alkyl, C 1 -C 8 alkoxy, halogen, nitro, cyano, phenyl, which can be substituted with C 1 -C 8 alkyl or C 1 -C 8 alkoxy one to three times, —NR 23 R 24 , wherein R 23 and R 24 represent hydrogen, C 1 -C 25 -alkyl, C 5 -C 12 -cycloalkyl or C 6 -C 24 -aryl, in particular phenyl or 1- or 2-naphthyl which can be substituted one to three times with C 1 -C 8 alkyl, C 1 -C 8 alkoxy, halogen or cyano, or phenyl, which can be substituted with C 1 -C 8 alkyl or C 1 -C 8 alkoxy one to three times, and m stands for 0, 1, 2, 3 or 4,

A 4 and A 5 independently from each other stand for

R 25 , R 26 , R 27 independently from each other stands for hydrogen, C 1 -C 25 alkyl, —CR 11 R 12 —(CH 2 ) m -A 6 , cyano, halogen, —OR 29 , —S(O) p R 30 , or phenyl, which can be substituted one to three times with C 1 -C 8 alkyl or C 1 -C 8 alkoxy, wherein R 29 stands for C 1 -C 25 -alkyl, C 5 -C 12 -cycloalkyl, —CR 11 R 12 —(CH 2 ) m -Ph, C 6 -C 24 -aryl, or a saturated or unsaturated heterocyclic radical comprising five to seven ring atoms, wherein the ring consists of carbon atoms and one to three hetero atoms selected from the group consisting of nitrogen, oxygen and sulfur, R 30 stands for C 1 -C 25 -alkyl, C 5 -C 12 -cycloalkyl, —CR 11 R 12 —(CH 2 ) m -Ph, R 28 stands for C 2 -C 20 -heteroaryl or C 6 -C 24 -aryl, p stands for 0, 1, 2 or 3, m and n stands for 0, 1, 2, 3 or 4.

10. A composition according to claim 9 , wherein the host chromophore is a diketopyrrolopyrrole represented by formula II wherein R 13 and R 14 independently from each other stand for C 1 -C 8 alkyl, 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, phenyl or 1- or 2-naphthyl which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, or —CR 11 R 12 —(CH 2 ) m -A 6 wherein R 11 and R 12 stand for hydrogen, or C 1 -C 4 alkyl, A 6 stands for phenyl or 1- or 2-naphthyl, which can be substituted one to three times with C 1 -C 8 alkyl and/or C 1 -C 8 alkoxy, and m stands for 0 or 1.

11. A composition according to claim 10 , wherein the host chromophore is a diketopyrrolopyrrole represented by formula II, wherein A 4 and A 5 independently from each other stand for

wherein R 25 is C 1 -C 8 -alkyl, phenyl, 1- or 2-naphthyl.

12. A composition according to claim 11 , wherein the host chromophore is a diketopyrrolopyrrole represented by formula II, wherein A 4 and A 5 independently from each other stand for

wherein R 25 is C 1 -C 8 -alkyl

and the guest chromophore is a fluorescent diketopyrrolopyrrole selected from

wherein R 1 and R 2 are independently of each other a C 1 -C 12 alkyl group.

Assignments (7)
NUNC PRO TUNC ASSIGNMENT Recorded Oct 9, 2023
From: BASF SE
To: CLAP CO., LTD.
Reel/Frame 065156/0122 →
SUBMISSION TO CORRECT ERRORS IN PREVIOUSLY-FILED DOCUMENTS THAT ERRONEOUSLY AFFECT PATENT Recorded Nov 8, 2010
From: BASF SE
To: BASF SE
Reel/Frame 025324/0472 →
ASSET TRANSFER AGREEMENT Recorded Oct 29, 2010
From: CIBA CORPORATION
To: BASF SE
Reel/Frame 025217/0436 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 27, 2010
From: BASF PERFORMANCE PRODUCTS LLC
To: BASF CORPORATION
Reel/Frame 025039/0693 →
CHANGE OF NAME Recorded Sep 27, 2010
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: CIBA CORPORATION
Reel/Frame 025039/0774 →
CHANGE OF NAME Recorded Sep 27, 2010
From: CIBA CORPORATION
To: BASF PERFORMANCE PRODUCTS LLC
Reel/Frame 025039/0744 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2008
From: YAMAMOTO, HIROSHI; DAN, NORIHISA
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 020464/0946 →
Priority Claims (1)
EP 03100972 · Apr 10, 2003 · regional
Continuity (1)
Related Publication 20070010672A1 · Jan 11, 2007