Patent Grant
8663821
This application is a U.S. national stage application under 35 U.S.C. §371 of International Application No. PCT/EP2009/059074 filed Jul. 15, 2009, which claims priority to European Application No. 08160492.8 filed Jul. 16, 2008, this application being herein incorporated by reference in its entirety for all purposes.
The present invention relates to a light-emitting material and the use of such material. The present invention further relates to a light-emitting device capable of converting electric energy to light.
Currently, various display devices are actively being researched and developed, particularly those based on electroluminescence (EL) from organic materials. Contrary to photoluminescence (i.e., light emission from an active material due to optical absorption and relaxation by radioactive decay of an excited state), EL refers to a non-thermal generation of light resulting from applying an electric field to a substrate. In the case of EL, excitation is accomplished by recombining the charge carriers of opposite signs (electrons and holes) injected into an organic semiconductor in the presence of an external circuit.
A simple prototype of an organic light-emitting diode (OLED), i.e., a single layer OLED, is typically composed of a thin film made from an active organic material, which is sandwiched between two electrodes. One electrode needs to be semitransparent in order to observe the light emission from the organic layer. Typically, an indium tin oxide (ITO)-coated glass substrate is used as an anode.
Many organic materials exhibit fluorescence, i.e., luminescence from a symmetry-allowed process, from singlet excitons, which may be efficient since this process occurs between states of the same symmetry. On the contrary, if the symmetry of an exciton is different from the one of the ground state, then the radioactive relaxation of the exciton is disallowed and the luminescence will be slow and inefficient. Since the ground state is usually anti-symmetric, the decay from a triplet breaks the symmetry. Thus, the process is disallowed and the efficiency of EL is very low. Therefore, the energy contained in the triplet states is mostly wasted.
Luminescence from a symmetry-disallowed process is known as phosphorescence. Typically, phosphorescence may last up to several seconds after excitation due to the low probability of the transition, which is different from fluorescence that originates in a rapid decay. However, only a few organic materials have been identified that show efficient room temperature phosphorescence from triplets.
If phosphorescent materials are successfully utilized, they hold enormous promises and benefits for organic electroluminescent devices. For example, the advantage of utilizing phosphorescent materials is that all excitons (formed by combining holes and electrons in an EL), which are, in part, triplet-based in phosphorescent devices, may participate in the energy transfer and luminescence. This can be achieved by phosphorescence emission itself or, alternatively, it can be accomplished by using phosphorescent materials to improve the efficiency of the fluorescence process as a phosphorescent host or a dopant in a fluorescent guest, with phosphorescence from a triplet state of the host enabling energy transfer from a triplet state of the host to a singlet state of the guest.
Iridium(III) complexes have recently attracted a lot of interest as potential triplet emitters in electronic devices and in biological applications as luminescent and electrochemiluminescent materials. Colors ranging from bluish green to red are generated by varying the ligands in the iridium complexes. However, iridium complexes having only one iridium atom have emitted light at a very narrow spectral region and, thus, are not suitable for white light emission, e.g., for replacing incandescent bulbs. If each light-emitting diode (LED) emits only at a narrow spectral region, a white light display would require multiple LEDs, and the multiple LEDs would then be incorporated into complicated and expensive LED modules to obtain the required broad band illumination necessary for providing white light. In this regard, there have been several studies on the development of iridium complexes having at least two iridium atoms.
Plummer et al., “Mono- and Di-nuclear Iridium(III) Complexes: Synthesis and Photophysics,” Dalton Trans., 2080-2084 (2003) discloses heteroleptic mono- and di-nuclear iridium(III) complexes containing two ortho-metalating ligands, 2-phenylpyridine with a bipyridine derivative. The iridium(III) complexes emit light in the range from a green region to a red region, as represented by the following formula:
Tsuboyama et al., “A Novel Dinuclear Cyclometalated Iridium Complex Bridged with 1,4-bis[pyridine-2-yl]benzene: Its Structure and Photophysical Properties,” Dalton Trans., 1115-1116 (2004) discloses a dinuclear iridium complex, which exhibits intense red phosphorescence in solutions, as represented by the following formula:
L. Yang., “Novel HEXOL-Type Cyclometallated Iridium(III) Complexes: Stereoselective Synthesis and Structure Elucidation,” Chem. Commun., 4155-4157 (2005) discloses the preparation of two diastereoisomers of tetranuclear cyclometallated iridium complexes, either having an inner core of HEXOL-type [Ir(IrCl2)3]6+ unit and a surface of six chiral, didentate, cyclometallated ligands from an enantiopure pinenopyridine derivative.
PCT International Publication No. WO 2004/043974 relates to a process for producing a trivalent hexadentate ortho-metallated iridium complex characterized in a monovalent iridium dinuclear complex having halogens as bridging ligands.
However, the above light-emitting materials containing iridium complexes disclosed in the art do not exhibit sufficiently high efficiency as well as broad emission to obtain white light. It would thus be desirable to develop light-emitting materials capable of effectively emitting light of a broad spectral range, especially in the orange, green, and blue regions.
The present invention relates to a light emitting material capable of emitting light of a broad spectral range efficient for white light emission, as described below.
Another aspect of the present invention relates to the use of said light emitting material and an organic light emitting device comprising said light emitting material.
The present invention provides a light emitting material comprising a multinuclear complex comprising at least two metal atoms, and a 2-connecting short metal bridging ligand bound to said at least two metal atoms, where the metal bridging ligand comprises coordinating atoms independently selected from nitrogen, phosphor, carbon, oxygen, sulphur and selenium in 1,2 or 1,3 mutual position.(1,2-μ or 1,3-μ bonding mode).
According to the invention, “2-connecting” means that the ligand connects to the metal atoms through 2 different atoms thereof, which may be vicinal (next to each other, which corresponds to 1,2-μ) or separated by one other atom (which corresponds to 1,3-μ).
More specifically, the multinuclear complex of the present invention can be represented by Formula (I): {-[L]2M-B-}n
In one, preferred embodiment, each B, which may be the same or different, is independently selected from short-bridging “pseudo-halide” ligands, preferably:
Preferably, L represents
wherein E1 represents an aromatic or heteroaromatic ring, optionally condensed with additional aromatic moieties or non aromatic cycles, said ring optionally having one or more substituents and coordinating to metal M via a sp2 hybridized carbon, optionally forming a condensed structure with a ring E2;
In one embodiment of the present invention, the multinuclear complex has the following formula:
wherein:
In another embodiment of the present invention, the multinuclear complex has the following formula:
wherein:
In another embodiment of the present invention, the multinuclear complex has the following formula:
wherein:
In another embodiment of the present invention, the multinuclear complex has the following formula:
wherein:
Other embodiments of the present invention relate to multinuclear complexes wherein each B, which may be the same or different, is selected from cyano and thiocyanate ligands (preferably cyano ligands) and n is specifically 4, i.e., tetranuclear complexes.
Specifically, other embodiments of the multinuclear complexes of the present invention include the following complexes represented by Formulae (III) and (V) having bluish green to deep blue emission:
It has been found that when a complex having at least two metals which bind both orthometallated ligands comprising E1 and B2 moieties and a bridged ligand, those metals faun a rigid structure in which the metal atoms are caged by the orthometallated ligands, thereby significantly broadening the emission in the visible region and simultaneously, enhancing the emission intensity of the solid state compared to the corresponding mononuclear complexes. It has also been found that cyclic structures as described above (where the at least two metals and their bridging ligands form a cycle) are very stable.
Further embodiments of the multinuclear complexes of the present invention include the following complexes represented by Formulae (VI) to (XII):
Excellent results can be obtained with light emitting materials comprising the above complexes of Formulae (VI) to (XII). Complexes of Formulae (VI) to (XII) comprising orthometallated ligands and a cyano bridged ligand are particularly advantageous due to their broad and intense emission in the various wavelength regions which is necessary for white light emission.
The synthesis of the complexes of Formula (I), i.e., metal complex comprising two orthometallated ligands (CAN ligands) and bridged ligands (B1 and B2), can be accomplished by any known method. The synthetic methods suitable for the preparation of the complexes of Formula (I) are described in detail in K. Dedian et al, Inorg. Chem., 30:1685 (1991); F. O. Garces, K. A. King, and R. J. Watts, Inorg. Chem., 27:3464 (1988); M. G. Colombo, et al, Inorg. Chem., 33:545 (1994); J H van Diemen, J G Haasnoot, R. Hage, E. Miiller and J. Reedijk, Inorg. Chem. Acta, 181:245 (1991); K. A. King, et al., J. Am. Chem. Soc., 107:1431 (1985), which are hereby incorporated by reference in their entirety.
Generally, an example of the multinuclear complexes of the present invention, such as tetranuclear complexes of Formula (I), can be prepared according to the following reaction scheme:
Orthometallated ligands (H—C^N) can be prepared with good to excellent yields by using Suzuki coupling of the substituted pyridine compound with corresponding arylboronic acids, as described in LOHSE et al., “The Palladium Catalyzed Suzuki Coupling of 2- and 4-chloropyridines,” Syn. Lett., 1:15-18 (1999) and in U.S. Pat. No. 6,670,645, which are hereby incorporated by reference in their entirety.
Synthetic methods, which are particularly adapted for the preparation of fluorinated orthometallated ligands (H—C^N), are described in Japanese Patent Publication Nos. 2003113164 A and 2003113163 A, which are hereby incorporated by reference in their entirety.
If the transition metal is iridium, trihalogenated iridium (III) compounds such as IrCl3.H2O, hexahalogenated iridium (III) compounds such as Mo3IrXo6, wherein Xo is a halogen, specifically Cl and Mo is an alkaline metal, specifically K, and hexahalogenated iridium (IV) compounds such as Mo2IrXo6, wherein Xo is a halogen, specifically Cl and Mo is an alkaline metal, specifically K (Ir halogenated precursors) can be used as starting materials to synthesize the complexes of the present invention.
[C^N]2Ir(CN)2 (compound X, wherein M=Ir) complexes can be prepared by the reaction of [Ir(ppy)2(CI)]2(ppy=2-phenylpyridine) with tetraalkylammonium cyanide, as described in NAZEERUDDIN et al. “Highly phosphorescent iridium complexes and their application in organic light-emitting devices,” J. Am. Chem. Soc. 125(29):8790-8797 (2003), which is hereby incorporated by reference in its entirety.
[C^N]2Ir(μ-Xo)2Ir[C^N]2 complexes (compound XIII, wherein M=Ir), with Xo being a halogen, specifically Cl (e.g., [(2-(2,4-difluorophenyl)-4-dimethylaminopyridine)2IrCl]2, [(2-(2,4-difluorophenyl)pyridine)2IrCl]2, [(2-phenylpyridine)2IrCl]2 and [(2-(2,4-difluorophenyl)-5-dimethylaminopyridine)2IrCl]2) can be prepared from said Ir halogenated precursors and the appropriate orthometalated ligand by resorting to procedures known in the literature, as described in King and Watts, J. Am. Chem. Soc. 109:1589-1590 (1987), which is hereby incorporated by reference in its entirety.
The preparation of tetranuclear complexes by reacting [C^N]2M(CN)2 and) [C^N]2M(μ-Xo)2M[C^N]2 is advantageously carried out in organic solvents. Polar aprotic solvents are generally used for this reaction. A solvent which gives particularly good results is methylene dichloride (CH2Cl2). The solvent can be used as such or in admixture with another solvent.
The reaction can be conducted at a temperature of from 0 to 100° C., specifically 20 to 80° C., more specifically 40 to 50° C., most specifically at the refluxing temperature of methylene dichloride, for 0.5 to 48 hours, specifically 2 to 24 hours, most specifically 4 to 12 hours.
The reaction can be carried out in the presence of a suitable metal salt, such as silver salts with non- or weakly-coordinating counterions, e.g., silver tetrafluoroborate (AgBF4) and silver hexafluorophosphate (AgPF6), particularly silver nitrate (AgNO3) or silver triflate (AgCF3SO3).
The present invention also relates to using the light emitting material comprising the multinuclear complexes, as described above, in the emitting layer of an organic light emitting device (OLED).
Furthermore, the present invention relates to using the light emitting material comprising the multinuclear complexes, as described above, as a dopant in a host layer, under conditions effective to function as an emissive layer in an organic light emitting device.
If the light emitting material is used as a dopant in a host layer, it is generally used in an amount of at least 1% wt, specifically of at least 3% wt, more specifically of least 5% wt with respect to the total weight of the host and the dopant, and generally at most 25% wt, specifically at most 20% wt, more specifically at most 15% wt.
The present invention also relates to an organic light emitting device (OLED) comprising an emissive layer (EML). The emissive layer comprises the light emitting material, as described above, optionally with a host material (wherein the light emitting material is specifically present as a dopant). The host material is notably adapted to luminesce when a voltage is applied across the device structure.
An OLED generally comprises:
a glass substrate;
an anode, which is a generally transparent anode such as an indium-tin oxide (ITO) anode;
a hole transporting layer (HTL);
an emissive layer (EML);
an electron transporting layer (ETL); and
a cathode, which is generally a metallic cathode such as an Al layer.
As for a hole conducting emissive layer, one may have an exciton blocking layer, notably a hole blocking layer (HBL) between the emissive layer and the electron transporting layer. As for an electron conducting emissive layer, one may have an exciton blocking layer, notably an electron blocking layer (EBL) between the emissive layer and the hole transporting layer. The emissive layer may be equal to the hole transporting layer (in which case the exciton blocking layer is near or at the anode) or to the electron transporting layer (in which case the exciton blocking layer is near or at the cathode).
The emissive layer may be formed with a host material in which the above-described light emitting material resides as a guest or the emissive layer may consist essentially of the light emitting material. In the &inner case, the host material may be a hole-transporting material selected from the group of substituted tri-aryl amines. Specifically, the emissive layer is formed with a host material in which the light emitting material resides as a guest. The host material may be an electron-transporting material selected from the group consisting of metal quinoxolates (e.g., aluminium quinolate (Alq3), lithium quinolate (Liq)), oxadiazoles, and triazoles. An example of a host material is 4,4′-N,N-dicarbazole-biphenyl [“CBP”], which has the following formula:
Optionally, the emissive layer may also contain a polarization molecule, which is present as a dopant in said host material and having a dipole moment, that generally affects the wavelength of light emitted when said light emitting material used as a dopant luminesces.
A layer formed of an electron transporting material is advantageously used to transport electrons into the emissive layer comprising the light emitting material and the (optional) host material. The electron transporting material may be an electron-transporting matrix selected from the group consisting of metal quinoxolates (e.g., Alq3, Liq), oxadiazoles and triazoles. An example of an electron transporting material is tris-(8-hydroxyquinoline)aluminium of formula [“Alq3”]:
A layer formed of a hole transporting material is advantageously used to transport holes into the emissive layer comprising the above-described light emitting material and the (optional) host material. An example of a hole transporting material is 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl [“α-NPD”].
An exciton blocking layer (“barrier layer”) can be used to confine excitons within the luminescent layer (“luminescent zone”). As for a hole-transporting host, the blocking layer may be placed between the emissive layer and the electron transport layer. An example of a material, which is used for such a barrier layer, is 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (also called bathocuproine or “BCP”) having the following formula:
Specifically, the OLED may have a multilayer structure, as depicted in
Another aspect of the present invention relates to a display device comprising the above OLED.
Cyclometalated Ir(III) m-chloro-bridge dimer with ligand (L), bis-cyclometalated Ir(III)(L)2(CN)2TBA and Ir(III)(L)2(acetonitrile)2CF3SO2 were obtained as described in the literatures which are cited herein.
Preparation of Homoleptic Complexes
The homoleptic multinuclear complexes, such as Formulae (X) and (XI), were prepared as shown below.
Method 1:
In a 250 mL two-necked round bottom flask equipped with a condenser were placed an [(L)2Ir(m-Cl)2Ir(L)2] complex (about 200 mg depending on the complex, 1 equivalent), tetrabutyl ammonium cyanide (1.9 equivalent) and silver (I) trifluoromethane sulfonate (2.2 equivalents), and dichloromethane (200 mL). The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main band was collected, concentrated under vacuum, and precipitated with hexane. The precipitate was filtered with fritted glass, washed with hexane, and dried to yield the expected tetranuclear complex in 30-70% yield as a solid.
Method 2:
In a 250 mL two-necked round bottom flask equipped with a condenser were placed an Ir(III)(L)2(CN)2TBA complex (about 200 mg depending on the complex, 1 equivalent), Ir(III)(L)2(acetonitrile)2CF3SO2 (about 200 mg depending on the complex, 1 equivalent) and dichloromethane (200 mL) The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main band was collected, concentrated under vacuum, and precipitated with hexane. The precipitate was filtered with fritted glass and washed with hexane and dried to yield the expected tetranuclear complex in 30-70% yield as a solid.
Preparation of Heteroleptic Complexes
The heteroleptic multinuclear complexes, such as Formulas (VII) and (VIII), are prepared in the same manner as shown below.
Type[Ir(L)2][Ir(L′)2][Ir(L)2][Ir(L′)2]: 1
Method 3:
Method 2 for the homoleptic complexes synthesis was used with Ir(III)(L)2(CN)2TBA and Ir(III)(L′)2(acetonitrile)2CF3SO2 as starting material.
Method 4:
In a 250 mL two-necked round bottom flask equipped with a condenser were placed an [(L)2Ir(m-Cl)2Ir(L)2] complex (about 200 mg depending on the complex, 0.5 equivalent), Ir(III)(L)2(CN)2TBA complex (about 100 mg depending on the complex, 1 equivalent) and silver (I) trifluoromethane sulfonate (1.2 equivalent), and dichloromethane (200 mL). The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main band was collected, concentrated under vacuum, and precipitated with hexane. The precipitate was filtered with fritted glass, washed with hexane, and dried to yield the expected heteroleptic tetranuclear complex in 20-70% yield as a solid.
Type[Ir(L)2][Ir(L′)2][Ir(L)2][Ir(L″)2]: 2
Method 5:
In a 250 mL two-necked round bottom flask equipped with a condenser were placed an [(L′)2Ir(m-Cl)2Ir(L′)2] complex (about 100 mg depending on the complex, 0.25 equivalent), [(L)2Ir(m-Cl)2Ir(L)2] complex (about 200 mg depending on the complex, 0.5 equivalent), [(L″)2Ir(m-Cl)2Ir(L″)2] complex (about 100 mg depending on the complex, 0.25 equivalent), tetrabutyl ammonium cyanide (1.9 equivalent) and silver (I) trifluoromethane sulfonate (2.2 equivalent), and dichloromethane (200 mL). The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main bands were collected, concentrated under vacuum, and precipitated with hexane. The precipitate was filtered with fritted glass, washed with hexane, and dried to yield different combinations of the expected tetranuclear complexes in 5-10% yield each, as solids.
Method 6:
First step: In a 250 mL two-necked round bottom flask equipped with a condenser were placed an Ir(III)(L)2(CN)2TBA complex (about 200 mg depending on the complex, 3 equivalents), Ir(III)(L′)2(acetonitrile)2CF3SO2 (about 60 mg depending on the complex, 1 equivalent) and dichloromethane (200 mL). The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main band was collected, concentrated under vacuum and precipitated with hexane. The precipitate was filtered with fritted glass, washed with hexane, and dried to yield the expected non-closed trinuclear complex [Ir(L)2][Ir(L′)2][Ir(L)2] in 30-70% yield as a solid.
Second step: In a 250 mL two-necked round bottom flask equipped with a condenser were placed an [Ir(L)2] [Ir(L′)2] [Ir(L)2] complex (about 200 mg depending on the complex, 1 equivalent), Ir(III)(L″)2(acetonitrile)2CF3SO2 (about 60 mg depending on the complex, 1 equivalent) and dichloromethane (200 mL) The flask was evacuated and filled with argon gas three times. The reaction mixture was refluxed for 8 hours under argon gas and cooled to room temperature. The reaction mixture was filtered with a short silica gel pad and subsequently washed with dichloromethane or a dichloromethane/methanol 3% mixture. The solvents were removed under vacuum and the complex further purified by a Sephadex chromatography column. The main band was collected, concentrated under vacuum and precipitated with hexane. The precipitate was filtered with fritted glass and washed with hexane and dried to yield the expected tetranuclear complex [Ir(L)2][Ir(L′)2][Ir(L)2][Ir(L″)2] in 30-70% yield as a solid.
A. Preparation of the Compounds of Formula (IX): [Ir(phenyl-pyridine)2(CN)]4
For the preparation of the multinuclear complex of Formula (IX), only one type of iridium complex is employed to obtain a homoleptic tetranuclear complex according to the scheme below (Method 1).
The compound of Formula (IX) was obtained as a bright green luminescent yellow solid with a 68% yield. MS: m/z: 1054.6112 (calcd. 1054.6986 for [MH]2+)
B. Preparation of the Compounds of Formula (X): [Ir(2-(2,4-difluoro-phenyl)-4-NMe2-pyridine)2(CN)]4
The compound of Formula (X) was prepared according to Method 1. After filtration and washing with hexane, a bright light-blue luminescent pale yellow solid was obtained with a 29% yield.
C. Preparation of the Compounds of Formula (VI): [Ir(2-phenyl-4-COOMe-pyridine)2(CN)]4
The compound of Foimula (VI) was prepared according to Method 1. After filtration and washing with hexane, a bright orange luminescent red solid was obtained with a 46% yield.
D. Preparation of the Compounds of Formula (XI): [Ir(2-(2,4-difluoro-phenyl)-pyridine)2(CN)]4
The compound of Formula (XI) was prepared according to Method 1. After filtration and washing with hexane, a light blue luminescent pale yellow solid was obtained with a 54% yield.
E. Preparation of the Compounds of Formula (XII): [Ir(1-phenyl-pyrazolyl)2(CN)]4
The compound of Formula (XII) was prepared according to Method 1. After filtration and washing with hexane, a bright light green luminescent colorless solid was obtained with a 38% yield.
F. Preparation of the Compounds of Formula (VII): [Ir(2-phenyl-pyridine)2(CN)2][Ir(2-phenyl-4-COOMe-pyridine)2][Ir(2-phenyl-pyridine)2(CN)2][Ir(2-phenyl-4-COOMe-pyridine)2]
The compound of Formula (VII) was prepared according to Method 4, using [(2-phenyl-4-COOMe-pyridine)2Ir(μ-Cl)2Ir(2-phenyl-4-COOMe-pyridine)2] complex and Ir(III)(2-phenyl-pyridine)2(CN)2TBA obtained as a bright orange luminescent orange solid in a 31% yield. MS: m/z=1169.1785 (calcd. 1169.7056 [M-H]2+).
G. Preparation of the Compounds of Formula (VIII): [Ir(2-phenyl-pyridine)2(CN)2][Ir(2-phenyl-4-COOMe-pyridine)2][Ir(2-phenyl-pyridine)2(CN)2][Ir(2-phenyl-pyridine)2]
The compound of Formula (VIII) was prepared according to Method 6, using Ir(III)(2-phenyl-4-COOMe-pyridine)2(acetonitrile)2CF3SO2 complex and Ir(III)(2-phenyl-pyridine)2(CN)2TBA in the first step and the Ir(III)(2-phenyl-pyridine)2(acetonitrile)2CF3SO2 complex in the second step, and obtained as a bright orange luminescent orange solid in 22% yield. MS: m/z=1111.0532 (calcd. 1111.7001 [M-H]2+).
The crude obtained was apparently highly luminescent, in particular in the solid state compared to the usual iridium complexes. However, the thin layer chromatography (TLC) analysis showed several defined spots, where the two main spots were separated by column chromatography as Formula (VII) and Formula (VIII). The 1H-NMR of those fractions were very complex but different from each other (see
Surprisingly, the mass spectrometry results showed a very clean product, with only one peak in each fraction corresponding to a double charged compound: Formula (VII) m/z=1169.18 and Formula (VIII) m/z=1111.05 (see
Crystals of the compound of Formula (IX) for X-ray analysis were successfully obtained by slow diffusion of methanol into an acetonitrile solution of Formula (IX). The crystal structure and a schematic drawing of the iridium centers are illustrated in
The crystal structure results showed that the compound was indeed a tetranuclear iridium complex bridged by cyanides, where it was not a square, but rather intermediate between a square and a tetrahedral. In this organization, the cyanide bridges are not bridging two iridium atoms in a linear fashion, but their distorted coordination leads to curves between two iridium atoms as shown in the schematic representation. Another way to look at this structure is to see it as two non-coplanar triangles attached by one side. This structure is sometimes called a “butterfly” in chemistry, and therefore this new family of molecules can be named as “iridium-butterflies.”
It should be noted that the coordination of the cyanide bridge leads to two different iridium complexes-type in the square: two iridium centres are coordinated with two nitrogen atoms of the cyanide bridges, and the two other iridium centres are connected with two carbon atoms of the cyanide bridge. However, due to the quality of the crystals used in the X-ray analysis, another coordination pattern where all four iridium centres are coordinated with one nitrogen atom and one carbon atom may be formed. According to the data, the structures of other compounds of the present invention, such as Formulas (VII), (VIII), (X), and (XI), may have almost identical structures to Formula (IX), i.e., the butterfly structure.
The photoluminescence quantum yield of Formula (IX) has been measured in acetonitrile and is fairly high, i.e., Φ=66%. In addition, the solid state luminescences for Formulae (VII), (VIII), and (IX), are easily seen with a naked eye, which points to possibly high quantum yield in the solid state (see
The four iridium centres which are “caged” by the phenyl pyridine ligands and the overall structure of the complexes of the present invention being certainly rigid as seen with the NMR analysis, can explain such observation of strong luminescence in the solid state. This makes this new family of phosphorescent molecules potentially interesting for solid-state devices.
It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit and scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.
Spincoated OLEDs
OLED structure:
ITO/CH8000/PVK:OXD7:Formula IX/TPBi/Cs2CO3/A1
Comparative OLED structure:
ITO/CH8000/PVK:PBD: Ir(mppy)3/TPBi/Cs2CO3/A1
Experimental Part.
OXD-7 (1,3-Bis[(p-tert-butyl)phenyl-1,3,4-oxadiazoyl]benzene) and PBD (2-(4-biphenylyl-5-(4-tertbutylphenyl)-1,2,3-oxadiazole) were obtained from Luminescence Technology Corp.
Poly(9-vinylcarbazole) (PVK, Mw=1.100.00) has been obtained from SP2.
Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Clevios CH8000) and 1,3,5-tris[N-(phenyl)benzimidazole]benzene (TPBI) were purchased from HC Starck and from Luminescence Technology Corp. respectively. The device structure consists of a 120 nm transparent ITO layer as the bottom electrode, supported on a glass substrate. A PEDOT:PSS layer and the emissive layer were spun in sequence on top of ITO, using a Delta6 RC spincoater from Suss Microtec. Then, TPBI, Cs2CO3 and the aluminum top metal contact were evaporated in sequence using a Lesker Spectros system. The ITO surface was treated for 10 min with O2-plasma cleaner prior to any further processing. The emissive layer was spun from a chlorobenzene solution containing PVK:OXD7 and different mass ratios of Formula IX. The OLEDs were characterized optically and electrically with a C9920-12 External Quantum Efficiency Measurement System from HAMAMATSU.
Results Summary
At 100 Cd/m2, the external quantum efficiency with the device containing 3% of Foiinula IX was 10.1%, with current and power efficiency of 31.6 Cd/A and 19 lm/W, respectively. However, negligible difference was found in the concentration range of 4-10%. For these devices the turn-on voltage is about 3.5 V. By comparison with another device having the same architecture and benchmark molecule Ir(mppy)3 in place of Formula IX, an improvement of the overall performances is evident. In Table 1, the performances of the devices with Formula IX vs Ir(mppy)3 measured at 100 and 1000 Cd/m2 are reported.
The normalized EL spectra of Formula IX and benchmark molecule Ir(mppy)3 [tris(2-(p-tolyl)pyridine)iridium(III)] are depicted in
Plots of the current efficiency and power efficiency versus luminance obtained for the device with Formula IX are depicted in
| Number | Date | Country | Kind |
|---|---|---|---|
| 08160492 | Jul 2008 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
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| PCT/EP2009/059074 | 7/15/2009 | WO | 00 | 1/14/2011 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2010/007098 | 1/21/2010 | WO | A |
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