Spirobifluorene compounds for light emitting devices

[0001] The present invention relates to compounds based on spirobifluorene and light emitting devices comprising said compounds.

[0002] Various organic light emitting devices have been under active study and development, particularly those based on electroluminescence (EL) from small organic materials. For such organic devices, the ability to form morphologically stable amorphous films is a key requirement for the development of small materials for organic light emitting diodes (OLEDs). That is because when a small molecule compound is used in the organic light-emitting layer, crystallization usually occurs if the molecule of the compound is too small and its structure is too symmetrical. Therefore, when applied in an organic light-emission layer, the small molecule compound is vulnerable to morphological change such as crystallization, and once the crystal is formed, it yields negative impacts upon the light- emitting nature and service life of the OLED.

[0003] Thermal stress during device operation can lead to such phase transitions from the amorphous state to the thermodynamically stable polycrystalline state leading to dramatic degradation of the device. As a result it is crucial to design materials featuring high glass transition temperature (Tg

>150°C) in order to stabilize the amorphous state. For improving the stability of devices in order to increase operational lifetime, several host materials have been reported. Especially, designing materials having a spiro linkage has been a very successful strategy to obtain OLEDs materials with enhanced morphological stability while keeping their electro- optical functionality.

[0004] US2006/0141287 discloses light-emitting layers which include a solid

organic material containing a mixture of at least two components. The first host component is an organic compound capable of transporting electrical charges and also forms an aggregate. The second component of the mixture is an organic compound capable of transporting electrical charges and, upon mixing with the first host component, is capable of forming a continuous and substantially pin-hole-free layer. In the reference, as the second component, various compounds such as substituted fluorene derivatives, and spirobifluorene derivatives, etc. are used.

[0005] Spirobifluorene, as used herein denotes a structural element of formula (1 ) and is referred to as SBF hereinafter, whereas Open SBF denotes a system of formula (2) below.

[0006] (1 ) (2)

[0007] The substitution of the SBF ring system in "para-position" (i.e. the 2, 7, 2' or T position of the SBF) by a heteroatom, which carries one or two substituents has been described in the prior art.

[0008] 2,7'-bis-N.N'-diphenylamino-SBF and various derivatives as well as

various derivatives of 2-N,N'-diphenylamino-SBF have been described by Salbeck et al., Chem.Rev. 2007, 107, 101 1 -1065.

[0009] 2,2'-disubstituted SBF derivatives with diarylamino-substitutents are also disclosed in US 7,714,145.

[0010] Spirobifluorenes with substituted diphenylamino-substituents in 4 and or 4'-position are disclosed in WO 201 1/006574. Such compounds may be referred to as orthosubstituted relative to the direct bond linking the phenyl rings of the SBF unit.

[001 1] European Patent Application 2 312 667 discloses compositions for organic electroluminescence elements comprising at least two different materials fulfilling a certain mathematical equation related to the solubility of the materials. Among an extended list of suitable materials having as a common structural feature substituted diphenylamino groups, 3,6-Bis-N,N'- di(4-tert.butylphenyl)amino-spirobifluorene as well as the respective Open SBF derivative are mentioned. [0012] None of the above-disclosed materials meets all the requirements necessary for OLED application, particularly suitable energy level for high phosphorescent efficiency (high triplet energy), high morphological stability, while maintaining other electro-optic and processing properties under operational conditions of the device, such as emission colour, dimensional stability, etc, in a fully satisfactory manner. Thus, there has been a need to develop new host materials, which are capable of satisfying all of the requirements indicated above.

[0013] Surprisingly, it has been found that spirobifluorene compounds as defined in claim 1 possess a property spectrum which makes them particularly suitable for use in organic electroluminescent devices.

[0014] Preferred compounds in accordance with the instant invention are

described in the dependent claims and the detailed specification hereinafter.

[0015] The compounds of the present invention are characterized by formulae 3 to 9 below

[0020]

wherein n, m and o may be the same or different and represent an integer of from 0 to 3,

each of the phenyl rings may carry no ligands other than L ¹ or may be substituted by ligands other than L ¹ ,

L ¹ , which may be the same or different in each position shown, L ¹ is represented by one of the following formulae

wherein R ¹ to R ⁹ independently from each other are represented by phenyl, biphenyl, and naphthyl, anthracenyl or terphenyl, all of which may be substituted or unsubstituted, a heteroaryl group selected from

2H-pyrrole 3H-pyrrole 1 -substituted 2H-imidazole ₄ H-imidazole

-imidazole

1 -substituted- 1 H-1 ,2,3-triazole

2-substituted-2H-1 ,2,3-triazole 1-substituted-1 H-1 ,2,4-triazole

1 -sub stituted-1 H-pyrazole

1 -substituted 1 H-1 ,2,3,4-tetrazole

1 ,3-disubstituted imidazol-2-ylidene or a heteroaryl group selected from

oxazole isoxazole thiazole isothiazole

1 ,2,3-oxadiazole 1 ,2,5-oxadiazole 1 ,2,3-thiadiazole 1 ,2,5-thiadiazole or a heteroaryl group selected from

pyridine pyridazine pyrimidine pyrazii triazine

1 ,2,4-triazine 1 ,2,3,4-tetrazine 1 ,2,3,5-tetrazine 1 ,2,4,5-tetrazine

with the following compounds being excluded:

[0022] Particularly preferred are compounds where L ¹ is selected from -NR ¹ R ² ,

OR ³ and SR ⁴ , especially preferably L ¹ is -NR ¹ R ² .

[0023] The aryl or heteroaryl group carried by the heteroatom is preferably

selected from C6 to Cie aryl or Ci to Cie heteroaryl groups.

[0024] Preferred aryl groups are phenyl, napththyl, anthracenyl, biphenyl or

terphenyl, which may be unsubstituted or substituted by substituents selected from the group consisting of halogen, alkyl, alkoxy, amino, cyano, alkenyl, alkynyl, arylalkyl, aryl and heteroaryl groups or the aryl group may be part of an annealed ring system.

[0025] Especially preferred aryl substituents are derived from the following

substituted or unsubstituted aryl systems

[0028] of which phenyl and biphenyl are especially preferred.

[0029] A particularly preferred group of heteroaryl groups are the following:

2H-pyrrole 3H-pyrrole 1 -substituted 1 H-imidazole 2H-imidazole 4H-imidazole

In all these ring systems one or more of the nitrogen atoms may be replaced by another heteroatom like O or S, to name only two exam as shown below:

oxazole isoxazole thiazole isothiazole

1 ,2,3-oxadiazole 1 ,2,5-oxadiazole 1 ,2,3-thiadiazole 1 ,2,5-thiadiazole

[0031] Still another preferred group of heteroaryl substituents comprises the 6- membered ring systems shown below:

pyridine pyridazine pyrimidine pyrazine -| 2 3-triazine

1 ,2,4-triazine 1 ,2,3,4-tetrazine 1 ,2,3,5-tetrazine 1 ,2,4,5-tetrazine

[0032] In the same manner as the aryl groups the aforementioned heteroaryl groups may be substituted, preferably by substituents selected from the group consisting of halogen, alkyl, alkoxy, amino, cyano, alkenyl, alkynyl, arylalkyl, aryl and heteroaryl groups or the heteroaryl group may be part of an annealed ring system.

[0033] A further group of preferred compounds in accordance with the present invention are those wherein at least one of n, m or o represents an integer of from 1 to 3. [0034] Also preferred are compounds wherein n, m and o are zero.

[0035] Further preferred amongst such compounds (where n, m and o are zero) are compounds of general formula

the compound

being especially preferred.

[0036] The SBF or open SBF ring system may or may not comprise further

substituents in addition to substituents L ¹ . If present, such additional substituents, which may be the same or different in each position they occur, are generally selected from of halogen, alkyl, alkoxy, amino, cyano, alkenyl, alkynyl, arylalkyl, aryl and heteroaryl groups.

[0037] The compounds in accordance with the present invention may be

synthesized by any known and suitable method.

[0038] Generally, the compounds of the present invention may be prepared by the following general reaction schemes, which show an exemplary way for compounds carrying one or two ligands L ¹

[0039] wherein X is a leaving group selected from known leaving groups for such reactions such as halogen, OH, OR, SR, OCN, SCN or CN, especially preferably halogen, in particular chlorine or bromine.

[0040] The skilled person will select the suitable reactants and reaction conditions based on the individual needs of a specific synthesis.

[0041] The starting materials for such synthesis with at least one leaving group in a meta-position of the SBF or Open SBF ring system may be synthesized in accordance with various process routes which the skilled person will select in accordance with the specific needs. Generally, such compounds are not easily accessible through introduction of the substituents directly into a SBF or Open SBF core as these routes generally yield the para- substituted products preferably due to their higher reactivity. Accordingly, the substituents X have to be introduced through suitable precursor substances e.g. fluorene derivatives, benzophenone derivatives or biphenyl derivatives, to mention only three examples, which are thereafter reacted to yield the SBF or Open SBF structure.

[0042] Thus respective compounds may for example be obtained from substituted fluorenone derivatives of formula

[0044] with suitable biphenyl compounds.

[0045] Another possibility for the synthesis of the compounds of the present invention is the reaction of fluorenones with suitable substituted biphenyl com ounds in accordance with the eneral reaction scheme

[0046]

[0047] which is described in more detail in JP 2006/089585 for X= OH and which may be adopted for other substituents X.

[0048] Another embodiment of the present invention is directed to the use of the compounds of the present invention in an organic light emitting device, especially an organic light emitting diode (OLED).

[0049] The compounds in accordance with the present invention may particularly be used as host in an emissive layer in an organic light emitting diode, it is also possible, however, to advantageously use the compounds in accordance with the present invention in other layers of organic light emitting diodes or organic

[0050] The present invention is also directed to an organic light emitting device (OLED) comprising an emissive layer (EML), said emissive layer comprising the compounds of the present invention as host material, together with an emitting material.

[0051] An OLED generally comprises :

a substrate, for example (but not limited to) glass, plastic, metal;

an anode, generally transparent anode, such as an indium-tin oxide (ITO) anode;

a hole injection layer (HIL) for example (but not limited to) PEDOT/PSS; a hole transporting layer (HTL); an ennissive layer (EML);

an electron transporting layer (ETL);

an electron injection layer (EIL) such as LiF, CS2CO3

a cathode, generally a metallic cathode, such as an Al layer.

[0052] For a hole conducting emissive layer, one may have a hole blocking layer (HBL) that can also act as an exciton blocking layer between the emissive layer and the electron transporting layer. For an electron conducting emissive layer, one may have an electron blocking layer (EBL) that can also act as an exciton blocking layer 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).

[0053] The compounds of the present invention may be used preferably used as hosts in an emissive layer.

[0054] Optionally, the emissive layer may also contain a polarization molecule, present as a dopant in said host material and having a dipole moment that generally affects the wavelength of light emitted.

[0055] 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 of metal quinoxolates (e.g. Alq3, Liq), oxadiazoles, triazoles and ketones (e.g. Spirobifluorene ketones SBFK). Examples of electron transporting materials are tris-(8-hydroxyquinoline)aluminum of formula ["Alq3"] and spirobifluoreneketone SBFK:

SBFK

A layer formed of a hole transporting material is advantageously used to transport holes into the emissive layer comprising the light emitting material as above described and the (optional) host material. An example of a hole transporting material is 4,4'-bis[N-(1 -naphthyl)-N- phenylamino]biphenyl ["a-NPD"].

The use of an exciton blocking layer ("barrier layer") to confine excitons within the luminescent layer ("luminescent zone") is greatly preferred. 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 for such a barrier layer is 2,9-dimethyl-4,7-diphenyl-1 ,10-phenanthroline (also called bathocuproine or "BCP"), which has the formula

BCP

[0058] The OLED has preferably a multilayer structure, as depicted in Figure 1 , wherein 1 is a glass substrate, 2 is an ITO layer, 3 is a HIL layer comprising PEDOT/PSS, 4 is a HTL layer comprising a-NPD, 5 is an EML comprising mCBP as host material and the light emitting material or mixture of these materials as above defined as dopant in an amount of about 15 % wt with respect to the total weight of host plus dopant; 6 is a HBL comprising BCP; 7 is an ETL comprising Alq3; 8 is an EIL comprising LiF and 9 is an Al layer cathode.

[0059] Some examples of the present invention are reported hereinafter, whose purpose is merely illustrative but not limitative of the scope of the invention itself.

[0060] Example 1

[0061] Synthesis of 3-Bromo-SBF

3-Bromofluorenone

[0064] In a three ways flask 60 ml of water were added to 8.9 ml of hydrochloric acid (HCI, 37 % w/w, 2.1 molar equivalents) and the medium was cooled to 0°C. NaNO2 (1.5 molar equivalents), dissolved in 50 ml of water, was added dropwise at 0°C. At the end of the addition, 4-amino-2- bromobenzophenone (one equivalent, 15.0 g, 51.6 mmole) solubilised in a mixture of acetone/water (400/230 ml), was added carefully. After 30 minutes at room temperature, the mixture was warmed up and kept at 60 °C for 3 hours.

[0065] After extraction with methylene chloride and evaporation of the organic phase, a brown solid was recovered (17.4 g) and a flash chromatography is realized. The pure compound was recovered after crystallization with hexane (4.2 g, 32 % yield).

[0066] Step 2: 3-bromo-SBF

[0067] ^^^^^^^Br

[0068] This compound was made in two steps from 3-bromofluorenone obtained in step 1. First, 2-bromobiphenyl (1.05 equivalents, 4.0 g, 16.5 mmol) was solubilised in 102 ml of anhydrous diethyl ether. This solution was cooled to -60°C and n-BuLi (1.16 eq.) is added dropwise. After 10 min at this temperature, a white precipitate appeared which was redissolved while the medium was warmed to room temperature. 3-Bromofluorenone was then added and the reaction mixture was kept at 45 °C for one night.

[0069] After addition of NH ₄ CI (5% aq. 260 ml) and extraction with diethyl ether, 7.0 g of an alcohol was obtained. This solid was solubilised in 141 ml of acetic acid and hydrolyzed by the addition of 78 ml of HCI/dioxane (10 % mol, 20 eq.). After evaporation of the solvents, the solid was subjected to normal phase flash chromatography to afford 5.86 g of the target compound (94 % yield).

[0070] Step 3: 3-N,N'-bis-(3-methylphenyl)amino -SBF

[0071]

[0072] In a 500 ml flask, 320 ml of toluene were degassed during 2 hours. 3-

Bromo SBF (9.9 g, 0.025 mol), sodium tert. butylate (tBuONa, 4.92 g, 0.05 mol) and 3,3'-dimethyldiphenylamine (5g, 0.025 mol) were added and after 30 min, a mixture of Bis-dibenzylideneacetone palladium (Pd(dba)2) and Tris-tert.-butylphosphine (P(tBu)3) previously prepared was slowly added.

[0073] The solution was warmed to 1 10 °C for one hour and then filtrated on a celite pad. After evaporation of the solvent, the solid recovered was recrystallised in ethanol to afford 5.5 g of a white solid (42 % yield).