Electroluminescent devices incorporating mixed metal organic complexes

Abstract

An electroluminescent device in which there is an electroluminescent which comprises a complex of general formula (Lα)nM1M2 or of general formula (Lα)n M1M2 (Lp), where Lp is a neutral ligand and where M1 is a rare earth, transition metal, lanthamide or an actimide, M2 is a non rare earth metal, Lαis an organic complex and n is the combined valence state of M1 and M2.

Description

The present invention relates to electroluminescent devices incorporating mixed metal complexes of transition metals and other metals.

Materials which emit light when an electric current is passed through them are well known and used in a wide range of display applications. Liquid crystal devices and devices which are based on inorganic semiconductor systems are widely used, however these suffer from the disadvantages of high energy consumption, high cost of manufacture, low quantum efficiency and the inability to make flat panel displays.

Organic polymers have been proposed as useful in electroluminescent devices, but it is not possible to obtain pure colours, they are expensive to make and have a relatively low efficiency.

Another compound which has been proposed is aluminium quinolate, but this requires dopants to be used to obtain a range of colours and has a relatively low efficiency.

Patent application WO98/58037 describes a range of lanthanide complexes which can be used in electroluminescent devices which have improved properties and give better results. Patent Applications PCT/GB98/01773, PCT/GB99/03619, PCT/GB99/04030, PCT/GB99/04024, PCT/GB99/04028, PCT/GB00/00268 describe electroluminescent complexes, structures and devices using rare earth chelates.

Hitherto electroluminescent metal complexes have been based on a rare earth, transition metal, lanthanide or an actinide or have been quinolates such as aluminium quinolate.

We have now invented new electroluminescent metal complexes which include a rare earth, transition metal, lanthanide or an actinide and a non rare earth, transition metal, lanthanide or an actinide.

According to the invention there is provided an electroluminescent device which incorporates a layer of an electroluminescent complex of general formula (_ααα)_nM₁M₂ where M₁ is a rare earth, transition metal, lanthanide or an actinide, M₂ is a non rare earth metal, L_αis an organic complex and n is the combined valence state of M₁ and M₂.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1–9 show exemplary ligands L_α and Lp as described in this application.

FIGS. 10 and 11 show exemplary quinolates and other electron transmitting materials as described in this application.

FIGS. 12–16 show exemplary hole transmitting materials as described in this application.

FIG. 17 is a diagrammatic section of an exemplary LED cell as described in this application.

FIG. 18 is a plot of intensity against voltage for the device of Example 2 as described in this application.

FIG. 19 is a plot of radiance against wavelength for the device of Example 2 as described in this application.

FIG. 20 is a plot of radiance against wavelength for the device of Example 4 as described in this application.

FIGS. 21 and 22 are, respectively, plots of brightness and currency efficiency against voltage for the device of Example 3a as described in this application.

FIGS. 23 and 24 are plots similar to FIGS. 21 and 22 for the device of Example 3b as described in this application.

FIGS. 25 and 26 are plots similar to FIGS. 23 and 24 for the device of Example 3c as described in this application.

FIGS. 27 and 28 are plots similar to FIGS. 25 and 26 for the device of Example 4a as described in this application.

FIGS. 29 and 30 are plots similar to FIGS. 27 and 28 for the device of Example 5 as described in this application.

Preferably the complex can also comprise one or more neutral ligands L_p so the complex has the general formula (L_α)_n M₁ M₂ (L_p), where L_pis a neutral ligand.

There can be more than one group L_αand more than one group L_p and each of which group may be the same or different.

M₁ can be any metal ion having an unfilled inner shell which can be used as the metal and the preferred metals are selected from Sm(III), Eu(II), Eu(III), Tb(III), Dy(III), Yb(III), Lu(III), Gd (III), U(III), U(VI)O₂, Tm(III), Th(IV), Ce (III), Ce(IV), Pr(III), Nd(III), Pm(III), Dy(III), Ho(III), Er(III).

The metal M₂ can be any metal which is not a rare earth, lanthanide or an actinide examples of metals which can be used include lithium, sodium, potassium, rubidium, caesium, beryllium, magnesium, calcium, strontium, barium, copper, silver, gold, zinc, cadmium, boron, aluminium, gallium, indium, germanium, tin, antimony, lead, and metals of the first, second and third groups of transition metals e.g. manganese, iron, ruthenium, osmium, cobalt, nickel, palladium, platinum, cadmium, chromium, titanium, vanadium, zirconium, tantulum, molybdenum, rhodium, iridium, niobium, scandium, yttrium etc.

The different groups (L_α) may be the same or different and can be selected from β diketones such as those of formulae

where R₁, R₂ and R₃ can be the same or different and are selected from hydrogen, hydrocarbyl groups, substituted and unsubstituted aliphatic groups substituted and unsubstituted aromatic, heterocyclic and polycyclic ring structures, fluorocarbons such as trifluoryl methyl groups, halogens such as fluorine or thiophenyl groups; R₁, R₂ and R₃ can also be copolymerisable with a monomer e.g. styrene and where X is Se, S or O and Y is hydrogen, hydrocarbyl groups, substituted and unsubstituted aromatic, heterocyclic and polycyclic ring structures, fluorine, fluorocarbons such as trifluoryl methyl groups, halogens such as fluorine or thiophenyl groups or nitrile.

Examples of R₁ and/or R₂ and/or R₃ include aliphatic, aromatic and heterocyclic alkoxy, aryloxy and carboxy groups, substituted and substituted phenyl, fluorophenyl, biphenyl, phenanthrene, anthacene, naphthyl and fluorene groups alkyl groups such as t-butyl, heterocyclic groups such as carbazole

R₁, R₂ and R₃ can also be

where X is O, S, Se or NH.

A preferred moiety R₁ is trifluoromethyl CF₃ and examples of such diketones are, banzoyltrifluoroacetone, p-chlorobenzoyltrifluoroacetone, p-bromotrifluoroacetore, p-phenyltriuoroacetone, 1-naphthoyltrifluoroacetone, 2-naphthoyltrifluoroacetone, 2-phenathoyltrifluoroacetone, 3-phenanthoyltrifluoroacetone, 9-anthroyltrifluoroacetonetrifluoroacetone, cinnamoyltrifluoroacetone, and 2-thenoyltrifluoroacetone.

The different groups (L_α) may be the same or different ligands of formulae

where X is O,S; or Se and R₁R₂ and R₃are as above

The different groups (L_α) may be the same or different quinolate derivatives such as

where R is hydrocarbyl, aliphatic, aromatic or heterocyclic carboxy, aryloxy, hydroxy or alkoxy e.g. the 8 hydroxy quinolate derivatives or

where R is as above or H or F or

The different groups (L_α) may also be the same or different carboxylate groups

where R₅ is a substituted or unsubstituted aromatic, polycyclic or heterocyclic ring a polypyridyl group, R₅ can also be a 2-ethyl hexyl group so L_α is 2-ethylhexanoate or R₅ can be a chair structure so that L_α is 2-acetyl cyclohexanoate or L can be

where R₁ and R₂ are as above e.g. alkyl, allenyl, amino or a fused ring such as a cyclic or polycyclic ring.

The different groups (L_α) may also be

Where R₁ and R₂ are as above.

The groups L_p can be selected from

where each Ph which can be the same or different and can be a phenyl (OPNP) or a substituted phenyl group, other substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic or polycyclic group, a substituted or unsubstituted fused aromatic group such as a naphthyl, anthracene, phenanthrene, perylene or pyrene group. The substituents can be for example an alkyl, aralkyl, alkoxy, aromatic, heterocyclic, polycyclic group, halogen such as fluorine, cyano, amino and substituted amino groups etc. Examples are given in FIGS. 1 and 2 of the drawings where R, R_1, R_2, R₃ and R₄ can be the same or different and are selected from hydrogen, hydrocarbyl groups, substituted and unsubstituted aromatic, heterocyclic and polycyclic ring structures, fluorocarbons such as trifluoryl methyl groups, halogens such as fluorine or thiophenyl groups; R, R_1, R_2, R₃ and R₄ can also form substituted and unsubstituted fused aromatic, heterocyclic and polycyclic ring structures and can be copolymerisable with a monomer e.g. styrene. R, R_1, R_2, R₃ and R₄ can also be unsaturated alkylene groups such as vinyl groups or groups—C—CH₂═CH₂—Rwhere R is as above.

L_p can also be compounds of formulae

where R₁, R₂ and R₃ are as referred to above, for example bathophen shown in FIG. 3 of the drawings in which R is as above.

L_p can also be

where Ph is as above.

Other examples of L_p are as shown in FIGS. 4 to 8

Specific examples of L_αand L_p are tripyridyl and TUMH, and TMHD complexes, α, α′, α″ tripyridyl, crown ethers, cyclans, cryptans phthalocyanans, porphoiyins ethylene diarnine tetramine (EDTA), DCTA, DTPA and TIHA. Where TMHD is 2,2,6,6-tetramethyl-3,5-heptanedionato and OPNP is diphenylphosphonimide triphenyl phosphorane. The formulae of the polyamines are shown in FIG. 9.

The first electrode is preferably a transparent substrate which is a conductive glass or plastic material which acts as the anode, preferred substrates are conductive glasses such as indium tin oxide coated glass, but any glass which is conductive or has a conductive layer can be used. Conductive polymers and conductive polymer coated glass or plastics materials can also be used as the substrate.

The electroluminescent material can be deposited on the substrate directly by evaporation from a solution of the material in an organic solvent. The solvent which is used will depend on the material but chlorinated hydrocarbons such as dichloromethane, n-methyl pyrrolidone, dimethyl sulphoxide, tetra hydrofiran dimethylformamide etc. are suitable in many cases.

Alternatively the material can be deposited by spin coating from solution or by vacuum deposition from the solid state e.g. by sputtering or any other conventional method can be used.

The mixed complexes can be made by reacting a mixture of salts of the metals with the organic complexes as in conventional methods of making the transition metal complexes.

Examples of complexes of the present invention include Eu(DBM)₃OPNP, Tb(tmhd)₃OPNP, Eu(Zn(DBM)₅OPNP etc.

Optionally there is a layer of an electron transmitting material between the cathode and the electroluminescent material layer, the electron transmitting material is a material which will transport electrons when an electric current is passed through electron transmitting materials include a metal complex such as a metal quinolate e.g. an aluminium quinolate, lithium quinolate a cyano anthracene such as 9,10 dicyano anthracene, a polystyrene sulphonate and compounds of formulae shown in FIGS. 10 and 11. Instead of being a separate layer the electron transmitting material can be mixed with the electroluminescent material and co-deposited with it.

In general the thickness of the layers is from 5 nm to 500 nm.

The second electrode functions as the cathode and can be any low work function metal e.g. aluminium, calcium, lithium, silver/magnesium alloys etc., aluminium is a preferred metal. Lithium fluoride can be used as the second electrode for example by having a lithium fluoride layer formed on a metal.

Preferably there is a hole transporting layer deposited on the transparent substrate and the electroluminescent material is deposited on the hole transporting layer. The hole transporting layer serves to transport holes and to block the electrons, thus preventing electrons from moving into the electrode without recombining with holes. The recombination of carriers therefore mainly takes place in the emitter layer.

Hole transporting layers are used in polymer electroluminescent devices and any of the known hole transporting materials in film form can be used.

In general the thickness of the layers is from 5 nm to 500 nm and preferably the thickness of the electroluminescent layer is from 20 to 50 mn.

The second electrode functions as the cathode and can be any low work function metal e.g. aluminium, calcium, lithium, silver/magnesium alloys etc., aluminium is a preferred metal. Lithium fluoride can be used as the second electrode for example by having a lithium fluoride layer formed on a metal.

Preferably there is a hole transporting layer deposited on the transparent substrate and the electroluminescent material is deposited on the hole transporting layer. The hole transporting layer serves to transport holes and to block the electrons, thus preventing electrons from moving into the electrode without recombining with holes. The recombination of carriers therefore mainly takes place in the emitter layer.

Preferably there is a hole transporting layer deposited on the transparent substrate and the electroluminescent material is deposited on the hole transporting layer. The hole transporting layer serves to transport holes and to block the electrons, thus preventing electrons from moving into the electrode without recombining with holes. The recombination of carriers therefore mainly takes place in the emitter layer.

Hole transporting layers are used in polymer electroluminescent devices and any of the known hole transporting materials in film form can be used.

Examples of such hole transporting materials are aromatic amine complexes such as poly (vinylcarbazole),N,N′-diphenyl-N, N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), an unsubstituted or substituted polymer of an amino substituted aromatic compound, a polyaniline, substituted polyanilines, polythiophenes, substituted polythiophenes, polysilanes etc. Examples of polyanilines are polymers of

where R is in the ortho—or meta-position and is hydrogen, C1–18 alkyl, C1–6 alkoxy, amino, chloro, bromo, hydroxy or the group

where R is ally or aryl and R′ is hydrogen, C1–6 alkyl or aryl with at least one other monomer of formula I above.

Polyanilines which can be used in the present invention have the general formula

where p is from 1 to 10 and n is from 1 to 20, R is as defined above and X is an anion, preferably selected from Cl, Br, SO₄, BF₄, PF₆, H₂PO₃, H₂PO₄, arylsulphonate, arenedicarboxylate, polystyrenesulphonate, polyacrylate alkysulphonate, vinylsulphonate, vinylbenzene sulphonate, cellulose sulphonate, camphor sulphonates, cellulose sulphate or a perfluorinated polyanion.

Examples of arylsulphonates are p-toluenesulphonate, benzenesulphonate, 9,10-anthraquinone-sulphonate and anthracenesulphonate, an example of an arenedicarboxylate is phthalate and an example of arenecarboxylate is benzoate.

We have found that protonated polymers of the unsubstituted or substituted polymer of an amino substituted aromatic compound such as a polyaniline are difficult to evaporate or cannot be evaporated, however we have surprisingly found that if the unsubstituted or substituted polymer of an amino substituted aromatic compound is deprotonated the it can be easily evaporated i.e. the polymer is evaporable.

Preferably evaporable deprotonated polymers of unsubstituted or substituted polymer of an amino substituted aromatic compound are used. The de-protonated unsubstituted or substituted polymer of an amino substituted aromatic compound can be formed by deprotonating the polymer by treatment with an alkali such as ammonium hydroxide or an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide.

The degree of protonation can be controlled by forming a protonated polyaniline and de-protonating. Methods of preparing polyanilines are described in the article by A. G. MacDiarmid and A. F. Epstein, Faraday Discussions, Chem Soc. 88 P319 1989.

The conductivity of the polyaniline is dependant on the degree of protonation with the maximum conductivity being when the degree of protonation is between 40 and 60% e.g. about 50% for example.

Preferably the polymer is substantially fully deprotonated

A polyaniline can be formed of octamer units i.e. p is four e.g.

The polyanilines can have conductivities of the order of 1×10⁻¹ Siemen cm⁻¹ or higher.

The aromatic rings can be unsubstituted or substituted e.g. by a C1 to 20 alkyl group such as ethyl.

The polyaniline can be a copolymer of aniline and preferred copolymers are the copolymers of aniline with o-anisidine, m-sulphanilic acid or o-aminophenol, or o-toluidine with o-aminophenol, o-ethylamine, o-phenylene diamine or with amino anthracenes.

Other polymers of an amino substituted aromatic compound which can be used include substituted or unsubstituted polyaminonapthalenes, polyaminoanthracenes, polyaminophenanthrenes, etc. and polymers of any other condensed polyaromatic compound. Polyaminoanthracenes and methods of making them are disclosed in U.S. Pat. No. 6,153,726. The aromatic rings can be unsubstituted or substituted e.g. by a group R as defined above.

The polyanilines can be deposited on the first electrode by conventional methods e.g. by vacuum evaporation, spin coating, chemical deposition, direct electrodeposition etc. preferably the thickness of the polyaniline layer is such that the layer is conductive and transparent and can is preferably from 20 nm to 200 nm. The polyanilines can be doped or undoped, when they are doped they can be dissolved in a solvent and deposited as a film, when they are undoped they are solids and can be deposited by vacuum evaporation i.e. by sublimation.

The polymers of an amino substituted aromatic compound such as polyanilines referred to above can also be used as buffer layers with or in conjunction with other hole transporting materials.

The structural formulae of some other hole transporting materials are shown in FIGS. 12 to 16 of the drawings, where R_1, R₂ and R₃ can be the same or different and are selected from hydrogen, and substituted and unsubstituted hydrocarbyl groups such as substituted and unsubstituted aliphatic groups, substituted and unsubstituted aromatic, heterocyclic and polycyclic ring structures, fluorocarbons such as trifluoryl methyl groups, halogens such as fluorine or thiophenyl groups; R_1, R₂ and R₃ can also form substituted and unsubstituted fused aromatic, heterocyclic and polycyclic ring structures and can be copolymerisable with a monomer e.g. styrene. X is Se, S or O, Y can be hydrogen, substituted or unsubstituted hydrocarbyl groups, such as substituted and unsubstituted aromatic, heterocyclic and polycyclic ring structures, fluorine, fluorocarbons such as trifluoryl methyl groups, halogens such as fluorine or thiophenyl groups or nitrile.

Examples of R₁ and/or R₂ and/or R₃ include aliphatic, aromatic and heterocyclic alkoxy, aryloxy and carboxy groups, substituted and substituted phenyl, fluorophenyl, biphenyl, phenanthrene, anthracene, naphthyl and fluorene groups alkyl groups such as t-butyl, heterocyclic groups such as carbazole.

The preparation of complexes according to the invention are illustrated in the following examples.

EXAMPLE 1

Preparation of EuZn(DBM)₅(OPNP)

A mixture of dibenzoylmethane (DBM) (4.1 g; 0.0 18 mole) and OPNP (3.5 g; 0.007 mole) was dissolved in ethanol (40 ml) by warming the magnetically stirred solution. A solution containing ZnCl₂ (0.5 g; 0.0037 mole) and EuCl₃ (1.34 g; 0.0037 mole) in water (10 ml) was added to the reaction mixture, followed by 2N NaOH solution until the pH was 6–7. The precipitate was filtered off, washed with water and ethanol and dried under vacuum at 80° C. for 16 hours. The product had a M.P. of 182° C. Films of the product were obtained by dissolving the product in a solvent and evaporating from the solution.

Elemental analysis: Found C 69.59, H 4.56, N 0.79. C₁₀₅H₈₀O₁₁NP₂EuZn requires C 69.63, H 4.45 and N 0.77. The elemental analysis suggests that there was only one OPNP.

The ultraviolet spectrum was

UV (λmax) nm (thick evaporated film): 356, 196

UV (λmax) nm (thin evaporated film): 362

UV (λmax) nm (thin film made from CH₂Cl₂ solution): 360, 195

TGA: ° C. (% weight loss): 350(11),444 (39) and 555 (80)

The photoluminescent colour had co-ordinates: x 0.66, y 0.33

EXAMPLE 2

EuAl(DBM)₆OPNP

A warm ethanolic solution (50 ml) of dibenzoylmethane (DBM) (3.67 g. 0.016 mole) was mixed with an ethanolic solution (30 ml) of OPNP (2.60 g. 0.005 mole). NaOH (0.65 g, 0.0 16 mole) in water (30 ml) was added to the ligand (DBM) solution while stirring. The solution became dark yellow. The solution was stirred for 10 minutes. After 10 minutes, a mixture of EuCl₃.6H₂O (1 g 0.0027 mole) in ethanol: water (1:1) (20 ml) and AlCl₃.6H₂O (0.658 g. 0.0027 mole) in water (20 ml) was slowly added while stirring. The reaction mixture was stirred for 5 hours at 60° C. The yellow colour product was suction filtered and thoroughly washed with water followed by ethanol. Product was vacuum dried at 80° C. Analysis showed it to be EuAL(DBM)₆OPNP.

EXAMPLE 3

Electroluminescent Device

An ITO coated glass piece (1×1 cm² ) had a portion etched out with concentrated hydrochloric acid to remove the ITO and was cleaned and dried. The device is shown in FIG. 17 where (1) is ITO; (2) CuPc; (3) α-NPB; (4) EuZn(DBM)₅(OPNP); (5) BCP; (6) Alq_3; (7) LiF; (8) Al was fabricated by sequentially forming on the ITO, by vacuum evaporation, layers comprising:

ITO(100Ω/sqr)|CuPc (6.6 nm)|α-NPB(35 mm)|EuZn(DBM)₅(OPNP)(35 nm)|BCP (8 nm)|Alq₃(10 nm)|LiF(3 nm)|Al (500 nm).

Where CuPc is copper phthalocyanine, BCP bathocupron and Alq₃ is aluminiumn quinolate.

The EuZn(DBM)₅(OPNP) was prepared as in Example 1.

The organic coating on the portion which had been etched with the concentrated hydrochloric acid was wiped with a cotton bud.

The coated electrodes were stored in a vacuum desiccator over a molecular sieve and phosphorous pentoxide until they were loaded into a vacuum coater (Edwards, 10⁻⁶ torr) and aluminium top contacts made. The active area of the LED's was 0.08 cm by 0.1 cm² the devices were then kept in a vacuum desiccator until the electroluminescent studies were performed.

The ITO electrode was always connected to the positive terminal. The current vs. voltage studies were carried out on a computer controlled Keithly 2400 source meter.

An electric current was applied across the device and a plot of the radiance and intensity against voltage is shown in the graph of FIG. 18.

A plot of radiance against wavelength is shown in FIG. 19, and the colour coordinates according to the CIE colour chart were x=0.65857; y=0.33356 which is reddish orange.

EXAMPLE 3a

Other devices were fabricated as above with the structure 100ΩITO and Al electrodes

Material	CuPc	α-NPB	EuZn(DBM)5(OPNP)	BCP	Alq3	LiF
Thickness/	1.4	6.9	36.3	4.0	11.5	0.8
nm

The electroluminescent properties were

		Current			Current
Voltage/	Current/	Density/		Brightness/	Efficiency/	Electroluminescent
V	mA	mAcm−2	x, y	cdm−2	cdA−1	Efficiency/lmW−1
19.0	10.10	168.33	0.55, 0.42	160.60	0.10	0.02

The results are shown graphically in FIGS. 21 and 22

EXAMPLE 3b

Other devices were fabricated as above with the structure 100Ω ITO and Al electrodes

Material	CuPc	α-NPB	EuZn(DBM)5(OPNP)	BCP	Alq3	LiF
Thickness/	4.2	20.2	117.9	4.0	11.5	0.8
nm

The electroluminescent properties were

		Current			Current
Voltage/	Current/	Density/		Brightness/	Efficiency/	Electroluminescent
V	mA	mAcm−2	x, y	cdm−2	cdA−	Efficiency/ImW−1
22.0	1.21	20.17	0.62, 0.37	53.78	0.27	0.040

The results are shown graphically in FIGS. 23 and 24

EXAMPLE 3c

Other devices were fabricated as above with the structure 47Ω ITO and Al electrodes

Material	CuPc	β-NPB	EuZn(DBM)5(OPNP)	BCP	Alq3	LiF
Thickness/	2.0	8.5	55.0	6.0	17.0	0.9
nm

The electroluminescent properties were

		Current			Current
Voltage/	Current/	Density/		Brightness/	Efficiency/	Electroluminescent
V	mA	mAcm−2	x, y	cdm−2	cdA−1	Efficiency/ImW−1
16.0	0.81	13.60	0.59, 0.40	29.74	0.22	0.043

The results are shown graphically in FIGS. 25 and 26

EXAMPLE 4

Electroluminescent Device

Example 3 was repeated using EuAl(DBM)₆OPNP prepared as in Example 2 and the plot of radiance against wavelength is shown in FIG. 20 and the colour coordinates according to the CIE colour chart were x=0.60622; y=0.3224 which is reddish orange.

EXAMPLE 4a

Other devices were fabricated as above with the structure 100Ω ITO and Al electrodes

Material	CuPc	α-NPB	EuA1(DBM)6OPNP	BCP	Alq3	LiF
Thickness/	2.2	18.3	55.0	6.0	12.0	0.9
nm

The electroluminescent properties were

		Current			Current
Voltage/	Current/	Density/		Brightness/	Efficiency/	Electroluminescent
V	mA	mAcm−2	x, y	cdm−2	cdA−1	Efficiency/ImW−1
21.0	3.60	60.0	0.43, 0.42	528.0	0.132	0.0880

The results are shown graphically in FIGS. 27 and 28

EXAMPLE 5

Example 4 was repeated using EuSc(DBM)₆OPNP 47Ω ITO and Al electrodes

Material	CuPc	α-NPB	EuSc(DBM)6OPNP	BCP	Alq3	LiF
Thickness	2.1	8.5	54.9	6.0	17.5	1.0
nm

The electroluminescent properties were

		Current			Current
Voltage/	Current/	Density/		Brightness/	Efficiency/	Electroluminescent
V	mA	mAcm−2	x, y	cdm−2	cdA−1	Efficiency/ImW−1
22.0	3.60	60.0	0.38, 0.37	43.79	0.73	1.04 × 10−2

The results are shown graphically in FIGS. 29 and 30.

Claims

1. An electroluminescent device comprising: (i) a first electrode;(ii) a second electrode: and,(iii) a layer of an electroluminescent material positioned between said first and second electrodes, wherein said electroluminescent material is selected from the group consisting of materials having the general chemical formula (Lα)nM1M2 and materials having the general chemical formula (Lα)nM1M2(Lp) wherein:M1 is selected from the group consisting of Sm(III), Eu(II), Eu(III), Tb(III), Dy(III), Yb(III), Lu(III), Gd(III), Tm(III), Th(IV), Ce(III), Ce(IV), Pr(III), Nd(III), Pm(III), Dy(III), Ho(III) or Er(III);M2 is selected from the group consisting of lithium, sodium, potassium, rubidium, caesium, magnesium, calcium, strontium, barium, boron, aluminum, gallium, indium, germanium, tin, lead, scandium, titanium, vanadium, chromium, nickel, copper, zinc, yttrium, zirconium, niobium, molybdenum, ruthenium, rhodium, palladium, silver, cadmium, tantalum, osmium, iridium, platinum and gold;n is an integer equal to the combined valence state of M1 and M2;Lαis selected from the group of materials consisting of (a) to (f) as follows:

2. The electroluminescent device according to claim 1 wherein the electroluminescent material comprises EuZn(DBM)5OPNP.

3. The electroluminescent device according to claim 1 wherein the electroluminescent material comprises EuAl(DBM)6OPNP.

4. The electroluminescent device according to claim 1 wherein the electroluminescent material comprises EuSc(DBM)6OPNP.

5. The electroluminescent device according to claim 1 wherein a layer of a hole transmitting material is positioned between the first electrode and the layer of the electroluminescent material.

6. The electroluminescent device according to claim 5 wherein the hole transmitting layer is formed from a material selected from the group consisting of poly(vinylcarbazole), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′diamine (TPD), polyaniline, and a substituted polyaniline.

7. The electroluminescent device according to claim 1 wherein a layer of an electron transmitting material is positioned between the second electrode and the layer of electroluminescent material.

8. The electroluminescent device according to claim 7 wherein the electron transmitting material is a metal quinolate.

9. The electroluminescent device according to claim 8 wherein the metal quinolate is selected from the group consisting of lithium quinolate, sodium quinolate, potassium quinolate, zinc quinolate, magnesium quinolate and aluminum quinolate.

10. The electroluminescent device according to claim 1 wherein a layer of a hole transmitting material is positioned between the first electrode and the layer of the electroluminescent material, and further wherein a layer of an electron transmitting material is positioned between the second electrode and the layer of electroluminescent material.

11. The electroluminescent device according to claim 10 wherein the hole transmitting layer comprises a copper phthalocyanine layer and the electron transmitting layer comprises lithium fluoride.