Fluorene compound and organic light-emitting device using same

[0001] 1. Field of the Invention

[0002] The present invention relates to a novel organic compound and an organic light-emitting device using the same.

[0003] 2. Related Background Art

[0004] An organic light-emitting device is a device in which a thin film comprising a fluorescent organic compound or a phosphorescent organic compound is sandwiched between an anode and a cathode and electrons and holes are injected from the respective electrodes to generate excitons of the fluorescent compound or the phosphorescent compound, whereby light emitted when the excitons return to a ground state is utilized.

[0005] According to a study at Kodak company in 1987 (Appl. Phys. Lett. 51, 913 (1987)), there has been reported a light emission of approximately 1000 cd/m² at an applied voltage of approximately 10 V in a device having a function-separation type two-layer structure using ITO as an anode, a magnesium-silver alloy as a cathode, an aluminum quinolinol complex as an electron-transporting material and a light-emitting material, and a triphenylamine derivative as a hole-transporting material. Related patents include U.S. Pat. Nos. 4,539,507, 4,720,432, and 4,885,211.

[0006] In addition, emission of a light within the range of from ultraviolet to infrared light can be generated by changing the type of fluorescent organic compound. In recent years extensive studies have been made on various kinds of compounds. For instance, such compounds are disclosed in U.S. Pat. Nos. 5,151,629, 5,409,783 and 5,382,477, and Japanese Patent Application Laid-Open Nos. H2-247278, H3-255190, H5-202356, H9-202878 and H9-227576.

[0007] In recent years, many studies have been made into the application of energy in a triplet state to EL by using a phosphorescent compound as a light-emitting material. A high emission efficiency exhibited by an organic light-emitting device using an iridium complex as a light-emitting material has been reported by a group at Princeton University (Nature 395, 151 (1998)).

[0008] Furthermore, in addition to the organic light-emitting device using a low molecular weight material as mentioned above, an organic light-emitting device using a conjugated polymer has been reported by a group at Cambridge University (Nature, 347, 539 (1990)). In this report, light emission from a single layer was confirmed using a film of polyphenylenevinylene (PPV) formed by application. Related patents to an organic light-emitting device using a conjugated polymer include U.S. Pat. Nos. 5,247,190, 5,514,878, 5,672,678, and Japanese Patent Application Laid-Open Nos. H4-145192 and H5-247460.

[0009] The recent progress in organic light-emitting devices is remarkable as described above and the characteristics of such devices enable a light-emitting device with a high luminance even at a low applied voltage, a wide range of emission wavelengths, a high-speed response, a small thickness and a light weight, thus suggesting the possibility of application to a variety of uses.

[0010] However, the present situation calls for optical output with even higher luminance or higher conversion efficiency. In addition, many problems still remain to be solved regarding durability against the change over time due to long-term use, deterioration caused by atmospheric gas containing oxygen, moisture, or the like. Furthermore, when considering application to a full color display or similar device, the present art is still insufficient against problems relating to the needs for light emission of blue, green, and red with a high color purity.

[0011] It is, therefore, an object of the present invention to provide a novel substituted fluorene compound.

[0012] It is another object of the present invention to provide an organic light-emitting device using a substituted fluorene compound and having an optical output with an extremely high efficiency and a high luminance.

[0013] It is still another object of the present invention to provide an organic light-emitting device having an extremely high durability.

[0014] It is yet another object of the present invention to provide an organic light-emitting device that can easily be produced at a relatively low cost.

[0015] Namely, the fluorene compound according to the present invention is represented by the general formula [I]:

[0016]
wherein the two pyrenyl groups are each independently bonded at position 1 or 4 thereof to the fluorenyl group;

[0017] each R₁ and R₂, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, a substituted amino group, cyano group, or a halogen atom;

[0018] each R₃ and R₄, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group;

[0019] each R₅ and R₆, independently, is substituted or unsubstituted isopropyl group, sec-butyl group, tert-butyl group, 1-adamantyl group, 2-adamantyl group, isoamyl group, trimethylsilyl group or triphenylsilyl group;

[0020] a and b are independently an integer of 0 to 9;

[0021] c and d are independently an integer of 1 to 9; and

[0022] n is an integer of 1 to 10.

[0023] That is, in the above general formula [I], R₁(s) and R₂(s) which are bonded to different fluorene rings may be the same or different, and R₁(s) and R₂(s) which are bonded to the same fluorene ring may be the same or different. Further, a and b may be the same or different, and when a and b are each an integer of 2 or more, R₁s and R₂s may be the same or different. Moreover, R₃(s) and R₄(s) which are bonded to different fluorene rings may be the same or different, and R₃ and R₄ which are bonded to the same fluorene ring may be the same or different. In addition, R₅(s) and R₆(s) may be the same or different; c and d may be the same or different; and when c and d are each an integer of 2 or more, R₅s and R₆s may be the same or different.

[0024] Further, the organic light-emitting device according to the present invention comprises a pair of electrodes including an anode and a cathode, and at least one layer comprising an organic compound sandwiched between the pair of electrodes, wherein at least one of the at least one layer comprising the organic compound contains at least one of the above-described fluorene compounds.

[0025] An organic light-emitting device which uses the fluorene compound represented by the general formula [I] can emit light at a high luminance with a low applied voltage and has excellent durability. In particular, an organic layer that contains the fluorene compound according to the present invention is excellent as an electron-transporting layer and as a light-emitting layer.

[0026] In addition, the device can be prepared by using a vacuum evaporation method or a casting method, so that a device having a large area can easily be prepared at a relatively low cost.

[0034] The present invention will now be described in detail.

[0035] First, the fluorene compound of the present invention will be described.

[0036] The fluorene compound of the present invention is represented by the above general formula [I].

[0037] Specific examples of the substituents in the above general formula [I] will be shown below.

[0038] Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, tert-butyl group, sec-butyl group, octyl group, 1-adamantyl group, 2-adamantyl group and the like.

[0039] Examples of the aralkyl group include benzyl group, phenethyl group and the like.

[0040] Examples of the aryl group include phenyl group, biphenyl group, terphenyl group and the like.

[0041] Examples of the heterocyclic group include thienyl group, pyrrolyl group, pyridyl group, oxazolyl group, oxadiazolyl group, thiazolyl group, thiadiazolyl group, terthienyl group and the like.

[0042] Examples of the substituted amino group include dimethylamino group, diethylamino group, dibenzylamino group, diphenylamino group, ditolylamino group, dianisoylamino group and the like.

[0043] Examples of the halogen atom include fluorine, chlorine, bromine, iodine and the like. Examples of the hydrogen atom include a radioisotope such as deuterium.

[0044] Examples of the substituents which the above-mentioned substituents may have include an alkyl group such as methyl group, ethyl group, and propyl group; an aralkyl group such as benzyl group and phenethyl group; an aryl group such as phenyl-group and biphenyl group; a heterocyclic group such as thienyl group, pyrrolyl group, and pyridyl group; amino groups such as dimethylamino group, diethylamino group, dibenzylamino group, diphenylamino group, ditolylamino group, and dianisoylamino group; an alkoxyl group such as methoxyl group, ethoxyl group, propoxyl group, and phenoxyl group; cyano group; a halogen atom such as fluorine, chlorine, bromine, and iodine; and the like.

[0045] Next, typical examples of the fluorene compound of the present invention will be given. However, the present invention is not limited thereto.

[0046]

[0047] Particularly preferable ones of these are the following compounds.

[0048]

[0049] The fluorene compound of the present invention is superior to the conventional compounds in electron-transporting properties, light mission properties and durability, which is useful for a layer containing an organic compound of an organic light-emitting device, in particular for an electron-transporting layer and a light-emitting layer. In addition, a layer formed by a vacuum evaporation method, a solution application method, etc., does not readily undergo crystallization or the like and is excellent in stability over time.

[0050] Furthermore, because substituted or unsubstituted isopropyl group, sec-butyl group, tert-butyl group, 1-adamantyl group, 2-adamantyl group, isoamyl group, trimethylsilyl group or triphenylsilyl group is incorporated into the pyrene ring, molecular association can be suppressed, lowering in emission efficiency or the like due to concentration quenching can be restrained, and solubility increases to enable an organic layer to be readily formed by a solution application method.

[0051] The fluorene compound of the present invention can be synthesized by a well-known method and obtained by using, for example, a synthesis method such as the Suzuki coupling method (e.g., Chem. Rev. 1995, 95, 2457-2483) using a palladium catalyst, the Yamamoto method (e.g., Bull. Chem. Soc. Jpn. 51, 2091, 1978) using a nickel catalyst, or a method in which synthesis is performed by using an aryl tin compound (e.g., J. Org. Chem., 52, 4296, 1987), or by alkylation using a Friedel-Crafts reaction.

[0052] Next, the organic light-emitting device of the present invention will be described in detail below.

[0053] The organic light-emitting device of the present invention comprises a pair of electrodes including an anode and a cathode, and at least one layer comprising an organic compound sandwiched between the pair of electrodes, wherein at least one of the at least one layer comprising the organic compound contains at least one of the fluorene compounds represented by the above general formula [I].

[0054] In the organic light-emitting device of the present invention, it is preferable that at least an electron-transporting layer or a light-emitting layer of the layer(s) comprising an organic compound comprises at least one of the above-mentioned fluorene compounds.

[0055] In the organic light-emitting device of the present invention, the fluorene compound represented by the above general formula [I] is formed between the anode and the cathode by a vacuum evaporation method or a solution application method. The organic layer is preferably formed into a thin film with a thickness of 10 μm or less, more preferably 0.5 μm or less, and most preferably 0.01 to 0.5 μm.

[0056] Further, according to a preferred embodiment of the organic light-emitting device of the present invention, at least a light-emitting layer of the layer(s) comprising the organic compound comprises at least one of the fluorene compounds represented by the above general formula [I] and either one of the arylamine compounds represented by the following general formulae [II] to [VII] or an acetylene compound represented by the following general formula [VIII].

[0057]
In the general formula [II],

[0058] each R₁₃ and R₁₄, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group;

[0059] each R₁₅ and R₁₆, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0060] e and f are each independently an integer of 1 to 3;

[0061] Ar₃, Ar₄, Ar₅, and Ar₆ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₃ and Ar₄, and Ar₅ and Ar₆ can respectively be joined to form a ring; and

[0062] r is an integer of 1 to 10.

[0063] That is, in the above general formula [II], R₁₃(s) and R₁₄(s) which are bonded to different fluorene rings may be the same or different, and R₁₃ and R₁₄ which are bonded to the same fluorene ring may be the same or different. Further, R₁₅(s) and R₁₆(s) which are bonded to different fluorene rings may be the same or different, and R₁₅(s) and R₁₆(s) which are bonded to the same fluorene ring may be the same or different. Moreover, e and f may be the same or different, and when e and f are each an integer of 2 or more, R₁₅s and R₁₆s may be the same or different. In addition, Ar₃, Ar₄, Ar₅, and Ar₆ may be the same or different.

[0064]
In the general formula [III],

[0065] each R₁₇ and R₁₈, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group;

[0066] each R₁₉ and R₂₀, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0067] g and h are each independently an integer of 1 to 3;

[0068] Ar₇ and Ar₈ are each independently a substituted or unsubstituted divalent aromatic group or heterocyclic group;

[0069] Ar₉, Ar₁₀, Ar₁₁, and Ar₁₂, are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₉ and Ar₁₀, and Ar₁₁ and Ar₁₂ can respectively be joined to form a ring; and

[0070] s is an integer of 1 to 10.

[0071] That is, in the above general formula [III], R₁₇(s) and R₁₈(s) which are bonded to different fluorene rings may be the same or different, and R₁₇ and R₁₈ which are bonded to the same fluorene ring may be the same or different. Further, R₁₉(s) and R₂₀(s) which are bonded to different fluorene rings may be the same or different, and R₁₉(s) and R₂₀(s) which are bonded to the same fluorene ring may be the same or different. Moreover, g and h may be the same or different, and when g and h are each an integer of 2 or more, R₁₉s and R₂₀s may be the same or different. In addition, Ar₇ and Ar₈ may be the same or different, and Ar₉, Ar₁₀, Ar₁₁, and Ar₁₂ may be the same or different.

[0072]
In the general formula [IV],

[0073] each R₂₁ and R₂₂, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group;

[0074] each R₂₃ and R₂₄, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0075] i and j are each independently an integer of 1 to 4;

[0076] Ar₁₃ and Ar₁₄ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₁₃ and Ar₁₄ can be joined to form a ring;

[0077] Ar₁₅ is a substituted or unsubstituted divalent aromatic group or heterocyclic group; and

[0078] t is an integer of 1 to 10.

[0079] That is, in the above general formula [IV], R₂₁(s) and R₂₂(s) which are bonded to different fluorene rings may be the same or different, and R₂₁ and R₂₂ which are bonded to the same fluorene ring may be the same or different. Further, R₂₃(s) and R₂₄(s) which are bonded to different fluorene rings may be the same or different, and R₂₃(s) and R₂₄(s) which are bonded to the same fluorene ring may be the same or different. Moreover, i and j may be the same or different, and when i and j are each an integer of 2 or more, R₂₃s and R₂₄s may be the same or different. In addition, Ar₁₃ and Ar₁₄ may be the same or different.

[0080]
In the general formula [V], each R₂₅, R₂₆, R₂₇, and R₂₈, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group;

[0081] each R₂₉, R₃₀, R₃₁, and R₃₂, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0082] k, l, m, and n are each independently an integer of 1 to 3;

[0083] Ar₁₆, Ar₁₇ and Ar₁₈ are each independently a substituted or unsubstituted divalent aromatic group or heterocyclic group, or Ar₁₆ and Ar₁₈ are each independently a bond;

[0084] Ar₁₉, Ar₂₀, Ar₂₁, and Ar₂₂ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₁₉ and Ar₂₀, and Ar₂₁ and Ar₂₂ can respectively be joined to form a ring; and

[0085] u and v are each independently an integer of 1 to 10.

[0086] That is, in the above general formula [V], R₂₅(s), R₂₆(s), R₂₇(s), and R₂₈(s) which are bonded to different fluorene rings may be the same or different, and R₂₅ and R₂₆, and R₂₇ and R₂₈ which are bonded to the same fluorene ring may respectively be the same or different. Further, R₂₉(s), R₃₀(s), R₃₁(s), and R₃₂(s) which are bonded to different fluorene rings may be the same or different, and R₂₉(s) and R₃₀(s), and R₃₁(s) and R₃₂(s) which are bonded to the same fluorene ring may respectively be the same or different. Moreover, k, l, m, and n may be the same or different, and when k, l, m, and n are each an integer of 2 or more, R₂₉s, R₃₀s, R₃₁s, and R₃₂s may be the same or different. In addition, Ar₁₉, Ar₂₀, Ar₂₁, and Ar₂₂ may be the same or different. Furthermore, u and v may be the same or different.

[0087]
In the general formula [VI],

[0088] each R₃₄, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0089] o is an integer of 1 to 4;

[0090] Ar₂₃ and Ar₂₄ are each independently a substituted or unsubstituted divalent aromatic group or heterocyclic group;

[0091] Ar₂₅, Ar₂₆, Ar₂₇, and Ar₂₈ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₂₅ and Ar₂₆, and Ar₂₇ and Ar₂₈ can respectively be joined to form a ring; and

[0092] w is an integer of 1 to 10.

[0093] That is, in the above general formula [VI], R₃₄s which are bonded to different benzene rings may be the same or different. Further, when o is an integer of 2 or more, R₃₄s may be the same or different. In addition, Ar₂₃ and Ar₂₄ may be the same or different, and Ar₂₅, Ar₂₆, Ar₂₇, and Ar₂₈ may be the same or different.

[0094]
In the general formula [VII],

[0095] each R₃₆, independently, is a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted alkoxyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, cyano group, or a halogen atom;

[0096] p is an integer of 1 to 4;

[0097] Ar₂₉ is a substituted or unsubstituted divalent aromatic group or heterocyclic group;

[0098] Ar₃₀ and Ar₃₁ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group, or Ar₃₀ and Ar₃₁ can be joined to form a ring; and

[0099] x is an integer of 1 to 10.

[0100] That is, in the above general formula [VII], R₃₆s which are bonded to different benzene may be the same or different. Further, when p is an integer of 2 or more, R₃₆ may be the same or different. In addition, Ar₃₀ and Ar₃₁ may be the same or different.
Ar₃₂[Image not available][Image not available]_yAr₃₃  [VIII]
In the general formula [VIII],

[0101] A₃₂ and Ar₃₃ are each independently a substituted or unsubstituted aromatic group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted fused polycyclic aromatic group, or a substituted or unsubstituted fused heteropolycyclic group; and y is an integer of 1 to 5.

[0102] That is, in the above general formula [VIII], Ar₃₂ and Ar₃₃ may be the same or different.

[0103] Here, specific examples of the substituents in the general formulae [II] to [XIII] will be given below. Further examples of the substituents are the same as those described above for the general formula [I].

[0104] Examples of the alkoxyl group include methoxy group, ethoxy group, tert-butoxy group, n-butyl group, isopropoxy group and the like.

[0105] Examples of the fused polycyclic aromatic group include fluorenyl group, naphthyl group, fluoranthenyl group, anthryl group, phenanthryl group, pyrenyl group, tetracenyl group, pentacenyl group, triphenylenyl group, perylenyl group and the like.

[0106] Examples of the fused heteropolycyclic group include carbazolyl group, acridinyl group, phenanthrolyl group and the like.

[0107] Typical examples of the arylamine compounds represented by the general formulae [II] to [VII] and the acetylene compound represented by the general formula [VIII] will be given below, but the present invention is not limited thereto.

[0108]
<Examples of Arylamine Compounds of General Formula [II]>

[0109]

[0110]
<Examples of Arylamine Compounds of General Formula [III]>

[0111]

[0112]
<Examples of Arylamine Compounds of General Formula [IV]>

[0113]

[0114]
<Examples of Arylamine Compounds of General Formula [V]>

[0115]

[0116]
<Examples of Arylamine Compounds of General Formula [VI]>

[0117]

[0118]
<Examples of Arylamine Compounds of General Formula [VII]>

[0119]

[0120]
<Examples of Acetylene Compounds of General Formula [VIII]>

[0121]

[0122] The content ratio of the fluorene compound represented by the general formula [I], and the arylamine compound represented by the general formulae [II] to [VII] or the acetylene compound represented by the general formula [VIII] is such that the arylamine compound or the acetylene compound is used in an amount of preferably 0.01 to 80 parts by weight, more preferably 1 to 40 parts by weight per 100 parts by weight of the fluorene compound.

[0123] FIGS. 1 to 7 show preferable examples of the organic light-emitting device of the present invention. In FIGS. 1 to 7, reference numeral 1 denotes a substrate, reference numeral 2 denotes an anode, reference numeral 3 denotes a light-emitting layer, reference numeral 4 denotes a cathode, reference numeral 5 denotes a hole-transporting layer, reference numeral 6 denotes an electron-transporting layer, reference numeral 7 denotes a hole-injecting layer, and reference numeral 8 denotes a hole/exciton blocking layer.

[0124] FIG. 1 is a cross-sectional view showing an example of the organic light-emitting device of the present invention. In FIG. 1, the device is composed of an anode 2, a light-emitting layer 3, and a cathode 4, which are provided on a substrate 1 in the mentioned order. The light-emitting device with this structure is advantageous when a compound having by itself a hole-transporting property, an electron-transporting property and a light-emitting property is used or when plural kinds of compounds possessing the respective properties are used as a mixture.

[0125] FIG. 2 is a cross-sectional view showing another example of the organic light-emitting device of the present invention. In FIG. 2, the device is composed of an anode 2, a hole-transporting layer 5, an electron-transporting layer 6, and a cathode 4, which are provided on a substrate 1 in the mentioned order. In this case, a light-emitting material having either or both of a hole-transporting property and an electron-transporting property is advantageously used for the corresponding one of the layers, in combination with a hole-transporting material or an electron-transporting material having no light-emitting property for the other layer. Incidentally, in this case, the light-emitting layer is composed of either of the hole-transporting layer 5 or the electron-transporting layer 6.

[0126] FIG. 3 is a cross-sectional view showing still another example of the organic light-emitting device of the present invention. In FIG. 3, the device is composed of an anode 2, a hole-transporting layer 5, a light-emitting layer 3, an electron-transporting layer 6, and a cathode 4, which are provided on a substrate 1 in the mentioned order. With this arrangement, the carrier-transporting function and the light-emitting function are separated from each other, and compounds having a hole-transporting property, an electron-transporting property, and a light-emitting property respectively are used appropriately in combination therewith. Thus, the degree of freedom in selection of materials greatly increases, and various kinds of compounds having different emission wavelengths can be used, thus allowing a variety of emission hues to be achieved. Furthermore, it also becomes possible to improve the emission efficiency by effectively confining carriers or excitons within the middle light-emitting layer 3.

[0127] FIG. 4 is a cross-sectional view showing still another example of the organic light-emitting device of the present invention. In FIG. 4, as compared with the example shown in FIG. 3, the device is constructed such that a hole-injecting layer 7 is provided on the anode 2 side, which is effective for improving adhesion between the anode 2 and the hole-transporting layer 5 or improving the hole-injecting property. Thus, this arrangement is effective for lowering the driving voltage.

[0128] FIGS. 5 and 6 are cross-sectional views showing other examples of the organic light-emitting device of the present invention, respectively. In FIGS. 5 and 6, as compared with the examples shown in FIGS. 3 and 4, the device is constructed such that a layer (a hole-blocking layer 8) serving to prevent holes or excitons from passing to the cathode 4 side is provided between the light-emitting layer 3 and the electron-transporting layer 6. The use of a compound having an extremely high ionization potential for the hole-blocking layer 8 is effective for improving the emission efficiency.

[0129] FIG. 7 is a cross-sectional view showing still another example of the organic light-emitting device of the present invention. In FIG. 7, the device is composed of an anode 2, a hole-transporting layer 5, a light-emitting layer 3, and a cathode 4, which are provided on a substrate 1 in the mentioned order. The light-emitting device with this structure is advantageous when a light-emitting material having by itself either or both of a hole-transporting property and an electron-transporting property is used for the corresponding layers, in combination with a mere hole-transporting material having no light-emitting property.

[0130] Note that, in FIGS. 1 to 7, there are shown common basic device structures. The structure of the organic light-emitting device using the compound of the present invention is not limited thereto. For example, it is possible to adopt various layer structures such as one in which an insulating layer is provided at an interface between an electrode and an organic layer, one in which an adhesive layer or an interference layer is additionally provided, and one in which a hole-transporting layer is composed of two layers with different ionization potentials.

[0131] The fluorene compound represented by the general formula [I] used in the present invention is a compound superior to the conventional compounds in electron-transporting property and durability, and can be used in any one of the embodiments shown in FIGS. 1 to 7.

[0132] In the present invention, the fluorene compound represented by the general formula [I] is used as a component for an electron-transporting layer or a light-emitting layer. However, hitherto known hole-transporting compounds, light-emitting compounds, electron-transporting compounds, or the like may be used in combination therewith as needed.

[0133] Examples of those compounds will be given below.

<Hole-Transporting Compounds>

[0134]
<Electron-transporting/Light-Emitting Compounds>

[0135]
<Light-Emitting Compounds>

[0136]
<Light-Emitting Layer Matrix Compounds and Electron-Transporting Compounds>

[0137]
<Polymeric Hole-Transporting Compounds>

[0138]
<Polymeric Light-Emitting Compounds and Charge-Transporting Compounds>

[0139]

[0140] In the organic light-emitting device of the present invention, the layer(s) containing the fluorene compound represented by the general formula [I] and the layer(s) containing other organic compound(s) are generally formed as thin films by a vacuum evaporation method or by an application method after dissolving in an appropriate solvent. In particular, in the case of forming a film with the application method, the film may be formed by additionally using an appropriate binder resin.

[0141] The binder resin can be selected from a wide variety of binder resins including, for example, polyvinyl carbazole resin, polycarbonate resin, polyester resin, polyarylate resin, polystyrene resin, acrylic resin, methacrylic resin, butyral resin, polyvinyl acetal resin, diallyl phthalate resin, phenolic resin, epoxy resin, silicone resin, polysulfone resin, and urea resin, although it is not limited thereto. In addition, one of the above resins may be used singularly, or two or more such resins may be combined with each other as a copolymer.

[0142] Preferably, the anode material has a work function that is as large as possible. For example, an elemental metal such as gold, platinum, nickel, palladium, cobalt, selenium, or vanadium, or an alloy thereof, or a metal oxide such as tin oxide, zinc oxide, indium tin oxide (ITO), or indium zinc oxide can be used. In addition, a conductive polymer such as polyaniline, polypyrrole, polythiophene, or polyphenylene sulfide can be also used. Any one of those electrode materials may be used singularly or plural electrode materials may be used in combination.

[0143] On the other hand, preferably, the cathode material may have a small work function. For example, an elemental metal such as lithium, sodium, potassium, cesium, calcium, magnesium, aluminum, indium, silver, lead, tin, or chromium, or an alloy of plural metals can be used therefor. It is also possible to use a metal oxide such as indium tin oxide (ITO). In addition, the cathode may take either a single-layer structure or a multi-layer structure.

[0144] The substrate used in the present invention may be, although not particularly limited, a non-transparent substrate such as a metallic substrate or a ceramic substrate, or a transparent substrate formed of glass, quartz, plastic sheet, or the like. In addition, it is also possible to control the emission color by using a color filter film, a fluorescent color-changing filter film, a dielectric reflection film or the like for the substrate.

[0145] Furthermore, a protective layer or an encapsulating layer may also be provided on the prepared device for preventing the device from coming into contact with oxygen, moisture, or the like. The protective layer may be a diamond thin film, a film made of an inorganic material such as a metal oxide or a metal nitride, or a polymer film made of fluororesin, poly-para-xylylene, polyethylene, silicone resin, polystyrene resin or the like. In addition, a photocurable resin or the like can be used therefor. Furthermore, it is also possible to cover the device with glass, a gas-impermeable film, a metal or the like or package the device itself with an appropriate encapsulating resin

[0146] The present invention will now be described in more detail based on examples. However, the present invention is not limited to those examples.

[Synthesis of Exemplified Compound No. 1]

[0147]

[0148] To a 500-ml three-neck flask, 2.0 g (5.68 mmol) of 2,7-dibromo-9,9-dimethylfluorene [1], 4.2 g (17.0 mmol) of pyrene-1-boronic acid [2], 120 ml of toluene, and 60 ml of ethanol were added. Then, an aqueous solution of 24 g of sodium carbonate in 120 ml of water was added dropwise therein with stirring in a nitrogen atmosphere at room temperature, followed by the addition of 0.33 g (0.28 mmol) of tetrakis (triphenylphosphine) palladium (0). After stirring the mixture for 30 minutes at room temperature, the temperature was raised to 77° C., followed by stirring for 5 hours. After the reaction, an organic layer was extracted with chloroform and then dried with anhydrous sodium sulfate, followed by purification with a silica gel column (hexane and toluene mixture developing solvent). Consequently, 3.0 g (89% yield) of a compound [3] (white crystal) was obtained.

[0149]

[0150] To a 500-ml three-neck flask, 3.51 g (5.89 mmol) of compound [3], 1.64 g (17.67 mmol) of tert-butyl chloride and 200 ml of dichloromethane were added. The resultant mixture was stirred at 0° C., and then 1.71 g (13.0 mmol) of aluminum chloride was slowly added thereto. After stirring the mixture for 30 minutes at 0° C., the temperature was raised to room temperature, followed by stirring for 5 hours. After the reaction, an organic layer was taken into 200 ml of water, extracted with chloroform and then dried with anhydrous sodium sulfate, followed by purification with a silica gel column (hexane and toluene mixture developing solvent). Consequently, 3.53 g (84% yield) of exemplified compound No. 1 (white crystal) was obtained.

[Synthesis of Exemplified Compound No. 14]

[0151]

[0152] To a 500-ml three-neck flask, 1.50 g (2.52 mmol) of compound [3], 1.61 g (7.55 mmol) of 1-bromoadamantane and 100 ml of dichloromethane were added. The resultant mixture was stirred at 0° C., and then 0.70 g (5.30 mmol) of aluminum chloride was slowly added thereto. After stirring the mixture for 30 minutes at 0° C., the temperature was raised to room temperature, followed by stirring for 5 hours. After the reaction, an organic layer was taken into 200 ml of water, extracted with chloroform and then dried with anhydrous sodium sulfate, followed by purification with a silica gel column (hexane and toluene mixture developing solvent). Consequently, 1.42 g (65% yield) of exemplified compound No. 14 (white crystal) was obtained.

[0153] A device having the structure shown in FIG. 2 was prepared.

[0154] On a glass substrate as the substrate 1, indium tin oxide (ITO) was deposited to form a film with a thickness of 120 nm by sputtering method to obtain the anode 2, so that the substrate thus formed was used as a transparent conductive support substrate. The substrate was subjected to ultrasonic cleaning sequentially with acetone and with isopropyl alcohol (IPA). Following this, the substrate was washed with IPA through boiling and then dried. Furthermore, the substrate after UV/ozone cleaning was used as the transparent conductive support substrate.

[0155] On the transparent conductive support substrate, a chloroform solution of the compound represented by the following structural formula was applied to form a film of 30 nm in thickness by a spin-coating method, thereby forming the hole-transporting layer 5.

[0156]

[0157] Furthermore, a fluorene compound represented as exemplified compound No. 1 was deposited to form a film of 50 nm in thickness by vacuum evaporation method, thereby forming the electron-transporting layer 6. The film formation was performed under the conditions such that the degree of vacuum at the time of evaporation was 1.0×10⁻⁴ Pa and the film formation rate was 0.2 to 0.3 nm/sec.

[0158] Next, a metal layer film of 50 nm in thickness was formed on the above organic layer as the cathode 4 using an evaporation material made of aluminum and lithium (lithium concentration: 1 atomic %) by vacuum evaporation method, and further an aluminum layer of 150 nm in thickness was formed by vacuum evaporation method. The film formation was performed under the conditions such that the degree of vacuum at the time of evaporation was 1.0×10⁻⁴ Pa and the film formation rate was 1.0 to 1.2 nm/sec.

[0159] Furthermore, the resultant structure was covered with a protective glass plate in a nitrogen atmosphere and was then encapsulated with an acrylic resin adhesive.

[0160] When a DC voltage of 4 V was applied to the device thus obtained with the ITO electrode (anode 2) being connected to a positive electrode and the Al—Li electrode (cathode 4) being connected to a negative electrode, an electric current flowed through the device at a current density of 38.5 mA/cm² and light emission of a blue color at a luminance of 900 cd/m² was observed.

[0161] Furthermore, when the current density was kept at 50.0 mA/cm² and the voltage was applied for 100 hours, the deterioration of luminance was small; an initial luminance of 1000 cd/m² was reduced to a luminance of 950 cd/m² after 100 hours.

[0162] Devices were prepared and evaluated following the same procedure as in Example 1 with the exception that the compounds shown in Table 2 were used in place of exemplified compound No. 1. The results are shown in Table 1.

[0163] Devices were prepared and evaluated following the same procedure as in Example 1 with the exception that compounds represented by the following structural formulae were used in place of exemplified compound No. 1. The results are shown in Table 1.

[0164]

TABLE 1
<Comparative Compound No. 1>
<Comparative Compound No. 2>
		Durability
	Initial Stage			Luminance
		Applied		Current	Initial	After 100
Example	Exemplified	Voltage	Luminance	Density	Luminance	Hours
No.	Compound No.	(V)	(cd/m2)	(mA/cm2)	(cd/m2)	(cd/m2)
Example 1	1	4	900	50.0	1000	950
Example 2	2	4	890	50.0	980	940
Example 3	7	4	870	50.0	950	890
Example 4	12	4	850	50.0	910	860
Com-	Comparative	4	400	50.0	450	200
parative	Compound 1
Example 1
Com-	Comparative	4	380	50.0	400	150
parative	Compound 2
Example 2

[0165] A device having the structure shown in FIG. 3 was prepared.

[0166] Similarly to Example 1, a hole-transporting layer 5 was formed on a transparent conductive support substrate.

[0167] Further, a fluorene compound represented by exemplified compound No. 1 was deposited to form a film of 20 nm in thickness by vacuum evaporation method, thereby forming a light-emitting layer 3. The film formation was performed under the conditions such that the degree of vacuum at the time of evaporation was 1.0×10⁻⁴ Pa and the film formation rate was 0.2 to 0.3 nm/sec.

[0168] Furthermore, bathophenanthroline (Bpen) was deposited into a film of 40 nm in thickness by vacuum evaporation method, thereby forming an electron-transporting layer 6. The film formation was performed under the conditions such that the degree of vacuum at the time of evaporation was 1.0×10⁻⁴ Pa and the film formation rate was 0.2 to 0.3 nm/sec.

[0169] Next, in the same manner as in Example 1, a cathode 4 was formed and the resultant structure was then encapsulated.

[0170] When a DC voltage of 4 V was applied to the device thus obtained with the ITO electrode (anode 2) being connected to a positive electrode and the Al—Li electrode (cathode 4) being connected to a negative electrode, an electric current flowed through the device at a current density of 70.0 mA/cm² and light emission of a blue color at a luminance of 11000 cd/m² was observed.

[0171] Furthermore, when a voltage was applied for 100 hours with the current density being kept at 100.0 mA/cm², the deterioration of luminance was small such that an initial luminance of 13000 cd/m² was reduced to a luminance of 11000 cd/m² after 100 hours.

[0172] Devices were prepared and evaluated in the same way as that of Example 5, except that the compounds shown in Table 2 were used in place of the exemplified compound No. 1. The results are shown in Table 2.

[0173] Devices were prepared and evaluated following the same procedure as in Example 5 with the exception that comparative compounds 1 and 2 were used in place of exemplified compound No. 1. The results are shown in Table 2.

[0174]

	TABLE 2
	Durability
	Initial Stage		Luminance
		Applied		Current	Initial	After 100
Example	Exemplified	voltage	Luminance	Density	Luminance	Hours
No.	Compound No.	(V)	(cd/m2)	(mA/cm2)	(cd/m2)	(cd/m2)
Example 5	1	4	11000	100.0	13000	11000
Example 6	3	4	10000	100.0	11000	10000
Example 7	7	4	9500	100.0	8700	7500
Example 8	12	4	11000	100.0	13000	11000
Comparative	Comparative	4	1800	100.0	2000	900
Example 3	Compound 1
Comparative	Comparative	4	4500	100.0	5000	2100
Example 4	Compound 2

[0175] A device having the structure shown in FIG. 3 was prepared.

[0176] On a transparent conductive support substrate similar to that in Example 1, a chloroform solution of a compound represented by the following structural formula was applied to form a film of 20 nm in thickness by spin-coating method, thereby forming a hole-transporting layer 5.

[0177]

[0178] Furthermore, the fluorene compound represented as exemplified compound No. 1 and the arylamine compound represented as exemplified compound No. AA-6 (weight ratio of 100:1) were deposited into a film with a thickness of 20 nm by vacuum evaporation method to form a light-emitting layer 3. The film formation was performed under the conditions such that the degree of vacuum at the time of evaporation was 1.0×10⁻⁴ Pa and the film formation rate was 0.2 to 0.3 nm/sec.

[0179] Next, in the same manner as in Example 5, an electron-transporting layer 6 and a cathode 4 were formed and the resultant structure was then encapsulated.

[0180] When a DC voltage of 4 V was applied to the device thus obtained with the ITO electrode (anode 2) being connected to a positive electrode and the Al—Li electrode (cathode 4) being connected to a negative electrode, an electric current was flowed through the device at a current density of 75.0 mA/cm² and light emission of a pure blue color at a luminance of 13000 cd/m² was observed.

[0181] Furthermore, when a voltage was applied for 100 hours while keeping the current density at 80.0 mA/cm², the deterioration of luminance was small such that an initial luminance of 15000 cd/m² was reduced to a luminance of 12000 cd/m² after 100 hours.

[0182] Devices were prepared and evaluated following the same procedure as in Example 9 with the exception that exemplified fluorene compound No. 1 and/or exemplified arylamine compound No. AA-6 were replaced with ones shown in Table 3. The results are shown in Table 3.

[0183] Devices were prepared and evaluated following the same procedure as in Example 9 with the exception that comparative compounds 1 and 2 were used in place of exemplified compound No. 1. The results are shown in Table 3.

[0184]

	TABLE 3
	Initial Stage	Durability
		Exemplified	Applied		Current	Initial	Luminance after
	Exemplified	Arylamine	Voltage	Luminance	Density	Luminance	100 hours
Example No.	Compound No.	Compound No.	(V)	(cd/m2)	(mA/cm2)	(cd/m2)	(cd/m2)
Example 9	1	AA-6	4	13000	80.0	15000	12000
Example 10	1	AA-11	4	13500	80.0	15200	12600
Example 11	1	AA-15	4	11500	80.0	13000	10100
Example 12	1	AA-25	4	10200	80.0	11900	10000
Example 13	1	AA-39	4	12800	80.0	13800	11200
Example 14	1	AA-50	4	11000	80.0	12200	10800
Example 15	1	AC-1	4	16200	80.0	19000	16000
Example 16	7	AA-15	4	13300	80.0	15100	13500
Example 17	7	AA-53	4	12200	80.0	14100	12200
Example 18	12	AC-1	4	16500	80.0	17800	16100
Example 19	33	AA-10	4	13500	80.0	14300	12500
Comparative	Comparative	AA-6	4	4000	80.0	4500	1800
Example 5	Compound 1
Comparative	Comparative	AA-6	4	3000	80.0	3500	1000
Example 6	Compound 2

[0185] A device having the structure shown in FIG. 7 was prepared.

[0186] On a transparent conductive support substrate which was similar to that of Example 1, a solution prepared by dissolving 1.00 g of poly-N-vinylcarbazole (weight average molecular weight=63,000) in 80 ml of chloroform was applied to form a film of 110 nm in thickness by spin-coating method (rotation speed=2000 rpm), thereby forming an organic layer (hole-transporting layer 5).

[0187] Next, a solution prepared by dissolving 0.050 g of the fluorene compound represented as exemplified compound No. 1 in 50 ml of toluene was applied to form a film of 120 nm in thickness by spin-coating method (rotation speed=2000 rpm) to thereby form an organic layer (light-emitting layer 3).

[0188] Next, in the same manner as in Example 1, a cathode 4 was formed and the resultant structure was then encapsulated.

[0189] When a DC current voltage of 4 V was applied to the device thus obtained with the ITO electrode (anode 2) being connected to a positive electrode and the Al—Li electrode (cathode 4) being connected to a negative electrode, an electric current flowed through the device at a current density of 35.5 mA/cm² and light emission of a blue color at a luminance of 2200 cd/m² was observed.

[0190] Furthermore, when a voltage was applied for 100 hours with the current density being kept at 50.0 mA/cm², the deterioration of luminance was small such that an initial luminance of 4100 cd/m² was reduced to a luminance of 3100 cd/m² after 100 hours.

[0191] Devices were prepared and evaluated following the same procedure as in Example 21 with the exception that the compounds shown in Table 4 were used in place of exemplified compound No. 1. The results are shown in Table 4.

[0192] Devices were prepared and evaluated following the same procedure as in Example 21 with the exception that comparative compounds 1 and 2 were used in place of exemplified compound No. 1. The results are shown in Table 4.

[0193]

	TABLE 4
	Initial Stage	Durability
		Applied		Current	Initial	Luminance after
	Exemplified	voltage	Luminance	Density	Luminance	100 hours
Example No.	Compound No.	(V)	(cd/m2)	(mA/cm2)	(cd/m2)	(cd/m2)
Example 20	1	4	2200	50.0	4100	3100
Example 21	12	4	2000	50.0	4000	3200
Example 22	16	4	2100	50.0	4200	3300
Example 23	32	4	2040	50.0	4090	3100
Comparative	Comparative	4	750	50.0	800	400
Example 7	Compound 1
Comparative	Comparative	4	620	50.0	710	310
Example 8	Compound 2