COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE

Abstract

Provided is an organic electronic element comprising a hole transport layer containing a compound of Formula (1) and an emitting auxiliary layer containing a compound of Formula (2), capable of improving the light emitting efficiency, stability, and life span of an electronic device using the same.

Claims

1. An organic electronic element comprising: a first electrode, a second electrode, and an organic layer formed between the first electrode and the second electrode, wherein the organic material layer includes an emitting auxiliary layer formed between the first electrode and the emitting layer, and a hole transport layer formed between the first electrode and the emitting auxiliary layer, wherein the hole transport layer contains a compound represented by the following Formula (1), and the emitting auxiliary layer contains a compound represented by the following Formula (2), ##STR00080## in Formulas (1) and (2), Ar.sup.1, Ar.sup.2, Ar.sup.4, Ar.sup.5 and Ar.sup.6 are each independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group; a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.1-C.sub.50 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group; a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (where, L′ may be selected from the group consisting of a single bond; a C.sub.6-C.sub.60 arylene group; a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic, and the R.sub.a and R.sub.b may be independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group, a fluorenyl group, a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group containing at least one heteroatom of O, N, S, Si, or P), and Ar.sup.3 is at least one of the Formula (1-a) or Formula (1-b) below, ##STR00081## wherein q, r and s are each an integer of 0 to 4, t is an integer of 0 to 3, and R.sup.1, R.sup.2, R.sup.3, R.sup.4 are the same or different, and are each independently selected from the group consisting of deuterium; halogen; a C.sub.6-C.sub.60 aryl group; a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.1-C.sub.50 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group; a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (wherein, L′, R.sub.a and R.sub.b are the same as indicated above), wherein in case q, r and s are each an integer of 2 or more, R.sup.1, R.sup.2 and R.sup.3 are each in plural and are the same or different, and a plurality of R.sup.1 or a plurality of R.sup.2 or a plurality of R.sup.3 or a plurality of R.sup.4 may combine to each other to form a ring, and L.sup.4 is selected from the group consisting of a C.sub.6-C.sub.60 arylene group, and a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P, and L.sup.5 is selected from the group consisting of a single bond; a C.sub.6-C.sub.60 arylene group; a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P, and Ar.sup.7 is independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group; a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.1-C.sub.50 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group; a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (wherein, L′, R.sub.a and R.sub.b are as defined above), and L.sup.1, L.sup.2, and L.sup.3 are selected from the group consisting of a single bond; a C.sub.6-C.sub.60 arylene group; a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P, wherein the aryl group, fluorenyl group, heterocyclic group, fused ring group, alkyl group, alkenyl group, alkynyl group, alkoxyl group, aryloxy group, arylene group and fluorenylene group may be substituted with one or more substituents selected from the group consisting of deuterium; halogen; a silane group; a siloxane group; boron group; a germanium group; a cyano group; a nitro group; -L′-N(R.sub.a)(R.sub.b); a C.sub.1-C.sub.20 alkylthio group; a C.sub.1-C.sub.20 alkoxyl group; a C.sub.1-C.sub.20 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.6-C.sub.60 aryl group; a C.sub.6-C.sub.60 aryl group substituted with deuterium; a fluorenyl group; a C.sub.2-C.sub.20 heterocyclic group; a C.sub.3-C.sub.20 cycloalkyl group; a C.sub.7-C.sub.20 arylalkyl group; and a C.sub.8-C.sub.20 arylalkenyl group, wherein the substituents may combine each other to form a saturated or unsaturated ring selected from the group consisting of a C.sub.3-C.sub.60 aliphatic ring, a C.sub.6-C.sub.60 aromatic ring, a C.sub.2-C.sub.60 heterocyclic ring, and a fused ring formed by the combination thereof.

2. The organic electronic element according to claim 1, wherein the compound represented by the Formula (1) is one of compounds of the following Formulas (3) to (4), ##STR00082## in Formula (3) and Formula (4), R.sup.1, R.sup.2, R.sup.3, R.sup.4, L.sup.4, L.sup.5, Ar.sup.1, Ar.sup.2, Ar.sup.7, q, r, s, and t are the same as defined in claim 1.

3. The organic electronic element according to claim 1, wherein the compound represented by the Formula (1) is one of compounds represented by the following of Formula (5) to Formula (7), ##STR00083## in Formula (5), Formula (6) and Formula (7), R.sup.3, R.sup.4, Ar, Ar.sup.2, Ar.sup.7, s, and t are the same as defined in claim 1.

4. The organic electronic element according to claim 1, wherein the compound represented by the Formula (2) of the emission-auxiliary layer is one of compounds of Formula (8) to Formula (12) below, ##STR00084## in Formula (8), Formula (9), Formula (10), Formula (11) and Formula (12), L.sup.1, L.sup.2, L.sup.3, Ar.sup.4, Ar.sup.5, and Ar.sup.6 are the same as defined in claim 1.

5. The organic electronic element according to claim 1, wherein L.sup.1, L.sup.2, L.sup.3, and L.sup.5 in the compounds represented by the Formula (1) and the Formula (2) are a single bond, or L.sup.1, L.sup.2, L.sup.3, L.sup.4 and L.sup.5 are represented by the following Formulas, ##STR00085##

6. The organic electronic element according to claim 2, wherein the compounds represented by the formula (1) of the hole transport layer or by the Formulas (3) to (7) are one of the following compounds, ##STR00086## ##STR00087## ##STR00088## ##STR00089## ##STR00090## ##STR00091## ##STR00092## ##STR00093## ##STR00094## ##STR00095## ##STR00096##

7. The organic electronic element according to claim 4, wherein the compounds represented by the formula (2) of the emitting-auxiliary layer or by the formulas (8) to (12) are one of the following compounds, ##STR00097## ##STR00098## ##STR00099## ##STR00100## ##STR00101## ##STR00102## ##STR00103## ##STR00104## ##STR00105## ##STR00106## ##STR00107## ##STR00108##

8. The organic electronic element according to claim 1, wherein all of Ar.sup.4 to Ar.sup.6 in the formula (2) are aryl groups of C.sub.6 to C.sub.60.

9. The organic electronic element according to claim 1, wherein at least one of Ar.sup.4 to Ar.sup.6 of the Formula (2) is an C.sub.6-C.sub.60 heteroaryl group.

10. The organic electronic element according to claim 2, wherein the hole transport layer comprises a compound represented by Formula (3) and the emitting auxiliary layer comprises a compound represented by Formula (2).

11. The organic electronic element according to claim 2, wherein the hole transport layer comprises a compound represented by Formula (4) and the emitting auxiliary layer comprises a compound represented by Formula (2).

12. The organic electronic element according to claim 1, wherein the emitting auxiliary layer comprises a mixture of two or more compounds represented by the formula (2).

13. A display device comprising the organic electronic element of claim 2; and a control part driving the display apparatus.

14. The display device according to claim 13, wherein the organic electronic element is at least one of an OLED, an organic solar cell, an organic photo conductor (OPC), Organic transistor (organic TFT) and an element for monochromic or white illumination.

Description

MODE FOR CARRYING OUT THE INVENTION

[0016] Hereinafter, some embodiments of the present invention will be described in detail. Further, in the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear.

[0017] In addition, terms, such as first, second, A, B, (a), (b) or the like may be used herein when describing components of the present invention. Each of these terminologies is not used to define an essence, order or sequence of a corresponding component but used merely to distinguish the corresponding component from other component(s). It should be noted that if a component is described as being “connected”, “coupled”, or “connected” to another component, the component may be directly connected or connected to the other component, but another component may be “connected”, “coupled” or “connected” between each component.

[0018] As used in the specification and the accompanying claims, unless otherwise stated, the following is the meaning of the term as follows.

[0019] Unless otherwise stated, the term “halo” or “halogen” as used herein includes F, Br, Cl, or I.

[0020] Unless otherwise stated, the term “alkyl” or “alkyl group” as used herein has a single bond of 1 to 60 carbon atoms, and means saturated aliphatic functional radicals including a linear alkyl group, a branched chain alkyl group, a cycloalkyl group (alicyclic), an cycloalkyl group substituted with a alkyl or an alkyl group substituted with a cycloalkyl.

[0021] Unless otherwise stated, the term “haloalkyl” or “halogen alkyl” as used herein means an alkyl group substituted with a halogen.

[0022] Unless otherwise stated, the term “heteroalkyl” as used herein means alkyl substituted one or more carbon atoms with heteroatom.

[0023] Unless otherwise stated, the term “alkenyl” or “alkynyl” as used herein has, but not limited to, double or triple bonds of 2 to 60 carbon atoms, and includes a linear alkyl group, or a branched chain alkyl group,

[0024] Unless otherwise stated, the term “cycloalkyl” as used herein means, but not limited to, alkyl forming a ring having 3 to 60 carbon atoms.

[0025] Unless otherwise stated, the term “alkoxyl group”, “alkoxy group” or “alkyloxy group” as used herein means an oxygen radical attached to an alkyl group, but not limited to, and has 1 to 60 carbon atoms.

[0026] Unless otherwise stated, the term “alkenoxyl group”, “alkenoxy group”, “alkenyloxyl group” or “alkenyloxy group” as used herein means an oxygen radical attached to an alkenyl group, but not limited to, and has 2 to 60 carbon atoms.

[0027] Unless otherwise stated, the term “aryloxyl group” or “aryloxy group” as used herein means an oxygen radical attached to an aryl group, but not limited to, and has 6 to 60 carbon atoms.

[0028] Unless otherwise stated, the term “aryl group” or “arylene group” as used herein has, but not limited to, 6 to 60 carbon atoms. Herein, the aryl group or the arylene group means a monocyclic or polycyclic aromatic group, and may include the aromatic ring formed in conjunction or reaction with an adjacent substituent. For examples, the aryl group may include a phenyl group, a biphenyl group, a fluorene group, or a spirofluorene group.

[0029] The prefix “aryl” or “ar” means a radical substituted with an aryl group. For example, an arylalkyl may be an alkyl substituted with an aryl, and an arylalkenyl may be an alkenyl

[0030] substituted with aryl, and a radical substituted with an aryl has a number of carbon atoms as defined herein.

[0031] Also, when prefixes are named subsequently, it means that substituents are listed in the order described first. For example, an arylalkoxy means an alkoxy substituted with an aryl, an alkoxylcarbonyl means a carbonyl substituted with an alkoxyl, and an arylcarbonylalkenyl also means an alkenyl substituted with an arylcarbonyl, wherein the arylcarbonyl may be a carbonyl substituted with an aryl.

[0032] Unless otherwise stated, the term “heteroalkyl” as used herein means alkyl containing one or more heteroatoms. Unless otherwise stated, the term “heteroaryl group” or “heteroarylene group” as used herein means, but not limited to, a C.sub.2 to C.sub.60 aryl or arylene group containing one or more heteroatoms, and includes at least one of monocyclic or polycyclic rings, and may also be formed in conjunction with an adjacent group.

[0033] Unless otherwise stated, the term “heterocyclic group” as used herein contains one or more heteroatoms, but not limited to, has 2 to 60 carbon atoms, includes both monocyclic and polycyclic rings, and may include heteroaliphadic ring and/or heteroaromatic ring. Also, the heterocyclic group may also be formed in conjunction with an adjacent group.

[0034] Unless otherwise stated, the term “heteroatom” as used herein represents at least one of N, O, S, P, or Si.

[0035] Also, the term “heterocyclic group” may include SO.sub.2 instead of carbon consisting of cycle. For example, “heterocyclic group” includes compound below.

##STR00002##

[0036] Unless otherwise stated, the term “aliphatic” as used herein means an aliphatic hydrocarbon having 1 to 60 carbon atoms, and the term “aliphatic ring” as used herein means an aliphatic hydrocarbon ring having 3 to 60 carbon atoms.

[0037] Unless otherwise stated, the term “ring” means an aliphatic ring having 3 to 60 carbon atoms, or an aromatic ring having 6 to 60 carbon atoms, or a hetero ring having 2 to 60 carbon atoms, or a fused ring formed by the combination of them, and includes a saturated or unsaturated ring.

[0038] Other hetero compounds or hetero radicals other than the above-mentioned hetero compounds contain, but are not limited to, one or more heteroatoms.

[0039] Unless otherwise stated, the term “carbonyl” as used herein is represented by —COR′, wherein R′ may be hydrogen, an alkyl having 1 to 20 carbon atoms, an aryl having 6 to 30 carbon atoms, a cycloalkyl having 3 to 30 carbon atoms, an alkenyl having 2 to 20 carbon atoms, an alkynyl having 2 to 20 carbon atoms, or the combination of these.

[0040] Unless otherwise stated, the term “ether” as used herein is represented by —R—O—R′, wherein R or R′ may be independently hydrogen, an alkyl having 1 to 20 carbon atoms, an aryl having 6 to 30 carbon atoms, a cycloalkyl having 3 to 30 carbon atoms, an alkenyl having 2 to 20 carbon atoms, an alkynl having 2 to 20 carbon atoms, or the combination of these.

[0041] Unless otherwise expressly stated, the term “substituted or unsubstituted” as used herein means that “substitution” is substituted with at least one substituent selected from the group consisting of, but not limited to, deuterium, halogen, an amino group, a nitrile group, a nitro group, a C.sub.1-C.sub.20 alkyl group, a C.sub.1-C.sub.20 alkoxyl group, a C.sub.1-C.sub.20 alkylamine group, a C.sub.1-C.sub.20 alkylthiophene group, a C.sub.6-C.sub.20 arylthiophene group, a C.sub.2-C.sub.20 alkenyl group, a C.sub.2-C.sub.20 alkynyl group, a C.sub.3-C.sub.20 cycloalkyl group, a C.sub.6-C.sub.60 aryl group, a C.sub.6-C.sub.20 aryl group substituted by deuterium, a C.sub.8-C.sub.20 arylalkenyl group, a silane group, a boron group, a germanium group, and a C.sub.2-C.sub.20 heterocyclic group.

[0042] Unless otherwise expressly stated, the formula used in the present invention is applied in the same manner as the substituent definition according to the definition of the exponent of the following Formula.

##STR00003##

[0043] Wherein, when a is an integer of zero, the substituent R.sup.1 is absent, when a is an integer of 1, the sole R.sup.1 is linked to any one of the carbon atoms constituting the benzene ring, when a is an integer of 2 or 3, each substituent R.sup.1s are linked to the benzene ring as follows and may be the same and different. When a is an integer of 4 to 6, the substituent R.sup.1s are linked to carbon atoms of the benzene ring in a similar manner, and the indication of hydrogen bound to the carbon forming the benzene ring is omitted.

##STR00004##

[0044] Further, the organic electronic element according to the present invention may be any one of an organic light emitting diode (OLED), an organic solar cell, an organic photo conductor (OPC), an organic transistor (organic TFT), and an element for monochromatic or white illumination.

[0045] Another embodiment of the present invention may include an electronic device including the display device which includes the described organic electronic element of the present invention, and a control unit for controlling the display device. Here, the electronic device may be a wired/wireless communication terminal which is currently used or will be used in the future, and covers all kinds of electronic devices including a mobile communication terminal such as a cellular phone, a personal digital assistant (PDA), an electronic dictionary, a point-to-multipoint (PMP), a remote controller, a navigation unit, a game player, various kinds of TVs, and various kinds of computers.

[0046] Hereinafter, an organic electronic element according to an aspect of the present invention will be described.

[0047] According to an embodiment of the present invention, there is provided an organic electronic element comprising a first electrode, a second electrode, and an organic layer formed between the first electrode and the second electrode, wherein the organic material layer includes an emitting auxiliary layer formed between the first electrode and the emitting layer, and a hole transport layer formed between the first electrode and the emitting auxiliary layer, wherein the hole transport layer contains a compound represented by the following Formula (1), and the emitting auxiliary layer contains a compound represented by the following Formula (2).

##STR00005##

[0048] In the Formulas (1) and (2), wherein Ar.sup.1, Ar.sup.2, Ar.sup.4, Ar.sup.5 and Ar.sup.6 are each independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group; a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring, a C.sub.1-C.sub.50 alkyl group, a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group, a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (where, L′ may be selected from the group consisting of a single bond; a C.sub.6-C.sub.60 arylene group; a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic, and the R.sub.a and R.sub.b may be independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group, a fluorenyl group, a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group containing at least one heteroatom of O, N, S, Si, or P)

[0049] Ar.sup.3 is at least one of the Formula (1-a) or Formula (1-b) below.

##STR00006##

[0050] q, r and s are integer of 0 to 4, t is an integer of 0 to 3, and R.sup.1, R.sup.2, R.sup.3, R.sup.4 may be the same or different, and are each independently selected from the group consisting of deuterium; halogen; a C.sub.6-C.sub.60 aryl group; a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.1-C.sub.50 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group; a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (wherein, L′, R.sub.a and R.sub.b are the same as indicated above), or in case q, r and s are 2 or more, R.sup.1, R.sup.2 and R.sup.3 are each in plural and are the same or different, and a plurality of R.sup.1 or a plurality of R.sup.2 or a plurality of R.sup.3 or a plurality of R.sup.4 may combine to each other to form a ring.

[0051] L.sup.4 may be selected from the group consisting of a C.sub.6-C.sub.60 arylene group, and a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P.

[0052] L.sup.5 may be selected from the group consisting of a single bond, a C.sub.6-C.sub.60 arylene group, and a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; and a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P.

[0053] Ar.sup.7 may be independently selected from the group consisting of a C.sub.6-C.sub.60 aryl group, and a fluorenyl group; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.1-C.sub.50 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.1-C.sub.30 alkoxyl group; a C.sub.6-C.sub.30 aryloxy group; and -L′-N(R.sub.a)(R.sub.b) (wherein, L′, R.sub.a and R.sub.b are as defined above).

[0054] L.sup.1, L.sup.2, L.sup.3 may be selected from the group consisting of a single bond, a C.sub.6-C.sub.60 arylene group; a fluorenylene group; a fused ring group of a C.sub.3-C.sub.60 aliphatic ring and a C.sub.6-C.sub.60 aromatic ring; a C.sub.2-C.sub.60 heterocyclic group including at least one heteroatom of O, N, S, Si or P.

[0055] Aryl group, fluorenyl group, heterocyclic group, fused ring group, alkyl group, alkenyl group, alkynyl group, alkoxyl group, aryloxy group, arylene group and fluorenylene group may be substituted with one or more substituents selected from deuterium; halogen; a silane group; a siloxane group; boron group; a germanium group; a cyano group; a nitro group; -L′-N(R.sub.a)(R.sub.b); a C.sub.1-C.sub.20 alkylthio group; a C.sub.1-C.sub.20 alkoxyl group; a C.sub.1-C.sub.20 alkyl group; a C.sub.2-C.sub.20 alkenyl group; a C.sub.2-C.sub.20 alkynyl group; a C.sub.6-C.sub.60 aryl group; a C.sub.6-C.sub.60 aryl group substituted with deuterium; a fluorenyl group; a C.sub.2-C.sub.20 heterocyclic group; a C.sub.3-C.sub.20 cycloalkyl group; the group consisting of a C.sub.7-C.sub.20 arylalkyl group and a C.sub.8-C.sub.20 arylalkenyl group, and also, these substituents may combine each other and form a ring, wherein the term ‘ring’ means a C.sub.3-C.sub.60 aliphatic ring or a C.sub.6-C.sub.60 aromatic ring or a C.sub.2-C.sub.60 heterocyclic ring or a fused ring formed by the combination of them, and includes a saturated or unsaturated ring.

[0056] In another example of the present invention, the compound represented by the Formula (1) may be one of compounds of the following Formulas (3) to (4).

##STR00007##

[0057] Hereinafter, R.sup.1, R.sup.2, R.sup.3, R.sup.4, L.sup.4, L.sup.5, Ar.sup.1, Ar.sup.2, Ar.sup.7, q, r, s, and t are the same as R.sup.1, R.sup.2, R.sup.3, R.sup.4, L.sup.4, L.sup.5, Ar.sup.1, Ar.sup.2, Ar.sup.7, q, r, s, and t defined in the Formula (1).

[0058] In another example of the present invention, the compound represented by the Formula (1) is one of compounds of the following Formulas (5) to (7).

##STR00008##

[0059] Hereinafter, R.sup.3, R.sup.4, Ar.sup.1, Ar.sup.2, Ar.sup.7, s, and t are the same as R.sup.3, R.sup.4, Ar.sup.1, Ar.sup.2, Ar.sup.7, s, and t defined in the Formula (1).

[0060] In another specific example of the present invention, the compound represented by the Formula (2) of the emission-auxiliary layer may be any one of compounds of Formula (8) to Formula (12) below.

##STR00009##

[0061] Hereinafter, L.sup.1, L.sup.2, L.sup.3, Ar.sup.4, Ar.sup.5, and Ar.sup.6 are the same as L.sup.1, L.sup.2, L.sup.3, Ar.sup.4, Ar.sup.5, and Ar.sup.6 defined by the Formula (1).

[0062] In another specific example of the present invention, L, L.sup.2, L.sup.3, and L.sup.5 in the compounds represented by the Formula (1) and the Formula (2) may be a single bond, or L.sup.1, L.sup.2, L.sup.3, L.sup.4 and L.sup.5 may be represented by the following Formulas.

##STR00010##

[0063] In another specific example of the present invention, the compounds represented by the formula (1) of the hole transport layer or by the Formulas (3) to (7) further specified the formula (1) may be one of the following compounds.

##STR00011## ##STR00012## ##STR00013## ##STR00014## ##STR00015## ##STR00016## ##STR00017## ##STR00018## ##STR00019## ##STR00020## ##STR00021##

[0064] In another specific example of the present invention, the compounds represented by the formula (2) of the emitting-auxiliary layer or by the formulas (8) to (12) further specified the formula (2) may be one of the following compounds.

##STR00022## ##STR00023## ##STR00024## ##STR00025## ##STR00026## ##STR00027## ##STR00028## ##STR00029## ##STR00030## ##STR00031## ##STR00032## ##STR00033##

[0065] In another specific example of the present invention, the emitting auxiliary layer includes one of the compounds in which Ar.sup.4 to Ar.sup.6 in the formula (2) are aryl groups of C.sub.6 to C.sub.60.

[0066] In another specific example of the present invention, the emitting auxiliary layer provides one of compounds in which at least one of Ar.sup.4 to Ar.sup.6 of the Formula (2) is C.sub.6-C.sub.60 heteroaryl group.

[0067] In another specific example of the present invention, the hole transport layer comprises a compound represented Formula (3) and the emitting auxiliary layer comprises a compound represented Formula (2).

[0068] In another specific example of the present invention, the hole transport layer comprises a compound represented Formula (4) and the emitting auxiliary layer comprises a compound represented Formula (2).

[0069] In another specific example of the present invention, the emitting auxiliary layer comprises a mixture of two or more compounds represented by the formula (2).

[0070] In another specific example of the present invention, an electronic element includes a display device comprising the organic electronic element; and a control part driving the display apparatus characterized in that an organic electronic element comprising a first electrode, a second electrode, and an organic layer formed between the first electrode and the second electrode, wherein the organic material layer includes an emitting auxiliary layer formed between the first electrode and the emitting layer, and a hole transport layer formed between the first electrode and the emitting auxiliary layer, wherein the hole transport layer contains a compound represented by the following Formula (1), and the emitting auxiliary layer contains a compound represented by the following Formula (2).

[0071] In another specific example of the present invention, the organic electronic element may be at least one of an OLED, an organic solar cell, an organic photo conductor (OPC), Organic transistor (organic TFT) and an element for monochromic or white illumination.

[0072] Hereinafter, the synthesis examples of the compounds represented by the formulas (1) and (2) comprised in the organic electronic element of the present invention and the preparation examples of an organic electronic element of the present invention will be described in detail by way of examples. However, the following examples are only for illustrative purposes and are not intended to limit the following examples of the invention.

Synthesis Example 1

[0073] The final product 1 represented by Formula (1) according to the present invention can be synthesized by reaction between Sub 1 or Sub 2 and Sub 3 as illustrated in the following Reaction Scheme 1.

##STR00034##

[0074] *L is L.sup.4 or L.sup.5 defined as the Formula (1-a), and the Formula (1-b).

1. Synthesis Example of Sub 1

[0075] ##STR00035##

1) Synthesis Example of Sub 1-1-1 (L=Biphenyl)

[0076] ##STR00036##

[0077] The starting material 9H-carbazole (50.16 g, 300 mmol) in 4-bromo-4′-iodo-1,1′-biphenyl (129.2 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 80.05 g (yield: 67%) was obtained.

2) Synthesis Examples of Sub 1-1-2 (L=9,9-Dimethyl-9H-Fluorene)

[0078] ##STR00037##

[0079] The starting material 9H-carbazole (50.16 g, 300 mmol) in 2-bromo-7-iodo-9,9-dimethyl-9H-fluorene (143.7 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 88.11 g (yield: 67%) was obtained.

3) Synthesis Examples of Sub 1-1-3 (L=9,9-Dimethyl-9H-Fluorene)

[0080] ##STR00038##

[0081] The starting material 7H-benzo[c]carbazole (65.18 g, 300 mmol) in 4-bromo-4′-iodo-1,1′-biphenyl (129.2 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 92.8 g (yield: 69%) was obtained.

4) Synthesis Examples of Sub 1-1-4 (L=9,9-Dimethyl-9H-Fluorene)

[0082] ##STR00039##

[0083] The starting material 7H-benzo[c]carbazole (65.18 g, 300 mmol) in 2-bromo-7-iodo-9,9-dimethyl-9H-fluorene (143.7 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 95.24 g (yield: 65%) was obtained.

5) Synthesis Examples of Sub 1-1-5 (L=Biphenyl)

[0084] ##STR00040##

[0085] The starting material 11H-benzo[a]carbazole (65.18 g, 300 mmol) in 4-bromo-4′-iodo-1,1′-biphenyl (129.2 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 80.05 g (yield: 62%) was obtained.

6) Synthesis Examples of Sub 1-1-6 (L=9,9-Dimethyl-9H-Fluorene)

[0086] ##STR00041##

[0087] The starting material 5H-benzo[b]carbazole (65.18 g, 300 mmol) in 2-bromo-7-iodo-9,9-dimethyl-9H-fluorene (143.7 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 93.78 g (yield: 64%) was obtained.

7) Synthesis Examples of Sub 1-1-7 (L=Biphenyl)

[0088] ##STR00042##

[0089] The starting material 9H-dibenzo[a,c]carbazole (80.2 g, 300 mmol) in 4-bromo-4′-iodo-1,1′-biphenyl (129.2 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 98.7 g (yield: 66%) was obtained.

8) Synthesis Examples of Sub 1-1-9 (L=9,9-Dimethyl-9H-Fluorene)

[0090] ##STR00043##

[0091] The starting material 7H-dibenzo[c,g]carbazole (80.2 g, 300 mmol) in 2-bromo-7-iodo-9,9-dimethyl-9H-fluorene (143.7 g, 360 mmol), Na.sub.2SO.sub.4 (42.6 g, 300 mmol), K.sub.2CO.sub.3 (41.4 g, 300 mmol), Cu (5.72 g, 90 mmol), nitrobenzene using the synthesis method Sub 1, the product 98.5 g (yield: 61%) was obtained.

2. Synthesis Examples of Sub 2

[0092] Sub 2 of the reaction scheme 1 can be synthesized by the reaction path of the reaction scheme 2 below.

##STR00044##

1) Synthesis Examples of M2-2-1

[0093] ##STR00045##

[0094] After 3-bromo-9-phenyl-9H-carbazole (45.1 g, 140 mmol) was dissolved in DMF 980 mL, followed by being adding Bispinacolborate (39.1 g, 154 mmol), PdCl.sub.2(dppf) catalyst (3.43 g, 4.2 mmol), KOAc (41.3 g, 420 mmol) in order, followed by stirring for 24 hours, to synthesize a borate compound, and then the resulting compound was separated over silicagel column and recrystallization to give the borate compound 35.2 g (68%).

2) Synthesis Examples of M2-2-2

[0095] ##STR00046##

[0096] The same procedure as described in the synthesis method of M2-2-1 above was carried out to obtain 40 g (64%).

3) Synthesis Examples of Sub 2-1-1

[0097] ##STR00047##

[0098] After M2-2-1 (29.5 g, 80 mmol) was dissolved in THF 360 mL, followed by being added 4-bromo-4′-iodo-1,1′-biphenyl (30.16 g, 84 mmol), Pd(PPh.sub.3).sub.4 (2.8 g, 2.4 mmol), NaOH (9.6 g, 240 mmol), 180 mL of water, followed by reflux and stirring. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired 26.56 g (70%).

4) Synthesis Examples of Sub 2-1-2

[0099] ##STR00048##

[0100] After M2-2-1 (29.5 g, 80 mmol) was dissolved in THF 360 mL, followed by being added 1-bromo-4-iodobenzene (23.8 g, 84 mmol), Pd(PPh.sub.3).sub.4 (2.8 g, 2.4 mmol), NaOH (9.6 g, 240 mmol), 180 mL of water, followed by reflux and stirring. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired 22.9 g (72%).

5) Synthesis Examples of Sub 2-1-3

[0101] ##STR00049##

[0102] After M2-2-1 (29.5 g, 80 mmol) was dissolved in THF 360 mL, followed by being added 4′-bromo-3-iodo-1,1′-biphenyl (30.16 g, 84 mmol), Pd(PPh.sub.3).sub.4 (2.8 g, 2.4 mmol), NaOH (9.6 g, 240 mmol), 180 mL of water, followed by reflux and stirring. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired 24.7 g (65%).

6) Synthesis Examples of Sub 2-1-4

[0103] ##STR00050##

[0104] After M2-2-2 (35.63 g, 80 mmol) obtained by the synthesis was dissolved in THF 360 mL, followed by being added 4-bromo-4′-iodo-1,1′-biphenyl (30.16 g, 84 mmol), Pd(PPh.sub.3).sub.4 (2.8 g, 2.4 mmol), NaOH (9.6 g, 240 mmol), 180 mL of water, followed by reflux and stirring. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired 29.51 g (67%).

3. Synthesis Examples of Sub 3

[0105] Sub 3 of the reaction scheme 1 can be synthesized by the reaction path of the reaction scheme 3 below.

##STR00051##

[0106] Synthesis Method of Sub 3

[0107] After [1,1′-biphenyl]-4-amine (1 equiv) and 4-bromo-1,1′-biphenyl (1.1 equiv) were dissolved in toluene, followed by being added respectively Pd.sub.2(dba).sub.3 (0.05 equiv), PPh.sub.3 (0.1 equiv), NaOt-Bu (3 equiv), followed by reflux and stirring at 100° C. for 24 hours. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired di([1,1′-biphenyl]-4-yl)amine.

[0108] The examples of Sub 3 include, but are not limited to, the following compounds.

##STR00052## ##STR00053## ##STR00054## ##STR00055## ##STR00056## ##STR00057## ##STR00058## ##STR00059## ##STR00060## ##STR00061## ##STR00062## ##STR00063##

TABLE-US-00001 TABLE 1 compound FD-MS compound FD-MS Sub 3-1 m/z = 169.09(C12H11N = 169.22) Sub 3-2 m/z = 219.10(C16H13N = 219.28) Sub 3-3 m/z = 219.10(C16H13N = 219.28) Sub 3-4 m/z = 245.12(C18H15N = 245.32) Sub 3-5 m/z = 170.08(C11H10N2 = 170.21) Sub 3-6 m/z = 199.10(C10H13NO = 199.25) Sub 3-7 m/z = 225.15(C16H19N = 225.33) Sub 3-8 m/z = 285.15(C21H19N = 285.38) Sub 3-9 m/z = 409.18(C31H23N = 409.52) Sub 3-10 m/z = 407.17(C31H21N = 407.51) Sub 3-11 m/z = 269.12(C20H15N = 269.34) Sub 3-12 m/z = 269.12(C20H15N = 269.34) Sub 3-13 m/z = 295.14(C22H17N = 295.38) Sub 3-14 m/z = 220.10(C15H12N2 = 220.27) Sub 3-15 m/z = 249.12(C17H12NO = 249.31) Sub 3-16 m/z = 275.17(C20H21N = 275.39) Sub 3-17 m/z = 335.17(C25H21N = 335.44) Sub 3-18 m/z = 459.20(C35H25N = 459.58) Sub 3-19 m/z = 457.18(C35H23N = 457.56) Sub 3-20 m/z = 269.12(C20H15N = 269.34) Sub 3-21 m/z = 295.14(C22H17N = 295.38) Sub 3-22 m/z = 220.10(C15H2N2 = 220.27) Sub 3-23 m/z = 249.12(C17H15NO = 249.31) Sub 3-24 m/z = 275.17(C20H21N = 275.39) Sub 3-25 m/z = 335.17(C25H21N = 335.44) Sub 3-26 m/z = 459.20(C35H25N = 459.58) Sub 3-27 m/z = 457.18(C35H23N = 457.56) Sub 3-28 m/z = 321.15(C24H19N = 321.41) Sub 3-29 m/z = 246.12(C17H14N2 = 246.31) Sub 3-30 m/z = 275.13(C19H17NO = 275.34) Sub 3-31 m/z = 301.18(C22H23N = 301.42) Sub 3-32 m/z = 361.18(C27H23N = 361.48) Sub 3-33 m/z = 485.21(C37H27N = 485.62) Sub 3-34 m/z = 483.20(C37H25N = 483.60) Sub 3-35 m/z = 171.08(C10H09N3 = 171.20) Sub 3-36 m/z = 200.09(C12H12N2O = 200.24) Sub 3-37 m/z = 226.15(C15H18N2 = 226.32) Sub 3-38 m/z = 286.15(C20H18N2 = 286.37) Sub 3-39 m/z = 410.18(C30H22N2 = 410.51) Sub 3-40 m/z = 408.16(C30H20N2 = 408.49) Sub 3-41 m/z = 229.11(C14H15NO2 = 229.27) Sub 3-42 m/z = 255.16(C17H21NO = 255.35) Sub 3-43 m/z = 315.16(C22H21NO = 315.41) Sub 3-44 m/z = 439.19(C32H25NO = 439.55) Sub 3-45 m/z = 437.18(C32H23NO = 437.53) Sub 3-46 m/z = 281.21(C20H27N = 281.44) Sub 3-47 m/z = 341.21(C25H27N = 341.49) Sub 3-48 m/z = 465.25(C35H31N = 465.63) Sub 3-49 m/z = 463.23(C35H29N = 463.61) Sub 3-50 m/z = 401.21(C30H27N = 401.54) Sub 3-51 m/z = 525.25(C40H31N = 525.68) Sub 3-52 m/z = 523.23(C40H29N = 523.66)

[0109] Synthesis of Final Product of Formula (1)

[0110] After Sub 1 (1 equiv) or Sub 2 (1 equiv) was dissolved in toluene, followed by being added respectively Sub 3 (1.1 equiv), Pd.sub.2(dba).sub.3 (0.05 equiv), PPh.sub.3 (0.1 equiv), NaOt-Bu (3 equiv), followed by reflux and stirring at 100° C. for 24 hours. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired Final Product.

Synthesis Examples of 1-17

[0111] ##STR00064##

[0112] After 9-(4′-bromo-[1,1′-biphenyl]-4-yl)-9H-carbazole (9.6 g, 24 mmol) was dissolved in toluene, followed by being added respectively di([1,1′-biphenyl]-4-yl)amine (6.4 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.05 equiv), PPh.sub.3 (0.1 equiv), NaOt-Bu (3 equiv), followed by reflux and stirring at 100° C. for 24 hours. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired Final Product 12.9 g (yield: 84%).

Synthesis Examples of 1-32

[0113] ##STR00065##

[0114] After 3-(4-bromophenyl)-9-phenyl-9H-carbazole (9.6 g, 24 mmol) was dissolved in toluene, followed by being added respectively N-([1,1′-biphenyl]-4-yl)-9,9-dimethyl-9H-fluoren-2-amine (7.2 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.05 equiv), PPh.sub.3 (0.1 equiv), NaOt-Bu (3 equiv) followed by reflux and stirring at 100° C. for 24 hours. Upon completion of the reaction, the reaction product was extracted with ether and water. The organic layer was dried with MgSO.sub.4 and concentrated, and then the produced organic material was purified by silicagel column and recrystallized to obtain desired Final Product 13.8 g (yield: 85%).

[0115] A part of the obtained product above was confirmed by the following Mass Data

TABLE-US-00002 TABLE 2 compound FD-MS compound FD-MS 1-17 m/z = 638.27 (C48H34N2 = 638.80) 1-20 m/z = 678.30 (C51H38N2 = 678.86) 1-21 m/z = 802.33 (C61H42N2 = 803.00) 1-22 m/z = 800.32 (C61H40N2 = 800.98) 1-32 m/z = 678.30 (C51H38N2 = 678.86) 1-33 m/z = 802.33 (C61H42N2 = 803.00) 1-34 m/z = 800.32 (C61H40N2 = 800.98) 1-43 m/z = 714.30 (C54H38N2 = 714.89) 1-44 m/z = 754.33 (C57H42N2 = 754.96) 1-45 m/z = 878.37 (C67H46N2 = 879.10) 1-46 m/z = 876.35 (C67H44N2 = 877.08) 1-47 m/z = 744.26 (C54H36N2S = 744.94) 1-52 m/z = 826.33 (C63H42N2 = 827.02) 1-53 m/z = 824.32 (C63H40N2 = 825.01) 1-54 m/z = 688.29 (C52H36N2 = 688.86) 1-55 m/z = 728.32 (C55H40N2 = 728.92) 1-57 m/z = 778.33 (C59H42N2 = 778.98) 1-58 m/z = 902.37 (C69H46N2 = 903.12) 1-59 m/z = 900.35 (C69H44N2 = 901.10)

Synthesis Examples 2

[0116] The final product 2 represented by Formula (2) according to the present invention can be synthesized by reaction between Sub 4 and Sub 5 as illustrated in the following Reaction Scheme 4.

##STR00066##

Synthesis Examples Sub 4

[0117] Sub 4 of Reaction Scheme 4 can be synthesized, but not limited to, by the Reaction Path of the following Reaction Scheme 5,

##STR00067##

Example of Sub 4(1)

[0118] ##STR00068##

[0119] Synthesis of Sub 4-3(1)

[0120] In a round-bottom flask, Sub 4-1(1) (0.3 g, 20 mmol), Sub 4-2(1) (4.7 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.5 g, 0.6 mmol), P(t-Bu).sub.3 (0.2 g, 2 mmol), t-BuONa (5.8 g, 60 mmol), and toluene (300 mL) were placed and allowed to react at 100° C. After completion of the reaction, the reaction product was extracted with CH.sub.2Cl.sub.2 and water, and the extracted organic layer was dried with MgSO.sub.4 and concentrated. And the produced organic material was purified by a silicagel column and recrystallized, to give 2.5 g of Sub 4-3(1) (yield: 75%).

[0121] Synthesis of Sub 4(1)

[0122] In a round-bottom flask, Sub 4-3(1) (2.5 g, 15 mmol), Sub 4-4(1) (3.5 g, 15 mmol), Pd.sub.2(dba).sub.3 (0.5 g, 0.5 mmol), P(t-Bu).sub.3 (0.2 g, 2 mmol), t-BuONa (5.8 g, 60 mmol), toluene (300 mL) were placed and allowed to react at 100° C. After completion of the reaction, the product was extracted with CH.sub.2Cl.sub.2 and water, and the extracted organic layer was dried over MgSO.sub.4 and concentrated, after which the product was purified by a silicagel column and recrystallized, to give 3.8 g of Sub 4(1) (yield: 78%).

[0123] The examples of Sub 4 include, but are not limited to, the followings.

##STR00069## ##STR00070## ##STR00071## ##STR00072## ##STR00073## ##STR00074##

TABLE-US-00003 TABLE 3 compound FD-MS compound FD-MS Sub 4(1) m/z = 321.15(C24H19N = 321.41) Sub 4(2) m/z = 508.20(C36H20D5NS = 508.69) Sub 4(3) m/z = 492.22(C36H20D5NO = 492.62) Sub 4(4) m/z = 492.22(C36H20D5NO = 492.62) Sub 4(5) m/z = 508.20(C36H20D5NS = 508.69) Sub 4(6) m/z = 569.21(C48H31NOS = 669.83) Sub 4(7) m/z = 517.15(C36H23NOS = 517.64) Sub 4(8) m/z = 517.15(C36H23NOS = 517.64) Sub 4(9) m/z = 669.21(C48H31NOS = 669.83) Sub 4(10) m/z = 669.21(C48H31NOS = 669.83) Sub 4(11) m/z = 533.13(C36H23NS2 = 533.70) Sub 4(12) m/z = 501.17(C36H23NO2 = 501.57) Sub 4(13) m/z = 517.15(C36H23NOS = 517.64) Sub 4(14) m/z = 532.26(C39H24D5NO = 532.68) Sub 4(15) m/z = 548.23(C39H24D5NS = 548.74) Sub 4(16) m/z = 543.20(C39H29NS = 543.72) Sub 4(17) m/z = 456.22(C33H20D5NO = 456.59) Sub 4(18) m/z = 665.22(C49H31NS = 665.84) Sub 4(19) m/z = 477.16(C34H23NS = 477.62) Sub 4(20) m/z = 589.19(C43H27NS = 589.75) Sub 4(21) m/z = 573.21(C43H27NO = 573.68) Sub 4(22) m/z = 639.20(C47H29NS = 639.80) Sub 4(23) m/z = 639.20(C47H29NS = 639.80) Sub 4(24) m/z = 695.17(C49H29NS2 = 695.89) Sub 4(25) m/z = 645.16(C45H27NS2 = 645.83) Sub 4(26) m/z = 645.16(C45H27NS2 = 645.83) Sub 4(27) m/z = 589.19(C43H27NS = 589.75) Sub 4(28) m/z = 589.19(C43H27NS = 589.75) Sub 4(29) m/z = 381.06(C24H15NS2 = 381.51) Sub 4(30) m/z = 583.23(C45H29N = 583.72) Sub 4(31) m/z = 583.23(C45H29N = 583.72) Sub 4(32) m/z = 645.25(C50H31N = 645.79) Sub 4(33) m/z = 421.18(C32H23N = 421.53) Sub 4(34) m/z = 503.17(C36H25NS = 503.66) Sub 4(35) m/z = 421.18(C32H23N = 421.53) Sub 4(36) m/z = 473.21(C36H27N = 473.61) Sub 4(37) m/z = 523.23(C40H29N = 523.66) Sub 4(38) m/z = 523.23(C40H29N = 523.66) Sub 4(39) m/z = 421.18(C32H23N = 421.53) Sub 4(40) m/z = 321.15(C24H19N = 321.41)

Synthesis Example of Sub 5

[0124] The examples of Sub 5 of Reaction Scheme 4 include, but are not limited to, the followings.

##STR00075## ##STR00076##

[0125] Synthesis of Final Product 2

Synthesis Examples 2-34

[0126] ##STR00077##

[0127] In a round-bottom flask, Sub 4(19) (9.5 g, 20 mmol), Sub 5(4) (4.7 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.5 g, 0.6 mmol), P(t-Bu).sub.3 (0.2 g, 2 mmol), t-BuONa (5.8 g, 60 mmol), and toluene (300 mL) were placed and allowed to react at 100° C. After completion of the reaction, the product was extracted with CH.sub.2Cl.sub.2 and water, and the extracted organic layer was dried with MgSO.sub.4 and concentrated. And the product was purified by a silicagel column and recrystallized to give 9.8 g of 2-34 (yield: 78%).

Synthesis Examples 2-58

[0128] ##STR00078##

[0129] In a round-bottom flask, Sub 4(35) 8.4 g, 20 mmol), Sub 5(7) (5.7 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.5 g, 0.6 mmol), P(t-Bu).sub.3 (0.2 g, 2 mmol), t-BuONa (5.8 g, 60 mmol), and toluene (300 mL) were placed and using the synthetic method 2-34, to obtain the product of 2-58 10.4 g (yield: 83%)

Synthesis Examples 2-59

[0130] ##STR00079##

[0131] In a round-bottom flask, Sub 4(32) (12.9 g, 20 mmol), Sub 5(11) (7.9 g, 20 mmol), Pd.sub.2(dba).sub.3 (0.5 g, 0.6 mmol), P(t-Bu).sub.3 (0.2 g, 2 mmol), t-BuONa (5.8 g, 60 mmol), and toluene (300 mL) were placed and using the synthetic method of 2-34, to obtain the product of 2-59 5.2 g (yield: 79%)

TABLE-US-00004 TABLE 4 compound FD-MS compound FD-MS 2-1 m/z = 473.21(C36H27N = 473.61) 2-2 m/z = 660.26(C48H28D5NS = 660.88) 2-3 m/z = 644.29(C48H28D5NO = 644.81) 2-4 m/z = 644.29(C48H28D5NO = 644.81) 2-5 m/z = 660.26(C48H28D5NS = 660.88) 2-6 m/z = 821.28(C60H39NOS = 822.02) 2-7 m/z = 669.21(C48H31NOS = 669.83) 2-8 m/z = 669.21(C48H31NOS = 669.83) 2-9 m/z = 821.28(C60H39NOS = 822.02) 2-10 m/z = 821.28(C60H39NOS = 822.02) 2-11 m/z = 761.22(C54H35NS2 = 761.99) 2-12 m/z = 685.19(C48H31NS2 = 685.90) 2-13 m/z = 685.19(C48H31NS2 = 685.90) 2-14 m/z = 837.25(C60H39NS2 = 838.09) 2-15 m/z = 761.22(C54H35NS2 = 761.99) 2-16 m/z = 837.25(C60H39NS2 = 838.09) 2-17 m/z = 669.21(C48H31NOS = 669.83) 2-18 m/z = 669.21(C48H31NOS = 669.83) 2-19 m/z = 669.21(C48H31NOS = 669.83) 2-20 m/z = 821.28(C60H39NOS = 822.02) 2-21 m/z = 684.32(C51H32D5NO = 684.88) 2-22 m/z = 700.30(C51H32D5NS = 700.94) 2-23 m/z = 695.26(C51H37NS = 695.91) 2-24 m/z = 608.29(C45H28D5NO = 608.78) 2-25 m/z = 817.28(C61H39NS = 818.03) 2-26 m/z = 629.22(C46H31NS = 629.81) 2-27 m/z = 741.25(C55H35NS = 741.94) 2-28 m/z = 725.27(C55H35NO = 725.87) 2-29 m/z = 629.22(C46H31NS = 629.81) 2-30 m/z = 725.27(C55H35NO = 725.87) 2-31 m/z = 791.26(C59H37NS = 792.00) 2-32 m/z = 791.26(C59H37NS = 792.00) 2-33 m/z = 847.24(C61H37NS2 = 848.08) 2-34 m/z = 629.22(C46H31NS = 629.81) 2-35 m/z = 791.26(C59H37NS = 792.00) 2-36 m/z = 613.24(C46H31NO = 613.74) 2-37 m/z = 613.24(C46H31NO = 613.74) 2-38 m/z = 613.24(C46H31NO = 613.74) 2-39 m/z = 613.24(C46H31NO = 613.74) 2-40 m/z = 797.22(C57H35NS2 = 798.02) 2-41 m/z = 797.22(C57H35NS2 = 798.02) 2-42 m/z = 741.25(C55H35NS = 741.94) 2-43 m/z = 741.25(C55H35NS = 741.94) 2-44 m/z = 665.22(C49H31NS = 665.84) 2-45 m/z = 695.17(C49H29NS2 = 695.89) 2-46 m/z = 695.17(C49H29NS2 = 695.89) 2-47 m/z = 563.08(C36H21NS3 = 563.75) 2-48 m/z = 735.29(C57H37N = 735.91) 2-49 m/z = 735.29(C57H37N = 735.91) 2-50 m/z = 635.26(C49H33N = 635.79) 2-51 m/z = 735.29(C57H37N = 735.91) 2-52 m/z = 797.31(C62H39N = 797.98) 2-53 m/z = 663.29(C51H37N = 663.85) 2-54 m/z = 623.26(C48H33N = 623.78) 2-55 m/z = 903.30(C68H41NS = 904.12) 2-56 m/z = 655.23(C48H33NS = 655.85) 2-57 m/z = 741.25(C55H35NS = 741.94) 2-58 m/z = 623.26(C48H33N = 623.78) 2-59 m/z = 959.36(C75H45N = 960.17) 2-60 m/z = 625.28(C48H35N = 625.80) 2-61 m/z = 679.23(C50H33NS = 679.87) 2-62 m/z = 675.29(C52H37N = 675.86) 2-63 m/z = 725.31(C56H39N = 725.92) 2-64 m/z = 725.31(C56H39N = 725.92) 2-65 m/z = 473.21(C36H27N = 473.61) 2-66 m/z = 623.26(C48H33N = 623.78) 2-67 m/z = 623.26(C48H33N = 623.78) 2-68 m/z = 473.21(C36H27N = 473.61)

[0132] Manufacture and Evaluation of Organic Electronic Element

Example 1) Manufacture and Test of Blue OLED (EBL)

[0133] On an ITO layer (anode) formed on a glass substrate, 2-TNATA was vacuum deposited to form a hole injection layer with a thickness of 60 nm, and N,N′-bis(1-naphthalenyl)-N,N′-bis-phenyl-(1,1′-biphenyl)-4,4′-diamine (hereinafter will be abbreviated as NPB) was vacuum deposited on the hole injection layer to form a hole transport layer with a thickness of 60 nm. Then, the compound of the present invention was vacuum deposited on the hole transport layer to form an EBL with a thickness of 20 nm. On the EBL, an light emitting layer with a thickness of 30 nm was deposited using 9,10-di(naphthalen-2-yl)anthracene as a host doped with BD-052X (Idemitsukosan) as a dopant in a weight ratio of 96:4. (1,1′-bisphenyl)-4-olato)bis(2-methyl-8-quinolinolato)aluminum (hereinafter will be abbreviated as BAlq) was vacuum deposited to form a hole blocking layer with a thickness of 40 nm, and an electron transport layer was formed using tris(8-quinolinol)aluminum (hereinafter will be abbreviated as Alq3) to a thickness of 40 nm. After that, an alkali metal halide, LiF was deposited as an electron injection layer to a thickness of 0.2 nm, and Al was deposited as a cathode to a thickness of 150 nm to manufacture an OLED.

[0134] To the OLEDs which were manufactured in examples and comparative examples, a forward bias direct current voltage was applied, and electroluminescent (EL) properties were measured using PR-650 of Photoresearch Co., and T95 life was measured using a life measuring apparatus manufactured by McScience Inc. with a reference luminance of 500 cd/m.sup.2. In the following table, the results on the manufacture of a device and evaluation are shown.

Comparative Example 1 and 2

[0135] Except for not using the emitting auxiliary layer, an OLED was manufactured in the same manner as described in the embodiment 1.

Comparative Example 3

[0136] Except for forming a hole transport layer using the compound 2-1 instead of the compound represented by Formula (1) and except for not using the emitting auxiliary layer and, an OLED was manufactured in the same manner as described in the embodiment 1.

TABLE-US-00005 TABLE 5 compounds of compounds of the hole the emitting Current Brightness Lifetime transport layer auxiliary layer Voltage Density (cd/m2) Efficiency T(95) Comparative compound(1-17) — 4.7 13.9 500.0 3.6 93.2 Example(1) Comparative compound(1-32) — 4.2 12.2 500.0 4.1 95.8 Example(2) Comparative compound(2-58) — 4.9 15.6 500.0 3.2 84.3 Example(3) Example(1) compound(1-17) compound(2-1) 4.8 8.8 500.0 5.7 115.1 Example(2) compound(1-17) compound(2-12) 4.8 8.9 500.0 5.6 132.0 Example(3) compound(1-17) compound(2-54) 4.8 9.1 500.0 5.5 142.6 Example(4) compound(1-17) compound(2-56) 4.8 8.8 500.0 5.7 132.4 Example(5) compound(1-17) compound(2-58) 4.8 8.1 500.0 6.2 154.8 Example(6) compound(1-17) compound(2-60) 4.8 9.4 500.0 5.3 114.1 Example(7) compound(1-17) compound(2-61) 4.8 9.7 500.0 5.2 130.2 Example(8) compound(1-17) compound(2-62) 4.9 9.1 500.0 5.5 123.6 Example(9) compound(1-17) compound(2-63) 4.8 8.6 500.0 5.8 140.8 Example(10) compound(1-17) compound(2-64) 4.8 9.6 500.0 5.2 139.0 Example(11) compound(1-17) compound(2-66) 4.8 9.1 500.0 5.5 114.7 Example(12) compound(1-17) compound(2-67) 4.8 9.2 500.0 5.5 125.3 Example(13) compound(1-32) compound(2-1) 4.3 7.4 500.0 6.7 133.6 Example(14) compound(1-32) compound(2-12) 4.3 8.0 500.0 6.2 147.0 Example(15) compound(1-32) compound(2-54) 4.5 7.2 500.0 7.0 144.2 Example(16) compound(1-32) compound(2-56) 4.2 7.4 500.0 6.8 110.7 Example(17) compound(1-32) compound(2-58) 4.3 7.0 500.0 7.1 150.9 Example(18) compound(1-32) compound(2-60) 4.2 7.3 500.0 6.8 122.9 Example(19) compound(1-32) compound(2-61) 4.3 7.3 500.0 6.9 144.4 Example(20) compound(1-32) compound(2-62) 4.3 8.1 500.0 6.2 147.8 Example(21) compound(1-32) compound(2-63) 4.2 8.3 500.0 6.0 136.8 Example22) compound(1-32) compound(2-64) 4.4 8.0 500.0 6.3 138.6 Example(23) compound(1-32) compound(2-66) 4.4 7.4 500.0 6.8 127.7 Example(24) compound(1-32) compound(2-67) 4.4 7.2 500.0 7.0 138.0

Example 2) Manufacture and Test of Green Organic Light Emitting Diode

[0137] First, on an ITO layer (anode) formed on a glass substrate, N.sup.1-(naphthalen-2-yl)-N.sup.4,N.sup.4-bis(4-(naphthalen-2-yl(phenyl)amino)phenyl)-N.sup.1-phenylbenzene-1,4-diamine (hereinafter will be abbreviated as 2-TNATA) was vacuum-deposited to form a thickness of 60 nm, and subsequently, the inventive compound represented by the formula (1) was vacuum-deposited on the film as a hole transport compound to a thickness of 60 nm to form a hole transport layer. Then, the inventive compound represented by the formula (2) was vacuum-deposited as an emitting auxiliary layer material to a thickness of 20 nm to form an emitting auxiliary layer.

[0138] After forming the emitting auxiliary layer, CBP [4,4′-N, N′-dicarbazole-biphenyl] was used as a host on the emitting auxiliary layer, and Ir (ppy) 3 [tris (2-phenylpyridine)-iridium] was doped as a dopant at a weight ratio of 95:5 to deposit an emitting layer with a thickness of 30 nm on the emitting auxiliary layer. (1,1′-bisphenyl)-4-olato)bis(2-methyl-8-quinolinolato)aluminum (hereinafter will be abbreviated as BAlq) was vacuum deposited to form a hole blocking layer with a thickness of 10 nm, and Tris (8-quinolinol) aluminum (hereinafter abbreviated as Alq3) was deposited to a thickness of 40 nm as an electron transport layer. Next, LiF as halogenated alkali metal was deposited with a thickness of 0.2 nm on the electron transport layer to form an electron injection layer, and then Al was deposited with a thickness of 150 nm on the electron injection layer to form a cathode. In this way, the OLED was completed.

[0139] To the OLEDs which were manufactured in examples and comparative examples, a forward bias direct current voltage was applied, and electroluminescent (EL) properties were measured using PR-650 of Photoresearch Co., and T95 life was measured using a life measuring apparatus manufactured by McScience Inc. with a reference luminance of 5000 cd/m.sup.2. In the following table, the results on the manufacture of a device and evaluation are shown.

Comparative Example 4, 5

[0140] Except for not using the emitting auxiliary layer, an OLED was manufactured in the same manner as described in the embodiment 1 above.

Comparative Example 6

[0141] Except for forming a hole transport layer using the compound 2-1 instead of the compound represented by Formula (1) and except for not using the emitting auxiliary layer and, an OLED was manufactured in the same manner as described in the embodiment 1.

TABLE-US-00006 TABLE 6 compounds of compounds of the hole the emitting Current Brightness Lifetime transport layer auxiliary layer Voltage Density (cd/m2) Efficiency T(95) comparative compound(1-17) — 5.5 17.9 5000.0 28.0 93.0 example(4) comparative compound(1-32) — 5.0 14.3 5000.0 35.0 97.3 example(5) comparative compound(2-58) — 5.8 20.0 5000.0 25.0 89.1 example(6) example(25) compound(1-17) compound(2-7) 5.6 13.5 5000.0 37.1 148.2 example(26) compound(1-17) compound(2-12) 5.5 13.7 5000.0 36.5 110.9 example(27) compound(1-17) compound(2-54) 5.5 13.9 5000.0 36.1 117.8 example(28) compound(1-17) compound(2-56) 5.6 12.2 5000.0 41.0 111.5 example(29) compound(1-17) compound(2-58) 5.7 11.2 5000.0 44.5 135.3 example(30) compound(1-17) compound(2-60) 5.7 11.2 5000.0 44.5 137.0 example(31) compound(1-17) compound(2-61) 5.7 12.8 5000.0 39.1 150.0 example(32) compound(1-17) compound(2-62) 5.7 12.2 5000.0 40.9 125.4 example(33) compound(1-17) compound(2-63) 5.7 12.0 5000.0 41.6 130.8 example(34) compound(1-17) compound(2-64) 5.5 13.5 5000.0 37.1 122.1 example(35) compound(1-17) compound(2-66) 5.8 11.9 5000.0 42.2 143.4 example(36) compound(1-17) compound(2-67) 5.6 11.8 5000.0 42.3 115.5 example(37) compound(1-32) compound(2-7) 5.2 11.1 5000.0 44.9 116.0 example(38) compound(1-32) compound(2-12) 5.1 11.8 5000.0 42.5 125.2 example(39) compound(1-32) compound(2-54) 5.2 13.2 5000.0 38.0 132.4 example(40) compound(1-32) compound(2-56) 5.1 13.8 5000.0 36.1 138.3 example(41) compound(1-32) compound(2-58) 5.1 12.7 5000.0 39.3 132.6 example(42) compound(1-32) compound(2-60) 5.2 11.4 5000.0 43.8 122.0 example(43) compound(1-32) compound(2-61) 5.3 14.3 5000.0 35.0 146.0 example(44) compound(1-32) compound(2-62) 5.1 12.7 5000.0 39.5 145.3 example(45) compound(1-32) compound(2-63) 5.0 11.6 5000.0 43.2 113.9 example(46) compound(1-32) compound(2-64) 5.3 13.1 5000.0 38.1 139.5 example(47) compound(1-32) compound(2-66) 5.2 14.1 5000.0 35.6 131.6 example(48) compound(1-32) compound(2-67) 5.3 14.2 5000.0 35.2 133.2

[0142] As can be seen from the results of Table 5 and Table 6, when the compound of the Formula (1) is used as the hole transport layer, and the compound of the Formula (2) is used as the emitting auxiliary layer, the efficiency and the lifetime were remarkably improved, even though the driving voltage was about the same or slightly higher, than that of the comparative example using the compound of formula (1) as the hole transport layer without using the luminescent auxiliary layer.

[0143] Further, comparing the comparative examples (1), (2), (4), and (5) without emitting auxiliary layer, wherein the compound 1-17 and 1-32 represented by the formula (1) were respectively used as the hole transport layer, and the examples (1) to (24), (25), and (48) using the compound represented by Formula (2), it can be seen that the efficiency and the life span are remarkably improved. This is because when the compound of the present invention is used as an emitting auxiliary layer, due to the deep HOMO energy levels inherent to the inventive compounds, a suitable amount of holes in the emitting layer can be efficiently transferred from the hole transport layer, and the holes and electrons in the emitting layer make a charge balance and it is considered that the interface deterioration at the interface of the emitting layer are prevented and the efficiency and life span are increased. Also, as the charge balance in the emitting layer increases, the surplus polaron in the emitting layer decreases, and the light emitting material deformation decreases, it is considered that color purity improvement, life span, and efficiency increase.

[0144] As can be seen from the results of Comparative Examples (3) or (6) and Examples (1) to (24), (25) and (48), when the compound represented by the formula (2) is used alone as the hole transport layer, the efficiency and the life span were lower than that of the example using the compound of formula (1) as the hole transporting layer, but it can be confirmed that excellent results are obtained in efficiency and life span when used as an emitting auxiliary layer. That is, unlike the case of using the compound of formula (2) as the hole transport layer, the result of the device was improved when used as the emitting auxiliary layer, and this indicates that the characteristics of the device can be significantly changed by using a compound in a specific layer, in particular, it shows that the performance varies depending on the combination of the hole transport layer material and the emitting auxiliary layer material.

[0145] Although exemplary embodiments of the present invention have been described for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims. Therefore, the embodiment disclosed in the present invention is intended to illustrate the scope of the technical idea of the present invention, and the scope of the present invention is not limited by the embodiment.

[0146] The scope of the present invention shall be construed on the basis of the accompanying claims, and it shall be construed that all of the technical ideas included within the scope equivalent to the claims belong to the present invention.