Organic light emitting diode having high efficiency

1. An organic light-emitting diode, comprising:

a first electrode; a second electrode facing the first electrode;

a hole injecting layer or a hole transport layer interposed between the first electrode and the second electrode; and

a light-emitting layer,

wherein the hole injecting layer or the hole transport layer comprises at least one of the amine compounds represented by the following Chemical Formula A or B:

wherein,

A 1 , A 2 , E, and F, which may be the same or different, are each independently a substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms, or a substituted or unsubstituted heteroaromatic ring of 2 to 40 carbon atoms;

wherein two adjacent carbon atoms within the aromatic ring of A 1 and two adjacent carbon atoms within the aromatic ring of A 2 form a 5-membered ring with a carbon atom connected to both substituents R 1 and R 2 , thus establishing a fused ring structure;

linkers L 1 to L 6 , which may be the same or different, are each independently selected from among a single bond and a substituted or unsubstituted arylene of 6 to 60 carbon atoms;

M is selected from among N-R 3 , CR 4 R 5 , SiR 6 R 7 , O, and S;

R 1 to R 7 and Ar 1 to Ar 4 , which may be the same or different, are each independently selected from among a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl of 1 to 30 carbon atoms, a substituted or unsubstituted aryl of 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl of 3 to 30 carbon atoms, a substituted or unsubstituted heteroaryl of 2 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl of 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl of 6 to 30 carbon atoms, a cyano, a nitro, and a halogen,

wherein R 1 and R 2 may be connected to each other to form a five-membered ring, which may be part of a monocyclic or polycyclic aliphatic or aromatic ring system;

p1 and p2, r1 and r2, and s1 and s2 are each independently an integer of 1 to 3, under which when any of them is 2 or greater, the corresponding linkers L 1 to L 6 may be the same or different,

Ar 1 and Ar 2 may be connected to each other to form a ring and Ar 3 and Ar 4 may be connected to each other to form a ring;

two adjacent carbon atoms within the A 2 ring in Chemical Formula A are linked to respective * of structure formula Q 1 to form a fused ring, and

two adjacent carbon atoms within the A 1 ring in Chemical Formula B are linked to respective * of structure formula Q 2 to form a fused ring and two adjacent carbon atoms within the A 2 ring in Chemical Formula B are linked to respective * of structure formula Q 1 to form a fused ring,

wherein the term “substituted” in the expression “substituted or unsubstituted” used for [Chemical Formula A] and [Chemical Formula B] means having at least one substituent selected from the group consisting of a deuterium atom, a cyano, a halogen, a nitro, an alkyl of 1 to 24 carbon atoms, a halogenated alkyl of 1 to 24 carbon atoms, an aryl of 6 to 24 carbon atoms, an arylalkyl of 7 to 24 carbon atoms, a heteroaryl of 2 to 24 carbon atoms or a heteroarylalkyl of 2 to 24 carbon atoms, an alkylsilyl of 1 to 24 carbon atoms, and an arylsilyl of 6 to 24 carbon atoms.

2. The organic light-emitting diode of claim 1 , wherein A 1 , A 2 , E, and F in [Chemical Formula A] or [Chemical Formula B], which may be the same or different, are independently respective substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms.

3. The organic light-emitting diode of claim 2 , wherein the substituted or unsubstituted aromatic hydrocarbon rings of 6 to 50 carbon atoms are same or different and are each independently any one selected from [Structural Formula 10] to [Structural Formula 21]:

wherein

“-*” denotes a bonding site for forming a 5-membered ring bearing the carbon atom connected to the substituents R 1 and R 2 or a bonding site for forming a 5-membered ring bearing M of Structural Formula Q 1 and Q 2 ;

when one of the aromatic hydrocarbon rings of [Structural Formula 10] to [Structural Formula 21] for A 1 or A 2 is bonded to Structural Formula Q 1 or Structural Formula Q 2 , two adjacent carbon atoms of the aromatic hydrocarbon ring occupy respective positions * of Structural Formula Q 1 or Q 2 to form a fused ring;

R is as defined for R 1 and R 2 above; and m is an integer of 1 to 8 wherein when m is 2 or greater or when R exists as multiple radicals, the resulting R's may be the same or different.

4. The organic light-emitting diode of claim 1 , wherein the amine compound represented by Chemical Formula A or B is contained in the hole transport layer.

5. The organic light-emitting diode of claim 1 , wherein the linkers L 1 to L 6 in Chemical Formulas A and B are same or different and are each independently a single bond or any one selected from among the following Structural Formulas 22, 23, 25, 27, 28, and 30, and p1 and p2, r1 and r2, and s1 and s2 are each 1 or 2:

wherein, each of the unsubstituted carbon atoms of the aromatic ring moiety is bound with a hydrogen atom or a deuterium atom.

6. The organic light-emitting diode of claim 1 , wherein R 1 and R 2 are same or different and are connected to each other to form a ring or are each a substituted or unsubstituted aryl of 6 to 50 carbon atoms which remains unconnected.

7. The organic light-emitting diode of claim 1 , wherein the amine compound represented by Chemical Formula A or B is any one of the compounds represented by the following Chemical Formulas 1 to 144:

8. The organic light-emitting diode of claim 1 , wherein one or two of A 1 , A 2 , E, and F in Chemical Formulas A and B are each independently a substituted or unsubstituted heteroaromatic ring of 2 to 40 carbon atoms.

9. The organic light-emitting diode of claim 8 , wherein one of A 1 , A 2 , E, and F in Chemical Formulas A and B is a substituted or unsubstituted heteroaromatic ring of 2 to 40 carbon atoms.

10. The organic light-emitting diode of claim 1 , wherein the light-emitting layer comprises at least one of the amine compounds represented by the following Chemical Formulas D1 and D2:

wherein,

A 31 , A 32 , E 1 , and F 1 , which may be the same or different, are each independently a substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms, or a substituted or unsubstituted heteroaromatic ring of 2 to 40 carbon atoms;

wherein two adjacent carbon atoms within the aromatic ring of A 31 and two adjacent carbon atoms within the aromatic ring of A 32 form a 5-membered ring with a carbon atom connected to both substituents R 31 and R 32 , thus establishing a fused ring structure;

linkers L 21 to L 32 , which may be the same or different, are each independently selected from among a single bond, a substituted or unsubstituted alkylene of 1 to 60 carbon atoms, a substituted or unsubstituted alkenylene of 2 to 60 carbon atoms, a substituted or unsubstituted alkynylene of 2 to 60 carbon atoms, a substituted or unsubstituted cycloalkylene of 3 to 60 carbon atoms, a substituted or unsubstituted heterocycloalkylene of 2 to 60 carbon atoms, a substituted or unsubstituted arylene of 6 to 60 carbon atoms, and a substituted or unsubstituted heteroarylene of 2 to 60 carbon atoms;

W is selected from among N-R 33 , CR 34 R 35 , SiR 36 R 37 , GeR 38 R 39 , O, S, and Se;

R 31 to R 39 and Ar 21 to Ar 28 , which may be the same or different, are each independently selected from among a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl of 1 to 30 carbon atoms, a substituted or unsubstituted aryl of 6 to 50 carbon atoms, a substituted or unsubstituted alkenyl of 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl of 2 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl of 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl of 5 to 30 carbon atoms, a substituted or unsubstituted heteroaryl of 2 to 50 carbon atoms, a substituted or unsubstituted heterocycloalkyl of 2 to 30 carbon atoms, a substituted or unsubstituted alkoxy of 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy of 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy of 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy of 5 to 30 carbon atoms, a substituted or unsubstituted alkylamine of 1 to 30 carbon atoms, a substituted or unsubstituted arylamine of 5 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl of 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl of 5 to 30 carbon atoms, a substituted or unsubstituted alkyl germanium of 1 to 30 carbon atoms, a substituted or unsubstituted aryl germanium of 1 to 30 carbon atoms, a cyano, a nitro, and a halogen,

wherein R 31 and R 32 may be connected to each other to form a mono- or polycyclic aliphatic or aromatic ring which may bear at least one heteroatom selected from among N, O, P, Si, S, Ge, Se, and Te as a ring member;

p11 to p14, r11 to r14, and s11 to s14 are each independently an integer of 1 to 3, under which when any of them is 2 or greater, the corresponding linkers L21 to L32 may be the same or different,

x1 is an integer of 1 or 2, and y1 and z1, which may be the same or different, are each independently an integer of 0 to 3,

a connection may be made between Ar 21 and Ar 22 , between Ar 23 and Ar 24 , between Ar 25 and Ar 26 , and between Ar 27 and Ar 28 to form respective rings;

two adjacent carbon atoms within the A 32 ring in Chemical Formula D1 are linked to respective * of structure formula Q 11 to form a fused ring, and

two adjacent carbon atoms within the A 31 ring in Chemical Formula D2 are linked to respective * of structure formula Q 12 to form a fused ring and two adjacent carbon atoms within the A 32 ring in Chemical Formula D2 are linked to respective * of structure formula Q 11 to form a fused ring.

11. The organic light-emitting diode of claim 10 , wherein A 31 , A 32 , E 1 , and F 1 in the compounds represented by Chemical Formula D1 and Chemical Formula D2 are same or different and are each independently a substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms.

12. The organic light-emitting diode of claim 10 , wherein the linkers L 21 to L 32 in Chemical Formulas D1 and D2 are same or different and are each independently a single bond or any one selected from the following [Structural Chemical 22] to [Structural Chemical 30], p11 to p14, r11 to r14, and s11 to s14 are each 1 or 2, and x1 is 1:

wherein each of unsubstituted carbon atoms of the aromatic ring moiety can be bound with a hydrogen atom or a deuterium atom.

13. The organic light-emitting diode of claim 12 , wherein the amine compound represented by Chemical Formula D1 or D2 is any one selected from the following Compound 401 to Compound 639:

14. The organic light-emitting diode of claim 1 , further comprising at least one of a hole injection layer, a hole transport layer, a functional layer capable of both hole injection and hole transport, an electron transport layer, and an electron injecting layer in addition to the light-emitting layer.

15. The organic light-emitting diode of claim 14 , wherein the at least one selected from among the layers is formed using a deposition process or a solution process.

16. The organic light-emitting diode of claim 1 , wherein the organic light-emitting diode is used for a device selected from among a flat display device, a flexible display device, a monochrome or grayscale flat illumination device, and a monochrome or grayscale flexible illumination device.