Electron transport material and organic electroluminescent device using the same
Provided are a new electron transport material and an organic electroluminescent device including the same. The electron transport material according to the present invention may have the excellent luminescence property and reduce the driving voltage to increase the power efficiency, such that the organic electroluminescent device using less consumption power may be manufactured.
1. An electron transport material represented by the following Chemical Formula 1,
wherein in Chemical Formula 1,
A and C are N, B and D are independently C-(L 1 ) m -Ar 1 , and each of -(L 1 ) m -Ar 1 are the same as or different from each other, but two -(L 1 ) m -Ar 1 are not hydrogen at the same time;
L is (C 1 -C 2 )alkylene or (C 2 )alkenylene;
R 1 to R 4 each are independently hydrogen, (C1-C30)alkyl, (C3-C30)cycloalkyl, (C6-C30)aryl, or (C3-C30)heteroaryl;
L 1 (s) each are independently a single bond, (C6-C30)arylene, or (C3-C30)heteroarylene;
m is an integer of 1 to 3, and when m is an integer of 2 or more, L 1 (s) are the same as or different from each other;
Art(s) each are independently hydrogen, (C1-C30)alkyl, (C6-C30)aryl, or (C3-C30)heteroaryl; alkyl, cycloalkyl, aryl, heteroaryl of R 1 to R 4 , alkylene or alkenylene of L, arylene and heteroarylene of L 1 , and aryl and heteroaryl of Ar 1 are substituted with at least one selected from a group consisting of (C1-C30)alkyl, halo(C1-C30)alkyl, halogen, cyano, (C3-C30)cycloalkyl, (C1-C30)alkoxy, (C6-C30)aryloxy, (C6-C30)aryl, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyl(C6-C30)aryl, (C3-C30)heteroaryl, (C3-C30)heteroaryl substituted with (C1-C30)alkyl, (C3-C30)heteroaryl substituted with (C6-C30)aryl, mono or di(C1-C30)alkylamino, mono or di(C6-C30)arylamino, tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, nitro, and hydroxy; and
heteroarylene and heteroaryl contains at least one hetero atom selected from B, N, O, S, P(═O), Si, and P.
2. The electron transport material of claim 1 , wherein it is represented by the following Chemical Formula 2:
wherein in Chemical Formulas 2,
R 1 to R 4 and L each has the same definition in Chemical Formula 1 of claim 1 ;
L 2 and L 3 each are independently a single bond, (C6-C30)arylene, or (C3-C30)heteroarylene;
x and y each are independently an integer of 1 to 3, wherein when x is an integer of 2 or more, L 2 (s) are the same as or different from each other, and when y is an integer of 2 or more, L 3 (s) are the same as or different from each other;
Ar 2 and Ar 3 each are independently hydrogen, (C1-C30)alkyl, (C6-C30)aryl, or (C3-C30)heteroaryl;
arylene and heteroarylene of L 2 and L 3 , and aryl and heteroaryl of Ar 2 and Ar 3 are substituted with at least one selected from a group consisting of (C1-C30)alkyl, halo(C1-C30)alkyl, halogen, cyano, (C3-C30)cycloalkyl, (C1-C30)alkoxy, (C6-C30)aryloxy, (C6-C30)aryl(C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyl(C6-C30)aryl, (C3-C30)heteroaryl, (C3-C30)heteroaryl substituted with (C1-C30)alkyl, (C3-C30)heteroaryl substituted with (C6-C30)aryl, mono or di(C1-C30)alkylamino, mono or di(C6-C30)arylamino, tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, nitro, and hydroxy; and
-(L 2 ) x -Ar 2 and -(L 3 ) Y -Ar 3 are not hydrogen at the same time.
3. The electron transport material of claim 2 , wherein it is represented by the following Chemical Formulas 4 to 6:
wherein in Chemical Formulas 4 to 6,
R 1 to R 6 each are independently hydrogen, (C1-C30)alkyl, (C3-C30)cycloalkyl, (C6-C30)aryl, or (C3-C30)heteroaryl;
L 2 and L 3 each are independently a single bond, (C6-C30)arylene, or (C3-C30)heteroarylene;
x is an integer of 1 to 3, and when x is an integer of 2 or more, L 2 (s) are the same as or different from each other;
Ar 2 and Ar 3 each are independently hydrogen, (C1-C30)alkyl, (C6-C30)aryl, or (C3-C30)heteroaryl; and
arylene of L 2 and L 3 and aryl and heteroaryl of Ar 2 and Ar 3 are further substituted with at least one selected from a group consisting of (C1-C30)alkyl, (C6-C30)aryl, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyl(C6-C30)aryl, and (C3-C30)heteroaryl.
4. The electron transport material of claim 3 , wherein L 2 and L 3 each are a single bond, phenylene, biphenylene, 9,9-dimethylfluorenylene, naphthylene, anthrylene, pyridinylene, or pyrimidinylene;
Ar 2 and Ar 3 each are independently hydrogen, (C1-C30)alkyl, or selected from the following structure:
and
R′, R″, and R′″ each are independently hydrogen, (C1-C30)alkyl, (C6-C30)aryl, (C3-C30)heteroaryl, or (C1-C30)alkyl(C6-C30)aryl.
5. The electron transport material of claim 4 , wherein the electron transport material is selected from the following compounds:
6. An organic electroluminescent device containing the electron transport material of claim 1 .
7. The organic electroluminescent device of claim 6 , wherein it includes:
a first electrode; a second electrode; and at least one organic layer interposed between the first and second electrodes, the organic layer including an electron transport layer in which the electron transport material is contained.