Organic material composition and applications thereof
The present invention provides an organic material composition and applications thereof. By the combination of the compounds comprised in the organic material composition, the organic material composition makes the element have a lower driving voltage, a higher current efficiency and a longer service life.
1 . An organic material composition, wherein the organic material composition comprises at least one compound having a structure represented by Formula 1 and at least one compound having a structure represented by Formula 2-1:
wherein, R is selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group;
R 1 is -L 1 Ar 1 ; R 2 is -L 2 Ar 2 ; R 3 is -L 3 Ar 3 ; R 4 is -L 4 Ar 4 ;
L 1 to L 4 are each independently selected from a bond, a substituted or unsubstituted C6-C30 arylene group, and a substituted or unsubstituted C3-C30 heteroarylene group; and
Ar 1 to Ar 4 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C6-C60 arylamino group, a substituted or unsubstituted C3-C60 heteroarylamino group, a substituted or unsubstituted C6-C60 aryl group, and a substituted or unsubstituted C3-C60 heteroaryl group;
wherein at least two of Z 1 , Z 3 and Z 5 are N;
wherein, in Z 1 , Z 3 and Z 5 ,
Z 1 and Z 3 are N, and Z 5 is CL Y5 Ar Y5 , in which L Y5 Ar Y5 and L Y6 Ar Y6 are present individually without forming a ring, or joined to form a substituted or unsubstituted benzene ring; or
Z 1 , Z 3 , and Z 5 are N; and
wherein, Ar Y2 , Ar Y4 , Ar Y5 and Ar Y6 are each independently selected from hydrogen, deuterium, halogen, a cyano group, and a group selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenylnaphthyl group, a naphthylphenyl group, a triphenylenylene group, an anthryl group, a phenanthryl group, a chrysenyl group, each of which is substituted or unsubstituted; and a group represented by Formula 3:
Y is selected from O, S, and CR W1 R W2 ;
when at least one of Ar Y2 , Ar Y4 , Ar Y5 and Ar Y6 is selected from Formula 3,
any one of R Y1 to R Y8 , R W1 and R W2 in Formula 3 is connected to L Y2 , L Y4 or L Y6 in Formula 2-1 by chemical bonding;
Ar Y2 , Ar Y4 , Ar Y5 and Ar Y6 are the same or different;
R Y1 to R Y8 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a C1-C30 alkyl group in which one or more methylene groups are independently substituted by —O— and/or —S— in a manner that O atom and/or S atom are not adjacent to each other, a substituted or unsubstituted C7-C30 arylalkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C3-C30 heteroaryl group, a substituted or unsubstituted C4-C30 heteroarylalkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C3-C30 heterocycloalkyl group, a substituted or unsubstituted C3-C30 cycloalkenyl group, a substituted or unsubstituted C1-C30 alkoxy group, and a substituted or unsubstituted C6-C30 aryloxy group;
R Y1 to R Y8 are present individually without forming a ring, or any adjacent two of R Y1 to R Y8 joined to form a ring A, and the ring A is a substituted or unsubstituted C6-C30 aromatic ring;
R W1 and R W2 are selected from a substituted or unsubstituted C1-C30 alkyl group, and a substituted or unsubstituted C6-C30 aryl group;
L Y2 , L Y4 , L Y5 and L Y6 are each independently selected from a bond, a substituted or unsubstituted C6-C30 arylene group, and a substituted or unsubstituted C3-C30 heteroarylene group.
2 . The organic material composition according to claim 1 , wherein in Formula 1, at least one of Ar 1 to Ar 4 is a group represented by Formula b:
Ar 5 and Ar 6 are each independently selected from a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group.
3 . The organic material composition according to claim 1 , wherein in Formula 1, at least one of Ar 1 to Ar 4 is
the remaining ones of Ar 1 to Ar 4 are each independently selected from hydrogen, deuterium, and a group selected from a phenyl group, a naphthyl group, a biphenylyl group, a terphenylyl group, a phenanthryl group, a fluoranthenyl group, a triphenylenylene group, a dimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, a benzodimethylfluorenyl group, a benzodiphenylfluorenyl group, a benzo-spiro-bifluorenyl group, a dibenzofuryl group, a dibenzothiophenyl group, a carbazolyl group, a benzocarbazolyl group, and a dibenzocarbazolyl group, each of which is substituted or unsubstituted;
R T1 to R T8 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a C1-C30 alkyl group in which one or more methylene groups are independently substituted by —O— and/or —S— in a manner that O atom and/or S atom are not adjacent to each other, a substituted or unsubstituted C7-C30 arylalkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C3-C30 heteroaryl group, a substituted or unsubstituted C4-C30 heteroarylalkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C3-C30 heterocycloalkyl group, a substituted or unsubstituted C3-C30 cycloalkenyl group, a substituted or unsubstituted C1-C30 alkoxy group, and a substituted or unsubstituted C6-C30 aryloxy group;
R T1 to R T8 are present individually without forming a ring, or any adjacent two of R T1 to R T8 joined to form a ring B, and the ring B is a substituted or unsubstituted C6-C30 aromatic ring.
4 . The organic material composition according to claim 1 , wherein in Formula 1, R is selected from a phenyl group and a biphenylyl group, each of which is substituted or unsubstituted;
at least one of R 1 , R 2 , R 3 and R 4 is hydrogen;
when R 1 , R 2 , R 3 or R 4 is not hydrogen, L 1 to L 4 are each independently selected from a bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted naphthylene group, a substituted or unsubstituted biphenylene group, and a substituted or unsubstituted terphenylene group; and
at least one of Ar 1 to Ar 4 is a group represented by Formula b, and Formula b is any one selected from b-1, b-2, b-3, b-4, b-5 and b-6 as below:
R T1 to R T8 are each independently selected from hydrogen, deuterium, and a group selected from a methyl group, an ethyl group, a tert-butyl group, an adamantly, a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenanthryl group, an anthryl group, a triphenylenylene group, a phenylnaphthyl group, a naphthylphenyl group, a pyridyl group, a bipyridyl group, a dibenzofuryl group, a dibenzothiophenyl group, a benzonaphthofuryl group, a benzonaphthothiophenyl group, a dinaphthofuryl group, a dinaphthothiophenyl group, a dibenzofurylphenyl group, a dibenzothiophenylphenyl group, a dimethylfluorenyl group, a benzodimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, and a dimethylfluorenylphenyl group, each of which is substituted or unsubstituted;
Ar 1 to Ar 4 are each independently selected from hydrogen, deuterium, and a group selected from a phenyl group, a naphthyl group, a biphenylyl group, a terphenylyl group, a phenanthryl group, a fluoranthenyl group, a triphenylenylene group, a dimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, a benzodimethylfluorenyl group, a benzodiphenylfluorenyl group, a benzo-spiro-bifluorenyl group, a dibenzofuryl group, a dibenzothiophenyl group, a carbazolyl group, a benzocarbazolyl group, and a dibenzocarbazolyl group, each of which is substituted or unsubstituted.
5 . The organic material composition according to claim 1 , wherein the compound having a structure represented by Formula 1 is selected from the following compounds:
6 . The organic material composition according to claim 1 , wherein the group represented by Formula 3 is any one selected from the following groups:
R W1 and R W2 are each independently selected from a methyl group and a phenyl group; or R W1 and R W2 joined to form a spiro ring;
R Y1 -R Y8 are each independently selected from hydrogen, deuterium, and a group selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenylnaphthyl group, a naphthylphenyl group, an anthryl group, a phenanthryl group, a benzophenanthryl group, a pyridyl group, a dibenzofuryl group, a dibenzothiophenyl group, a dibenzofurylphenyl group, a dibenzothiophenylphenyl group, a dimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, a benzonaphthofuryl group, and a benzonaphthothiophenyl group, each of which is substituted or unsubstituted; R Y1 to R Y8 are present individually without forming a ring, or any adjacent two of R Y1 to R Y8 joined to form a ring A, and the ring A is a substituted or unsubstituted benzene ring;
L Y1 , L Y2 , L Y3 , L Y4 , L Y5 and L Y6 are each independently selected from a bond, a phenylene group, a biphenylene group, and a naphthylene group.
7 . The organic material composition according to claim 1 , wherein the compound having a structure represented by Formula 2-1 is selected from the compounds shown as below:
and the compound having a structure represented by Formula 1 and the compound having a structure represented by Formula 2-1 have a weight ratio of 1:9 to 9:1.
8 . The organic material composition according to claim 7 , wherein the compound having a structure represented by Formula 1 and the compound having a structure represented by Formula 2-1 have a weight ratio of 4:6 to 6:4.
9 . An organic electroluminescence material, wherein the organic electroluminescence material comprises the organic material composition according to claim 1 .
10 . A method for preparing an optical element comprising an emitting layer, the method comprising: co-depositing a light-emitting host material and a guest material to form the emitting layer; wherein the light-emitting host material comprises the organic material composition according to claim 1 , and the guest material comprises a phosphorescence dopant.
11 . An organic electroluminescence element, wherein the organic electroluminescence element comprises an anode, a cathode and an organic layer disposed between the anode and the cathode; and the organic layer comprises the organic material composition according to claim 1 .
12 . An electronic device, wherein the electronic device comprises the organic electroluminescence element according to claim 11 .