CN109180569A - A kind of compound and its organic luminescent device of the class formation containing pyrene - Google Patents
A kind of compound and its organic luminescent device of the class formation containing pyrene Download PDFInfo
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- CN109180569A CN109180569A CN201811118271.1A CN201811118271A CN109180569A CN 109180569 A CN109180569 A CN 109180569A CN 201811118271 A CN201811118271 A CN 201811118271A CN 109180569 A CN109180569 A CN 109180569A
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Abstract
The invention discloses the compounds and its organic luminescent device of a kind of class formation containing pyrene, a kind of compound for class formation containing pyrene that pyrene ring structure is formed in conjunction with fluorenes alkenyl group, on the one hand, possess extensible three-dimensional structure, so that this kind of compound has certain distortion on stereoeffect, its film forming is improved；On the other hand, pyrene ring structure triplet with higher and wider energy gap show the blue light performance haveing excellent performance, it is connected with the fluorenes alkene of electron-withdrawing energy, green light or feux rouges are issued after red shift.Moreover, this compound has suitable HOMO and LUMO value, and it is effective to stop transmission of the hole to electron transfer layer, it effectively shines to improve it.It is applied to organic luminescent device, is used as luminescent layer or hole blocking layer, device shows the advantage that driving voltage is low, luminous efficiency is high.
Description
Technical field
The present invention relates to the compounds of organic photoelectrical material technical field more particularly to a kind of class formation containing pyrene and its organic
Luminescent device.
Background technique
Organic electroluminescent LED (Organic Light Emitting Diode, OLED) is to utilize electrons and holes
The recombination luminescence in organic film and the luminescent device prepared, have the advantage that (1) from main light emission, does not need backlight；
(2) brightness is high, there is high contrast, pure in colour, the problem of almost without visible angle；(3) ultra-thin, by very thin organic
Material coating and basis material are constituted, small in size to be suitable for portable product；(4) power consumption is very small, environmental protection and energy saving；(5) it rings
It answers speed fast, is the one thousandth of LCD；(6) use temperature range is wide, remains to normally show at -40 DEG C.
Electroluminescent organic material is constantly realized in recent years to be broken through, and the progress to attract people's attention is achieved, to traditional
Display material constitutes strong challenge.After flexible OLED commercialization, associated scientific research and business in the world at present
Strength is all in the work for the development this respect done one's utmost.Although electroluminescent organic material research have been achieved with it is huge at
Fruit, but there are also some urgent problems to be solved during commercialized by OLED.
It is adjusted so how to design the better electroluminescent organic material of new performance, is always art technology
Personnel's urgent problem to be solved.
Summary of the invention
The object of the present invention is to provide the compounds and its organic luminescent device of a kind of class formation containing pyrene.It is provided by the invention
The compound thermal stability of the class formation containing pyrene is high, glass transition temperature is high, is not easy to crystallize, which is used for hole blocking layer
Or manufactured organic luminescent device in luminescent layer, the advantage that driving voltage is low, luminous efficiency is high is shown, is function admirable
Luminous organic material.
The present invention provides a kind of compounds of class formation containing pyrene, and general formula of molecular structure is as shown in I-1:
Wherein, Ar1、Ar2It is independent to be selected from hydrogen, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C3~
C30One of heteroaryl, the two simultaneously for hydrogen and at least one be selected from following group:
In formula, RaSelected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl,
Substituted or unsubstituted C3~C30One of heteroaryl；L is selected from singly-bound, substituted or unsubstituted C6~C30Aryl in
It is a kind of；X is selected from structure as follows:
In formula, Y is selected from CN, CF3、C2F5Or NO2；RbSelected from CN, CF3、C2F5、NO2, substituted or unsubstituted C6~C30Virtue
Base, substituted or unsubstituted C3~C30One of heteroaryl；
* binding site is represented.
Preferably, the general formula of molecular structure is as follows:
Wherein, R is selected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl, take
Generation or unsubstituted C3~C30One of heteroaryl.
Further preferably, the RbSelect structure as follows:
R1~R7Independent one in hydrogen, halogen atom, cyano, nitro, trifluoromethyl, pentafluoroethyl group, pentafluorophenyl group
Kind；
* binding site is represented.
Preferably, the X is selected from C (CN)2、NCN、C(NO2)2、(CF3)C(CN)、(NO2)C(CN)、C(CF3)2Or it is as follows
Shown in structure:
* binding site is represented.
Preferably, X is selected from C (CN)2, NCN or structure as follows:
* binding site is represented.
Preferably, the R be selected from hydrogen, methyl, ethyl, isopropyl, tert-butyl, substituted or unsubstituted phenyl, substitution or
Unsubstituted naphthalene, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, takes substituted or unsubstituted anthryl
Generation or unsubstituted acridinyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted carbazyl, substituted or unsubstituted pyrene
Base, substituted or unsubstituted pyridyl group, substituted or unsubstituted triazine radical, substituted or unsubstituted thienyl, substitution do not take
The furyl in generation, substituted or unsubstituted benzothienyl, substituted or unsubstituted benzofuranyl, substituted or unsubstituted two
One of benzothienyl, substituted or unsubstituted dibenzofuran group；L is selected from singly-bound, substituted or unsubstituted phenyl, takes
Generation or unsubstituted naphthalene, substituted or unsubstituted anthryl, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene
One of base, substituted or unsubstituted fluorenyl, substituted or unsubstituted pyrenyl.
Most preferably, any one of the specific structure in chemical structure as follows:
The present invention also provides a kind of organic luminescent device, including first electrode, second electrode and it is placed in two electrode
Between one or more organic compound layers, the organic compound layer contains a kind of described in any item class formations containing pyrene
Compound.
Preferably, organic compound layer includes luminescent layer, and a kind of chemical combination of class formation containing pyrene is contained in luminescent layer
Object.
Preferably, organic compound layer includes hole blocking layer, contains one kind knot of class containing pyrene in hole blocking layer
The compound of structure.
Beneficial effects of the present invention:
The present invention provides a kind of compounds of class formation containing pyrene, on the one hand, pyrene ring structure is because of its higher triplet state energy
Grade and wider energy gap, show the luminescent properties haveing excellent performance.On the one hand, fluorenes alkenyl group is the space structure of 3 D stereo,
It can effectively prevent intermolecular aggregation, it made to be not easy to crystallize；Connection one is that class has electrophilic group in fluorenes alkene double bond,
Such as fluorine, cyano, trifluoromethyl make the electronic transmission performance of structure increase.
On the other hand, a kind of compound for class formation containing pyrene that pyrene ring structure is formed in conjunction with fluorenes alkenyl group, not only possesses
Extensible three-dimensional structure improves its film forming so that this kind of compound has certain distortion on stereoeffect；And
The excellent pyrene ring of luminescent properties is connected with the fluorenes alkene of electron-withdrawing energy, and green light or feux rouges are issued after red shift.In addition, the compound has
There is suitable HOMO and LUMO value, effective to stop transmission of the hole to electron transfer layer, hole and electronics meet in luminescent layer,
It effectively shines to improve it.
It is applied to organic luminescent device, is used as luminescent layer or hole blocking layer, device shows driving voltage
Advantage low, luminous efficiency is high is better than existing common OLED device, when it is both electron transport material and hole barrier materials
When, making devices process is convenient, saves material to save cost.The good application effect shown in OLED luminescent device
Fruit, this point show it with good industrialization prospect.
Specific embodiment:
It is clearly and completely described below in conjunction with the technical solution of the embodiment of the present invention, it is clear that described implementation
Example is only a part of the embodiment of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, art technology
Personnel's every other embodiment obtained without making creative work, belongs to protection scope of the present invention.
Alkyl of the present invention refers to alkyl made of minusing a hydrogen atom in alkane molecule, can be straight chain alkane
Base, branched alkyl, naphthenic base, example may include methyl, ethyl, propyl, isopropyl, normal-butyl, isobutyl group, sec-butyl, tertiary fourth
Base, amyl, isopentyl, cyclopenta, cyclohexyl etc., but not limited to this.
Aryl of the present invention refers to remove a hydrogen atom on the aromatic core carbon of aromatic hydrocarbon molecule after, be left the total of univalent perssad
Claiming, can be monocyclic aryl or fused ring aryl, example may include phenyl, xenyl, naphthalene, anthryl, phenanthryl or pyrenyl etc., but
It is without being limited thereto.
Heteroaryl of the present invention refers to the group that one or more aromatic core carbon in aryl are substituted by hetero atom
General name, the hetero atom include but is not limited to oxygen, sulphur or nitrogen-atoms, and the heteroaryl can be bicyclic heteroaryl or condensed ring heteroaryl
Base, example may include pyridyl group, pyrrole radicals, pyridyl group, thienyl, furyl, indyl, quinolyl, isoquinolyl, benzo thiophene
Pheno base, benzofuranyl, dibenzofuran group, dibenzothiophene, carbazyl etc., but not limited to this.
The present invention provides a kind of compounds of class formation containing pyrene, and general formula of molecular structure is as shown in I-1:
Wherein, Ar1、Ar2It is independent to be selected from hydrogen, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C3~
C30One of heteroaryl, the two simultaneously for hydrogen and at least one be selected from following group:
In formula, RaSelected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl,
Substituted or unsubstituted C3~C30One of heteroaryl, it is preferred that RaSelected from hydrogen, methyl, ethyl, isopropyl, tert-butyl,
Substituted or unsubstituted phenyl, substituted or unsubstituted naphthalene, substituted or unsubstituted anthryl, substituted or unsubstituted phenanthryl,
It is substituted or unsubstituted triphenylene, substituted or unsubstituted acridinyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted
Carbazyl, substituted or unsubstituted pyrenyl, substituted or unsubstituted pyridyl group, substituted or unsubstituted triazine radical, substitution or not
Substituted thienyl, substituted or unsubstituted furyl, substituted or unsubstituted benzothienyl, substituted or unsubstituted benzo
One of furyl, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted dibenzofuran group；L is selected from single
Key, substituted or unsubstituted C6~C30One of aryl；X is selected from structure as follows:
In formula, Y is selected from CN, CF3、C2F5Or NO2；RbSelected from CN, CF3、C2F5、NO2, substituted or unsubstituted C6~C30Virtue
Base, substituted or unsubstituted C3~C30One of heteroaryl；
* binding site is represented.
According to the present invention, the substituted alkyl, substituted aryl, substituted heterocycle, the independent choosing of substituent group
From methyl, ethyl, isopropyl, tert-butyl, phenyl, naphthalene, anthryl, phenanthryl, benzo phenanthryl, base, pyrenyl, benzyl, methoxy
Base, methyl mercapto, phenoxy group, thiophenyl, fluorenyl, 9,9- dimethyl fluorenyl, hexichol amido, dimethylamino, carbazyl, 9- phenyl click
Oxazolyl, furyl, thienyl, cyano, fluorine-based, deuterium base, triphenyl silicon substrate, trimethyl silicon substrate, phenothiazinyl, phenoxazine base, a word used for translation
Piperidinyl, piperidyl, pyridyl group, pyrimidine radicals, xenyl, terphenyl, nitro etc., but not limited to this.
Preferably, its described general formula of molecular structure is as follows:
Wherein, R is selected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl, take
Generation or unsubstituted C3~C30One of heteroaryl.
Preferably, the RbSelect structure as follows:
R1~R7Independent one in hydrogen, halogen atom, cyano, nitro, trifluoromethyl, pentafluoroethyl group, pentafluorophenyl group
Kind；
* binding site is represented.
Preferably, X is selected from C (CN)2、NCN、C(NO2)2、(CF3)C(CN)、(NO2)C(CN)、C(CF3)2Or it is as follows
Structure:
* binding site is represented.
Preferably, the X is selected from C (CN)2, NCN or structure as follows:
* binding site is represented.
Preferably, the R be selected from hydrogen, methyl, ethyl, isopropyl, tert-butyl, substituted or unsubstituted phenyl, substitution or
Unsubstituted naphthalene, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, takes substituted or unsubstituted anthryl
Generation or unsubstituted acridinyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted carbazyl, substituted or unsubstituted pyrene
Base, substituted or unsubstituted pyridyl group, substituted or unsubstituted triazine radical, substituted or unsubstituted thienyl, substitution do not take
The furyl in generation, substituted or unsubstituted benzothienyl, substituted or unsubstituted benzofuranyl, substituted or unsubstituted two
One of benzothienyl, substituted or unsubstituted dibenzofuran group；L is selected from singly-bound, substituted or unsubstituted phenyl, takes
Generation or unsubstituted naphthalene, substituted or unsubstituted anthryl, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene
One of base, substituted or unsubstituted fluorenyl, substituted or unsubstituted pyrenyl.
Further preferably, the compound of a kind of class formation containing pyrene, specific structure is in chemical structure as follows
Any one:
A kind of compound of class formation containing pyrene of the invention, specific synthetic route are as follows:
Wherein, Ar1、Ar2It is independent to be selected from hydrogen, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C3~
C30One of heteroaryl, the two simultaneously for hydrogen and at least one be selected from following group:
In formula, RaSelected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl,
Substituted or unsubstituted C3~C30One of heteroaryl；L is selected from singly-bound, substituted or unsubstituted C6~C30Aryl in
It is a kind of；X is selected from structure as follows:
In formula, Y is selected from CN, CF3、C2F5Or NO2；RbSelected from CN, CF3、C2F5、NO2, substituted or unsubstituted C6~C30Virtue
Base, substituted or unsubstituted C3~C30One of heteroaryl；
* binding site is represented.
Above-mentioned synthesis is to be coupled to obtain target product I-1 via a series of C-C using hypoboric acid pyrene as starting material, is recommended
Using Suzuki coupling reaction, under nitrogen protection, using tetra-triphenylphosphine palladium as catalyst, potassium carbonate is alkali, and tetrahydrofuran is molten
Agent, reflux are reacted.If intermediate has and sells, can be directly used for reacting.
The present invention does not have special limitation to coupling reaction, is using popular response well-known to those skilled in the art
Can, the preparation method is easy to operate, is readily produced.
The present invention also provides a kind of organic luminescent device, including first electrode, second electrode and it is placed in two electrode
Between one or more organic compound layers, organic compound layer include hole injection layer, hole transmission layer, electronic blocking
At least one layer of layer, luminescent layer, hole blocking layer, electron transfer layer, electron injecting layer；At least one in the organic compound layer
Layer includes a kind of compound of the class formation containing pyrene of the present invention.
Preferably, a kind of compound of class formation containing pyrene can be used as the hole barrier material in organic luminescent device
Material.The device architecture of use is preferred specifically: and NPB-DPA is used as hole injection layer substance, and NPB is used as hole transmission layer substance,
ADN is used as main substance, and DPAVBi is used as dopant, and a kind of compound of class formation containing pyrene is used as hole barrier object
Matter, Alq3As electron transfer layer substance, to manufacture the organic luminescent device of construction same as below: ITO/NPB-DPA/
A kind of compound/Alq of class formation containing pyrene of NPB/ADN:DPAVBi (doping concentration 2wt%)/described3/LiF/Al。
Preferably, a kind of compound of class formation containing pyrene can be used as the master in the luminescent layer in organic luminescent device
Body substance.The device architecture of use is preferred specifically: NPB-DPA is used as hole injection layer substance, and NPB is used as hole transmission layer object
Matter, a kind of compound of class formation containing pyrene are used as main substance, and DPAVBi is used as dopant, Alq3It is passed as electronics
Defeated layer substance, to manufacture the organic luminescent device of construction same as below: one kind described in ITO/NPB-DPA/NPB/ contains pyrene
The compound of class formation: DPAVBi (doping concentration 2wt%)/Alq3/LiF/Al。
Wherein, the preparation method of any organic layer can be vapor deposition, spin coating or inkjet printing in organic electroluminescence device,
It is without being limited thereto.The organic electroluminescence device can be used for the application neck such as flat-panel monitor, lighting source, direction board, signal lamp
Domain.
The synthesis of [embodiment 1] compound 1
The synthesis of compound a 1
Into 250mL twoport flask be added 200mLDMF (dimethylformamide), be then added five fluorine pyridines (17.5g,
103.5mmol), potassium carbonate (17.2g, 124.3mmol) and ethyl cyanoacetate (11.7g, 103.5mmol), stir 48 at room temperature
Hour.Distilled water and acetic acid is added dropwise into mixture to terminate reaction, is then extracted with dichloromethane, merges and dry organic
Phase, concentration, recrystallizes to obtain compound a 1 (24.4g, yield 90%).
Mass spectrum m/z:262.12 (calculated value: 262.16).Theoretical elemental content (%) C10H6F4N2O2: C, 45.81；H,
2.31；F,28.99；N,10.69；O, 12.21 actual measurement constituent content (%): C, 45.81；H,2.31；F,28.99；N,10.67；
O,12.22.The above results confirm that obtaining product is target product.
The synthesis of compound b1
It is bis- that compound a 1 (26.7g, 102.4mmol), 50% acetic acid (42mL) and sulfuric acid (2.08mL) are added to 250mL
In mouth flask, it is stirred at reflux 16 hours.Reaction system is cooled to room temperature, 60mL cold distilled water is added dropwise to terminate reaction, then
Continue stirring 30 minutes.Reaction mixture is extracted with chloroform, merges and dry organic phase, is concentrated to get solid, i.e. compound
B1 (17.5g, 90%).
Mass spectrum m/z:190.12 (calculated value: 190.10).Theoretical elemental content (%) C7H2F4N2: C, 44.23；H,1.06；
F,39.98；N, 14.74 actual measurement constituent content (%): C, 44.25；H,1.05；F,39.97；N,14.73.The above results confirmation obtains
Obtaining product is target product.
The synthesis of compound c1
Into 250mL round-bottomed flask be added compound b1 (1.9g, 10mmol), the bromo- 9H- Fluorenone of 2- (2.6g,
10.1mmol), sodium ethoxide (2.0g, 30mmol) and 100ml ethyl alcohol, then heating stirring.After reaction terminates, add into system
Enter tetrahydrofuran dilution, extracted after water is added, collects organic phase, remove moisture through anhydrous magnesium sulfate, then filtration residue exists
The lower concentration of decompression, recrystallizes with prepare compound c1 (2.8g, yield 65%).
Mass spectrum m/z:431.12 (calculated value: 431.18).Theoretical elemental content (%) C20H7BrF4N2: C, 55.71；H,
1.64；Br,18.53；F,17.62；N, 6.50 actual measurement constituent content (%): C, 55.73；H,1.61；Br,18.52；F,17.62；
N,6.52.The above results confirm that obtaining product is target product.
The synthesis of compound 1
Tetra-triphenylphosphine palladium (2.1g, 1.83mmol) and potassium carbonate (75.7g, 549mmol) are added to 2- pyrene boric acid
The solution of (46.0g, 187mmol) and compound c1 (78.8g, 183mmol) in degassing tetrahydrofuran (500mL), and will
The mixture heats 4 hours under reflux.It filters while hot, obtains a large amount of solids, with solvent dissolved solid, be concentrated later, via
Silica gel column chromatography obtains compound 1 (60.6g, yield 60%).
Mass spectrum m/z:552.55 (calculated value: 552.52).Theoretical elemental content (%) C36H16F4N2: C, 78.26；H,
2.92；F,13.75；N, 5.07 actual measurement constituent content (%): C, 78.25；H,2.92；F,13.75；N,5.08.The above results card
The real product that obtains is target product.
The synthesis of [embodiment 2] compound 13
Change five fluorine pyridines in embodiment 1 into equimolar cyanuric fluoride, other steps with the synthesis phase of embodiment 1
Together, target product compound 13 is obtained.Mass spectrum m/z:518.56 (calculated value: 518.51).Theoretical elemental content (%)
C34H16F2N4: C, 78.76；H,3.11；F,7.33；N, 10.81 actual measurement constituent content (%): C, 78.75；H,3.11；F,7.33；
N,10.82.The above results confirm that obtaining product is target product.
The synthesis of [embodiment 3] compound 18
Change the compound b1 in embodiment 1 into equimolar 2- (perfluorophenyl) acetonitrile, other steps with embodiment 1
Synthesis it is identical, obtain target product compound 18.Mass spectrum m/z:569.56 (calculated value: 569.52).Theoretical elemental content
(%) C37H16F5N:C, 78.03；H,2.83；F,16.68；N, 2.46 actual measurement constituent content (%): C, 78.04；H,2.84；F,
16.65；N,2.47.The above results confirm that obtaining product is target product.
The synthesis of [embodiment 4] compound 19-1
Change the compound b1 in embodiment 1 into equimolar 4- (cyanogen methyl) -2,3,5,6,-tetrafluoro benzonitrile, 2- pyrene
Boric acid changes equimolar 1- pyrene boric acid into, other steps are identical as the synthesis of embodiment 1, obtains target product compound 19-
1.Mass spectrum m/z:576.56 (calculated value: 576.54).Theoretical elemental content (%) C38H16F4N2: C, 79.16；H,2.80；F,
13.18；N, 4.86 actual measurement constituent content (%): C, 79.17；H,2.82；F,13.15；N,4.86.The above results confirmation is produced
Object is target product.
The synthesis of [embodiment 5] compound 25-1
The synthesis of compound c2
Into 250mL round-bottomed flask be added malononitrile (0.66g, 10mmol), the bromo- 9H- Fluorenone of 2- (2.6g,
10.1mmol), sodium ethoxide (2.0g, 30mmol) and 100ml ethyl alcohol, then heating stirring.After reaction terminates, add into system
Enter tetrahydrofuran dilution, extracted after water is added, collects organic phase, remove moisture through anhydrous magnesium sulfate, then filtration residue exists
The lower concentration of decompression, recrystallizes with prepare compound c2 (2.1g, yield 70%).
Mass spectrum m/z:307.12 (calculated value: 307.14).Theoretical elemental content (%) C16H7BrN2: C, 62.57；H,
2.30；Br,26.02；N, 9.12 actual measurement constituent content (%): C, 55.73；H,1.61；Br,18.52；F,17.62；N,6.52.
The above results confirm that obtaining product is target product.
The synthesis of compound d1
Tetra-triphenylphosphine palladium (2.1g, 1.83mmol) and potassium carbonate (75.7g, 549mmol) are added to 1- pyrene boric acid
(46.0g, 187mmol) and to bromo-iodobenzene (51.6g, 183mmol) degassing tetrahydrofuran (500mL) in solution, and will
The mixture heats 4 hours under reflux.It filters while hot, obtains a large amount of solids, with solvent dissolved solid, be concentrated later, via
Silica gel column chromatography obtains compound d1 (39.2g, yield 60%).
Mass spectrum m/z:357.25 (calculated value: 357.24).Theoretical elemental content (%) C22H13Br:C, 73.97；H,3.67；
Br, 22.37 actual measurement constituent content (%): C, 73.98；H,3.63；Br,22.39.The above results confirm to obtain product as target production
Product.
The synthesis of compound e1
The addition 100mL THF into the there-necked flask equipped with compound d1 (15.1g, 42.4mmol), nitrogen protection, -78 DEG C
Then 21mL n-BuLi (2.5M) is added in stirring 30 minutes, react 1 hour, add triisopropyl borate ester 14g, low temperature is anti-
It answers 1 hour, is gradually recovered room temperature.Last handling process, 2M hydrochloric acid is added in system makes solution pH value 4-5, standing liquid separation, water layer
It is extracted with ethyl acetate, merges organic layer, be spin-dried for, obtain compound e1 (10.9g, yield 80%).
The synthesis of compound 25-1
Tetra-triphenylphosphine palladium (2.1g, 1.83mmol) and potassium carbonate (75.7g, 549mmol) are added to compound e1
The solution of (60.2g, 187mmol) and compound c2 (56.2g, 183mmol) in degassing tetrahydrofuran (500mL), and will
The mixture heats 4 hours under reflux.It filters while hot, obtains a large amount of solids, with solvent dissolved solid, be concentrated later, via
Silica gel column chromatography obtains compound 25-1 (73.8g, yield 80%).
Mass spectrum m/z:504.55 (calculated value: 504.58).Theoretical elemental content (%) C38H20N2: C, 90.45；H,4.00；
N, 5.55 actual measurement constituent content (%): C, 90.44；H,4.03；N,5.53.The above results confirm that obtaining product is target product.
The synthesis of [embodiment 6] compound 35-1
Change the malononitrile in embodiment 5 into equimolar 4- (cyanogen methyl) -2,3,5,6,-tetrafluoro benzonitrile, to bromine iodine
Benzene changes the bromo- 10- iodine anthracene of equimolar 9- into, other steps are identical as the synthesis of embodiment 5, obtain target product compound
35-1.Mass spectrum m/z:752.76 (calculated value: 752.75).Theoretical elemental content (%) C52H24F4N2: C, 82.97；H,3.21；F,
10.10；N, 3.72 actual measurement constituent content (%): C, 82.96；H,3.21；F,10.11；N,3.72.The above results confirmation is produced
Object is target product.
The synthesis of [embodiment 7] compound 17-2
Changing the compound b1 in embodiment 1 into equimolar the third two eyeball, 2- pyrene boric acid changes equimolar 4- pyrene boric acid into,
Other steps are identical as the synthesis of embodiment 1, obtain target product compound 17-2.Mass spectrum m/z:428.56 (calculated value:
428.48).Theoretical elemental content (%) C32H16N2: C, 89.70；H,3.76；N, 6.54 actual measurement constituent content (%): C, 89.72；
H,3.75；N,6.53.The above results confirm that obtaining product is target product.
The synthesis of [embodiment 8] compound 19-2
Change the compound b1 in embodiment 1 into equimolar 4- (cyanogen methyl) -2,3,5,6,-tetrafluoro benzonitrile, 2- pyrene
Boric acid changes equimolar 4- pyrene boric acid into, other steps are identical as the synthesis of embodiment 1, obtains target product compound 19-
2.Mass spectrum m/z:576.56 (calculated value: 576.54).Theoretical elemental content (%) C38H16F4N2: C, 79.16；H,2.80；F,
13.18；N, 4.86 actual measurement constituent content (%): C, 79.15；H,2.81；F,13.17；N,4.87.The above results confirmation is produced
Object is target product.
The synthesis of [embodiment 9] compound 50
The synthesis of compound c3
4- (cyanogen methyl) -2,3,5,6,-tetrafluoro benzonitrile (2.1g, 10mmol), 2- are added into 250mL round-bottomed flask
Bromo- 9H- Fluorenone (2.6g, 10.1mmol), sodium ethoxide (2.0g, 30mmol) and 100ml ethyl alcohol, then heating stirring.Reaction knot
After beam, tetrahydrofuran dilution is added into system, is extracted after water is added, collects organic phase, removes moisture through anhydrous magnesium sulfate,
Then filtration residue is concentrated under reduced pressure, recrystallize with prepare compound c3 (3.2g, yield 70%).
Mass spectrum m/z:455.12 (calculated value: 455.20).Theoretical elemental content (%) C16H7BrN2: C, 58.05；H,
1.55；Br,17.55；F,16.69；N, 6.15 actual measurement constituent content (%): C, 58.05；H,1.56；Br,17.55；F,16.67；
N,6.16.The above results confirm that obtaining product is target product.
The synthesis of compound 50
Tetra-triphenylphosphine palladium (2.1g, 1.83mmol) and potassium carbonate (75.7g, 549mmol) are added to 1,6- pyrene, two boron
The solution of sour (53.1g, 183mmol) and compound c3 (174.7g, 384mmol) in degassing tetrahydrofuran (500mL), and
The mixture is heated 4 hours under reflux.It filters while hot, obtains a large amount of solids, with solvent dissolved solid, be concentrated later, pass through
Compound 50 (130.4g, yield 75%) is obtained by silica gel column chromatography.
Mass spectrum m/z:950.85 (calculated value: 950.83).Theoretical elemental content (%) C60H22F8N4: C, 75.79；H,
2.33；F,15.98；N, 5.89 actual measurement constituent content (%): C, 75.77；H,2.34；F,15.99；N,5.89.The above results card
The real product that obtains is target product.
The synthesis of [embodiment 10] compound 71
The synthesis of compound c4
4- (cyanogen methyl) -2,3,5,6,-tetrafluoro benzonitrile (2.1g, 10mmol), 2,7- are added into 250mL round-bottomed flask
Two bromo- 9H- Fluorenones (3.4g, 10.1mmol), sodium ethoxide (2.0g, 30mmol) and 100ml ethyl alcohol, then heating stirring.Reaction
After end, tetrahydrofuran dilution is added into system, is extracted after water is added, collects organic phase, removes water through anhydrous magnesium sulfate
Point, then filtration residue is concentrated under reduced pressure, recrystallize with prepare compound c4 (3.2g, yield 70%).
Mass spectrum m/z:534.12 (calculated value: 534.10).Theoretical elemental content (%) C22H6Br2N2: C, 49.47；H,
1.13；Br,29.92；F,14.23；N, 5.24 actual measurement constituent content (%): C, 49.47；H,1.13；Br,29.91；F,14.23；
N,5.25.The above results confirm that obtaining product is target product.
The synthesis of compound 71
Tetra-triphenylphosphine palladium (2.1g, 1.83mmol) and potassium carbonate (75.7g, 549mmol) are added to 2- pyrene boric acid
The solution of (94.5g, 384mmol) and compound c4 (97.7g, 183mmol) in degassing tetrahydrofuran (500mL), and will
The mixture heats 4 hours under reflux.It filters while hot, obtains a large amount of solids, with solvent dissolved solid, be concentrated later, via
Silica gel column chromatography obtains compound 71 (99.4g, yield 70%).
Mass spectrum m/z:776.75 (calculated value: 776.78).Theoretical elemental content (%) C54H24F4N2: C, 83.50；H,
3.11；F,9.78；N, 3.61 actual measurement constituent content (%): C, 83.52；H,3.11；F,9.74；N,3.62.The above results confirm
Acquisition product is target product.
[comparison Application Example]
Transparent anode electrode ito substrate is cleaned by ultrasonic 15 minutes in isopropanol, and exposure 30 minutes under ultraviolet light,
Then handled 10 minutes with plasma.Then by treated, ito substrate is put into evaporated device.The 2- of one layer of 10nm is deposited first
Then TNATA is deposited the NPB of one layer of 40nm as hole transmission layer, steams as hole injection layer, evaporation rate 0.1nm/s
Plating rate is 0.1nm/s, then is the vapor deposition of luminescent layer, mixing vapor deposition CBP/Ir (PPy)3, doping concentration 5wt%, vapor deposition speed
Rate is 0.005nm/s, evaporation thickness 30nm, and the Alq of 50nm is then deposited3As electron transfer layer, evaporation rate is
0.1nm/s, successively vacuum evaporation LiF and Al is as cathode on the electron transport layer, with a thickness of 200nm.
[Application Example 1]
Transparent anode electrode ito substrate is cleaned by ultrasonic 15 minutes in isopropanol, and exposure 30 minutes under ultraviolet light,
Then handled 10 minutes with plasma.Then by treated, ito substrate is put into evaporated device.The 2- of one layer of 10nm is deposited first
Then TNATA is deposited the NPB of one layer of 40nm as hole transmission layer, steams as hole injection layer, evaporation rate 0.1nm/s
Plating rate is 0.1nm/s, then is the vapor deposition of luminescent layer, mixing vapor deposition compound 1/Ir (PPy)3, doping concentration 5wt%, steaming
Plating rate is 0.005nm/s, evaporation thickness 30nm, and the Alq of 50nm is then deposited3As electron transfer layer, evaporation rate is
0.1nm/s, successively vacuum evaporation LiF and Al is as cathode on the electron transport layer, with a thickness of 200nm.
[Application Example 2]
Change the main substance in 1 luminescent layer of Application Example into compound 13.
[Application Example 3]
Change the main substance in 1 luminescent layer of Application Example into compound 18.
[Application Example 4]
Change the main substance in 1 luminescent layer of Application Example into compound 25-1.
[Application Example 5]
Change the main substance in 1 luminescent layer of Application Example into compound 35-1.
[Application Example 6]
Change the main substance in 1 luminescent layer of Application Example into compound 17-2.
[Application Example 7]
Change the main substance in 1 luminescent layer of Application Example into compound 19-2.
[Application Example 8]
Transparent anode electrode ito substrate is cleaned by ultrasonic 15 minutes in isopropanol, and exposure 30 minutes under ultraviolet light,
Then handled 10 minutes with plasma.Then by treated, ito substrate is put into evaporated device.The 2- of one layer of 10nm is deposited first
Then TNATA is deposited the NPB of one layer of 40nm as hole transmission layer, steams as hole injection layer, evaporation rate 0.1nm/s
Plating rate is 0.1nm/s, then is the vapor deposition of luminescent layer, mixing vapor deposition CBP/Ir (PPy)3, doping concentration 5wt%, vapor deposition speed
Rate is 0.005nm/s, evaporation thickness 30nm, and the Alq of 50nm is then deposited3As electron transfer layer, evaporation rate is
0.1nm/s, then the compound 50 of 10nm is deposited as hole blocking layer, on the hole blocking layer successively vacuum evaporation LiF and Al
As cathode, with a thickness of 200nm.
[Application Example 9]
Change the hole blocking layer in Application Example 8 into compound 71.
[Application Example 10]
Change the hole blocking layer in Application Example 8 into compound 81.
[Application Example 11]
Change the hole blocking layer in Application Example 8 into compound 97.
[Application Example 12]
Change the hole blocking layer in Application Example 8 into compound 104.
[Application Example 13]
Change the hole blocking layer in Application Example 8 into compound 105.
[Application Example 14]
Transparent anode electrode ito substrate is cleaned by ultrasonic 15 minutes in isopropanol, and exposure 30 minutes under ultraviolet light,
Then handled 10 minutes with plasma.Then by treated, ito substrate is put into evaporated device.The 2- of one layer of 10nm is deposited first
Then TNATA is deposited the NPB of one layer of 40nm as hole transmission layer, steams as hole injection layer, evaporation rate 0.1nm/s
Plating rate is 0.1nm/s, then is the vapor deposition of luminescent layer, mixing vapor deposition compound 1/Ir (PPy)3, doping concentration 5wt%, steaming
Plating rate is 0.005nm/s, evaporation thickness 30nm, and the Alq of 50nm is then deposited3As electron transfer layer, evaporation rate is
0.1nm/s, then the compound 50 of 10nm is deposited as hole blocking layer, on the hole blocking layer successively vacuum evaporation LiF and Al
As cathode, with a thickness of 200nm.
[Application Example 15]
Change the hole blocking layer in Application Example 14 into compound 104.
[Application Example 16]
Change the hole blocking layer in Application Example 14 into compound 71, main substance changes compound into luminescent layer
13。
[Application Example 17]
Change the hole blocking layer in Application Example 14 into compound 104, main substance changes compound into luminescent layer
18。
The electron luminescence characteristic of the organic luminescent device of above method manufacture indicates in the following table:
The above result shows that a kind of compound of class formation containing pyrene of the invention is applied in organic luminescent device, it can be with
As hole barrier layer material or material of main part, the advantage that driving voltage is low, luminous efficiency is high is shown, is of good performance
Luminous organic material.
Obviously, the above description of the embodiment is only used to help understand the method for the present invention and its core ideas.It should refer to
It out, without departing from the principle of the present invention, can also be to this hair for the those of ordinary skill of the technical field
Bright some improvement and modification can also be carried out, and these improvements and modifications also fall within the scope of protection of the claims of the present invention.
Claims (10)
1. a kind of compound of class formation containing pyrene, which is characterized in that its general formula of molecular structure is as shown in I-1:
Wherein, Ar1、Ar2It is independent to be selected from hydrogen, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C3~C30's
One of heteroaryl, the two simultaneously for hydrogen and at least one be selected from following group:
In formula, RaSelected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl, replace or
Unsubstituted C3~C30One of heteroaryl；L is selected from singly-bound, substituted or unsubstituted C6~C30One of aryl；X
Selected from structure as follows:
In formula, Y is selected from CN, CF3、C2F5Or NO2；RbSelected from CN, CF3、C2F5、NO2, substituted or unsubstituted C6~C30Aryl takes
Generation or unsubstituted C3~C30One of heteroaryl；
* binding site is represented.
2. a kind of compound of class formation containing pyrene according to claim 1, which is characterized in that its general formula of molecular structure is as follows
It is shown:
Wherein, R is selected from hydrogen, substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C6~C30Aryl, replace or
Unsubstituted C3~C30One of heteroaryl.
3. a kind of compound of class formation containing pyrene according to claim 1, which is characterized in that RbSelect structure as follows:
R1~R7It is independent to be selected from one of hydrogen, halogen atom, cyano, nitro, trifluoromethyl, pentafluoroethyl group, pentafluorophenyl group；
* binding site is represented.
4. a kind of compound of class formation containing pyrene according to claim 1, which is characterized in that X is selected from C (CN)2、NCN、C
(NO2)2、(CF3)C(CN)、(NO2)C(CN)、C(CF3)2Or structure as follows:
* binding site is represented.
5. a kind of compound of class formation containing pyrene according to claim 1, which is characterized in that X is selected from C (CN)2, NCN or such as
Structure shown in lower:
* binding site is represented.
6. a kind of compound of class formation containing pyrene according to claim 2, which is characterized in that R be selected from hydrogen, methyl, ethyl,
Isopropyl, tert-butyl, substituted or unsubstituted phenyl, substituted or unsubstituted naphthalene, substituted or unsubstituted anthryl, substitution or
Unsubstituted phenanthryl, substituted or unsubstituted triphenylene, substituted or unsubstituted acridinyl, substituted or unsubstituted fluorenyl,
Substituted or unsubstituted carbazyl, substituted or unsubstituted pyrenyl, substituted or unsubstituted pyridyl group, substituted or unsubstituted three
Piperazine base, substituted or unsubstituted thienyl, substituted or unsubstituted furyl, substituted or unsubstituted benzothienyl, substitution
Or in unsubstituted benzofuranyl, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted dibenzofuran group
One kind；L is selected from singly-bound, substituted or unsubstituted phenyl, substituted or unsubstituted naphthalene, substituted or unsubstituted anthryl, takes
Generation or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, substituted or unsubstituted fluorenyl, substituted or unsubstituted pyrenyl
One of.
7. a kind of compound of class formation containing pyrene according to claim 1, which is characterized in that specific structure is selected from following institute
Show any one in chemical structure:
8. a kind of organic luminescent device, which is characterized in that the organic luminescent device include cathode, anode and be placed in it is described two electricity
One or more organic compound layers between pole, it is described in any item that the organic compound layer contains claim 1~7
A kind of compound of the class formation containing pyrene.
9. a kind of organic luminescent device according to claim 8, which is characterized in that the organic compound layer includes hair
Photosphere contains a kind of described in any item compounds of the class formation containing pyrene of claim 1~7 in luminescent layer.
10. a kind of organic luminescent device according to claim 9, which is characterized in that the organic compound layer includes
Hole blocking layer contains a kind of described in any item compounds of the class formation containing pyrene of claim 1~7 in hole blocking layer.
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| CN201811118271.1A Pending CN109180569A (en) | 2018-09-26 | 2018-09-26 | A kind of compound and its organic luminescent device of the class formation containing pyrene |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN109678731A (en) * | 2019-01-31 | 2019-04-26 | 北京诚志永华显示科技有限公司 | Organic compound, electroluminescent organic material, electronic equipment |
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| CN109678731A (en) * | 2019-01-31 | 2019-04-26 | 北京诚志永华显示科技有限公司 | Organic compound, electroluminescent organic material, electronic equipment |
| CN109678731B (en) * | 2019-01-31 | 2022-01-04 | 石家庄诚志永华显示材料有限公司 | Organic compound, organic electroluminescent material, and electronic device |
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