CN107778213A - One kind 1,4 2 substitutes naphthalene derivatives and application - Google Patents

One kind 1,4 2 substitutes naphthalene derivatives and application Download PDF

Info

Publication number
CN107778213A
CN107778213A CN201610730802.7A CN201610730802A CN107778213A CN 107778213 A CN107778213 A CN 107778213A CN 201610730802 A CN201610730802 A CN 201610730802A CN 107778213 A CN107778213 A CN 107778213A
Authority
CN
China
Prior art keywords
ring
phenyl
unsubstituted
substituted
nitrae
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201610730802.7A
Other languages
Chinese (zh)
Inventor
范洪涛
邢其锋
邵爽
任雪艳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Eternal Material Technology Co Ltd
Guan Eternal Material Technology Co Ltd
Original Assignee
Beijing Eternal Material Technology Co Ltd
Guan Eternal Material Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Eternal Material Technology Co Ltd, Guan Eternal Material Technology Co Ltd filed Critical Beijing Eternal Material Technology Co Ltd
Priority to CN201610730802.7A priority Critical patent/CN107778213A/en
Publication of CN107778213A publication Critical patent/CN107778213A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
    • C07C211/60—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton containing a ring other than a six-membered aromatic ring forming part of at least one of the condensed ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
    • C07C211/61—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D219/00—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
    • C07D219/02—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems with only hydrogen, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/46—Phenazines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
    • C07D265/38—[b, e]-condensed with two six-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D279/10—1,4-Thiazines; Hydrogenated 1,4-thiazines
    • C07D279/14—1,4-Thiazines; Hydrogenated 1,4-thiazines condensed with carbocyclic rings or ring systems
    • C07D279/18—[b, e]-condensed with two six-membered rings
    • C07D279/22—[b, e]-condensed with two six-membered rings with carbon atoms directly attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/72—Benzo[c]thiophenes; Hydrogenated benzo[c]thiophenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/76—Dibenzothiophenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1007—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1011—Condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C09K2211/1033—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with oxygen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C09K2211/1037—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with sulfur
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1096—Heterocyclic compounds characterised by ligands containing other heteroatoms

Abstract

The invention provides a kind of Isosorbide-5-Nitrae two to substitute naphthalene derivatives, and its general formula compound is as shown in following formula I：In formula I：R ' is selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl；Ar1Selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30Cycloalkyl, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C2~C30Heteroaryl；Ar2As shown in following formula II：In formula II：R1~R5It is each independently selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30Cycloalkyl, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C2~C30Heteroaryl, and R1~R5In at least one be not hydrogen.

Description

A kind of 1,4- bis- substitutes naphthalene derivatives and application
Technical field
The present invention relates to a kind of general formula compound with special nature, more particularly to one kind to be used for electronic device and light Learn the compound in film field.
Background technology
When incident light (the being typically ultraviolet or X ray) irradiation of certain material through certain wavelength, enter after absorbing luminous energy Excitation state, then by slow Henan and send the phenomenon of the emergent light longer than the wavelength of incident light and be called luminescence generated by light phenomenon, one As be divided into fluorescence and phosphorescence, its principle of luminosity is not quite similar.Many inorganic and organic materials all have this property, and wide General is applied to various fields, such as illumination, biochemical medical treatment, detection.Relative to inorganic material, organic material has more knots The possibility of structure optimum choice, can provide more assembled schemes, and glow color can also cover whole visible region.It is organic The glow color of molecule depends on the architectural feature of molecule in itself, and energy gap determines the glow color of molecule, can be by material The structure of material is designed, adjusts, optimized, and changes the size of its energy gap and then obtains various having with required glow color Machine material.Luminescent material can be widely used in electroluminescent, luminescence generated by light and various optical film fields.
Show and illuminate for OLED, development of the blue light material for OLED is always a bottleneck, and one side blue light is Indispensable part in display and lighting engineering, it is not high on the other hand also to receive conventional fluorescent material efficiency, blueness Although phosphor material efficiency high, less stable, while also lack dark blue luminescent material system.Fluorescence blue light material has very Good stability and quantity is more, and the emerging production of light extraction protects a series of blue light dyestuffs using pyrene as precursor structure, is shown below Blue light material, accompanying drawing 1 shows that the CIE coordinates of device of the blue light material are (0.14,0.25), is the pretty good day of a performance Blue light dyestuff.But dark blue luminescent material strengthens the whole structure tool of device for reducing display and the energy expenditure of illuminating device There is very important effect, and efficient dark blue luminescent material is relatively fewer.Therefore it is significant to develop such material.
The content of the invention
To solve the above problems, the present invention provides a kind of new general formula compound, general formula compound of the invention design is adopted By the use of Isosorbide-5-Nitrae-two substitute naphthalene structure be used as parent nucleus, its protrusion the advantages of be：Firstly, since α-H presence and arylamine on naphthalene nucleus The presence of big steric group on substituent, it can greatly change the three arylamine groups (including parent naphthyl) being connected with nitrogen-atoms Between and the conjugation with nitrogen-atoms lone electron pair, i.e., effectively interrupted the conjugation between group, a target will be played The purpose of the Absorption and emission spectra blue shift (reaching 450nm or so) of compound, so that it is guaranteed that obtaining sending the material of deeper blue light Material.Secondly, exactly because the presence of big steric group, can effectively weaken the rotation and vibration of intramolecular, so as at reduction In the heat Henan approach late of excited state molecule, the beneficial effect of the fluorescence quantum efficiency of reinforcing material can be obtained.
Shown in the general formula compound such as following formula (I) of the present invention：
In formula (I), R ' is independently selected from from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, preferably C1~C10Alkane Base, more preferably C1~C6Alkyl, such as can enumerate：Methyl, ethyl, n-propyl, isopropyl, normal-butyl, n-hexyl, n-octyl, Isobutyl group, the tert-butyl group, cyclopenta, cyclohexyl etc..
Ar1It is each independently selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30 Cycloalkyl, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C2~C30Heteroaryl.
As above-mentioned substituted or unsubstituted C1~C30Alkyl, preferably C1~C10Alkyl, more preferably substitution or it is unsubstituted C1~C6Alkyl, can be enumerated as preferable example：It is methyl, ethyl, n-propyl, isopropyl, normal-butyl, n-hexyl, different Butyl, tert-butyl group etc..As above-mentioned substituted or unsubstituted C3~C30Cycloalkyl, preferably C3~C10Cycloalkyl, more preferably take Generation or unsubstituted C3~C6Cycloalkyl, can be enumerated as preferable example：Cyclopropyl, cyclobutyl, cyclopenta, cyclohexyl Deng.
As above-mentioned substituted or unsubstituted C6~C30Aryl, preferably with 6-20 backbone carbon atoms, preferably described virtue Base is by phenyl, xenyl, terphenyl, naphthyl, phenanthryl, indenyl, fluorenyl and its derivative, fluoranthene base, Sanya phenyl, pyrene Base, base,Group and its derivative in the group that base is formed, can be enumerated as preferable example, benzene, 1- naphthalenes, 2- naphthalenes, 4- phenanthrene, 9- phenanthrene, 2- pyrenes, 2- biphenyl, 4- fluorenes, 4- spiro fluorenes, triphenylene,Fluoranthene.
As above-mentioned substituted or unsubstituted C2~C30Heteroaryl, it is preferably former with 2-20 skeleton carbon, it is preferably described Heteroaryl is furyl, thienyl, pyrrole radicals, benzofuranyl, benzothienyl, isobenzofuran-base, indyl, dibenzo Furyl, dibenzothiophenes base, carbazyl and its derivative, can be enumerated as preferable example, 1- dibenzofurans, 4- bis- Benzofuran, 3- dibenzothiophenes, 4- dibenzothiophenes, 2- benzothiophenes, N- carbazoles, 3- carbazoles, N- acridines, N- phenoxazines, N- phenthazine.Wherein, the carbazole radical derivative is preferably 9- phenyl carbazoles, 9- naphthyl carbazoles, benzo carbazole, dibenzo click Azoles, 3- phenyl carbazoles, 3,6- diphenyl carbazoles.
Ar2As shown in following formula (II)：
Wherein, R1~R5Identical or different and R1、R5At least one is not hydrogen, be each independently selected from hydrogen, halogen, substitution or Unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30Cycloalkyl, substituted or unsubstituted C6~C30Aryl, substitution or Unsubstituted C2~C30Heteroaryl；
As above-mentioned substituted or unsubstituted C1~C30Alkyl, preferably C1~C10Alkyl, more preferably methyl, ethyl, just Propyl group, isopropyl, normal-butyl, n-hexyl, isobutyl group, tert-butyl group etc..
As above-mentioned substituted or unsubstituted C3~C30Cycloalkyl, preferably C3~C10Cycloalkyl, more preferably cyclopropyl, ring Butyl, cyclopenta, cyclohexyl etc..
As above-mentioned substituted or unsubstituted C6~C30Aryl, preferably with 6-20 backbone carbon atoms, preferably described virtue Base be by phenyl, xenyl, naphthyl, phenanthryl, fluorenyl and its derivative, fluoranthene base, Sanya phenyl, pyrenyl andWhat base was formed Group in group；It can be enumerated as preferable example, benzene, 1- naphthalenes, 2- naphthalenes, 4- phenanthrene, 9- phenanthrene, 2- pyrenes, 2- biphenyl, 4- fluorenes, 4- Spiro fluorene, triphenylene,Fluoranthene.
As above-mentioned substituted or unsubstituted C2~C30Heteroaryl, it is preferably former with 2-20 skeleton carbon, it is preferably described Heteroaryl is furyl, thienyl, pyrrole radicals, benzofuranyl, benzothienyl, isobenzofuran-base, indyl, dibenzo Furyl, dibenzothiophenes base, carbazyl and its derivative；It can be enumerated as preferable example, 1- dibenzofurans, 4- bis- Benzofuran, 3- dibenzothiophenes, 4- dibenzothiophenes, 2- benzothiophenes, N- carbazoles, 3- carbazoles, N- acridines, N- phenoxazines, N- phenthazine.Wherein, the carbazole radical derivative be preferably 9- phenyl carbazoles, 9- naphthyl carbazoles benzo carbazole, dibenzo-carbazole, 3- phenyl carbazoles, 3,6- diphenyl carbazoles.
In the general formula compound of the present invention, the design addition chain-like alkyl conduct on parent naphthalene nucleus and arylamine substituents Substituted radical, its protrude the advantages of be：First, preferable chain-like alkyl can increase the dissolubility of material, reinforcing material The function of solution processability energy；Secondly, big steric hindrance substituent and chain alkyl can be effectively protected compound molecule, avoid With oxygen or other side reaction caused by the contact of center impurity molecule is quenched, can obtain and improve material uvioresistant, anti- The beneficial effect of aging.
In the general formula compound structure of the present invention, designed substituted radical can be connected with the substituted radical of adjacent position Form ring structure.That is Ar1With Ar2Between can form ring structure, R1With R2And R4With R5Between can form ring structure, and Each substituted radical relatively independent can connect and form ring structure.
In the general formula compound formula (I) of the present invention, wherein Ar1, Ar2It can connect to be formed by two adjacent groups Ring, the constituting atom of these rings can also be hetero atom in addition to carbon atom, and these rings can have substituent, form ring Carbon atom can also form ketone group.Preferably, Ar1, Ar2Connect to form five-membered ring, hexa-atomic by two groups of arbitrary neighborhood Ring, it can enumerate as an example, pyrrole ring, piperidine ring, morpholine ring, thiomorpholine ring, piperazine ring etc..
In the formula (II) of the present invention, R1~R2And/or R4~R5Adjacent group can be interconnected to form ring-type knot Structure, such ring structure can be aliphatic monocyclic or polycyclic, aromatic monocyclic or condensed ring, and miscellaneous original can be included in these rings Son, wherein, as the example of aliphatic monocyclic, for example, R1~R2And/or R4~R5Two groups connection shape of middle arbitrary neighborhood Into aliphatic five-membered ring, hexatomic ring, the constituting atom of these rings can also be hetero atom in addition to carbon atom, and these rings can So that with substituent, ketone group can also be formed by forming the carbon atom of ring.As the example of these rings, pentamethylene ring, ring can be enumerated Hexane ring, dicyclopentenyl ring, nafoxidine ring, tetrahydrofuran ring, piperidine ring and pentamethylene ring and hexamethylene nuclear carbon are former Ester ring that son substitutes to obtain by ketone group etc..As aromatic monocyclic or condensed ring, preferably C6~C30Monocyclic or condensed ring, as Example can enumerate phenyl ring, naphthalene nucleus etc.；As comprising heteroatomic monocyclic or polycyclic, preferably pyrrole ring, pyridine ring, indoles Ring, N- phenyl substituted indoles ring, thiphene ring, furan nucleus etc..
As the concrete preferred structure compound of general formula compound of the present invention, compound C1-C63 is listed below.This hair Bright preferable compound is not limited to following concrete structures.
In the present invention, it is preferred to particular compound raw material intermediate it is relative be easy to get, target compound can pass through two The Buchwald-Hartwig of arylamine and dihalo naphthalene derivatives reacts to obtain, and preparation is simple, and cost is relatively low；In addition Due to these compound molecular weights are larger, comprising the larger substituent group of steric hindrance, can effectively ensure to turn its vitrifying Temperature is high, has good heat endurance, there is very big advantage in the application process of material；Compound in the present invention is equal Adopt and substitute naphthalene derivatives for Isosorbide-5-Nitrae-two, there is effective conjugation of two N atoms in molecule, but still keep its PL spectrum In blue region, pass through the selection of substituted radical, it is possible to achieve in the luminous of deep blue region；Research is had shown that for luminescent material For, the polarity of luminous quantum efficiency and material has very big relation, has the compound of Isosorbide-5-Nitrae-symmetrical diaryl-amine base substitution, Due to the symmetry of structure, there can be less polarity, so as to have comparatively larger luminous quantum efficiency, for material Application in various illumination fields has great importance.
The general formula compound of the present invention and the preferred structure compound enumerated, may be used as functional membrane and electronics Active component in device.Described functional membrane includes photic display film, electroluminescent display film, filter coating, color conversion film etc.； The usual concept of described electronic device refers to include anode, negative electrode and at least one layer of device, and the wherein layer includes at least one Kind organic compound.Therefore the electronic device of the present invention includes anode, negative electrode and at least one layer, and the described layer includes at least one The preferred structure compound that the general formula compound and the present invention of the kind present invention has been enumerated.Preferred electronic device is selected from and had herein Organic electroluminescence devices (OLED, PLED), organic integrated circuits (O-IC), organic field effect tube (O-FET), organic film It is transistor (O-TFT), organic light-emitting transistor (O-LET), organic solar batteries (O-SC), organic optical detector, organic Photoreceptor, organic field quenching device (O-FQD), light-emitting electrochemical cell (LEC) and organic laser diode (O-laser), It includes at least one the compounds of this invention at least one layer.Particularly preferred organic electroluminescence device, organic film Transistor (O-TFT), organic light-emitting transistor (O-LET), can enumerate organic electroluminescence devices embodiment as an example.
Brief description of the drawings
From the detailed description to the embodiment of the present invention below in conjunction with the accompanying drawings, of the invention these and/or other side and Advantage will become clearer and be easier to understand, wherein：
Fig. 1 is the launching light spectrogram of the emerging production blue light dyestuff device of light extraction.
Fig. 2 is the launching light spectrogram of two compounds in comparative example 1.
Embodiment
In order that those skilled in the art more fully understand the present invention, with reference to the accompanying drawings and detailed description to this hair It is bright to be described in further detail.
Part I, the synthetic example of noval chemical compound of the present invention：
Various chemicals such as petroleum ether, ethyl acetate, n-hexane, toluene, tetrahydrofuran, dichloro used in the present invention Double (bromomethyl) benzene of methane, carbon tetrachloride, acetone, 1,2-, CuI, o-phthaloyl chloride, phenylhydrazine hydrochloride, trifluoroacetic acid, acetic acid, Trans-diaminocyclohexane, iodobenzene, cesium carbonate, potassium phosphate, ethylenediamine, benzophenone, cyclopentanone, 9-Fluorenone, sodium tert-butoxide, The bromo- 2- methyl naphthalenes of Loprazolam, 1-, o-dibromobenzene, butyl lithium, Bromofume, o-dibromobenzene, benzoyl peroxide, 1- (2- bromines Phenyl) -2- methyl naphthalenes, N- bromo-succinimides, methoxyl methyl San Jia Ji phosphonium chlorides, three (dibenzalacetone) two palladium, four (triphenylphosphine) palladium, 1,3- pairs of 2-phenyl-phosphine oxide nickel chloride, carbazole, 3,6- Dimethylcarbazoles, 3- (2- naphthyls) -6- phenyl clicks The basic chemical industry raw materials such as azoles, N- phenyl carbazole -3- boric acid, 9- (2- naphthyls) carbazole -3- boric acid can chemical products city at home Buy field.
Embodiment 1：
Compound C1 synthesis
Bromo- 3, the 7- diisopropyl naphthalenes (3.69g, 10mmol) of Isosorbide-5-Nitrae-two, N- phenyl-(9-N phenyl-benzo carbazole) amine (8.4g, 22mmol), sodium tert-butoxide 10.0g (10mmol, 5.0eq), toluene 500mL, nitrogen 30min is led under liquid level of solution, then Pd2 (dba) 31.2g (2mmol, 2%eq) is added, 10% tri-butyl phosphine 4ml (2mmol, 2%eq) is injected with syringe, opens Stirring is opened, is heated to 100 degrees Celsius, reacts 6h, reaction is completed, reaction solution concentration, through column chromatography for separation (petroleum ether：Acetic acid second Ester=50:1~10:1) faint yellow solid 7.9g, yield 74.7%, are obtained.
1H NMR(400MHz,Chloroform)δ9.89(s,3H),9.36(s,3H),8.54(s,3H),8.28(s, 6H), 7.90 (dd, J=26.5,12.3Hz, 15H), 8.03-7.65 (m, 25H), 7.60 (d, J=16.0Hz, 17H), 7.49 (d, J=8.0Hz, 18H), 7.25 (d, J=12.0Hz, 14H), 7.16 (d, J=16.0Hz, 7H), 7.10-6.84 (m, 27H), 6.40 (s, 3H), 2.87 (s, 2H), 1.25 (d, J=12.0Hz, 36H)
Embodiment 2：
Compound C2 synthesis
Using method prepare compound C2 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- phenyl of equivalent-(9-N phenyl-mesitylene and carbazole) amine, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two Bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are replaced with, after the completion of reaction, isolated faint yellow solid 8.2g, yield is 78.2%.
1H NMR(400MHz,Chloroform)δ9.96(s,3H),9.60(s,6H),9.41(s,3H),9.23(s, 3H), 9.15 (t, J=29.6Hz, 12H), 8.13 (s, 3H), 7.94 (s, 3H), 7.70 (d, J=4.0Hz, 13H), 7.66- 7.55 (m, 28H), 7.51 (d, J=8.0Hz, 22H), 7.25 (d, J=12.0Hz, 14H), 7.16 (d, J=16.0Hz, 7H), 7.04 (dd, J=26.0,6.0Hz, 27H), 6.40 (s, 3H), 2.70 (s, 9H), 2.41 (s, 9H)
Embodiment 3：
Compound C3 synthesis
Using method prepare compound C3 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 2, the 8- diisoamyl carbazolamines of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 6- di-t-butyl naphthalins of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 7.2g, yield 68.2%.
1H NMR(400MHz,Chloroform)δ8.25(s,1H),8.00–7.77(m,5H),7.74–7.46(m,4H), 7.44 (s, 1H), 7.11 (d, J=0.4Hz, 2H), 7.02 (dd, J=68.3,12.1Hz, 5H), 2.61 (s, 6H), 1.80- 1.44(m,21H),1.40(s,9H),0.90(s,15H).
Embodiment 4：
Compound C4 synthesis
Using method prepare compound C4 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- phenyl-(9-N phenyl -3- tert-butyl carbazoles) amine of equivalent, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two Replace with bromo- 2, the 7- bis- of Isosorbide-5-Nitrae-two (2- ethyls n-hexyl) naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 7.5g, yield 72.8%.
1H NMR(400MHz,Chloroform)δ8.91(s,2H),7.98(s,1H),7.47(s,10H),7.41(s, 5H), 7.94-7.01 (m, 82H), 7.29-7.18 (m, 20H), 7.53-7.01 (m, 61H), 7.11 (s, 3H), 7.02 (dd, J= 17.9,13.9Hz, 23H), 3.13 (s, 3H), 2.76 (d, J=69.8Hz, 4H), 2.60 (s, 4H), 2.11 (d, J=3.2Hz, 3H), 1.54 (s, 6H), 1.42 (s, 48H), 1.37 (d, J=0.8Hz, 6H), 1.29-1.07 (m, 19H), 0.91 (d, J= 15.9Hz,27H).
Embodiment 5：
Compound C5 synthesis
Using method prepare compound C5 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- phenyl-(9,9 '-di-n-octyl fluorenes) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced with Bromo- 2, the 6- di-t-butyl naphthalins of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.4g, yield is 65.3%.
1H NMR (400MHz, Chloroform) δ 7.89 (d, J=12.0Hz, 2H), 7.66 (d, J=10.1Hz, 1H), 7.44 (s, 4H), 7.34 (dd, J=14.3,2.4Hz, 3H), 7.21 (dd, J=8.5,7.5Hz, 6H), 7.08 (d, J= 19.9Hz, 3H), 6.97 (d, J=8.0Hz, 2H), 1.92 (s, 4H), 1.49 (s, 6H), 1.43 (s, 6H), 1.33 (s, 12H), 1.26(s,22H),0.89(s,9H).
Embodiment 6：
Compound C6 synthesis
Using method prepare compound C6 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- isopropyl phenyls)-(9,9 '-two spiro fluorene) amine of equivalent, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two Bromo- 3, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are replaced with, after the completion of reaction, isolated faint yellow solid 6.9g, yield is 69.2%.
1H NMR (400MHz, Chloroform) δ 8.00 (s, 1H), 8.22-7.60 (m, 16H), 7.56 (t, J= 5.4Hz,4H),7.47(s,5H),7.34(s,2H),7.27–6.95(m,28H),6.21(s,1H),2.87(s,1H),2.70 (s,4H),2.41(s,4H),1.20(s,17H).
Embodiment 7：
Compound C7 synthesis
Using method prepare compound C7 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3,5- diisopropyl phenyl)-benzophenanthrene amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are changed to, after the completion of reaction, isolated faint yellow solid 6.0g, yield is 56.2%.
1H NMR(400MHz,Chloroform)δ9.08(s,1H),8.98(s,1H),8.27(s,1H),8.01–7.72 (m,3H),8.01–7.34(m,10H),7.31(s,2H),6.80(s,1H),2.87(s,1H),2.49(s,3H),1.20(s, 12H).
Embodiment 8：
Compound C8 synthesis
Using method prepare compound C8 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replace with equivalent N- (4- trimethyl silicanes phenyl) -6- methyl bend amine, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are changed to, after the completion of reaction, isolated faint yellow solid 6.5g, yield is 70.1%.
1H NMR (400MHz, Chloroform) δ 9.13 (s, 3H), 9.00 (d, J=18.1Hz, 9H), 8.11 (s, 6H), 7.87(s,3H),7.68(s,4H),7.62(s,5H),7.39(s,3H),7.10(s,12H),2.97(s,9H),2.49(s, 9H),1.33(s,27H).
Embodiment 9：
Compound C9 synthesis
Using method prepare compound C9 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- cyclohexyl phenyls) -4- tert-butyl group naphthylamines of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are changed to, after the completion of reaction, isolated faint yellow solid 6.3g, yield is 64.4%.
1H NMR (400MHz, Chloroform) δ 8.15 (d, J=8.0Hz, 2H), 7.87 (s, 1H), 7.49 (d, J= 8.0Hz, 2H), 7.39 (s, 1H), 7.29 (s, 1H), 7.18 (s, 2H), 7.06 (s, 2H), 6.94 (s, 1H), 2.47 (d, J= 12.7Hz, 4H),1.95(s,1H),1.62–1.36(m,14H),1.40(s,2H),1.40(s,2H),1.12(s,3H).
Embodiment 10：
Compound C10 synthesis
Using method prepare compound C10 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- aminomethyl phenyls)-pyrene amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 6- di-t-butyl naphthalins of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 7.5g, yield 78.8%.
1H NMR (400MHz, Chloroform) δ 8.30 (d, J=13.0Hz, 3H), 8.13-7.93 (m, 10H), 7.93- 7.85 (m, 4H), 7.67 (d, J=4.0Hz, 3H), 7.11 (d, J=8.0Hz, 8H), 6.95 (s, 1H), 6.43 (s, 1H), 2.31 (s,6H),1.48(s,9H),1.42(s,9H).
Embodiment 11：
Compound C11 synthesis
Using method prepare compound C11 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2,4,6- trimethylphenyl) -9- phenanthrene amine of equivalent, and by Isosorbide-5-Nitrae-two bromo- 3,7- diisopropyl naphthalenes are replaced For bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 7.0g, yield is 80.2%.
1H NMR (400MHz, Chloroform) δ 8.98 (s, 1H), 8.84 (s, 1H), 8.11 (s, 1H), 7.88 (d, J= 12.0Hz, 2H), 7.65 (dd, J=21.2,2.8Hz, 5H), 7.39 (s, 1H), 6.76 (s, 2H), 2.49 (s, 3H), 2.26 (s, 3H),2.13(s,6H).
Embodiment 12：
Compound C12 synthesis
Using method prepare compound C12 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2,4,6- tri-tert phenyl) -4- phenanthrene amine of equivalent, and by Isosorbide-5-Nitrae-two bromo- 3,7- diisopropyl naphthalenes replace Isosorbide-5-Nitrae-dibromine naphthalene of equivalent is changed to, after the completion of reaction, isolated faint yellow solid 8.2g, yield 81.4%.
1H NMR(400MHz,Chloroform)δ8.95(s,1H),8.20(s,1H),7.92–7.85(m,1H),7.73 (s,1H),7.68–7.49(m,1H),7.47–7.40(m,1H),7.23(s,1H),1.37(s,1H),1.31(s,1H).
Embodiment 13：
Compound C13 synthesis
Using method prepare compound C13 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2- methyl -4- tert-butyl-phenyls)-(N- ethyl carbazoles) amine of equivalent, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 8.5g, Yield is 76.5%.
1H NMR(400MHz,Chloroform)δ8.16(s,2H),7.53(s,2H),7.42(s,2H),7.32(s, 2H), 7.95-6.52 (m, 23H), 7.26 (s, 2H), 7.60-6.52 (m, 19H), 7.11 (d, J=11.6Hz, 3H), 7.06- 6.96 (m,5H),6.92(s,2H),4.52(s,4H),2.70(s,3H),2.41(s,3H),2.13(s,6H),1.37(s, 3H),1.28(s,18H).
Embodiment 14：
Compound C14 synthesis
Using method prepare compound C14 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- cyclohexyl phenyls)-(N- phenyl bases carbazole) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.6g, and yield For 78.0%.
1H NMR (400MHz, Chloroform) δ 8.55 (s, 5H), 7.86 (d, J=8.0Hz, 10H), 7.60 (d, J= 16.0Hz, 14H), 7.51 (d, J=8.0Hz, 14H), 7.37 (d, J=16.0Hz, 9H), 7.13 (dd, J=34.0,14.0Hz, 36H), 2.48 (d, J=5.4Hz, 18H), 1.95 (s, 6H), 1.51 (d, J=74.0Hz, 20H), 1.40 (s, 1H), 1.12 (s, 13H).
Embodiment 15：
Compound C15 synthesis
Using method prepare compound C15 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2,4- diisopropyl phenyl)-dibenzofuranamines of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with bromo- 2, the 6- dicyclohexyls naphthalene of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 8.2g, receives Rate is 80.1%.
1H NMR (400MHz, Chloroform) δ 8.00 (d, J=3.7Hz, 1H), 7.98 (s, 1H), 7.81 (d, J= 8.0Hz, 2H), 7.67-7.31 (m, 9H), 7.31 (s, 4H), 7.30 (d, J=7.4Hz, 8H), 7.27-7.13 (m, 7H), 6.89 (d, J=8.0Hz, 4H), 3.67 (s, 1H), 2.87 (s, 2H), 2.44 (s, 1H), 1.91 (d, J=19.9Hz, 4H), 1.60 (s, 6H),1.39(s,2H),1.34(s,2H),1.20(s,32H),1.12(s,6H).
Embodiment 16：
Compound C16 synthesis
Using method prepare compound C16 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3- cyclohexyl phenyls) -4- dibenzothiophenes amine of equivalent, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent are replaced with, after the completion of reaction, isolated faint yellow solid 8.6g, yield is 88.0%.
1H NMR (400MHz, Chloroform) δ 8.45 (s, 5H), 8.11 (s, 5H), 7.86 (d, J=4.0Hz, 10H), 7.56 (s, 5H), 7.40 (d, J=8.0Hz, 10H), 7.30 (d, J=8.0Hz, 8H), 7.20 (s, 5H), 6.98 (t, J= 14.0Hz, 15H), 2.54 (s, 2H), 2.49 (s, 16H), 1.97 (s, 6H), 1.51 (d, J=70.4Hz, 21H), 1.12 (s, 13H).
Embodiment 17：
Compound C17 synthesis
Using method prepare compound C17 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3- cyclohexyl phenyls) -4- (3- dibenzothiophenes) -2- aminomethyl phenyl amine of equivalent, and Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated pale yellow colored solid Body 6.4g, yield 69.2%.
1H NMR (400MHz, Chloroform) δ 9.54 (s, 2H), 8.45 (s, 2H), 8.07 (d, J=80.0Hz, 3H), 7.95 (s, 1H), 7.86 (d, J=4.0Hz, 4H), 7.70-7.46 (m, 8H), 7.38 (d, J=8.0Hz, 4H), 7.29 (d, J= 16.0Hz,4H),7.25–7.12(m,12H),2.49(s,6H),2.34(s,6H),2.13(s,6H).
Embodiment 18：
Compound C18 synthesis
Using method prepare compound C18 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (5- cyclohexyl naphthyl) -4- (3- dibenzothiophenes) -2- aminomethyl phenyl amine of equivalent, and Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated pale yellow colored solid Body 7.5g, yield 74.7%.
1H NMR(400MHz,Chloroform)δ8.44(s,2H),8.37(s,1H),8.16(s,2H),7.93–7.83 (m, 5H), 7.79 (s, 1H), 7.73 (s, 2H), 8.14-6.99 (m, 12H), 7.64 (d, J=4.0Hz, 3H), 7.94-6.99 (m, 12H), 7.56 (d, J=8.0Hz, 5H), 7.51-7.02 (m, 9H), 7.31 (d, J=4.0Hz, 3H), 7.36-7.02 (m, 5H), 7.04 (d, J=79.9Hz, 2H), 3.20 (s, 3H), 2.85 (s, 1H), 2.77 (s, 1H), 2.58 (s, 3H), 2.49 (s, 6H), 2.13 (s, 3H), 2.03 (d, J=3.9Hz, 4H), 1.62-1.36 (m, 11H), 1.36-1.12 (m, 4H), 1.12 (s, 3H).
Embodiment 19：
Compound C19 synthesis
Using method prepare compound C19 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (the 6- tert-butyl group -2- naphthyls) -4- (3- dibenzofurans) -2- aminomethyl phenyl amine of equivalent, by Isosorbide-5-Nitrae-two Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two that bromo- 3,7- diisopropyl naphthalenes replace with equivalent, it is isolated yellowish after the completion of reaction Color solid 7.8g, yield 72.5%.
1H NMR (400MHz, Chloroform) δ 9.08 (s, 1H), 7.98 (s, 1H), 7.87 (s, 1H), 7.76 (d, J= 16.0Hz, 2H), 7.69-7.52 (m, 3H), 7.52-7.36 (m, 6H), 7.32 (d, J=4.0Hz, 3H), 6.99 (s, 1H), 2.49(s,3H),2.13(s,3H),1.49(s,9H).
Embodiment 20：
Compound C20 synthesis
Using method prepare compound C20 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- (4- (2-N- ethyl carbazoles) -6- aminomethyl phenyls) of equivalent-(7- isopropyls -2- is luxuriant and rich with fragrance) amine, by Isosorbide-5-Nitrae-two Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two that bromo- 3,7- diisopropyl naphthalenes replace with equivalent, it is isolated yellowish after the completion of reaction Color solid 6.4g, yield 76.3%.
1H NMR(400MHz,Chloroform)δ9.11–8.79(m,4H),8.16–7.90(m,6H),7.90–7.73 (m, 6H), 7.72 (s, 2H), 7.52 (d, J=15.1Hz, 2H), 7.47-7.37 (m, 4H), 7.33 (d, J=4.0Hz, 2H), 6.97(s,1H),4.53(s,2H),2.87(s,1H),2.49(s,4H),2.13(s,4H),1.37(s,2H),1.26(s, 16H).
Embodiment 21：
Compound C21 synthesis
Using method prepare compound C21 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- (2- phenyl-benzothiophene) -6- aminomethyl phenyls)-(2,7- dimethylphenanthrene) amine of equivalent, by Isosorbide-5-Nitrae - Bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two that two bromo- 3,7- diisopropyl naphthalenes replace with equivalent are isolated light after the completion of reaction Yellow solid 5.8g, yield 58.6%.
1H NMR (400MHz, Chloroform) δ 8.87 (s, 4H), 8.45 (s, 2H), 7.87 (d, J=4.0Hz, 4H), 7.74 (s, 2H), 7.61-7.44 (m, 12H), 7.39 (s, 7H), 7.32 (dd, J=6.1,2.1Hz, 7H), 7.09 (s, 2H), 6.89(s,2H),2.70(s,12H),2.49(s,6H),2.13(s,6H).
Embodiment 22：
Compound C22 synthesis
Using method prepare compound C22 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- phenyl of equivalent-(3- bends -6- aminomethyl phenyls) amine, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced with The bromo- 7- methyl naphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.0g, yield 64.3%.
1H NMR (400MHz, Chloroform) δ 8.98 (s, 4H), 8.84 (d, J=2.2Hz, 8H), 8.05 (s, 2H), 7.91 (d, J=8.0Hz, 11H), 7.76 (s, 2H), 7.74-7.61 (m, 20H), 7.46 (d, J=12.0Hz, 4H), 7.37 (s, 4H), 7.23 (d, J=8.0Hz, 12H), 7.18-6.87 (m, 19H), 6.96 (t, J=3.3Hz, 1H), 2.70 (s, 6H), 2.13 (s,12H).
Embodiment 23：
Compound C23 synthesis
Using method prepare compound C22 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- phenyl-(4- (2- pyrenes) -2- phenyl benzene) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced For bromo- 3, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 7.2g, yield is 72.1%.
1H NMR(400MHz,Chloroform)δ9.24(s,1H),8.72(s,4H),8.22(s,1H),8.13(s, 4H), 8.00 (d, J=15.9Hz, 6H), 7.87 (d, J=7.9Hz, 5H), 7.65 (s, 1H), 7.59 (s, 2H), 7.50 (s, 2H), 7.36 (d, J=7.9Hz, 6H), 7.18 (s, 4H), 7.03 (s, 7H), 6.95 (d, J=4.0Hz, 3H), 6.58 (s, 1H), 2.68(s,3H),2.39(s,3H).
Embodiment 24：
Compound C24 synthesis
Using method prepare compound C24 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- phenyl-(4- fluoranthene -2- methylbenzenes) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced For bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 7.5g, yield is 71.2%.
1H NMR (400MHz, Chloroform) δ 8.42 (s, 5H), 8.10 (s, 5H), 7.87 (s, 3H), 7.75 (d, J= 8.0Hz, 6H), 7.71-7.44 (m, 10H), 7.43 (d, J=3.0Hz, 2H), 7.42-7.30 (m, 9H), 7.24 (s, 6H), 7.08(s,6H),7.00(s,2H),2.49(s,9H),2.13(s,9H).
Embodiment 25：
Compound C25 synthesis
Using method prepare compound C25 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- (3- (5- methyl)-dibenzo-carbazole) of equivalent-(4- (9- is luxuriant and rich with fragrance) -2- methylbenzenes) amine, by Isosorbide-5-Nitrae-two Bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two that bromo- 3,7- diisopropyl naphthalenes replace with equivalent, it is isolated yellowish after the completion of reaction Color solid 6.9g, yield 65.3%.
1H NMR(400MHz,Chloroform)δ9.08(s,4H),8.84(s,4H),8.27(s,4H),8.03(s, 4H), 7.94 (s, 3H), 7.90 (s, 3H), 7.90 (s, 3H), 7.92-7.42 (m, 40H), 7.29 (d, J=28.0Hz, 8H), 7.03 (d, J=17.2Hz, 6H), 6.46 (d, J=50.0Hz, 4H), 2.70 (s, 6H), 2.42 (d, J=8.0Hz, 18H), 2.13(s,12H).
Embodiment 26：
Compound C26 synthesis
Using method prepare compound C26 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (7- phenyl -2- dibenzofurans)-(4- (2- naphthalenes) -2- methylbenzenes) amine of equivalent, and Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated pale yellow colored solid Body 6.0g, yield 58.4%.
1H NMR (400MHz, Chloroform) δ 8.20 (d, J=19.0Hz, 2H), 8.08 (d, J=12.0Hz, 2H), 7.99 (s, 1H), 7.87 (d, J=3.1Hz, 2H), 7.85-7.67 (m, 5H), 7.63 (s, 2H), 7.57 (d, J=12.0Hz, 2H),7.53–7.36(m,7H),7.32(s,1H),2.49(s,3H),2.13(s,3H).
Embodiment 27：
Compound C27 synthesis
Using method prepare compound C27 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replace with equivalent N- (2- (9,9 '-dimethyl fluorene)-(2,6- dimethyl -3- xenyls benzene) amine, Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated pale yellow colored solid Body 8.3g, yield 79.5%.
1H NMR (400MHz, Chloroform) δ 7.95-7.62 (m, 2H), 7.51 (d, J=14.9Hz, 1H), 7.44- 7.30(m,2H),7.30–7.22(m,2H),2.49(s,1H),2.26(s,1H),2.13(s,1H),1.69(s,2H).
Embodiment 28：
Compound C28 synthesis
Using method prepare compound C28 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3- dibenzothiophenes)-(2- methyl -4- xenyls benzene) amine of equivalent, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 5.9g, Yield is 62.6%.
1H NMR (400MHz, Chloroform) δ 8.45 (s, 1H), 8.25 (d, J=7.1Hz, 2H), 7.94 (s, 1H), 7.86 (s, 1H), 7.81-7.66 (m, 11H), 7.56 (s, 1H), 7.54-6.97 (m, 24H), 7.02 (d, J=8.0Hz, 3H), 7.02 (d, J=8.0Hz, 3H), 6.17 (s, 1H), 2.70 (s, 3H), 2.43 (d, J=16.0Hz, 6H), 2.13 (s, 6H)
Embodiment 29：
Compound C29 synthesis
Using method prepare compound C29 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (7- phenyl -2- dibenzothiophenes)-(2- (2- xenyls benzene) amine, by Isosorbide-5-Nitrae-two bromo- 3,7- of equivalent Diisopropyl naphthalene replaces with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.3g, yield 68.2%.
1H NMR (400MHz, Chloroform) δ 9.24 (s, 1H), 8.30 (s, 1H), 8.11 (d, J=8.0Hz, 2H), 7.99(s,1H),7.87(s,1H),7.75(s,4H),7.70(s,1H),7.63–7.57(m,4H),7.49(s,3H),7.43– 7.34(m,4H),7.14(s,1H),7.01(s,1H),2.49(s,3H).
Embodiment 30：
Compound C30 synthesis
Using method prepare compound C30 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2- phenyl -2- dibenzothiophenes)-(2- phenyl benzene) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Base naphthalene replaces with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 7.2g, and yield 70.1%.
1H NMR (400MHz, Chloroform) δ 8.49 (s, 8H), 8.21 (s, 7H), 8.10 (d, J=8.0Hz, 16H), 7.86 (d, J=95.9Hz, 25H), 7.72 (dd, J=4.9,3.7Hz, 16H), 7.65-7.44 (m, 66H), 7.43-7.33 (m, 27H),7.24(s,32H),7.13(s,5H),7.00(s,8H).
Embodiment 31：
Compound C31 synthesis
Using method prepare compound C31 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2-N- ethyl carbazoles)-(2- phenyl benzene) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced Bromo- 6, the 7- diethyl naphthalene of Isosorbide-5-Nitrae-two of equivalent is changed to, after the completion of reaction, isolated faint yellow solid 6.3g, yield is 60.2%.
1H NMR (400MHz, Chloroform) δ 8.44-7.96 (m, 18H), 7.96 (s, 4H), 7.94 (d, J= 12.0Hz, 14H), 7.63 (d, J=76.0Hz, 14H), 7.49 (d, J=4.0Hz, 1H), 7.45-7.30 (m, 47H), 7.26 (d, J=8.0Hz, 15H), 7.14 (s, 5H), 7.08 (s, 12H), 4.53 (s, 14H), 2.82 (s, 14H), 1.37 (s, 11H), 1.24(s,11H).
Embodiment 32：
Compound C32 synthesis
Using method prepare compound C32 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3-N- phenyl carbazoles)-(2-methyl-4- tert-butyl benzenes) amine of equivalent, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with bromo- 2, the 6- di-t-butyl naphthalins of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.7g, yield 58.8%.
1H NMR (400MHz, Chloroform) δ 8.55 (s, 1H), 7.81 (d, J=8.0Hz, 1H), 7.69-7.47 (m, 3H), 7.35 (d, J=4.0Hz, 2H), 7.13 (d, J=20.0Hz, 1H), 6.99 (dd, J=8.0,4.0Hz, 4H), 6.93 (s, 1H),6.93(s,1H),2.13(s,3H),1.49(s,6H),1.43(s,496H),1.28(s,9H).
Embodiment 33：
Compound C33 synthesis
Using method prepare compound C33 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (3,5- di-tert-butyl)-(2-methyl-4- tert-butyl benzenes) amine of equivalent, by bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two Isopropyl naphthalene replaces with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, and after the completion of reaction, isolated faint yellow solid 6.8g, yield is 62.4%.
1H NMR(400MHz,Chloroform)δ8.22(s,1H),7.54(s,1H),7.47(s,1H),7.20(s, 1H),7.11(s,1H),7.05(s,1H),7.00(s,1H),6.93(s,1H),2.13(s,1H),1.41(s,1H),1.28(s, 1H).
Embodiment 34：
Compound C34 synthesis
Using method prepare compound C34 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- bis- (2-methyl-4- tert-butyl benzenes) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 7.4g, yield 68.5%.
1H NMR(400MHz,Chloroform)δ8.22(s,1H),7.54(s,1H),7.47(s,1H),7.05(s, 1H),7.00(s,1H),6.93(s,1H),2.13(s,1H),1.28(s,1H).
Embodiment 35：
Compound C35 synthesis
Using method prepare compound C35 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- xenyls-(2,4,6- trimethylbenzene) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced For Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 7.2g, yield 68.8%.
1H NMR(400MHz,Chloroform)δ8.22(s,1H),7.75(s,2H),7.61–7.45(m,6H),7.39 (d, J=16.0Hz, 3H), 6.76 (s, 2H), 2.26 (s, 3H), 2.13 (s, 6H)
Embodiment 36：
Compound C36 synthesis
Using method prepare compound C36 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N-3- xenyls-(2,4- di-tert-butyl) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced Isosorbide-5-Nitrae-dibromine naphthalene of equivalent is changed to, after the completion of reaction, isolated faint yellow solid 7.4g, yield 81.2%.
1H NMR(400MHz,Chloroform)δ8.22(s,1H),8.10(s,1H),7.54(s,1H),7.49–7.34 (m,7H),7.31(s,2H),7.14(s,1H),7.08(s,2H),6.80(s,1H),2.87(s,1H),1.20(s,14H).
Embodiment 37：
Compound C37 synthesis
Using method prepare compound C37 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2- (9,9 '-dimethyl) fluorenes)-(2- methyl -4- cyclohexyl phenyls) amine of equivalent, and Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 6.0g, and yield For 58.1%.
1H NMR (400MHz, Chloroform) δ 8.22 (s, 1H), 7.88 (d, J=16.0Hz, 2H), 7.57-7.37 (m, 5H), 7.34 (s, 1H), 7.25 (d, J=5.8Hz, 2H), 7.15 (t, J=1.4Hz, 1H), 7.13-6.90 (m, 3H), 2.51 (s, 1H), 2.13 (s, 3H), 1.95 (s, 1H), 1.69 (s, 8H), 1.51 (d, J=74.5Hz, 6H), 1.39-1.39 (m, 1H),1.12(s,3H).
Embodiment 38：
Compound C38 synthesis
Using method prepare compound C38 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- tert-butyl-phenyls)-(2- methyl -4- tert-butyl-phenyls) amine of equivalent, by bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two Isopropyl naphthalene replaces with bromo- 6, the 7- dihexyls naphthalene of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.4g yield 58.8%.
1H NMR(400MHz,Chloroform)δ7.88(s,1H),7.36(s,1H),7.08–6.93(m,6H),6.89 (s,1H),2.72(s,1H),2.12(s,3H),1.58(s,1H),1.35–1.25(m,24H),0.88(s,3H).
Embodiment 39：
Compound C39 synthesis
Using method prepare compound C39 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- carbazyls)-(3,5- di-t-butyl phenyl) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.9g, and yield For 62.3%.
1H NMR(400MHz,Chloroform)δ7.97(s,1H),7.86(s,1H),7.63(s,1H),7.53(s, 1H),7.42–7.36(m,1H),7.30(s,1H),7.22–7.15(m,1H),7.10(s,1H),2.49(s,1H),1.41(s, 1H).
Embodiment 40：
Compound C40 synthesis
Using method prepare compound C40 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (9,9 '-dimethyl fluorene)-(4- tert-butyl-phenyls) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with bromo- 3, the 7- dicyclohexyls naphthalene of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 7.2g, receives Rate is 65.8%.
1H NMR (400MHz, Chloroform) δ 7.91 (d, J=12.0Hz, 3H), 7.69 (s, 1H), 7.58-7.50 (m, 3H), 7.30 (dt, J=22.4,14.1Hz, 6H), 7.18 (s, 3H), 7.06 (s, 3H), 6.98 (s, 1H), 3.08 (s, 1H),2.87(s,1H),2.23(s,1H),1.88(s,1H),1.76(s,1H),1.69(s,8H),1.60(s,6H),1.35(s, 1H), 1.30 (s, 1H), 1.16 (d, J=32.0Hz, 12H)
Embodiment 41：
Compound C41 synthesis
Using method prepare compound C41 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (the 6- tert-butyl group -2- dibenzothiophenes)-(2- methyl -4- trimethyl silicanes phenyl) amine of equivalent, by Isosorbide-5-Nitrae - Two bromo- 3,7- diisopropyl naphthalenes replace with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 8.0g, yield 78.3%.
1H NMR (400MHz, Chloroform) δ 8.22 (s, 2H), 8.12 (s, 1H), 8.06 (s, 1H), 7.60 (d, J= 4.0Hz, 4H), 7.54 (s, 2H), 8.02-7.01 (m, 17H), 7.44 (t, J=12.0Hz, 4H), 7.65-7.01 (m, 15H), 7.08-6.97 (m, 6H), 6.93 (s, 2H), 2.13 (s, 6H), 1.43 (s, 9H), 1.30 (d, J=16.0Hz, 27H)
Embodiment 42：
Compound C42 synthesis
Using method prepare compound C42 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- (2,7- dimethyl dibenzofurans)-(4- aminomethyl phenyls) amine, by Isosorbide-5-Nitrae-two bromo- 3,7- of equivalent Diisopropyl naphthalene replaces with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 8.5g, yield 81.6%.
1H NMR(400MHz,Chloroform)δ7.87(s,1H),7.71(s,1H),7.67–7.36(m,3H),7.16 (dd, J=19.5,8.6Hz, 6H), 2.50 (d, J=4.0Hz, 6H), 2.31 (d, J=4.0Hz, 6H)
Embodiment 43：
Compound C43 synthesis
Using method prepare compound C43 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replace with equivalent N- (2- (9,9 '-dimethyl -7- tert-butyl groups fluorenes)-(4- dibenzothiophenes) amine, Isosorbide-5-Nitrae-two is bromo- 3,7- diisopropyl naphthalenes replace with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 7.8g, and yield For 72.3%.
1H NMR (400MHz, Chloroform) δ 8.45 (s, 6H), 8.22 (s, 5H), 8.00 (d, J=84.0Hz, 9H), 7.86 (s, 15H), 7.65 (s, 6H), 7.61-7.51 (m, 18H), 7.47 (s, 5H), 7.33 (dd, J=21.8,14.6Hz, 25H),7.25(s,2H),7.01(s,6H),2.87(s,2H),1.69(s,35H),1.20(s,36H).
Embodiment 44：
Compound C44 synthesis
Using method prepare compound C44 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (N- phenyl -4- carbazoles)-(4- cyclohexyl phenyls) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with bromo- 6, the 7- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 7.6g, and yield For 71.5%.
1H NMR(400MHz,Chloroform)δ8.54(s,2H),8.18(s,2H),7.86(s,4H),7.62(s, 8H), 7.59-7.47 (m, 12H), 7.39 (d, J=4.0Hz, 8H), 7.29-6.80 (m, 12H), 6.97 (s, 1H), 6.40 (s, 2H),2.49(s,12H),2.43(s,4H),1.91(s,9H),1.60(s,12H),1.35(s,6H),1.12(s,12H).
Embodiment 45：
Compound C45 synthesis
Using method prepare compound C45 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- phenyl-(4- dibenzothiophenes) amine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replaced with Bromo- 2, the 6- di-t-butyl naphthalins of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 8.3g, yield 79.4%.
1H NMR (400MHz, Chloroform) δ 8.45 (s, 6H), 8.11 (s, 3H), 8.09 (d, J=3.1Hz, 3H), 8.10-7.65 (m, 18H), 7.56 (s, 6H), 7.31 (s, 7H), 7.26 (d, J=20.0Hz, 16H), 7.08 (s, 13H), 7.04–6.88(m,14H),1.49(s,26H),1.43(s,26H).
Embodiment 46：
Compound C46 synthesis
Using method prepare compound C46 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- (4- cyclohexyl phenyls) of equivalent-(2,7- diisopropyl -9- are luxuriant and rich with fragrance) amine, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, and after the completion of reaction, isolated faint yellow solid 8.2g, yield is 79.5%.
1H NMR (400MHz, Chloroform) δ 8.92 (s, 4H), 8.22 (s, 6H), 8.14 (s, 6H), 8.00 (d, J= 0.5Hz, 6H), 7.74 (d, J=5.2Hz, 8H), 7.54 (s, 4H), 7.47 (s, 4H), 7.18 (s, 6H), 7.06 (s, 6H), 2.87 (s, 6H), 2.45 (s, 2H), 1.92 (s, 6H), 1.60 (s, 6H), 1.36 (s, 6H), 1.19 (d, J=16.0Hz, 32H), 1.09 (d, J=2.7Hz, 2H)
Embodiment 47：
Compound C47 synthesis
Using method prepare compound C47 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the N- (4- (2,4,6- trimethylphenyl) phenyl) of equivalent-(4- is luxuriant and rich with fragrance) amine, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, and after the completion of reaction, isolated faint yellow solid 6.6g, yield is 64.2%.
1H NMR (400MHz, Chloroform) δ 8.98 (s, 1H), 8.22 (s, 1H), 7.91 (d, J=8.0Hz, 2H), 7.78-7.30 (m, 12H), 7.47 (s, 1H), 7.42 (d, J=8.0Hz, 3H), 7.37 (s, 2H), 7.01 (s, 2H), 2.92 (s, 6H),2.48(s,3H).
Embodiment 48：
Compound C48 synthesis
Using method prepare compound C48 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- aminomethyl phenyls)-(5- phenyl -2- dibenzofurans) amine of equivalent, and bromo- 3, the 7- bis- of Isosorbide-5-Nitrae-two is different Propyl group naphthalene replaces with bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two of equivalent, after the completion of reaction, isolated faint yellow solid 6.0g, Yield is 56.3%.
1H NMR (400MHz, Chloroform) δ 8.05 (d, J=24.0Hz, 4H), 7.94 (s, 1H), 7.71 (s, 1H), 7.64 (s, 2H), 7.51 (s, 4H), 7.46 (s, 4H), 7.40 (d, J=6.1Hz, 5H), 7.26 (s, 1H), 7.21-7.05 (m, 10H), 7.00 (d, J=7.4Hz, 2H), 2.70 (s, 3H), 2.41 (s, 3H), 2.32 (s, 6H)
Embodiment 49：
Compound C49 synthesis
Using method prepare compound C49 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (2- xenyls)-(2,4- di-tert-butyl-phenyl) amine of equivalent, by bromo- 3, the 7- diisopropyls of Isosorbide-5-Nitrae-two Naphthalene replaces with Isosorbide-5-Nitrae-dibromine naphthalene of equivalent, after the completion of reaction, isolated faint yellow solid 6.4g, and yield 60.8%.
1H NMR(400MHz,Chloroform)δ8.22(s,2H),7.75(s,5H),7.59(s,1H),7.61–7.44 (m,12H),7.41(s,1H),7.28(s,1H),7.28–7.15(m,8H),7.28–6.78(m,12H),2.87(s,2H), 1.19 (d, J=12.0Hz, 24H)
Embodiment 50：
Compound C50 synthesis
Using method prepare compound C50 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with N- (4- (N-3,6- Dimethylcarbazole) phenyl)-(2,4,6- trimethylphenyl) amine of equivalent, by Isosorbide-5-Nitrae-two Bromo- 2, the 6- di-n-hexyls naphthalene of Isosorbide-5-Nitrae-two that bromo- 3,7- diisopropyl naphthalenes replace with equivalent is isolated light after the completion of reaction Yellow solid 6.5g, yield 61.0%.
1H NMR (400MHz, Chloroform) δ 8.79 (s, 8H), 8.00 (d, J=16.0Hz, 12H), 7.71 (d, J= 20.0Hz, 21H), 7.60-6.92 (m, 58H), 7.23 (s, 4H), 7.29-6.92 (m, 18H), 7.09 (d, J=56.7Hz, 12H), 6.75 (s, 16H), 2.74 (d, J=4.0Hz, 11H), 2.50 (s, 48H), 2.26 (s, 24H), 2.13 (s, 48H), 1.60 (d, J=8.0Hz, 10H), 1.29 (d, J=4.0Hz, 49H), 0.89 (s, 22H)
Embodiment 51：
Compound C51 synthesis
Using method prepare compound C51 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the dibenzo-carbazole of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with to Isosorbide-5-Nitrae-dibromo of equivalent Naphthalene, after the completion of reaction, isolated faint yellow solid 6.2g, yield 78.2%.
1H NMR (400MHz, Chloroform) δ 8.54 (s, 2H), 8.64-8.15 (m, 8H), 7.97 (d, J= 16.0Hz, 4H), 7.84 (s, 3H), 7.75 (s, 2H), 7.61 (s, 1H), 7.53 (s, 2H), 7.47 (d, J=4.0Hz, 3H), 7.28 (d, J=96.0Hz, 3H), 7.14 (d, J=2.9Hz, 1H)
Embodiment 52：
Compound C52 synthesis
Using method prepare compound C52 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 2,3,6,7- tetramethyl carbazoles of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 7.3g, yield 70.6%.
1H NMR(400MHz,Chloroform)δ8.75(s,4H),8.16(s,2H),7.98(s,4H),7.93(s, 4H), 7.84 (s, 1H), 7.52 (d, J=68.9Hz, 5H), 7.35 (s, 2H), 7.04 (s, 2H), 2.70 (s, 12H), 2.47 (s, 24H),2.29(s,24H).
Embodiment 53：
Compound C53 synthesis
Using method prepare compound C53 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- di-t-butyl carbazoles of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with the 1 of equivalent, 4- dibromine naphthalenes, after the completion of reaction, isolated faint yellow solid 7.6g, yield 74.5%.
1H NMR(400MHz,Chloroform)δ8.95(s,1H),8.36(s,1H),8.20(s,1H),7.84(s, 1H),7.62(s,1H),7.50–7.42(m,1H),7.36–7.30(m,1H),1.43(s,1H).
Embodiment 54：
Compound C54 synthesis
Using method prepare compound C54 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- di-t-butyl carbazoles of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with the 1 of equivalent, Bromo- 2, the 6- di-t-butyl naphthalins of 4- bis-, after the completion of reaction, isolated faint yellow solid 7.8g, yield 70.3%.
1H NMR(400MHz,Chloroform)δ8.96(s,4H),8.28(s,2H),8.19(s,4H),7.83(s, 2H), 7.59 (s, 2H), 7.52 (s, 4H), 7.40 (s, 4H), 7.29 (d, J=8.2Hz, 4H), 7.15 (s, 5H), 7.01 (s, 2H),2.87(s,3H),1.49(s,19H),1.41(s,19H),1.20(s,52H).
Embodiment 55：
Compound C55 synthesis
Using method prepare compound C55 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- dicyclohexyl carbazoles of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 6- dimethylnaphthalenes of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 7.0g, yield 69.1%.
1H NMR (400MHz, Chloroform) δ 8.15 (d, J=8.2Hz, 2H), 7.92 (d, J=8.0Hz, 2H), 7.69 (s, 1H), 7.61 (t, J=5.7Hz, 2H), 7.24 (d, J=0.5Hz, 1H), 7.06 (d, J=12.0Hz, 2H), 2.70 (s, 4H), 2.56 (d, J=3.0Hz, 2H), 1.99 (d, J=6.4Hz, 5H), 1.63-1.36 (m, 12H), 1.36-1.15 (m, 1H),1.12(s,6H).
Embodiment 56：
Compound C56 synthesis
Using method prepare compound C56 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3,6- bis- (trimethyl silicon substrate) carbazole of equivalent, and bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with etc. and worked as The bromo- 2,6-DIPN of Isosorbide-5-Nitrae-two of amount, after the completion of reaction, isolated faint yellow solid 7.6g, yield 72.5%.
1H NMR(400MHz,Chloroform)δ8.95(s,1H),8.36(s,1H),8.20(s,1H),7.83(s, 1H),7.64–7.57(m,1H),7.44(s,1H),7.37–7.29(m,1H),7.01(s,1H),2.87(s,1H),1.43(s, 1H),1.28–1.21(m,1H).
Embodiment 57：
Compound C57 synthesis
Using method prepare compound C57 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- diphenyl carbazoles of equivalent, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replace with the Isosorbide-5-Nitrae of equivalent- Two bromo- 2,6- di-t-butyl naphthalins, after the completion of reaction, isolated faint yellow solid 7.6g, yield 73.6%.
1H NMR (400MHz, Chloroform) δ 8.36 (s, 2H), 8.24 (d, J=1.0Hz, 7H), 7.79 (q, J= 16.0Hz,24H),7.62–7.26(m,31H),7.41(s,5H),7.41(s,4H),7.01(s,2H),1.49(s,16H), 1.41(s,16H).
Embodiment 58：
Compound C58 synthesis
Using method prepare compound C58 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the dibenzo-carbazole of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with to the Isosorbide-5-Nitrae-two of equivalent Bromo- 3,7- di-t-butyl naphthalins, after the completion of reaction, isolated faint yellow solid 6.7g, yield 64.3%.
1H NMR(400MHz,Chloroform)δ8.54(s,4H),8.39(s,1H),7.99(s,4H),7.83(s, 1H), 7.60 (d, J=8.0Hz, 5H), 7.53 (d, J=4.0Hz, 6H), 7.28 (d, J=8.0Hz, 23H), 7.01 (s, 2H), 1.49(s,9H),1.41(s,9H).
Embodiment 59：
Compound C59 synthesis
Using method prepare compound C59 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the 3- tert-butyl groups-benzo carbazole of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 3- dimethylnaphthalenes of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 6.4g, yield 63.6%.
1H NMR(400MHz,Chloroform)δ8.95(s,2H),8.54(s,2H),7.99(s,2H),7.68(s, 2H),7.61(s,1H),7.53(s,1H),7.44(s,3H),7.41–6.98(m,8H),2.57(s,6H),1.43(s,19H).
Embodiment 60：
Compound C60 synthesis
Using method prepare compound C60 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 9, the 9- dimethyl acridiniums of equivalent, by bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two replace with the Isosorbide-5-Nitrae of equivalent- Dibromine naphthalene, after the completion of reaction, isolated faint yellow solid 6.8g, yield 58.9%.
1H NMR(400MHz,Chloroform)δ8.22(s,1H),7.54(s,1H),7.47(s,1H),7.28–7.15 (m,6H),6.94(s,2H),1.69(s,6H).
Embodiment 61：
Compound C61 synthesis
Using method prepare compound C57 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- tert-butyl group phenoxazines of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with the 1 of equivalent, Bromo- 6, the 7- diethyl naphthalenes of 4- bis-, after the completion of reaction, isolated faint yellow solid 6.0g, yield 55.6%.
1H NMR(400MHz,Chloroform)δ7.93(s,1H),7.41(s,1H),7.06(s,1H),7.00(s, 1H),6.82(s,1H),2.82(s,1H),1.29–1.21(m,1H).
Embodiment 62：
Compound C62 synthesis
Using method prepare compound C62 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with the 5- toluphenazines of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with to the Isosorbide-5-Nitrae-two of equivalent Bromo- 2,6- dimethylnaphthalenes, after the completion of reaction, isolated faint yellow solid 7.3g, yield 68.9%.
1H NMR (400MHz, Chloroform) δ 7.94 (s, 3H), 7.71 (d, J=3.0Hz, 6H), 7.17 (s, 1H), 7.08 (d, J=52.0Hz, 20H), 6.95 (s, 10H), 3.20 (s, 16H), 2.70 (s, 9H), 2.41 (s, 9H)
Embodiment 63：
Compound C63 synthesis
Using method prepare compound C63 same as Example 1, difference is N- phenyl-(9-N phenyl-benzo click Azoles) amine replaces with 3, the 6- di-t-butyl phenthazine of equivalent, bromo- 3, the 7- diisopropyl naphthalenes of Isosorbide-5-Nitrae-two are replaced with into equivalent Bromo- 2, the 6- di-n-hexyls naphthalene of Isosorbide-5-Nitrae-two, after the completion of reaction, isolated faint yellow solid 6.6g, yield 70.2%.
1H NMR(400MHz,Chloroform)δ7.98(s,1H),7.73(s,1H),7.67(s,1H),7.55–7.49 (m, 1H),7.11(s,1H),7.07–6.99(m,1H),2.77–2.71(m,1H),1.63–1.56(m,1H),1.34–1.26 (m,1H),0.89(s,1H).
The analysis detecting data row of specific composite structure compound disclosed in the embodiment of the present invention are in table 1 below.
Table 1：
All structural compounds prepared in the embodiment of the present invention have completed the dissolubility in toluene and lighted The test of property, specific experiment result are as shown in table 2 below.
Table 2：
It can be clearly apparent by table 2, all structural compounds that the embodiment of the present invention 1 is prepared into embodiment 63 are in the solution All there is good luminosity.
Comparative example 1：
The present embodiment is test and com-parison and analysis the compounds of this invention C36 and the spectrum of the known compound 1 of prior art.
The structural formula of two control compounds is as follows：
The emission spectrum of two control compounds refers to accompanying drawing 1.
From accompanying drawing 2, from the point of view of emission spectrum, the PL emission peaks of known compound 1 are contrasted in 467nm.In this hair In bright compound C36 molecular structure, the position of substitution of phenyl becomes ortho position from contraposition on phenyl ring so that compound C36 Emission peak wavelength blue shift to 454nm, obtained a kind of deeper blue light.
Its mechanism is that ortho-substituent is introduced between the aromatic ring for causing to be connected with N atoms, and aromatic ring and N originals Conjugation between lone electron pair on son weakens, and then causes the band gap of molecule to improve, so there occurs the blue shift of emission spectrum.
Fully demonstrated by the comparative example embodiment, it is of the invention in the molecular structure innovative design of mutual-through type compound, Ensure that the wavelength of the emission peak of the compounds of this invention obtains blue shift using the scheme for introducing big steric hindrance substituent, and then obtain this hair Improving eyesight target lights a kind of new compound of deeper blue light.
Part II, it is the Application Example of noval chemical compound of the present invention：
By applying practical technique effect of the embodiment in organic electroluminescence device to the compounds of this invention below It is described in detail.
Comparative example 2
The glass plate for being coated with transparent conductive layer is ultrasonically treated in commercial detergent, rinsed in deionized water, In acetone: alcohol mixed solvent (volume ratio 1:1) ultrasonic oil removing in, it is baked under clean environment and removes moisture content completely, with purple Outer light and ozone clean, and with low energy cation beam bombarded surface；
The above-mentioned glass substrate with anode is placed in vacuum chamber, 1 × 10-5~9 × 10-3Pa is evacuated to, upper State vacuum evaporation 2-TNATA on anode tunic and, as hole injection layer, evaporation rate 0.1nm/s, thickness 10nm is deposited；
Hole transmission layers of the vacuum evaporation NPB as device on hole injection layer, evaporation rate 0.1nm/s, steam Plating total film thickness is 80nm；
The luminescent layer of vacuum evaporation device on hole transmission layer, luminescent layer include material of main part and dye materials, profit The method steamed altogether with multi-source, regulation material of main part ADN evaporation rates are 0.1nm/s, and the ratio of dyestuff DSA-Ph evaporation rates 3% is set Fixed, evaporation total film thickness is 30nm；
The electron transport layer materials Bphen of vacuum evaporation device on luminescent layer, its evaporation rate are 0.1nm/s, are steamed Plating total film thickness is 30nm；
Vacuum evaporation thickness is 0.5nm LiF as electron injecting layer, thickness 150nm on electron transfer layer (ETL) Negative electrode of the Al layers as device.
The structure of organic electroluminescence device is in comparative example 2 of the present invention：
ITO/2-TNATA(10nm)/NPB(80nm)/ADN：DSA-Ph(30nm)/Bphen(30nm)/LiF(1nm)/Al.
Each functional layer material molecular structure is as follows：
Comparative example 3
Organic electroluminescence device is prepared using with the identical method of comparative example 2, difference is, by blue light dyestuff DSA-Ph replaces with known compound 1.
Embodiment 64
Organic electroluminescence device is prepared using with the identical method of comparative example 2, difference is, by blue light dyestuff DSA-Ph replaces with C34.
Embodiment 65
Organic electroluminescence device is prepared using with the identical method of comparative example 2, difference is, by blue light dyestuff DSA-Ph replaces with C35.
Device embodiments 66
Organic electroluminescence device is prepared using the method same with comparative example 2, difference is, by blue light dyestuff DSA- Ph replaces with C48.
Device embodiments 67
Organic electroluminescence device is prepared using with the identical method of comparative example 2, difference is, by blue light dyestuff DSA-Ph replaces with C49.
Device embodiments 68
Organic electroluminescence device is prepared using with the identical method of comparative example 2, difference is, by blue light dyestuff DSA-Ph replaces with compound C51.
Under same brightness 1000cd/m2, the organic electroluminescence device being prepared in device embodiments 64-68 is determined Driving voltage and current efficiency and CIE coordinate values, corresponding performance indications refer to table 3 below.
Table 3：
It is required that brightness cd/m2 Voltage V Current efficiency cd/A CIE(x,y)
Comparative example 2 1000.00 5.7 8.5 0.14,0.35
Comparative example 3 1000.00 5.4 8.0 0.14,0.17
Embodiment 64 1000.00 5.2 8.5 0.13,0.14
Embodiment 65 1000.00 5.3 8.6 0.14,0.13
Embodiment 66 1000.00 5.4 8.4 0.13,0.13
Embodiment 67 1000.00 5.2 7.9 0.14,0.11
Embodiment 68 1000.00 5.5 8.2 0.14,0.12
Result above is visible, existing with using when the new organic materials of the present invention are practically applicable into organic electroluminescence device There is the organic electroluminescence device prepared by the day blue light material DSA-Ph in technology to carry out performance comparision, the chromaticity coordinates y of device Value is reduced to 0.11-0.14 from 0.35.When with using the known chemical combination with the compounds of this invention structure proximate in the prior art When corresponding device prepared by thing 1 carries out performance comparision, y values there has also been obvious reduction, can obtain the indigo plant of higher color purity Optical device.Prove that preferred compounds of the invention possesses excellent electroluminescence characters by this group of embodiment, be dark blue well Luminescent material.
The preferred embodiment of the present invention described in detail above, still, the present invention are not limited in above-mentioned embodiment Detail, in the range of the technology design of the present invention, a variety of simple variants can be carried out to technical scheme, this A little simple variants belong to protection scope of the present invention.
It is further to note that each particular technique feature described in above-mentioned embodiment, in not lance In the case of shield, can be combined by any suitable means, in order to avoid unnecessary repetition, the present invention to it is various can The combination of energy no longer separately illustrates.
In addition, various embodiments of the present invention can be combined randomly, as long as it is without prejudice to originally The thought of invention, it should equally be considered as content disclosed in this invention.

Claims (13)

1. a kind of general formula compound is as shown in following formula I：
In formula I：
R ' is selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl；
Ar1Selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30Cycloalkyl, substitution or Unsubstituted C6~C30Aryl, substituted or unsubstituted C2~C30Heteroaryl；
Ar2As shown in following formula II：
In formula II：
R1~R5It is each independently selected from hydrogen, halogen, substituted or unsubstituted C1~C30Alkyl, substituted or unsubstituted C3~C30Ring Alkyl, substituted or unsubstituted C6~C30Aryl, substituted or unsubstituted C2~C30Heteroaryl, and R1、R5In at least one not For hydrogen.
2. according to the general formula compound described in claim 1,
In formula I, the Ar1With Ar2Connect to form substituted or unsubstituted ring structure by two adjacent groups, the ring structure Constituting atom be selected from carbon atom, nitrogen-atoms, oxygen atom or sulphur atom, the ring structure is selected from five-membered ring or hexatomic ring.
3. general formula compound according to claim 2,
In formula I, the Ar1With Ar2The ring structure to be formed, which is connected, by two adjacent groups is selected from pyrrole ring, piperidine ring, morpholine Ring, thiomorpholine ring, piperazine ring.
4. according to the general formula compound described in claim 1,
In formula II, the R1With R2、R4With R5Connect to form substituted or unsubstituted ring structure by two adjacent groups, the ring The constituting atom of structure is selected from carbon atom, nitrogen-atoms, oxygen atom or sulphur atom, and the ring structure is selected from C6~C30Aliphatic list Ring, C6~C30Aliphatic is polycyclic, C6~C30Aromatic monocyclic or C6~C30Aromatic fused ring.
5. general formula compound according to claim 4,
In formula II, the R1With R2、R4With R5Connected by two adjacent groups and to form substituted or unsubstituted ring structure and be selected from Pentamethylene ring, cyclohexane ring, dicyclopentenyl ring, nafoxidine ring, tetrahydrofuran ring, piperidine ring, pentamethylene ring and cyclohexane ring In carbon atom the ester ring, phenyl ring, naphthalene nucleus, pyrrole ring, pyridine ring, indole ring, the N- phenyl substituted indoles that substitute to obtain by ketone group Ring.
6. general formula compound according to claim 2,
In formula II, the R1With R2、R4With R5Connect to form substituted or unsubstituted ring structure by two adjacent groups, the ring The constituting atom of structure is selected from carbon atom, nitrogen-atoms, oxygen atom or sulphur atom, and the ring structure is selected from C6~C30Aliphatic list Ring, C6~C30Aliphatic is polycyclic, C6~C30Aromatic monocyclic or C6~C30Aromatic fused ring.
7. general formula compound according to claim 6,
In formula II, the R1With R2、R4With R5Connected by two adjacent groups and to form substituted or unsubstituted ring structure and be selected from Pentamethylene ring, cyclohexane ring, dicyclopentenyl ring, nafoxidine ring, tetrahydrofuran ring, piperidine ring, pentamethylene ring and cyclohexane ring In carbon atom the ester ring, phenyl ring, naphthalene nucleus, pyrrole ring, pyridine ring, indole ring, the N- phenyl substituted indoles that substitute to obtain by ketone group Ring, thiphene ring, furan nucleus.
8. according to the general formula compound described in one of claim 1,2,4 or 6,
In formula I：
The R ' is selected from substituted or unsubstituted C1~C10Alkyl；
The Ar1Selected from substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C3~C10Cycloalkyl, substitution or Unsubstituted C6~C20Aryl, substituted or unsubstituted C2~C20Heteroaryl；
In formula II：
The R1~R5It is each independently selected from substituted or unsubstituted C1~C10Alkyl, substituted or unsubstituted C3~C10Cycloalkyl, Substituted or unsubstituted C6~C20Aryl, substituted or unsubstituted C2~C20Heteroaryl, and R1~R5In at least one be not Hydrogen.
9. general formula compound according to claim 8,
In formula I：
The R ' is selected from substituted or unsubstituted C1~C6Alkyl；
The Ar1Selected from substituted or unsubstituted C1~C6Alkyl, substituted or unsubstituted C3~C6Cycloalkyl, phenyl, connection Phenyl, terphenyl, naphthyl, phenanthryl, indenyl, fluorenyl and its derivative, fluoranthene base, Sanya phenyl, pyrenyl, base,Base, furan Mutter base, thienyl, pyrrole radicals, benzofuranyl, benzothienyl, isobenzofuran-base, indyl, dibenzofuran group, two Benzothienyl, carbazyl and its derivative；
In formula II：
The R1~R5It each is selected from substituted or unsubstituted C1~C6Alkyl, substituted or unsubstituted C3~C6Cycloalkyl, Phenyl, xenyl, terphenyl, naphthyl, phenanthryl, indenyl, fluorenyl and its derivative, fluoranthene base, Sanya phenyl, pyrenyl, base,Base, furyl, thienyl, pyrrole radicals, benzofuranyl, benzothienyl, isobenzofuran-base, indyl, dibenzo furan Mutter base, dibenzothiophenes base, carbazyl and its derivative, and R1~R5In at least one be not hydrogen.
10. general formula compound according to claim 8,
In formula I：
The R ' is selected from hydrogen, halogen, methyl, ethyl, n-propyl, isopropyl, normal-butyl, n-hexyl, n-octyl, isobutyl group, uncle Butyl, cyclopenta, cyclohexyl；
The Ar1Selected from hydrogen, halogen, methyl, ethyl, n-propyl, isopropyl, normal-butyl, n-hexyl, isobutyl group, the tert-butyl group, ring Propyl group, cyclobutyl, cyclopenta, cyclohexyl, benzene, 1- naphthalenes, 2- naphthalenes, 4- phenanthrene, 9- phenanthrene, 2- pyrenes, 2- biphenyl, 4- fluorenes, 4- spiro fluorenes, Sanya Benzene,, fluoranthene, 1- dibenzofurans, 4- dibenzofurans, 3- dibenzothiophenes, 4- dibenzothiophenes, 2- benzothiophenes, N- carbazoles, 3- carbazoles, N- acridines, N- phenoxazines, N- phenthazine, 9- phenyl carbazoles, 9- naphthyl carbazoles, benzo carbazole, dibenzo Carbazole, 3- phenyl carbazoles, 3,6- diphenyl carbazoles；
In formula II：
The R1~R5Be each independently selected from methyl, ethyl, n-propyl, isopropyl, normal-butyl, n-hexyl, isobutyl group, the tert-butyl group, Cyclopropyl, cyclobutyl, cyclopenta, cyclohexyl, benzene, 1- naphthalenes, 2- naphthalenes, 4- phenanthrene, 9- phenanthrene, 2- pyrenes, 2- biphenyl, 4- fluorenes, 4- spiro fluorenes, three Sub- benzene,, fluoranthene, 1- dibenzofurans, 4- dibenzofurans, 3- dibenzothiophenes, 4- dibenzothiophenes, 2- benzo thiophenes Fen, N- carbazoles, 3- carbazoles, N- acridines, N- phenoxazines, N- phenthazine, 9- phenyl carbazoles, 9- naphthyl carbazoles, benzo carbazole, hexichol And carbazole, 3- phenyl carbazoles, 3,6- diphenyl carbazoles, and R1~R5In at least one be not hydrogen.
11. general formula compound according to claim 8, selected from following concrete structure formulas：
12. general formula compound according to claim 8, apply photic display film, electroluminescent display film, filter coating, Color conversion film, organic electroluminescence device, OTFT, organic light-emitting transistor and Organic Light Emitting Devices In.
13. structural compounds according to claim 11, apply photic display film, electroluminescent display film, filter coating, Color conversion film, organic electroluminescence device, OTFT, organic light-emitting transistor and Organic Light Emitting Devices In.
CN201610730802.7A 2016-08-26 2016-08-26 One kind 1,4 2 substitutes naphthalene derivatives and application Withdrawn CN107778213A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610730802.7A CN107778213A (en) 2016-08-26 2016-08-26 One kind 1,4 2 substitutes naphthalene derivatives and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610730802.7A CN107778213A (en) 2016-08-26 2016-08-26 One kind 1,4 2 substitutes naphthalene derivatives and application

Publications (1)

Publication Number Publication Date
CN107778213A true CN107778213A (en) 2018-03-09

Family

ID=61439062

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610730802.7A Withdrawn CN107778213A (en) 2016-08-26 2016-08-26 One kind 1,4 2 substitutes naphthalene derivatives and application

Country Status (1)

Country Link
CN (1) CN107778213A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111875551A (en) * 2019-09-02 2020-11-03 广东聚华印刷显示技术有限公司 Organic compound, electronic device and corresponding preparation method
JP2021031496A (en) * 2019-08-26 2021-03-01 北京夏禾科技有限公司 Aromatic amine derivative and organic electroluminescent devices containing the same
WO2021036851A1 (en) * 2019-08-27 2021-03-04 陕西莱特光电材料股份有限公司 Nitrogen-containing compound, organic electroluminescent device and photoelectric conversion device

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1412864A (en) * 2001-10-18 2003-04-23 日本电气株式会社 Organic thin film transistor
CN1906153A (en) * 2004-06-28 2007-01-31 出光兴产株式会社 Aromatic amine derivative and organic electroluminescent device using the same
CN1980884A (en) * 2004-08-31 2007-06-13 出光兴产株式会社 Aromatic amine derivative and organic electroluminescent device using the same
WO2008056722A1 (en) * 2006-11-09 2008-05-15 Idemitsu Kosan Co., Ltd. Organic el material-containing solution, method for forming thin film of organic el material, thin film of organic el material, and organic el device
WO2009008351A1 (en) * 2007-07-07 2009-01-15 Idemitsu Kosan Co., Ltd. Organic el device
KR20100008947A (en) * 2008-07-17 2010-01-27 덕산하이메탈(주) Fluorenecarbazole derivative and organic electroluminescent device comprising same
KR20160078765A (en) * 2014-12-24 2016-07-05 솔브레인 주식회사 COMPOUND, ORGANIC LiGHT EMITTING DIODE INCLUDING THE SAME AND DISPLAY INCLUDING THE ORGANIC LiGHT EMITTING DIODE

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1412864A (en) * 2001-10-18 2003-04-23 日本电气株式会社 Organic thin film transistor
CN1906153A (en) * 2004-06-28 2007-01-31 出光兴产株式会社 Aromatic amine derivative and organic electroluminescent device using the same
CN1980884A (en) * 2004-08-31 2007-06-13 出光兴产株式会社 Aromatic amine derivative and organic electroluminescent device using the same
WO2008056722A1 (en) * 2006-11-09 2008-05-15 Idemitsu Kosan Co., Ltd. Organic el material-containing solution, method for forming thin film of organic el material, thin film of organic el material, and organic el device
WO2009008351A1 (en) * 2007-07-07 2009-01-15 Idemitsu Kosan Co., Ltd. Organic el device
KR20100008947A (en) * 2008-07-17 2010-01-27 덕산하이메탈(주) Fluorenecarbazole derivative and organic electroluminescent device comprising same
KR20160078765A (en) * 2014-12-24 2016-07-05 솔브레인 주식회사 COMPOUND, ORGANIC LiGHT EMITTING DIODE INCLUDING THE SAME AND DISPLAY INCLUDING THE ORGANIC LiGHT EMITTING DIODE

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021031496A (en) * 2019-08-26 2021-03-01 北京夏禾科技有限公司 Aromatic amine derivative and organic electroluminescent devices containing the same
JP7175023B2 (en) 2019-08-26 2022-11-18 北京夏禾科技有限公司 Aromatic amine derivative and organic electroluminescent device containing the same
US11937499B2 (en) 2019-08-26 2024-03-19 Beijing Summer Sprout Technology Co., Ltd. Aromatic amine derivative and organic electroluminescent devices containing the same
WO2021036851A1 (en) * 2019-08-27 2021-03-04 陕西莱特光电材料股份有限公司 Nitrogen-containing compound, organic electroluminescent device and photoelectric conversion device
CN111875551A (en) * 2019-09-02 2020-11-03 广东聚华印刷显示技术有限公司 Organic compound, electronic device and corresponding preparation method
CN111875551B (en) * 2019-09-02 2022-04-15 广东聚华印刷显示技术有限公司 Organic compound, electronic device and corresponding preparation method

Similar Documents

Publication Publication Date Title
CN109251176B (en) Organic electroluminescent device
CN107833974B (en) A kind of novel electroluminescent device
CN110498765B (en) Compound, organic electroluminescent material and organic electroluminescent device
CN105503622A (en) Benzo[c]phenanthrene derivative with electron donor-acceptor structure and application thereof and electroluminescent device
CN107778212A (en) One kind 1,5 2 substitutes naphthalene derivatives and its application
CN109776542A (en) A kind of electroluminescent organic material and its application
CN112490391B (en) Organic electroluminescent device and display device
CN107954942A (en) Benzopyrazines substitutes anthracene derivant and organic electroluminescence device
CN104628623A (en) 2,6,6,8-tetra-substituted-6H-benzo[cd]pyrene compound and organic electroluminescence device containing same
CN107778213A (en) One kind 1,4 2 substitutes naphthalene derivatives and application
CN109942541B (en) Fluorenocarbazole derivative and preparation method and application thereof
CN108727389B (en) Pyrene derivative and application thereof in organic luminescent material
CN107840834A (en) A kind of benzopyrenes compound and application
TW201332943A (en) Aromatic amine derivative and organic electroluminescence device using same
CN109400603A (en) Compound and its application in organic light emission field
CN109836421B (en) A compound of general formula and its application
CN112442037A (en) Luminescent material and application thereof
CN111943942A (en) Compound, thermal activation sensitized fluorescent material, organic electroluminescent device and application
CN111354855A (en) Organic electroluminescent device
CN110128329A (en) Nitrogenous heterocyclic aromatic amino-derivative and its application and organic electroluminescence device
WO2022078250A1 (en) Organic compound for light-emitting device, use of organic compound, and organic light-emitting device
CN109411631A (en) Class terpyridyl derivative and its application in luminous organic material
CN109251203A (en) Pyrazolo indazole derivative and its application
CN115703747A (en) Organic compound having spirofluorene structure for light emitting device, organic electroluminescent device
CN107759527B (en) Compound, application thereof and organic electroluminescent device

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20180309