WO2021120835A1 - 含氮化合物、有机电致发光器件和电子装置 - Google Patents

含氮化合物、有机电致发光器件和电子装置 Download PDF

Info

Publication number
WO2021120835A1
WO2021120835A1 PCT/CN2020/122846 CN2020122846W WO2021120835A1 WO 2021120835 A1 WO2021120835 A1 WO 2021120835A1 CN 2020122846 W CN2020122846 W CN 2020122846W WO 2021120835 A1 WO2021120835 A1 WO 2021120835A1
Authority
WO
WIPO (PCT)
Prior art keywords
carbon atoms
group
substituted
nitrogen
independently selected
Prior art date
Application number
PCT/CN2020/122846
Other languages
English (en)
French (fr)
Inventor
杨敏
马天天
南朋
Original Assignee
陕西莱特光电材料股份有限公司
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 陕西莱特光电材料股份有限公司 filed Critical 陕西莱特光电材料股份有限公司
Priority to KR1020217042823A priority Critical patent/KR102442362B1/ko
Priority to US17/623,211 priority patent/US11608311B2/en
Publication of WO2021120835A1 publication Critical patent/WO2021120835A1/zh

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • 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
    • C07C211/54—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 two or three six-membered aromatic rings
    • 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
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
    • 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
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/82—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • 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
    • C07D333/76—Dibenzothiophenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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 Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • 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
    • H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
    • 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
    • H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/624—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing six or more rings
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
    • 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
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • 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
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
    • 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
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H10K85/636—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
    • 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
    • H10K85/652—Cyanine 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
    • H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
    • 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
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05—Isotopically modified compounds, e.g. labelled
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
    • C07C2603/18—Fluorenes; Hydrogenated fluorenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
    • C07C2603/42—Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
    • C07C2603/50—Pyrenes; Hydrogenated pyrenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/56—Ring systems containing bridged rings
    • C07C2603/58—Ring systems containing bridged rings containing three rings
    • C07C2603/70—Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74—Adamantanes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/56—Ring systems containing bridged rings
    • C07C2603/90—Ring systems containing bridged rings containing more than four rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/93—Spiro compounds
    • C07C2603/94—Spiro compounds containing "free" spiro atoms
    • 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
    • C09K2211/1044—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
    • C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only 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
    • C09K2211/1092—Heterocyclic compounds characterised by ligands containing sulfur as the only heteroatom
    • 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells

Definitions

  • This application relates to the technical field of organic materials, in particular to a nitrogen-containing compound, an organic electroluminescent device using the nitrogen-containing compound, and an electronic device using the organic electroluminescent device.
  • Organic electroluminescent devices also known as organic light-emitting diodes, refer to the phenomenon that organic light-emitting materials are excited by current to emit light under the action of an electric field. It is a process of converting electrical energy into light energy.
  • organic electroluminescent diodes OLED have the advantages of active light emission, large optical path range, low driving voltage, high brightness, high efficiency, low energy consumption, and simple manufacturing process. It is precisely because of these advantages that organic light-emitting materials and devices have become one of the most popular scientific research topics in the scientific and industrial circles.
  • blue materials are an indispensable part of display and lighting technology. Blue materials play a very important role in reducing the energy consumption of display and lighting devices and enhancing the overall effect of the devices.
  • blue materials The development of China has always been a problem. The existing blue phosphorescent materials have few types and poor stability, so the development of such materials is of great significance.
  • the blue light materials disclosed in patents CN108129332A, US20190074449A and CN109651174A have improved light-emitting characteristics, they are not enough to meet actual needs.
  • the purpose of this application is to provide a nitrogen-containing compound, organic electroluminescent device and electronic device to improve the performance of the organic electroluminescent device and electronic device.
  • a nitrogen-containing compound is provided, and the structure of the nitrogen-containing compound is shown in Chemical Formula 1:
  • Ar 1 , Ar 2 , Ar 3 and Ar 4 are the same or different, and are each independently selected from substituted or unsubstituted aryl groups having 6 to 30 carbon atoms, and substituted or unsubstituted carbon atoms of 3 30 heteroaryl groups, and at least one of Ar 1 , Ar 2 , Ar 3 and Ar 4 is
  • p is selected from 1, 2, 3, 4, when p is greater than or equal to 2, any two R 10 are the same or different;
  • q is selected from 1, 2, 3, when q is greater than or equal to 2, any two R 9 are the same or different;
  • R 1 to R 10 are the same or different, and are each independently selected from: hydrogen, deuterium, halogen, cyano, substituted or unsubstituted silyl, substituted or unsubstituted alkyl with 1-10 carbon atoms, substituted Or an unsubstituted aryl group with 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group with 3-30 carbon atoms, and a substituted or unsubstituted cycloalkyl group with 1-20 carbon atoms.
  • an organic electroluminescent device comprising an anode and a cathode arranged oppositely, and a functional layer arranged between the anode and the cathode; the functional layer includes the above-mentioned containing Nitrogen compounds.
  • an electronic device including the above-mentioned organic electroluminescent device.
  • the nitrogen-containing compound of this application includes a fluorene group spiro-connected with a pyrene group and adamantane.
  • the pyrene group has a larger rigid conjugated structure, strong chemical stability, blue light emission, high fluorescence quantum efficiency, etc.
  • this application uses large groups to modify it, and sterically hinders it to avoid the ⁇ aggregation or excimer formed by the direct stacking of the conjugate plane.
  • Aromatic amine compounds with adamantane spiro-linked fluorene group have a large molecular weight, which can effectively increase the glass transition temperature of nitrogen-containing compounds, and the large steric hindrance of its structure makes it difficult for nitrogen-containing compounds to crystallize Or agglomerate, so that the nitrogen-containing compound has a better lifetime in the device.
  • the nitrogen atom on the aromatic amine has a strong electron donating ability, which improves the hole mobility, so that the electrons and holes move quickly to the recombination area, recombine light, and achieve dynamic equilibrium, thereby improving the efficiency of the device.
  • FIG. 1 is a schematic structural diagram of an organic electroluminescent device according to an embodiment of the present application.
  • FIG. 2 is a schematic structural diagram of an electronic device according to an embodiment of the present application.
  • Electron transport layer 360, electron injection layer; 400, electronic device.
  • the present application provides a nitrogen-containing compound, the structure of the nitrogen-containing compound is shown in Chemical Formula 1:
  • Ar 1 , Ar 2 , Ar 3 and Ar 4 are the same or different, and are each independently selected from substituted or unsubstituted aryl groups having 6 to 30 carbon atoms, and substituted or unsubstituted carbon atoms of 3 30 heteroaryl groups, and at least one of Ar 1 , Ar 2 , Ar 3 and Ar 4 is
  • p is selected from 1, 2, 3, 4, when q is greater than or equal to 2, any two R 9 are the same or different;
  • q is selected from 1, 2, 3, when q is greater than or equal to 2, any two R 9 are the same or different;
  • R 1 to R 10 are the same or different, and are each independently selected from: hydrogen, deuterium, halogen, cyano, substituted or unsubstituted silyl, substituted or unsubstituted alkyl with 1-10 carbon atoms, substituted Or an unsubstituted aryl group with 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group with 3-30 carbon atoms, and a substituted or unsubstituted cycloalkyl group with 1-20 carbon atoms.
  • At least one of Ar 1 , Ar 2 , Ar 3 and Ar 4 is "Means that one of Ar 1 , Ar 2 , Ar 3 and Ar 4 is Or two of Ar 1 , Ar 2 , Ar 3 and Ar 4 are Or three of Ar 1 , Ar 2 , Ar 3 and Ar 4 are Or four of Ar 1 , Ar 2 , Ar 3 and Ar 4 are
  • silyl refers to trialkylsilyl and triarylsilyl, and specific examples include, but are not limited to, trimethylsilyl, triethylsilyl, triphenylsilyl, and the like.
  • R 9 and R 10 are selected from hydrogen, adamantane spirofluorene is not substituted.
  • the nitrogen-containing compound of this application includes a fluorene group spiro-connected with a pyrene group and adamantane.
  • the pyrene group has a larger rigid conjugated structure, strong chemical stability, blue light emission, high fluorescence quantum efficiency, etc.
  • this application uses large groups to modify it, and sterically hinders it to avoid the ⁇ aggregation or excimer formed by the direct stacking of the conjugate plane.
  • Aromatic amine compounds with adamantane spiro-linked fluorene group have a large molecular weight, which can effectively increase the glass transition temperature of nitrogen-containing compounds, and the large steric hindrance of its structure makes it difficult for nitrogen-containing compounds to crystallize Or agglomerate, so that the nitrogen-containing compound has a better lifetime in the device.
  • the nitrogen atom on the aromatic amine has a strong electron donating ability, which improves the hole mobility, so that the electrons and holes move quickly to the recombination area, recombine light, and achieve dynamic equilibrium, thereby improving the efficiency of the device.
  • each... are independently” and “... are independently” and “... are independently selected from” are interchangeable, and should be understood in a broad sense, which can be either It means that in different groups, the specific options expressed between the same symbols do not affect each other, or it can mean that the specific options expressed between the same symbols do not affect each other in the same group.
  • each q is independently 0, 1, 2 or 3, and each R" is independently selected from hydrogen, deuterium, fluorine, and chlorine", and its meaning is:
  • formula Q-1 represents q substituents R" on the benzene ring , Each R" can be the same or different, and the options of each R" do not affect each other;
  • formula Q-2 means that there are q substituents R" on each benzene ring of biphenyl, and R on two benzene rings The number q of "substituents can be the same or different, and each R" can be the same or different, and the options of each R" do not affect each other.
  • substituted or unsubstituted means that the functional group described after the term may or may not have a substituent (hereinafter, for ease of description, the substituents are collectively referred to as Rc).
  • Rc substituents
  • the "substituted or unsubstituted aryl group” refers to an aryl group having a substituent Rc or an unsubstituted aryl group.
  • the above-mentioned substituent Rc can be, for example, deuterium, fluorine, chlorine, bromine, cyano, heteroaryl with 3-20 carbon atoms, aryl with 6-20 carbon atoms, and 3 carbon atoms.
  • trialkylsilyl group arylsilyl group with 8-12 carbon atoms, alkyl group with 1-10 carbon atoms, haloalkyl group with 1-10 carbon atoms, 2 carbon atoms -6 alkenyl, carbon 2-6 alkynyl, carbon 3-10 cycloalkyl, carbon 2-10 heterocycloalkyl, carbon 5-10 Cycloalkenyl, heterocycloalkenyl with 4-10 carbon atoms, alkoxy with 1-10 carbon atoms, alkylamino with 1-10 carbon atoms, and alkane with 1-10 carbon atoms Thio group, aryloxy group with 6-18 carbon atoms, arylthio group with 6-18 carbon atoms, alkylsulfonyl group with 6-18 carbon atoms, trioxane with 3-18 carbon atoms Phosphine group, trialkylboron group with 3-18 carbon atoms.
  • the "substituted" functional group may be substituted by one or more of the above-mentioned Rc substituents; when two substituents Rc are attached to the same atom, these two substituents Rc may exist independently or They are connected to each other to form a ring with the atom; when there are two adjacent substituents Rc on the functional group, the adjacent substituents Rc may exist independently or be condensed with the functional group to which they are connected to form a ring.
  • the substituents on the Ar 1 , Ar 2 , Ar 3 , Ar 4 , R 1 to R 10 are the same or different, and are independently selected from deuterium, cyano, halogen, and the number of carbon atoms is 1- 3 straight chain alkyl groups, branched chain alkyl groups with 3-7 carbon atoms, aryl groups with 6-18 carbon atoms, heteroaryl groups with 3-18 carbon atoms, 3-10 carbon atoms A cycloalkyl group, a heterocycloalkyl group having 2-7 carbon atoms, and an alkoxy group having 1-7 carbon atoms.
  • the number of carbon atoms of Ar 1 , Ar 2 , Ar 3 , Ar 4 , and R 1 to R 10 refers to the number of all carbon atoms.
  • Ar 1 , Ar 2 , Ar 3 , Ar 4 , R 1 to R 10 are selected from substituted aryl groups with 18 carbon atoms, then all the carbon atoms of the aryl group and the substituents thereon are 18.
  • hetero means that a functional group includes at least one heteroatom such as B, O, N, P, Si, Se, or S, and the remaining atoms are carbon and hydrogen.
  • the unsubstituted alkyl group may be a "saturated alkyl group" without any double or triple bonds.
  • an aryl group refers to an optional functional group or substituent derived from an aromatic hydrocarbon ring.
  • the aryl group can be a monocyclic aryl group or a polycyclic aryl group.
  • the aryl group can be a monocyclic aryl group, a condensed ring aryl group, two or more monocyclic aryl groups conjugated by a carbon-carbon bond, and A monocyclic aryl group and a condensed ring aryl group conjugated by carbon bonds, and two or more fused ring aryl groups conjugated by a carbon-carbon bond. That is, two or more aromatic groups conjugated through carbon-carbon bonds can also be regarded as aryl groups in the present application.
  • aryl group does not contain heteroatoms such as B, O, N, P, Si, Se, or S.
  • aryl groups may include phenyl, naphthyl, fluorenyl, anthryl, phenanthryl, biphenyl, terphenyl, tetraphenyl, pentaphenyl, hexaphenyl, benzo[9 ,10] Phenanthryl, pyrenyl, benzofluoranthene, fluorenyl, fluorenyl, etc., but not limited thereto.
  • the involved arylene group refers to a divalent group formed by further losing one hydrogen atom of an aryl group.
  • the non-positioned connecting bond refers to the single bond protruding from the ring system It means that one end of the link can be connected to any position in the ring system that the bond penetrates, and the other end is connected to the rest of the compound molecule.
  • the naphthyl group represented by the formula (f) is connected to other positions of the molecule through two non-positional linkages that penetrate the bicyclic ring, and the meaning represented by the formula (f) -1) Any possible connection method shown in formula (f-10).
  • the phenanthryl group represented by the formula (X') is connected to other positions of the molecule through a non-localized bond extending from the middle of the benzene ring on one side, which represents The meaning of includes any possible connection modes shown in formula (X'-1) to formula (X'-4).
  • the non-positional substituent in this application refers to a substituent connected by a single bond extending from the center of the ring system, which means that the substituent can be attached to any possible position in the ring system.
  • the substituent R'represented by the formula (Y) is connected to the quinoline ring through a non-localized linkage, and its meaning includes the following formula (Y-1) ⁇ Any possible connection mode shown in formula (Y-7).
  • the alkyl group having 1-10 carbon atoms may be a straight-chain alkyl group or a branched-chain alkyl group.
  • the alkyl group having 1 to 10 carbon atoms may be a linear alkyl group having 1 to 10 carbon atoms, or a branched alkyl group having 3 to 10 carbon atoms.
  • the number of carbon atoms of the alkyl group may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, for example.
  • alkyl groups having 1-10 carbon atoms include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl Base, neopentyl, cyclopentyl, n-hexyl, heptyl, n-octyl, 2-ethylhexyl, nonyl, decyl, 3,7-dimethyloctyl, etc.
  • the alkyl group having 1 to 5 carbon atoms may be a straight-chain alkyl group or a branched-chain alkyl group.
  • the alkyl group having 1 to 5 carbon atoms may be a linear alkyl group having 1 to 5 carbon atoms, or a branched alkyl group having 3 to 5 carbon atoms.
  • the number of carbon atoms of the alkyl group may be 1, 2, 3, 4, or 5, for example.
  • alkyl groups having 1-5 carbon atoms include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isoamyl Base, neopentyl, cyclopentyl, etc.
  • the alkyl group having 1 to 3 carbon atoms may be a straight-chain alkyl group or a branched-chain alkyl group.
  • the alkyl group having 1 to 10 carbon atoms may be a linear alkyl group having 1 to 3 carbon atoms, or a branched alkyl group having 3 carbon atoms.
  • the number of carbon atoms of the alkyl group may be 1, 2, or 3, for example.
  • Specific examples of the alkyl group having 1 to 3 carbon atoms include, but are not limited to, methyl, ethyl, n-propyl, and isopropyl.
  • a substituted aryl group means that one or more hydrogen atoms in the aryl group are replaced by other groups.
  • at least one hydrogen atom is replaced by a deuterium atom, F, Cl, Br, I, CN, aryl, heteroaryl, hydroxyl, amino, branched alkyl, linear alkyl, cycloalkyl, alkoxy, alkylamine Group or other groups.
  • aryl substituted aryl include, but are not limited to, naphthyl substituted phenyl, phenyl substituted naphthyl, and the like.
  • heteroaryl-substituted aryl groups include, but are not limited to, dibenzofuranyl-substituted phenyl groups, dibenzothiophene-substituted phenyl groups, pyridine-substituted phenyl groups, and the like. It can be understood that the substituted aryl group with 18 carbon atoms means that the total number of carbon atoms of the aryl group and the substituent on the aryl group is 18. For example, the number of carbon atoms of 9,9-dimethylfluorenyl is 15.
  • the aryl group as a substituent is, for example, phenyl, biphenyl, naphthyl, 9,9-dimethylfluorenyl, 9,9-diphenylfluorenyl, spirobifluorenyl, anthracene Gee, Fiki, base.
  • a heteroaryl group refers to a monovalent aromatic ring containing at least one heteroatom in the ring or a derivative thereof.
  • the heteroatom may be at least one of B, O, N, P, Si, Se, and S.
  • the heteroaryl group can be a monocyclic heteroaryl group or a polycyclic heteroaryl group.
  • the heteroaryl group can be a single aromatic ring system or multiple aromatic ring systems conjugated through carbon-carbon bonds, and any aromatic
  • the ring system is an aromatic monocyclic ring or an aromatic fused ring.
  • heteroaryl groups may include thienyl, furyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, oxadiazolyl, triazolyl, pyridyl, bipyridyl, pyrimidinyl, triazinyl, Acridinyl, pyridazinyl, pyrazinyl, quinolinyl, quinazolinyl, quinoxalinyl, phenoxazinyl, phthalazinyl, pyridopyrimidinyl, pyridopyrazinyl, pyrazinopyrazine Azinyl, isoquinolinyl, indolyl, carbazolyl, N-arylcarbazolyl, N-heteroarylcarbazolyl, N-alkylcarbazolyl, benzoxazolyl, benzimidazole Group, benzothiazolyl, benzo, be
  • thienyl, furanyl, phenanthrolinyl, etc. are heteroaryl groups of a single aromatic ring system
  • N-arylcarbazolyl and N-heteroarylcarbazolyl are polycyclic rings conjugated through carbon-carbon bonds.
  • System type of heteroaryl In this application, the involved heteroarylene group refers to a divalent group formed by the heteroaryl group further losing one hydrogen atom.
  • the substituted heteroaryl group may be one or more hydrogen atoms in the heteroaryl group, such as deuterium atom, halogen group, -CN, aryl, heteroaryl, trialkylsilyl, alkane Group, cycloalkyl, alkoxy, alkylthio and other groups are substituted.
  • aryl-substituted heteroaryl groups include, but are not limited to, phenyl-substituted dibenzofuranyl, phenyl-substituted dibenzothienyl, phenyl-substituted pyridyl, and the like. It should be understood that the number of carbon atoms of the substituted heteroaryl group refers to the total number of carbon atoms of the heteroaryl group and the substituents on the heteroaryl group.
  • the heteroaryl group as a substituent is, for example, pyridyl, pyrimidinyl, carbazolyl, dibenzofuranyl, and dibenzothienyl.
  • the substituents on Ar 1 , Ar 2 , Ar 3 , Ar 4 , and R 1 to R 10 are the same or different, and are independently selected from deuterium, cyano, halogen, and the number of carbon atoms is 1- 3 straight-chain alkyl groups, branched-chain alkyl groups with 3-5 carbon atoms, aryl groups with 6-18 carbon atoms, heteroaryl groups with 3-12 carbon atoms, 3-10 carbon atoms ⁇ cycloalkyl.
  • the halogen group can be, for example, fluorine, chlorine, bromine, or iodine.
  • the R 1 to R 10 are the same or different, and are each independently selected from: hydrogen, deuterium, fluorine, cyano, substituted or unsubstituted silyl, and the number of substituted or unsubstituted carbon atoms is 1- 5 alkyl groups, substituted or unsubstituted aryl groups with 6-18 carbon atoms, substituted or unsubstituted heteroaryl groups with 3-12 carbon atoms, and substituted or unsubstituted carbon atoms with 1-10 ⁇ cycloalkyl.
  • the R 2 and R 6 are not hydrogen, and the R 1 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , and R 10 are all hydrogen.
  • Ar 1 , Ar 2 , Ar 3 and Ar 4 are the same or different, and are each independently selected from substituted or unsubstituted aryl groups having 6-25 carbon atoms, and the number of substituted or unsubstituted carbon atoms is 5-20 heteroaryl.
  • Ar 1 , Ar 2 , Ar 3 or Ar 4 are each independently selected from the group consisting of the following structures (i-1) to (i-9):
  • n 1 , n 4 , n 7 , and n 9 are the same or different, and are independently selected from 1, 2, 3, 4, and 5;
  • n 2 , n 3 , and n 11 are the same or different, and are independently selected from 1, 2, 3, 4, 5, 6, and 7;
  • n 5 , n 6 , and n 8 are the same or different, and are independently selected from 1, 2, 3, and 4;
  • n 10 is selected from 1, 2, 3, 4, 5, 6, 7, 8, 9;
  • X 1 and X 2 are the same or different, and are independently selected from C and N.
  • X 1 and X 2 are selected from C, it means that X 1 and X 2 are CH;
  • Y is selected from O, S, Si (E 12 E 13 ), C (E 14 E 15 ), N (E 16 ), Se;
  • Z 1 and Z 2 are the same or different, and are independently selected from O, S, N (E 17 ), and C (E 18 E 19 );
  • E 1 , E 4 , E 5 are the same or different, and are independently selected from deuterium, halogen, cyano, alkyl with 1-5 carbon atoms, heteroaryl with 3-18 carbon atoms, carbon atoms A cycloalkyl group of 3-10;
  • E 2 , E 3 , E 6 to E 19 are the same or different, and are each independently selected from hydrogen, deuterium, halogen, cyano, alkyl with 1-5 carbon atoms, aromatic with 6-18 carbon atoms Group, heteroaryl group with 3-18 carbon atoms, cycloalkyl group with 3-10 carbon atoms; or E 12 and E 13 can be connected to form a ring, or E 14 and E 15 can be connected to form a ring, or E 18 And E 19 can be connected to form a ring;
  • X 3 to X 7 are the same or different, and are independently selected from C(R') or N, and at least one of X 3 to X 7 is N, wherein R'in X 3 to X 7 is the same or Different and independently selected from alkyl groups having 1-5 carbon atoms, aryl groups having 6-18 carbon atoms, heteroaryl groups having 3-18 carbon atoms, and cycloalkyl groups having 3-10 carbon atoms , Or adjacent R'can be connected to form a ring.
  • n 1 is greater than or equal to 2, E 1 is the same or different; when n 2 is greater than or equal to 2, E 2 is the same or different; when n 3 is greater than or equal to 2, E 3 is the same or different;
  • n 4 is greater than or equal to 2, E 4 is the same or different; when n 5 is greater than or equal to 2, E 5 is the same or different; when n 6 is greater than or equal to 2, E 6 is the same or different; when n 7 is greater than or When equal to 2, E 7 is the same or different; when n 8 is greater than or equal to 2, E 8 is the same or different; when n 9 is greater than or equal to 2, E 9 is the same or different; when n 10 is greater than or equal to 2, E 10 is the same or different; when n 11 is greater than or equal to 2, E 11 is the same or different.
  • n 7 and n 9 are selected from 1, 2, 3, 4, and 5, and n 8 is selected from 1, 2, 3; in formula i-6-b , N 7 is selected from 1, 2, 3, 4, and 5, and n 8 and n 9 are selected from 1, 2, 3, and 4.
  • n 1 to n 11 are selected from 0, the benzene ring is not substituted.
  • Adjacent R' can be connected to form a ring, which means that X 3 and X 4 form a ring, or X 4 and X 5 form a ring, or X 5 and X 6 form a ring, or X 6 and X 7 form a ring, which of course also includes X 3 and X 4 form a ring, and X 5 and X 6 form a ring.
  • a and B "capable of being connected to form a ring" includes that A and B are independent of each other and not connected; it also includes that A and B are connected to each other to form a ring.
  • E 12 and E 13 can be connected to form a ring, including E 12 and E 13 are independent of each other and not connected, and E 12 and E 13 can be connected to each other to form a ring;
  • E 14 and E 15 can be connected to form a ring, including E 14 and E 15 are independent of each other and not connected, including E 14 and E 15 are connected to each other to form a ring;
  • E 18 and E 19 can be connected to form a ring, including E 18 and E 19 are independent of each other and not connected, also including E 18 and E 19 are connected to each other to form a ring.
  • X 3 and X 4 can be connected to form a ring, including R'of X 3 and R'of X 4 are independent of each other and not connected, and it also includes the connection of R'of X 3 and R'of X 4 and R'.
  • the atoms are connected to form a ring.
  • the ring refers to a saturated or unsaturated ring, for example Etc., but not limited to this.
  • Ar 1 , Ar 2 , Ar 3 or Ar 4 are each independently selected from the group consisting of the following groups:
  • Ar 1 , Ar 2 , Ar 3 or Ar 4 are each independently selected from the group consisting of the following groups:
  • the Ar 1 , Ar 2 , Ar 3 or Ar 4 are each independently selected from the following substituted or unsubstituted groups: phenyl, naphthyl, biphenyl, terphenyl, phenanthryl, anthracenyl , 9,9-spirobifluorenyl, 9,9-dimethylfluorenyl, pyridyl, carbazolyl, pyrimidinyl, 1,10-phenanthroline, pyridazinyl, triazinyl, quinolinyl, Quinazolinyl, phenylpyridyl, quinoxalinyl, pyrenyl, N-phenylcarbazolyl, dibenzofuranyl, dibenzothienyl or adamantane fluorenyl,
  • substitution is substituted by a group selected from the group consisting of deuterium, fluorine, chlorine, cyano, trimethylsilyl, methyl, ethyl, isopropyl, tert-butyl, phenyl, naphthyl, pyridyl , Dibenzofuranyl, carbazolyl or dibenzothienyl; when there are multiple substituents, the multiple substituents are the same or different.
  • the nitrogen-containing compound is selected from the group consisting of the following compounds:
  • the application also provides an organic electroluminescence device, which includes an anode and a cathode arranged oppositely, and a functional layer arranged between the anode and the cathode; the functional layer includes the nitrogen-containing compound of the application.
  • the organic light emitting device of the present application is a blue light device.
  • an organic electroluminescent device includes an anode 100 and a cathode 200 disposed oppositely, and a functional layer 300 disposed between the anode 100 and the cathode 200; the functional layer 300 includes the containing material provided in the present application. Nitrogen compounds.
  • the functional layer 300 includes an organic electroluminescent layer 330, and the organic electroluminescent layer 330 includes the nitrogen-containing compound of the present application.
  • the organic light-emitting layer 330 may be composed of a single light-emitting material, and may also include a host material and a guest material.
  • the organic light-emitting layer 330 is composed of a host material and a guest material. The holes injected into the organic light-emitting layer 330 and the electrons injected into the organic light-emitting layer 330 can recombine in the organic light-emitting layer 330 to form excitons, and the excitons transfer energy to The host material, the host material transfers energy to the guest material, so that the guest material can emit light.
  • the host material of the organic light-emitting layer 330 can be a metal chelate compound, a bisstyryl derivative, an aromatic amine derivative, a dibenzofuran derivative or other types of materials, which are not particularly limited in this application .
  • the host material of the organic light-emitting layer 330 may be ⁇ , ⁇ -ADN.
  • the guest material of the organic light-emitting layer 330 can be a compound with a condensed aryl ring or a derivative thereof, a compound with a heteroaryl ring or a derivative thereof, an aromatic amine derivative or other materials.
  • the organic The guest material of the light-emitting layer 330 is the nitrogen-containing compound of the application.
  • the organic electroluminescent device may include an anode 100, a hole transport layer 321, an electron blocking layer 322, an organic electroluminescent layer 330 as an energy conversion layer, and an electron transport layer which are sequentially stacked. 350 and cathode 200.
  • the nitrogen-containing compound provided in the present application can be applied to the organic electroluminescent layer 330 of an organic electroluminescent device, which can effectively improve the luminous efficiency and lifetime of the organic electroluminescent device, and reduce the driving voltage of the organic electroluminescent device.
  • the anode 100 includes the following anode material, which is preferably a material with a large work function (work function) that facilitates injection of holes into the functional layer.
  • anode materials include: metals such as nickel, platinum, vanadium, chromium, copper, zinc, and gold or their alloys; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); Combined metals and oxides such as ZnO:Al or SnO 2 :Sb; or conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene ] (PEDT), polypyrrole and polyaniline, but not limited thereto. It is preferable to include a transparent electrode containing indium tin oxide (ITO) as an anode.
  • ITO indium tin oxide
  • the hole transport layer 321 may include one or more hole transport materials, and the hole transport materials may be selected from carbazole polymers, carbazole-linked triarylamine compounds or other types of compounds. This does not make special restrictions.
  • the hole transport layer 321 is composed of the compound NPB.
  • the electron blocking layer 322 includes one or more electron blocking materials, and the electron blocking materials may be selected from carbazole polymers or other types of compounds, which are not specifically limited in this application.
  • the electron blocking layer 322 is composed of the compound TCTA.
  • the electron transport layer 350 can be a single-layer structure or a multi-layer structure, which can include one or more electron transport materials, which can be selected from benzimidazole derivatives and oxadiazole derivatives. , Quinoxaline derivatives or other electron transport materials, this application does not make any special restrictions.
  • the electron transport layer 340 may be composed of DBimiBphen and LiQ.
  • the cathode 200 includes the following cathode material, which is a material with a small work function that facilitates injection of electrons into the functional layer.
  • cathode materials include: metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead or their alloys; or multilayer materials such as LiF/Al, Liq/ Al, LiO 2 /Al, LiF/Ca, LiF/Al, and BaF 2 /Ca, but not limited thereto. It is preferable to include a metal electrode containing magnesium and silver as a cathode.
  • a hole injection layer 310 may be further provided between the anode 100 and the first hole transport layer 321 to enhance the ability to inject holes into the first hole transport layer 321.
  • the hole injection layer 310 can be selected from benzidine derivatives, starburst arylamine compounds, phthalocyanine derivatives or other materials, which are not particularly limited in this application.
  • the hole injection layer 310 may be composed of m-MTDATA.
  • an electron injection layer 360 may be further provided between the cathode 200 and the electron transport layer 350 to enhance the ability to inject electrons into the electron transport layer 350.
  • the electron injection layer 360 may include inorganic materials such as alkali metal sulfides and alkali metal halides, or may include complexes of alkali metals and organic substances.
  • the electron injection layer 360 may include LiQ.
  • a hole blocking layer 340 may also be provided between the organic electroluminescent layer 330 and the electron transport layer 350.
  • the embodiments of the present application also provide an electronic device, which includes the above-mentioned organic electroluminescent device. Since the electronic device has the above-mentioned organic electroluminescent device, it has the same beneficial effects, and the details are not repeated here in this application.
  • the present application provides an electronic device 400 including the above-mentioned organic electroluminescent device.
  • the electronic device 400 may be a display device, a lighting device, an optical communication device or other types of electronic devices, such as but not limited to computer screens, mobile phone screens, televisions, electronic paper, emergency lighting, light modules, etc. Since the electronic device 400 has the above-mentioned organic electroluminescent device, it has the same beneficial effects, which will not be repeated in this application.
  • the nuclear magnetic data of Intermediate 1-B are: 1 HNMR (400MHz, CDCl 2 ): 8.11 (d, 1H), 8.03 (d, 1H), 7.41-7.63 (m, 2H), 7.37-7.39 (m, 1H), 7.30-7.33 (m, 1H), 7.23-7.24 (m, 1H), 2.88-2.93 (m, 2H), 2.81-2.85 (m, 2H), 2.19 (s, 2H), 1.99 (s, 2H), 1.77-1.83 (m, 4H), 1.54 (s, 2H).
  • Intermediate-1-X-1 and Intermediate-1-X are synthesized by the same method as the synthesis method of Intermediate-1-A and Intermediate-1-B, where X can be C ,
  • X can be C
  • the other compound SM-1 in Table 1 is used instead of 2'-bromo-3-chlorobiphenyl.
  • the compound SM-1 can be 2-bromo-2'-chloro-1,1'- Biphenyl, and each compound SM-1 can produce its unique intermediate -1-X.
  • the synthesis process can be as shown in Reaction Formula 1, which can be:
  • SMZ-Y in the same way as the synthesis method of Intermediate-2-A, where Y can be 1 and 2, X is O or S, for example, SMZ-1-Y can be 1-bromo-diphenyl And furan and 1-bromodibenzothiophene.
  • SMZ is used instead of 1,6-dibromopyrene and aniline is used instead of diphenylamine.
  • each SMZ formed by X can prepare the corresponding SMZ-Y.
  • Intermediate-2-X is synthesized by the same method as the synthesis method of Intermediate-2-A, where X is B, C, D, E, F, G, H, I, and different
  • X is B, C, D, E, F, G, H, I, and different
  • the point is to use compound SM-2 instead of diphenylamine.
  • compound SM-2 can be N-phenyl-3-benzidine, N-phenyl-2 (9,9-dimethyl-9H-fluorene) Amine, 1-naphthylaminobenzene, 2-methyldiphenylamine, bis(3-biphenyl)amine, N-(4-(1-naphthyl)phenyl)-4-benzidine, N-2,6 -Diphenyl-2-naphthylamine and N-phenyl-2-naphthylamine, SMZ-1 and SMZ-2, and each compound SM-2 can be prepared as the only corresponding intermediate -2- X.
  • Reaction Formula 2 is shown in Reaction Formula 2, which is:
  • Intermediate-3-X is synthesized by the same method as the synthesis method of Intermediate-3-A, where X is B, C, D, E, F, G, H, I, G, K and L, the difference is that the other compound SM-3 in Table 3 is used instead of aniline.
  • compound SM-3 can be aniline, o-toluidine, 3-amino-1,1-biphenyl, 2- Naphthylamine, 4-fluoroaniline, 4-cyanoaniline, p-toluidine, 3-methylaniline, 4-amino-1,1-biphenyl, and each compound SM-3 can be prepared as unique The corresponding intermediate -3-X.
  • reaction formula 3 is shown in reaction formula 3, which is:
  • compound X is synthesized by the same method as that of compound 107, except that Intermediate-2-X is used instead of Intermediate-2-H, and Intermediate-3-X is used instead of Intermediate- 3-A, for example, Intermediate-2-X can be Intermediate-2-A, Intermediate-2-B, Intermediate-2-C, Intermediate-2-D, etc., Intermediate-3- X can be Intermediate-3-B, Intermediate-3-C, Intermediate-3-D, etc., from which the uniquely corresponding compound X can be prepared, the specific compound number, structure, raw material, and last step The synthesis yield and characterization data are shown in Table 4.
  • the blue organic electroluminescent device is prepared by the following method
  • the ITO substrate manufactured by Corning
  • the photolithography process was used to prepare it into an experimental substrate with cathode, anode and insulating layer patterns.
  • Ozone and O 2 :N 2 plasma are used for surface treatment to increase the work function of the anode (experimental substrate) and remove scum.
  • M-MTDATA (4,4',4"-tris(N-3-methylphenyl-N-phenylamino)triphenylamine) was vacuum-evaporated on the experimental substrate (anode) to form a thickness of The hole injection layer (HIL), and the compound NPB is vacuum-evaporated on the hole injection layer to form a thickness of The hole transport layer.
  • HIL hole injection layer
  • TCTA 4,4',4”-tris(carbazol-9-yl)triphenylamine
  • the thickness is formed by vapor deposition with a film thickness ratio of 20:1
  • DBimiBphen (4,7-diphenyl-2,9-bis(4-(1-phenyl-1H-benzo(d)imidazol-2-yl)phenyl)-1,10-phenanthroline)
  • LiQ (8-hydroxyquinoline-lithium) is formed by evaporation with a film thickness ratio of 1:1 Thick electron transport layer (ETL), LiQ is vapor-deposited on the electron transport layer to form a thickness of The electron injection layer (EIL), and then magnesium (Mg) and silver (Ag) are vapor-deposited on the electron injection layer with a film thickness ratio of 1:9 to form a thickness of The cathode.
  • the vapor deposition thickness on the above cathode is CP-1 to form an organic cover layer (CPL) to complete the manufacture of organic light-emitting devices.
  • each material used is as follows:
  • the corresponding blue organic electroluminescent device was prepared according to the method of Example 1 for the compound 1 where the light-emitting layer and ⁇ , ⁇ -ADN were co-evaporated.
  • Compound A was used to replace Compound 1 in Example 1 where the light-emitting layer and ⁇ , ⁇ -ADN were co-evaporated, and the corresponding blue organic electroluminescent device was prepared according to the method of Example 1.
  • Compound B was used to replace Compound 1 in Example 1 where the light-emitting layer and ⁇ , ⁇ -ADN were co-evaporated, and the corresponding blue organic electroluminescent device was prepared according to the method of Example 1.
  • Compound C was used to replace Compound 1 in Example 1 where the light-emitting layer and ⁇ , ⁇ -ADN were co-evaporated, and the corresponding blue organic electroluminescent device was prepared according to the method of Example 1.
  • Compound D was used to replace Compound 1 in Example 1 where the light-emitting layer and ⁇ , ⁇ -ADN were co-evaporated, and the corresponding blue organic electroluminescent device was prepared according to the method of Example 1.
  • the working voltage of the blue organic electroluminescent device prepared in Examples 1-24 is reduced by at least 0.27V, the luminous efficiency is increased by at least 44.9%, and the external quantum efficiency is at least increased.
  • the operating voltage of the blue organic electroluminescent device prepared in Examples 1-24 was reduced by at least 0.19V, and the luminous efficiency was increased by at least 27.1%.
  • the external quantum efficiency is increased by at least 26.7%, and the life span is increased by at least 25.4%.
  • the working voltage of the blue organic electroluminescent device prepared in Examples 1-24 is reduced by at least 0.30V, and it emits light.
  • the efficiency is increased by at least 35.4%, the external quantum efficiency is increased by at least 34.7%, and the lifetime is increased by at least 18.5%.
  • the operating voltage of the blue organic electroluminescent device prepared in Examples 1-24 is at least Reduced by 0.22V, the luminous efficiency is increased by at least 29.8%, the external quantum efficiency is increased by at least 29.3%, and the life span is increased by at least 38.4%.
  • the compounds with substituents at positions 1, 4 (Examples 1 to 5, 8 to 13, and 16 to 22) are better than the compounds with substituents at positions 2, 3 in all performance tests. (Examples 6 to 7, 14 to 15, 23 to 24)
  • the device performance test is high.
  • the average voltage difference is 0.10V
  • the average luminous efficiency difference is 0.4Cd/A
  • the average external quantum efficiency difference is 0.7 %
  • the average life difference is 30h; therefore, using the nitrogen-containing compound of the application as a guest material in the light-emitting layer can prepare blue organic electroluminescent devices with high luminous efficiency and long life.
  • Compounds with position substituents are preferred materials for device preparation.
  • the nitrogen-containing compound of this application includes a fluorene group spiro-connected with a pyrene group and adamantane.
  • the pyrene group has a larger rigid conjugated structure, strong chemical stability, blue light emission, high fluorescence quantum efficiency, etc.
  • this application uses large groups to modify it, and sterically hinders it to avoid the ⁇ aggregation or excimer formed by the direct stacking of the conjugate plane.
  • Aromatic amine compounds with adamantane spiro-linked fluorene group have a large molecular weight, which can effectively increase the glass transition temperature of nitrogen-containing compounds, and the large steric hindrance of its structure makes it difficult for nitrogen-containing compounds to crystallize Or agglomerate, so that the nitrogen-containing compound has a better lifetime in the device.
  • the nitrogen atom on the aromatic amine has a strong electron donating ability, which improves the hole mobility, so that the electrons and holes move quickly to the recombination area, recombine light, and achieve dynamic equilibrium, thereby improving the efficiency of the device.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Optics & Photonics (AREA)
  • Electroluminescent Light Sources (AREA)
  • Luminescent Compositions (AREA)

Abstract

提供了一种化学式1所示的含氮化合物、有机电致发光器件和电子装置，属于有机材料技术领域。该含氮化合物能够改善有机电致发光器件的性能。

Description

含氮化合物、有机电致发光器件和电子装置
相关申请的交叉引用
本申请要求申请日为2019年12月20日、申请号为CN201911328979.4、发明名称为“含氮化合物、有机电致发光器件和电子装置”的中国发明专利申请以及申请日为2020年09月03日、申请号为CN202010914703.0、发明名称为“含氮化合物、有机电致发光器件和电子装置”的中国发明专利申请的优先权，将其内容并入本申请作为本申请的一部分
技术领域
本申请涉及有机材料技术领域，尤其涉及一种含氮化合物、使用该含氮化合物的有机电致发光器件和应用该有机电致发光器件的电子装置。
背景技术
有机电致发光器件又称为有机发光二极管，是指有机发光材料在电场作用下，受到电流的激发而发光的现象。它是一种将电能转换为光能的过程。相比于无机发光材料，有机电致发光二极管OLED具有主动发光、光程范围大、驱动电压低、亮度大、效率高、耗能少以及制作工艺简单等优点。正是由于这些优点，有机发光材料与器件已经成为科学界和产业界十分热门的科研课题之一。
在有机电致发光器件中，蓝光材料在显示和照明技术中是不可缺少的组成部分，蓝光材料对于降低显示和照明器件的能量消耗，增强器件的整体效果具有非常重要的作用，但目前蓝光材料的发展一直是一个难题。现有的蓝色磷光材料种类少且稳定性差，因此发展此类材料具有重要意义。在专利CN108129332A、US20190074449A和CN109651174A中公开的蓝光材料，虽然发光特性有改良，但都不够满足实际需求。
发明内容
本申请的目的在于提供一种含氮化合物、有机电致发光器件和电子装置，以改善有机电致发光器件和电子装置的性能。
为实现上述发明目的，本申请采用如下技术方案：
根据本申请的第一个方面，提供一种含氮化合物，所述含氮化合物的结构如化学式1所示：
Figure PCTCN2020122846-appb-000001
其中，Ar 1、Ar 2、Ar 3和Ar 4相同或不同，且分别独立地选自取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基，且Ar 1、Ar 2、Ar 3和Ar 4中的至少一个为
Figure PCTCN2020122846-appb-000002
其中，
Figure PCTCN2020122846-appb-000003
表示化学键，
p选自1、2、3、4，当p大于等于2时，任意两个R 10相同或不同；
q选自1、2、3，当q大于等于2时，任意两个R 9相同或不同；
R 1至R 10相同或不同，且分别独立地选自：氢、氘、卤素、氰基、取代或未取代的硅基、取代或未取代的碳原子数为1-10的烷基、取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基、取代或未取代的碳原子数为1-20的环烷基。
根据本申请的第二个方面，提供一种有机电致发光器件，包括相对设置的阳极和阴极，以及设于所述阳极和所述阴极之间的功能层；所述功能层包含上述的含氮化合物。
根据本申请的第三个方面，提供一种电子装置，包括上述有机电致发光器件。
本申请的含氮化合物包括有芘基团和金刚烷螺接的芴基团，芘基团有较大的刚性共轭结构、较强的化学稳定性、发蓝光、高的荧光量子效率等优良的荧光性质和具有良好的热稳定性。为了避免芘的聚集，本申请通过大的基团对其进行修饰，通过空间立体位阻来避免共轭平面的直接堆积形成的π聚集或激基缔合物。带有金刚烷螺接的芴基团的芳胺化合物有大的分子量，可以有效的提升含氮化合物的玻璃化转变温度，而其结构所具有的大的空间位阻，使含氮化合物不易结晶或聚集，使得含氮化合物在器件中具有更好的寿命。且其中的芳胺上的氮原子具有很强的给电子能力，提高了空穴迁移率，从而使电子和空穴快速的运动到复合区域，复合发光，并达到动态平衡，进而提高器件效率。
附图说明
通过参照附图详细描述其示例实施方式，本申请的上述和其它特征及优点将变得更加明显。
图1是本申请实施方式的有机电致发光器件的结构示意图。
图2是本申请一实施方式的电子装置的结构示意图。
图中主要元件附图标记说明如下：
100、阳极；200、阴极；300、功能层；310、空穴注入层；321、空穴传输层；322、电子阻挡层；330、有机电致发光层；340、空穴阻挡层；350、电子传输层；360、电子注入层；400、电子装置。
具体实施方式
现在将参考附图更全面地描述示例性实施例。然而，示例性实施例能够以多种形式实施，且不应被理解为限于在此阐述的范例；相反，提供这些实施例使得本申请将更加全面和完整，并将示例性实施例的构思全面地传达给本领域的技术人员。所描述的特征、结构或特性可以以任何合适的方式结合在一个或更多实施例中。在下面的描述中，提供许多具体细节从而给出对本申请的实施例的充分理解。
在图中，为了清晰，可能夸大了区域和层的厚度。在图中相同的附图标记表示相同或类似的结构，因而将省略它们的详细描述。
所描述的特征、结构或特性可以以任何合适的方式结合在一个或更多个实施例中。在下面的描述中，提供许多具体细节从而给出对本申请的实施例的充分理解。然而，本领域技术人员将意识到，可以实践本申请的技术方案而没有所述特定细节中的一个或更多个，或者可以采用其它的方法、组元、材料等。在其它情况下，不详细示出或描述公知结构、材料或者操作以避免模糊本申请的主要技术创意。
本申请提供一种含氮化合物，所述含氮化合物的结构如化学式1所示：
Figure PCTCN2020122846-appb-000004
其中，Ar 1、Ar 2、Ar 3和Ar 4相同或不同，且分别独立地选自取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基，且Ar 1、Ar 2、Ar 3和Ar 4中的至少一个为
Figure PCTCN2020122846-appb-000005
其中，
Figure PCTCN2020122846-appb-000006
表示化学键，
p选自1、2、3、4，当q大于等于2时，任意两个R 9相同或不同；
q选自1、2、3，当q大于等于2时，任意两个R 9相同或不同；
R 1至R 10相同或不同，且分别独立地选自：氢、氘、卤素、氰基、取代或未取代的硅基、取代或未取代的碳原子数为1-10的烷基、取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基、取代或未取代的碳原子数为1-20的环烷基。
在本申请中，“Ar 1、Ar 2、Ar 3和Ar 4中的至少一个为
Figure PCTCN2020122846-appb-000007
”是指Ar 1、Ar 2、Ar 3和Ar 4中的一个为
Figure PCTCN2020122846-appb-000008
或者Ar 1、Ar 2、Ar 3和Ar 4中的两个个为
Figure PCTCN2020122846-appb-000009
或者Ar 1、Ar 2、Ar 3和Ar 4中的三个为
Figure PCTCN2020122846-appb-000010
或者Ar 1、Ar 2、Ar 3和Ar 4中的四个为
Figure PCTCN2020122846-appb-000011
在本申请中，硅基指的是三烷基硅基和三芳基硅基，且具体实例包括但不限于，三甲基硅基、三乙基硅基、三苯基硅基等。
在本申请中，R 9和R 10选自氢时，金刚烷螺芴没有被取代。
本申请的含氮化合物包括有芘基团和金刚烷螺接的芴基团，芘基团有较大的刚性共轭结构、较强的化学稳定性、发蓝光、高的荧光量子效率等优良的荧光性质和具有良好的热稳定性。为了避免芘的聚集，本申请通过大的基团对其进行修饰，通过空间立体位阻来避免共轭平面的直接堆积形成的π聚集或激基缔合物。带有金刚烷螺接的芴基团的芳胺化合物有大的分子量，可以有效的提升含氮化合物的玻璃化转变温度，而其结构所具有的大的空间位阻，使含氮化合物不易结晶或聚集，使得含氮化合物在器件中具有更好的寿命。且其中的芳胺上的氮原子具有很强的给电子能力，提高了空穴迁移率，从而使电子和空穴快速的运动到复合区域，复合发光，并达到动态平衡，进而提高器件效率。
在本申请中，所采用的描述方式“各……独立地为”与“……分别独立地为”和“……独立地选自”可以互换，均应做广义理解，其既可以是指在不同基团中，相同符号之间所表达的具体选项之间互相不影响，也可以表示在相同的基团中，相同符号之间所表达的具体选项之间互相不影响。例如，“
Figure PCTCN2020122846-appb-000012
其中，各q独立地为0、1、2或3，各R”独立地选自氢、氘、氟、氯”，其含义是：式Q-1表示苯环上有q个取代基R”，各个R”可以相同也可以不同，每个R”的选项之间互不影响；式Q-2表示联苯的每一个苯环上有q个取代基R”，两个苯环上的R”取代基的个数q可以相同或不同，各个R”可以相同也可以不同，每个R”的选项之间互不影响。
在本申请中，“取代或未取代的”这样的术语是指，在该术语后面记载的官能团可以具有或不具有取代基(下文为了便于描述，将取代基统称为Rc)。例如，“取代或未取代的芳基”是指具有取代基Rc的芳基或者非取代的芳基。其中，上述的取代基即Rc例如可以为氘、氟、氯、溴、氰基、碳原子数为3-20的杂芳基、碳原子数为6-20的芳基、碳原子数为3-12的三烷基硅基、碳原子数为8-12的芳基甲硅基、碳原子数为1-10的烷基、碳原子数为1-10的卤代烷基、碳原子数为2-6的烯基、碳原子数为2-6的炔基、碳原子数为3-10的环烷基、碳原子数为2-10的杂环烷基、碳原子数为5-10的环烯基、碳原子数为4-10的杂环烯基、碳原子数为1-10的烷氧基、碳原子数为1-10的烷胺基、碳原子数为1-10的烷硫基、碳原子数为6-18的芳氧基、碳原子数为6-18的芳硫基、碳原子数为6-18的烷基磺酰基、碳原子数为3-18的三烷基膦基、碳原子数为3-18的三烷基硼基。在本申请中，“取代的”官能团可以被上述Rc中的一个或2个以上取代基取代；当同一个原子上连接有两个取代基Rc时，这两个取代基Rc可以独立地存在或者相互连接以与所述原子形成环；当官能团上存在两个相邻的取代基Rc时，相邻的个取代基Rc可以独立地存在或者与其所连接的官能团稠合成环。
可选地，所述Ar 1、Ar 2、Ar 3、Ar 4、R 1至R 10上的取代基相同或不同，且分别独立地选自氘、氰基、卤素、碳原子数为1-3的直链烷基、碳原子数为3-7的支链烷基、碳原子数为6-18的芳基、碳原子数为3-18的杂芳基、碳原子数为3-10的环烷基、碳原子数为2-7的杂环烷基、碳原子数为1-7的烷氧基。如甲基、乙基、丙基、异丙基、叔丁基、2-甲基丁基、2-甲基戊基、2,3-二甲基戊基、环丙基、环丁基、环己基、甲基环戊基、环氧丁基、乙氧基、庚氧基、甲硫基、丙硫基、戊硫基等。
在本申请中，Ar 1、Ar 2、Ar 3、Ar 4、R 1至R 10的碳原子数，指的是所有碳原子数。举例而言，若Ar 1、Ar 2、Ar 3、Ar 4、R 1至R 10选自取代的碳原子数为18的芳基，则芳基及其上的取代基的所有碳原子数为18。
在本申请中，当没有另外提供具体的定义时，“杂”是指在一个官能团中包括至少1个B、O、N、P、Si、Se或S等杂原子且其余原子为碳和氢。未取代的烷基可以是没有任何双键或三键的“饱和烷基基团”。
在本申请中，芳基指的是衍生自芳香烃环的任选官能团或取代基。芳基可以是单环芳基或多环芳基，换言之，芳基可以是单环芳基、稠环芳基、通过碳碳键共轭连接的两个或者多个单环芳基、通过碳碳键共轭连接的单环芳基和稠环芳基、通过碳碳键共轭连接的两个或者多个稠环芳基。即，通过碳碳键共轭连接的两个或者多个芳香基团也可以视为本申请的芳基。其中，芳基中不含有B、O、N、P、Si、Se或S等杂原子。举例而言，芳基可以包括苯基、萘基、芴基、蒽基、菲基、联苯基、三联苯基、四联苯基、五联苯基、六联苯基、苯并[9,10]菲基、芘基、苯并荧蒽基、基、芴基等，而不限于此。本申请中，涉及的亚芳基是指芳基进一步失去一个氢原子所形成的二价基团。
本申请中，不定位连接键是指从环体系中伸出的单键
Figure PCTCN2020122846-appb-000013
其表示该连接键的一端可以连接该键所贯穿的环体系中的任意位置，另一端连接化合物分子其余部分。
举例而言，如下式(f)中所示地，式(f)所表示的萘基通过两个贯穿双环的不定位连接键与分子其他位置连接，其所表示的含义，包括如式(f‐1)～式(f‐10)所示出的任一可能的连接方式。
Figure PCTCN2020122846-appb-000014
再举例而言，如下式(X')中所示地，式(X')所表示的菲基通过一个从一侧苯环中间伸出的不定位连接键与分子其他位置连接，其所表示的含义，包括如式(X'‐1)～式(X'‐4)所示出的任一可能的连接方式。
Figure PCTCN2020122846-appb-000015
本申请中的不定位取代基，指的是通过一个从环体系中央伸出的单键连接的取代基，其表示该取代基可以连接在该环体系中的任何可能位置。例如，如下式(Y)中所示地，式(Y)所表示的取代基R'通过一个不定位连接键与喹啉环连接，其所表示的含义，包括如式(Y‐1)～式(Y‐7)所示出的任一可能的连接方式。
Figure PCTCN2020122846-appb-000016
在本申请中，碳原子数为1-10的烷基可以为直链烷基或支链烷基。具体而言，碳原子数为1-10的烷基可以为碳原子数1至10的直链烷基，或碳原子数3至10的支链烷基。烷基的碳原子数 例如可以为1、2、3、4、5、6、7、8、9、10。碳原子数为1-10的烷基的具体实例包括但不限于，甲基、乙基、正丙基、异丙基、正丁基、异丁基、叔丁基、正戊基、异戊基、新戊基、环戊基、正己基、庚基、正辛基、2-乙基己基、壬基、癸基、3,7-二甲基辛基等。
在本申请中，碳原子数为1-5的烷基可以为直链烷基或支链烷基。具体而言，碳原子数为1-5的烷基可以为碳原子数1至5的直链烷基，或碳原子数3至5的支链烷基。烷基的碳原子数例如可以为1、2、3、4、5。碳原子数为1-5的烷基的具体实例包括但不限于，甲基、乙基、正丙基、异丙基、正丁基、异丁基、叔丁基、正戊基、异戊基、新戊基、环戊基等。
在本申请中，碳原子数为1-3的烷基可以为直链烷基或支链烷基。具体而言，碳原子数为1-10的烷基可以为碳原子数1至3的直链烷基，或碳原子数3的支链烷基。烷基的碳原子数例如可以为1、2、3。碳原子数为1-3的烷基的具体实例包括但不限于，甲基、乙基、正丙基、异丙基。
在本申请中，取代的芳基，指的是芳基中的一个或者多个氢原子被其它基团所取代。例如至少一个氢原子被氘原子、F、Cl、Br、I、CN、芳基、杂芳基、羟基、氨基、支链烷基、直链烷基、环烷基、烷氧基、烷胺基或者其他基团取代。芳基取代的芳基的具体实例包括但不限于，萘基取代的苯基、苯基取代的萘基等。杂芳基取代的芳基的具体实例包括但不限于，二苯并呋喃基取代的苯基、二苯并噻吩取代的苯基、吡啶取代的苯基等。可以理解的是，取代的碳原子数为18的芳基，指的是芳基和芳基上的取代基的碳原子总数为18个。举例而言，9,9-二甲基芴基的碳原子数为15。
在本申请中，作为取代基的芳基为，例如苯基、联苯基、萘基、9,9-二甲基芴基、9,9-二苯基芴基、螺二芴基、蒽基、菲基、
Figure PCTCN2020122846-appb-000017
基。
在本申请中，杂芳基是指环中包含至少一个杂原子的一价芳香环或其衍生物，杂原子可以是B、O、N、P、Si、Se和S中的至少一种。杂芳基可以是单环杂芳基或多环杂芳基，换言之，杂芳基可以是单个芳香环体系，也可以是通过碳碳键共轭连接的多个芳香环体系，且任一芳香环体系为一个芳香单环或者一个芳香稠环。示例地，杂芳基可以包括噻吩基、呋喃基、吡咯基、咪唑基、噻唑基、噁唑基、噁二唑基、三唑基、吡啶基、联吡啶基、嘧啶基、三嗪基、吖啶基、哒嗪基、吡嗪基、喹啉基、喹唑啉基、喹喔啉基、吩噁嗪基、酞嗪基、吡啶并嘧啶基、吡啶并吡嗪基、吡嗪并吡嗪基、异喹啉基、吲哚基、咔唑基、N-芳基咔唑基、N-杂芳基咔唑基、N-烷基咔唑基、苯并噁唑基、苯并咪唑基、苯并噻唑基、苯并咔唑基、苯并噻吩基、二苯并噻吩基、噻吩并噻吩基、苯并呋喃基、菲咯啉基、异噁唑基、噻二唑基、苯并噻唑基、吩噻嗪基、硅芴基、二苯并呋喃基以及N-芳基咔唑基(如N-苯基咔唑基)、N-杂芳基咔唑基(如N-吡啶基咔唑基)、N-烷基咔唑基(如N-甲基咔唑基)等，而不限于此。其中，噻吩基、呋喃基、菲咯啉基等为单个芳香环体系的杂芳基，N-芳基咔唑基、N-杂芳基咔唑基为通过碳碳键共轭连接的多环体系类型的杂芳基。本申请中，涉及的亚杂芳基是指杂芳基进一步失去一个氢原子所形成的二价基团。
在本申请中，取代的杂芳基可以是杂芳基中的一个或者两个以上氢原子被诸如氘原子、卤素基团、-CN、芳基、杂芳基、三烷基硅基、烷基、环烷基、烷氧基、烷硫基等基团取代。芳基取代的杂芳基的具体实例包括但不限于，苯基取代的二苯并呋喃基、苯基取代的二苯并噻吩基、苯基取代的吡啶基等。应当理解地是，取代的杂芳基的碳原子数，指的是杂芳基和杂芳基上的取代基的碳原子总数。
在本申请中，作为取代基的杂芳基为，例如吡啶基、嘧啶基、咔唑基、二苯并呋喃基、二苯并噻吩基。
可选地，所述Ar 1、Ar 2、Ar 3、Ar 4、R 1至R 10上的取代基相同或不同，且分别独立地选自氘、 氰基、卤素、碳原子数为1-3的直链烷基、碳原子数为3-5的支链烷基、碳原子数为6-18的芳基、碳原子数为3-12的杂芳基、碳原子数为3-10的环烷基。
在本申请中，卤素基团例如可以为氟、氯、溴、碘。
可选地，所述R 1至R 10相同或不同，且分别独立地选自：氢、氘、氟、氰基、取代或未取代的硅基、取代或未取代的碳原子数为1-5的烷基、取代或未取代的碳原子数为6-18的芳基、取代或未取代的碳原子数为3-12的杂芳基、取代或未取代的碳原子数为1-10的环烷基。
可选地，所述R 2、R 6不为氢，所述R 1、R 3、R 4、R 5、R 7、R 8、R 9、R 10均为氢。
可选地，Ar 1、Ar 2、Ar 3和Ar 4相同或不同，且分别独立地选自取代或未取代的碳原子数为6-25的芳基、取代或未取代的碳原子数为5-20的杂芳基。
可选地，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下结构(i-1)至(i-9)所组成的组：
Figure PCTCN2020122846-appb-000018
其中，
n 1、n 4、n 7、n 9相同或不同，且分别独立地选自1、2、3、4、5；
n 2、n 3、n 11相同或不同，且分别独立地选自1、2、3、4、5、6、7；
n 5、n 6、n 8相同或不同，且分别独立地选自1、2、3、4；
n 10选自1、2、3、4、5、6、7、8、9；
X 1和X 2相同或不同，且分别独立地选自C、N，其中当X 1和X 2选自C时，是指X 1和X 2是CH；
Y选自O、S、Si(E 12E 13)、C(E 14E 15)、N(E 16)、Se；
Z 1和Z 2相同或不同，且分别独立地选自O、S、N(E 17)、C(E 18E 19)；
E 1、E 4、E 5相同或不同，且分别独立地选自氘、卤素、氰基、碳原子数为1-5的烷基、碳原子数为3-18的杂芳基、碳原子数3-10的环烷基；
E 2、E 3、E 6至E 19相同或不同，且分别独立地选自氢、氘、卤素、氰基、碳原子数为1-5的烷基、碳原子数为6-18的芳基、碳原子数为3-18的杂芳基、碳原子数3-10的环烷基；或者E 12和E 13能够连接成环，或者E 14和E 15能够连接成环，或者E 18和E 19能够连接成环；
X 3至X 7相同或不同，且分别独立地选自C(R’)或N，且X 3至X 7中至少一个为N，其中，所述X 3至X 7中的R’相同或不同，且分别独立地选自碳原子数为1-5烷基、碳原子数为6-18芳基、 碳原子数为3-18的杂芳基、碳原子数3-10的环烷基，或者相邻的R’能够连接成环。
在本申请中，当n 1大于或等于2时，E 1相同或不同；当n 2大于或等于2时，E 2相同或不同；当n 3大于或等于2时，E 3相同或不同；当n 4大于或等于2时，E 4相同或不同；当n 5大于或等于2时，E 5相同或不同；当n 6大于或等于2时，E 6相同或不同；当n 7大于或等于2时，E 7相同或不同；当n 8大于或等于2时，E 8相同或不同；当n 9大于或等于2时，E 9相同或不同；当n 10大于或等于2时，E 10相同或不同；当n 11大于或等于2时，E 11相同或不同。
在本申请中，式
Figure PCTCN2020122846-appb-000019
是指式
Figure PCTCN2020122846-appb-000020
和式
Figure PCTCN2020122846-appb-000021
两者结构，其中，在式i-6-a中，n 7、n 9选自1、2、3、4、5，n 8选自1、2、3；在式i-6-b中，n 7选自1、2、3、4、5，n 8、n 9选自1、2、3、4。
在本申请中，n 1至n 11选自0时，苯环没有被取代。
相邻的R’能够连接成环，是指X 3和X 4成环，或X 4和X 5成环，或X 5和X 6成环，或X 6和X 7成环，当然也包括X 3和X 4成环且X 5和X 6成环等情况。
在本申请中，A与B“能够连接成环”的含义包括A与B相互独立，不连接；也包括A与B相互连接成环。例如，E 12和E 13能够连接成环，包括E 12和E 13相互独立，不连接的方式，也包括E 12和E 13相互连接成环；E 14和E 15能够连接成环，包括E 14和E 15相互独立，不连接的方式，也包括E 14和E 15相互连接成环；E 18和E 19能够连接成环，包括E 18和E 19相互独立，不连接的方式，也包括E 18和E 19相互连接成环。
例如，X 3和X 4能够连接成环，包括X 3的R’与X 4的R’相互独立，不连接的方式，也包括X 3的R’与X 4的R’以及R’所连接的原子连接成环。
在本申请中，所述的环指的是饱和或不饱和的环，例如
Figure PCTCN2020122846-appb-000022
等，但不限于此。
具体地，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下基团所组成的组：
Figure PCTCN2020122846-appb-000023
Figure PCTCN2020122846-appb-000024
可选地，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下基团所组成的组：
Figure PCTCN2020122846-appb-000025
可选地，所述Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自取代或未取代的如下基团：苯基、萘基、联苯基、三联苯基、菲基、蒽基、9,9-螺二芴基、9,9-二甲基芴基、吡啶基、咔唑基、嘧啶基、1,10-菲罗啉、哒嗪基、三嗪基、喹啉基、喹唑啉基、苯基吡啶基、喹喔啉基、芘基、N-苯基咔唑基、二苯并呋喃基、二苯并噻吩基或者金刚烷芴基，
所述取代是被选自如下基团所取代：氘、氟、氯、氰基、三甲基硅基、甲基、乙基、异丙基、叔丁基、苯基、萘基、吡啶基、二苯并呋喃基、咔唑基或者二苯并噻吩基；取代基有多个时，多个取代基相同或不同。
可选地，所述含氮化合物选自如下化合物所组成的组：
Figure PCTCN2020122846-appb-000026
Figure PCTCN2020122846-appb-000027
Figure PCTCN2020122846-appb-000028
Figure PCTCN2020122846-appb-000029
Figure PCTCN2020122846-appb-000030
Figure PCTCN2020122846-appb-000031
Figure PCTCN2020122846-appb-000032
本申请还提供一种有机电致发光器件，包括相对设置的阳极和阴极，以及设于所述阳极和所述阴极之间的功能层；所述功能层包含本申请的含氮化合物。
可选地，本申请的有机发光器件为为蓝光器件。
举例而言，如图1所示，有机电致发光器件包括相对设置的阳极100和阴极200，以及设于阳极100和阴极200之间的功能层300；功能层300包含本申请所提供的含氮化合物。
可选地，功能层300包括有机电致发光层330，有机电致发光层330包含本申请的含氮化合物。
可选地，有机发光层330可以由单一发光材料组成，也可以包括主体材料和客体材料。可选地，有机发光层330由主体材料和客体材料组成，注入有机发光层330的空穴和注入有机发光层330的电子可以在有机发光层330复合而形成激子，激子将能量传递给主体材料，主体材料将能量传递给客体材料，进而使得客体材料能够发光。
有机发光层330的主体材料可以为金属螯合物类化合物、双苯乙烯基衍生物、芳香族胺衍生物、二苯并呋喃衍生物或者其他类型的材料，本申请对此不做特殊的限制。在本申请的一种实施方式中，有机发光层330的主体材料可以为α,β-ADN。
有机发光层330的客体材料可以为具有缩合芳基环的化合物或其衍生物、具有杂芳基环的化合物或其衍生物、芳香族胺衍生物或者其他材料，在本申请实施例中，有机发光层330的客体材料为本申请的含氮化合物。
在本申请的一种实施方式中，有机电致发光器件可以包括依次层叠设置的阳极100、空穴传输层321、电子阻挡层322、作为能量转化层的有机电致发光层330、电子传输层350和阴极200。本申请提供的含氮化合物可以应用于有机电致发光器件的有机电致发光层330，可以有效改善有机电致发光器件的发光效率和寿命，降低有机电致发光器件的驱动电压。
可选地，阳极100包括以下阳极材料，其优选地是有助于空穴注入至功能层中的具有大逸出功(功函数，work function)材料。阳极材料具体实例包括：金属如镍、铂、钒、铬、铜、锌和金或它们的合金；金属氧化物如氧化锌、氧化铟、氧化铟锡(ITO)和氧化铟锌(IZO)；组合的金属和氧化物如ZnO:Al或SnO 2:Sb；或导电聚合物如聚(3-甲基噻吩)、聚[3,4-(亚乙基-1,2-二氧基)噻吩](PEDT)、聚吡咯和聚苯胺，但不限于此。优选包括包含氧化铟锡(铟锡氧化物，indium tin oxide)(ITO)作为阳极的透明电极。
可选地，空穴传输层321可以包括一种或者多种空穴传输材料，空穴传输材料可以选自咔唑多聚体、咔唑连接三芳胺类化合物或者其他类型的化合物，本申请对此不做特殊的限定。举例而言，在本申请的一种实施方式中，空穴传输层321由化合物NPB组成。
可选地，电子阻挡层322包括一种或多种电子阻挡材料，电子阻挡材料可以选自咔唑多聚体或者其他类型化合物，本申请对此不特殊的限定。举例而言，在本申请的一些实施方式中，电子阻挡层322由化合物TCTA组成。
可选地，电子传输层350可以为单层结构，也可以为多层结构，其可以包括一种或者多种电子传输材料，电子传输材料可以选自苯并咪唑衍生物、噁二唑衍生物、喹喔啉衍生物或者其他电子传输材料，本申请对此不做特殊的限定。举例而言，在本申请的一种实施方式中，电子传输层340可以由DBimiBphen和LiQ组成。
可选地，阴极200包括以下阴极材料，其是有助于电子注入至功能层中的具有小逸出功的材料。阴极材料的具体实例包括：金属如镁、钙、钠、钾、钛、铟、钇、锂、钆、铝、银、锡和铅或它们的合金；或多层材料如LiF/Al、Liq/Al、LiO 2/Al、LiF/Ca、LiF/Al和BaF 2/Ca，但不限于此。优选包括包含镁和银的金属电极作为阴极。
可选地，如图1所示，在阳极100和第一空穴传输层321之间还可以设置有空穴注入层310，以增强向第一空穴传输层321注入空穴的能力。空穴注入层310可以选用联苯胺衍生物、星爆状芳基胺类化合物、酞菁衍生物或者其他材料，本申请对此不做特殊的限制。在本申请的一种实施方式中，空穴注入层310可以由m-MTDATA组成。
可选地，如图1所示，在阴极200和电子传输层350之间还可以设置有电子注入层360，以增强向电子传输层350注入电子的能力。电子注入层360可以包括有碱金属硫化物、碱金属卤化物等无机材料，或者可以包括碱金属与有机物的络合物。在本申请的一种实施方式中，电子注入层360可以包括LiQ。
可选地，在有机电致发光层330和电子传输层350之间还可以设置有空穴阻挡层340。
本申请实施方式还提供一种电子装置，该电子装置包括上述有机电致发光器件。由于该电子装置具有上述有机电致发光器件，因此具有相同的有益效果，本申请在此不再赘述。
举例而言，如图2所示，本申请提供一种电子装置400，该电子装置400包括上述有机电致发光器件。该电子装置400可以为显示装置、照明装置、光通讯装置或者其他类型的电子装置，例如可以包括但不限于电脑屏幕、手机屏幕、电视机、电子纸、应急照明灯、光模块等。由于该电子装置400具有上述有机电致发光器件，因此具有相同的有益效果，本申请在此不再赘述。
以下，通过实施例对本申请进一步详细说明。但是，下述实施例仅是本申请的例示，而并非限定本申请。
化合物合成
中间体-1-A的合成：
Figure PCTCN2020122846-appb-000033
将2’-溴-3-氯联苯(100g，373.8mmol)加入盛有THF(1L)的三口瓶中，降温至-80℃后滴加正丁基锂(19.15g，299.06mmol)，滴加完后保温1h，滴加金刚烷酮(44.92g，299.06mmol)，完毕后继续保温1h升温至室温搅拌过夜。加入盐酸(2mol/L)调节PH至中性，过滤反应液得到白色粗品，粗品用正庚烷打浆得为白色固体的中间体-1-A-1(92.86g，收率87％)。
中间体-1-B的合成：
Figure PCTCN2020122846-appb-000034
将中间体-1-A-1(92.86g，275.63mmol)、三氟乙酸(94.28g，826.89mmol)和二氯甲烷(900mL)加入三口烧瓶中，氮气保护下室温搅拌2小时；向反应瓶中加入氢氧化钠水溶液至反应液呈中性，反应液进行分液，有机相使用无水硫酸镁进行干燥，过滤，减压除去溶剂；所得粗品使用二氯甲烷/正庚烷(1:2)进行硅胶柱色谱分离，得到白色固体状中间体-1-A(50.43g，收率：54％)和中间体-1-B(42.42g，收率：46％)。
其中，中间体1-B的核磁数据为： 1HNMR(400MHz,CDCl 2):8.11(d,1H),8.03(d,1H),7.41-7.63(m,2H),7.37-7.39(m,1H),7.30-7.33(m,1H),7.23-7.24(m,1H),2.88-2.93(m,2H),2.81-2.85(m,2H),2.19(s,2H),1.99(s,2H),1.77-1.83(m,4H),1.54(s,2H).
在下列实施方式中，以与中间体-1-A和中间体-1-B的合成方法相同的方法合成中间体-1-X-1和中间体-1-X，其中，X可为C，不同之处在于使用表1中其他化合物SM-1代替2’-溴-3-氯联苯，举例而言，化合物SM-1可以是2-溴-2’-氯-1,1’-联苯，且每一种化合物SM-1可以制备出与之为唯一 对应的中间体-1-X。举例而言，其合成过程可如反应式1所示，该反应式1可以为：
Figure PCTCN2020122846-appb-000035
合成的中间体-1-X如表1所示：
表1 中间体-1-X合成列表
Figure PCTCN2020122846-appb-000036
中间体-2-A的合成：
Figure PCTCN2020122846-appb-000037
向500mL的反应瓶中投入1,6-二溴芘(50.00g，138.87mmol)、二苯胺(23.50g，138.87mmol)、三(二亚苄基丙酮)二钯(1.27g，1.38mmol)、2-二环己基膦-2',4',6'-三异丙基联苯(1.14g，2.77mmol)、叔丁醇钠(20.01g，208.31mmol)和甲苯溶剂(500mL)，氮气保护下升温至110℃，加热回流搅拌3h。反应液冷却至室温后，二氯甲烷和水萃取反应溶液，有机层经无水硫酸镁干燥有机层，并过滤，过滤后将滤液通过短硅胶柱，减压除去溶剂，使用二氯甲烷/正庚烷体系(1：3)对粗品进行重结晶提纯，得到中间体-2-A(50.43g，收率81％)。
Figure PCTCN2020122846-appb-000038
以与中间体-2-A的合成方法相同的方法合成SMZ-Y，其中Y可以是1和2，X为O或者S，举例而言，SMZ-1-Y可为1-溴-二苯并呋喃和1-溴二苯并噻吩。不同之处在于用SMZ代替1,6-二溴芘，用苯胺代替二苯胺。且每个X形成的SMZ都可以制备与之对应的SMZ-Y。
Figure PCTCN2020122846-appb-000039
Figure PCTCN2020122846-appb-000040
在下列实施方式中，以与中间体-2-A的合成方法相同的方法合成中间体-2-X，其中，X为B、C、D、E、F、G、H、I，不同之处在于用化合物SM-2代替二苯胺，举例而言，化合物SM-2可以是N-苯基-3-联苯胺、N-苯基-2(9,9-二甲基-9H-芴)胺、1-萘氨基苯、2-甲基二苯胺、二(3-联苯基)胺、N-(4-(1-萘基)苯基)-4-联苯胺、N-2,6-二苯基-2-萘胺和N-苯基-2-萘胺、SMZ-1和SMZ-2，且每一种化合物SM-2可以制备出与之为唯一对应的中间体-2-X。举例而言，其合成过程如反应式2所示，该反应式2为：
Figure PCTCN2020122846-appb-000041
合成的中间体-2-X如表2所示：
表2 中间体-2-X合成列表
Figure PCTCN2020122846-appb-000042
Figure PCTCN2020122846-appb-000043
中间体-3-A的合成：
Figure PCTCN2020122846-appb-000044
向100mL的反应瓶中投入中间体-1-A(5.0g，15.58mmol)、苯胺(1.45g，15.58mmol)、三(二亚苄基丙酮)二钯(0.14g，0.15mmol)、2-二环己基膦-2',4',6'-三异丙基联苯(0.12g，0.31mmol)、叔丁醇钠(2.25g，23.37mmol)和甲苯溶剂(50mL)，氮气保护下升温至110℃，加热回流搅拌5h。反应液冷却至室温后，二氯甲烷和水萃取反应溶液，有机层经无水硫酸镁干燥有机层，并过滤，过滤后将滤液通过短硅胶柱，减压除去溶剂，使用二氯甲烷/正庚烷体系(1:5)对粗品进行重结晶提 纯，得到中间体-3-A(4.70g，收率80％)。
Figure PCTCN2020122846-appb-000045
向100mL的反应瓶中投入中间体-1-C(5.0g，14.8mmol)、氨水(0.25g，14.84mmol)、三(二亚苄基丙酮)二钯(0.67g，0.74mmol)、2-二环己基膦-2',4',6'-三异丙基联苯(9.12g，22.26mmol)、叔丁醇钠(0.07g，0.74mmol)和甲苯溶剂(50mL)，氮气保护下升温至110℃，加热回流搅拌5h。反应液冷却至室温后，二氯甲烷和水萃取反应溶液，有机层经无水硫酸镁干燥有机层，并过滤，过滤后将滤液通过短硅胶柱，减压除去溶剂，使用二氯甲烷/正庚烷体系(1:5)对粗品进行重结晶提纯，得到中间体-1-C-1(3.91g，收率83％)。
在下列实施方式中，以与中间体-3-A的合成方法相同的方法合成中间体-3-X，其中，X为B、C、D、E、F、G、H、I、G、K、L，不同之处在于用表3中的其他化合物SM-3代替苯胺，举例而言，化合物SM-3可以是苯胺、邻甲苯胺、3-氨基-1,1-联苯、2-萘胺、4-氟苯胺、4-氰基苯胺、对甲苯胺、3-甲基苯胺、4-氨基-1,1-联苯，且每一种化合物SM-3可以制备出与之为唯一对应的中间体-3-X。举例而言，其合成过程如反应式3所示，该反应式3为：
Figure PCTCN2020122846-appb-000046
合成的中间体-3-X如表3所示：
表3 中间体-3-X合成列表
Figure PCTCN2020122846-appb-000047
Figure PCTCN2020122846-appb-000048
Figure PCTCN2020122846-appb-000049
化合物107的合成：
Figure PCTCN2020122846-appb-000050
向100mL的反应瓶中投入中间体-2-H(5.0g，9.49mmol)、中间体-3-A(3.59g，9.49mmol)、三(二亚苄基丙酮)二钯(0.08g，0.095mmol)、2-二环己基膦-2',4',6'-三异丙基联苯(0.07g，0.18mmol)、叔丁醇钠(1.37g，14.24mmol)和甲苯溶剂(50mL)，氮气保护下升温至110℃，加热回流搅拌10h。反应液冷却至室温后，二氯甲烷和水萃取反应溶液，有机层经无水硫酸镁干燥有机层，并过滤，过滤后将滤液通过短硅胶柱，减压除去溶剂，使用二氯甲烷/正庚烷体系(1:3)对粗品进行重结晶提纯，得到化合物107(6.16g，收率79％)，m/z＝823.4[M+H] +。
在下列实施方式中，以与化合物107的合成方法相同的方法合成化合物X，不同之处在于使用中间体-2-X代替中间体-2-H，使用中间体-3-X代替中间体-3-A，举例而言，中间体-2-X可以是中间体-2-A、中间体-2-B、中间体-2-C、中间体-2-D等，中间体-3-X可以是中间体-3-B、中间体-3-C、中间体-3-D等，由此可以制备出与之为唯一对应的化合物X，具体的化合物编号、结构、原料、最后一步的合成收率、表征数据等展示在表4中。
表4：化合物结构、制备及表征数据
Figure PCTCN2020122846-appb-000051
Figure PCTCN2020122846-appb-000052
Figure PCTCN2020122846-appb-000053
Figure PCTCN2020122846-appb-000054
Figure PCTCN2020122846-appb-000055
化合物1的核磁数据：
1H NMR(400Hz,CD 2Cl 2):8.20(d,1H),7.95(d,1H),7.81-7.72(m,4H),7.58-7.48(m,5H),7.46-7.39(m, 2H),7.34-7.21(m,8H),7.18(d,1H),7.15-7.08(m,1H),7.6(d,1H),6.99(s,1H),6.93(d,1H),6.91-6.89(m,7H),6.87(d,1H),2.84(d,2H),2.76(d,2H),2.16(s,1H),2.13(s,1H),1.96(s,2H),1.75(t,4H),1.46(s,2H).
化合物36的核磁数据：
1H NMR(400Hz,CD 2Cl 2):8.21(d,2H),7.90(d,1H),7.80-7.73(m,6H),7.68(d,1H),7.56-7.47(m,6H),7.43-7.36(m,7H),7.27-7.20(m,5H),7.19-7.13(m,3H),7.08(d,1H),7.03(d,2H),6.99-6.93(m,4H),6.90(d,2H),2.83(d,2H),2.74(d,2H),2.16(s,1H),2.13(s,1H),1.96(s,2H),1.75(t,4H),1.46(s,2H).
有机电致发光器件制备及评估
实施例1
通过如下方法制备蓝色有机电致发光器件
将厚度为
Figure PCTCN2020122846-appb-000056
的ITO基板(康宁制造)切割成40mm(长)×40mm(宽)×0.7mm(厚)的尺寸，采用光刻工序，将其制备成具有阴极、阳极以及绝缘层图案的实验基板，利用紫外臭氧以及O 2:N 2等离子进行表面处理，以增加阳极(实验基板)的功函数的和清除浮渣。
在实验基板(阳极)上真空蒸镀m-MTDATA(4,4',4”-三(N-3-甲基苯基-N-苯基氨基)三苯胺)以形成厚度为
Figure PCTCN2020122846-appb-000057
的空穴注入层(HIL)，并且在空穴注入层上真空蒸镀化合物NPB，以形成厚度为
Figure PCTCN2020122846-appb-000058
的空穴传输层。
在空穴传输层上蒸镀TCTA(4,4',4”-三(咔唑-9-基)三苯胺)，形成厚度为
Figure PCTCN2020122846-appb-000059
的电子阻挡层(EBL)。
将α,β-ADN作为主体材料，同时掺杂化合物1作为客体材料，以20:1的膜厚比蒸镀形成了厚度为
Figure PCTCN2020122846-appb-000060
的发光层(EML)。
将DBimiBphen(4,7-二苯基-2,9-双(4-(1-苯基-1H-苯并[d]咪唑-2-基)苯基)-1,10-菲咯啉)和LiQ(8-羟基喹啉-锂)以1:1的膜厚比蒸镀形成了
Figure PCTCN2020122846-appb-000061
厚的电子传输层(ETL)，将LiQ蒸镀在电子传输层上以形成厚度为
Figure PCTCN2020122846-appb-000062
的电子注入层(EIL)，然后将镁(Mg)和银(Ag)以1:9的膜厚比蒸镀在电子注入层上，形成厚度为
Figure PCTCN2020122846-appb-000063
的阴极。
此外，在上述阴极上蒸镀厚度为
Figure PCTCN2020122846-appb-000064
的CP-1，形成有机覆盖层(CPL)，从而完成有机发光器件的制造。
其中，在制备蓝色有机电致发光器件时，所使用的各个材料的结构如下：
Figure PCTCN2020122846-appb-000065
实施例2-24
用化合物3、4、7、8、28、36、79、82、83、106、107、108、116、117、121、122、124、125、126、128、133、134、135替代实施例1中发光层与α,β-ADN共蒸镀的化合物1，按照实施例1的 方法制备相应的蓝色有机电致发光器件。
对比例1
用化合物A替代实施例1中发光层与α,β-ADN共蒸镀的化合物1，按照实施例1的方法制备相应的蓝色有机电致发光器件。
对比例2
用化合物B替代实施例1中发光层与α,β-ADN共蒸镀的化合物1，按照实施例1的方法制备相应的蓝色有机电致发光器件。
对比例3
用化合物C替代实施例1中发光层与α,β-ADN共蒸镀的化合物1，按照实施例1的方法制备相应的蓝色有机电致发光器件。
对比例4
用化合物D替代实施例1中发光层与α,β-ADN共蒸镀的化合物1，按照实施例1的方法制备相应的蓝色有机电致发光器件。
其中，化合物A、化合物B和化合物C的结构如下：
Figure PCTCN2020122846-appb-000066
对实施例2-24和对比例1-3制备所得的蓝色有机电致发光器件进行性能测试，其中IVL(电流、电压、亮度)数据对比是在10mA/cm 2下的测试结果，寿命是15mA/cm 2电流密度下的测试结果，具体结果如表5所示。
表5 蓝色有机电致发光器件的性能测试结果
Figure PCTCN2020122846-appb-000067
Figure PCTCN2020122846-appb-000068
根据上表可知，相较于对比例1而言，实施例1-24制备的蓝色有机电致发光器件的工作电压至少降低了0.27V，发光效率至少提高了44.9％，外量子效率至少提高了43.8％，寿命至少提高了31.1％；相较于对比例2而言，实施例1-24制备的蓝色有机电致发光器件的工作电压至少降低了0.19V，发光效率至少提高了27.1％，外量子效率至少提高了26.7％，寿命至少提高了25.4％；相较于对比例3而言，实施例1-24制备的蓝色有机电致发光器件的工作电压至少降低了0.30V，发光效率至少提高了35.4％，外量子效率至少提高了34.7％，寿命至少提高了18.5％；相较于对比例4而言，实施例1-24制备的蓝色有机电致发光器件的工作电压至少降低了0.22V，发光效率至少提高了29.8％，外量子效率至少提高了29.3％，寿命至少提高了38.4％。在实施例1-24中在1，4位取代基的化合物(实施例1至5、8至13、16至22)制备的器件各项性能测试又均比在2，3位取代基的化合物(实施例6至7、14至15、23至24)器件各项性能测试高，在已测的器件中，电压平均相差0.10V，发光效率平均相差0.4Cd/A，外量子效率平均相差0.7％，寿命平均相差30h；因此，在发光层中使用本申请的含氮化合物作为客体材料能够制备得到高发光效率、长寿命的蓝色有机电致发光器件，同时又优先选择在1位，4位取代基的化合物作为器件制备的优选材料。
本申请的含氮化合物包括有芘基团和金刚烷螺接的芴基团，芘基团有较大的刚性共轭结构、较强的化学稳定性、发蓝光、高的荧光量子效率等优良的荧光性质和具有良好的热稳定性。为了避免芘的聚集，本申请通过大的基团对其进行修饰，通过空间立体位阻来避免共轭平面的直接堆积形成的π聚集或激基缔合物。带有金刚烷螺接的芴基团的芳胺化合物有大的分子量，可以有效的提升含氮化合物的玻璃化转变温度，而其结构所具有的大的空间位阻，使含氮化合物不易结晶或聚集，使得含氮化合物在器件中具有更好的寿命。且其中的芳胺上的氮原子具有很强的给电子能力，提高了空穴迁移率，从而使电子和空穴快速的运动到复合区域，复合发光，并达到动态平衡，进而提高器件效率。

Claims (14)

  1. 一种含氮化合物，其特征在于，所述含氮化合物的结构如化学式1所示：
    Figure PCTCN2020122846-appb-100001
    其中，Ar 1、Ar 2、Ar 3和Ar 4相同或不同，且分别独立地选自取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基，且Ar 1、Ar 2、Ar 3和Ar 4中的至少一个为
    Figure PCTCN2020122846-appb-100002
    其中，
    Figure PCTCN2020122846-appb-100003
    表示化学键，
    p选自1、2、3、4，当p大于等于2时，任意两个R 10相同或不同；
    q选自1、2、3，当q大于等于2时，任意两个R 9相同或不同；
    R 1至R 10相同或不同，且分别独立地选自：氢、氘、卤素、氰基、取代或未取代的硅基、取代或未取代的碳原子数为1-10的烷基、取代或未取代的碳原子数为6-30的芳基、取代或未取代的碳原子数为3-30的杂芳基、取代或未取代的碳原子数为1-20的环烷基。
  2. 根据权利要求1所述的含氮化合物，其特征在于，所述Ar 1、Ar 2、Ar 3、Ar 4、R 1至R 10上的取代基相同或不同，且分别独立地选自氘、氰基、卤素、碳原子数为1-3的直链烷基、碳原子数为3-7的支链烷基、碳原子数为6-18的芳基、碳原子数为3-18的杂芳基、碳原子数为3-10的环烷基、碳原子数为2-7的杂环烷基、碳原子数为1-7的烷氧基。
  3. 根据权利要求1所述的含氮化合物，其特征在于，所述R 1至R 10相同或不同，且分别独立地选自：氢、氘、氟、氰基、取代或未取代的硅基、取代或未取代的碳原子数为1-5的烷基、取代或未取代的碳原子数为6-18的芳基、取代或未取代的碳原子数为3-12的杂芳基、取代或未取代的碳原子数为1-10的环烷基。
  4. 根据权利要求1至3中任一项所述的含氮化合物，其特征在于，所述R 2、R 6不为氢，所述R 1、R 3、R 4、R 5、R 7、R 8、R 9、R 10均为氢。
  5. 根据权利要求1所述的含氮化合物，其特征在于，Ar 1、Ar 2、Ar 3和Ar 4相同或不同，且分别独立地选自取代或未取代的碳原子数为6-25的芳基、取代或未取代的碳原子数为5-20的杂芳基。
  6. 根据权利要求1或5所述的含氮化合物，其特征在于，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下结构(i-1)至(i-9)所组成的组：
    Figure PCTCN2020122846-appb-100004
    其中，
    n 1、n 4、n 7、n 9相同或不同，且分别独立地选自1、2、3、4、5；
    n 2、n 3、n 11相同或不同，且分别独立地选自1、2、3、4、5、6、7；
    n 5、n 6、n 8相同或不同，且分别独立地选自1、2、3、4；
    n 10选自1、2、3、4、5、6、7、8、9；
    X 1和X 2相同或不同，且分别独立地选自C、N；
    Y选自O、S、Si(E 12E 13)、C(E 14E 15)、N(E 16)、Se；
    Z 1和Z 2相同或不同，且分别独立地选自O、S、N(E 17)、C(E 18E 19)；
    E 1、E 4、E 5相同或不同，且分别独立地选自氘、卤素、氰基、碳原子数为1-5的烷基、碳原子数为3-18的杂芳基、碳原子数3-10的环烷基；
    E 2、E 3、E 6至E 19相同或不同，且分别独立地选自氢、氘、卤素、氰基、碳原子数为1-5的烷基、碳原子数为6-18的芳基、碳原子数为3-18的杂芳基、碳原子数3-10的环烷基；或者E 12和E 13能够连接成环，或者E 14和E 15能够连接成环，或者E 18和E 19能够连接成环；
    X 3至X 7相同或不同，且分别独立地选自C(R’)或N，且X 3至X 7中至少一个为N，其中，所述X 3至X 7中的R’相同或不同，且分别独立地选自氢、碳原子数为1-5烷基、碳原子数为6-18芳基、碳原子数为3-18的杂芳基、碳原子数3-10的环烷基，或者相邻的R’能够连接成环。
  7. 根据权利要求1所述的含氮化合物，其特征在于，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下基团所组成的组：
    Figure PCTCN2020122846-appb-100005
    Figure PCTCN2020122846-appb-100006
  8. 根据权利要求1所述的含氮化合物，其特征在于，Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自如下基团所组成的组：
    Figure PCTCN2020122846-appb-100007
  9. 根据权利要求1所述的含氮化合物，其特征在于，所述Ar 1、Ar 2、Ar 3或Ar 4分别独立地选自取代或未取代的如下基团：苯基、萘基、联苯基、三联苯基、菲基、蒽基、9,9-螺二芴基、9,9-二甲基芴基、吡啶基、咔唑基、嘧啶基、1,10-菲罗啉、哒嗪基、三嗪基、喹啉基、喹唑啉基、苯基吡啶基、喹喔啉基、芘基、N-苯基咔唑基、二苯并呋喃基、二苯并噻吩基或者金刚烷芴基，
    所述取代是被选自如下基团所取代：氘、氟、氯、氰基、三甲基硅基、甲基、乙基、异丙基、叔丁基、苯基、萘基、吡啶基、二苯并呋喃基、咔唑基或者二苯并噻吩基；取代基有多个时，多个取代基相同或不同。
  10. 根据权利要求1所述的含氮化合物，其特征在于，所述含氮化合物选自如下化合物所组成的组：
    Figure PCTCN2020122846-appb-100008
    Figure PCTCN2020122846-appb-100009
    Figure PCTCN2020122846-appb-100010
    Figure PCTCN2020122846-appb-100011
    Figure PCTCN2020122846-appb-100012
    Figure PCTCN2020122846-appb-100013
    Figure PCTCN2020122846-appb-100014
  11. 一种有机电致发光器件，其特征在于，包括相对设置的阳极和阴极，以及设于所述阳极和所述阴极之间的功能层；
    所述功能层包含权利要求1-10任一项所述的含氮化合物。
  12. 根据权利要求11所述的有机电致发光器件，其特征在于，所述功能层包括有机电致发光层，所述有机电致发光层包含权利要求1-10任一项所述的含氮化合物。
  13. 根据权利要求12所述的有机电致发光器件，其特征在于，所述有机电致发光层包含客体材料，所述客体材料含有权利要求1-10任一项所述的含氮化合物。
  14. 一种电子装置，其特征在于，包括权利要求11-13任一项所述的有机电致发光器件。
PCT/CN2020/122846 2019-12-20 2020-10-22 含氮化合物、有机电致发光器件和电子装置 WO2021120835A1 (zh)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1020217042823A KR102442362B1 (ko) 2019-12-20 2020-10-22 함질소 화합물, 유기 전계 발광 소자 및 전자 장치
US17/623,211 US11608311B2 (en) 2019-12-20 2020-10-22 Nitrogen-containing compound, organic electroluminescent device, and electronic apparatus

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
CN201911328979 2019-12-20
CN201911328979.4 2019-12-20
CN202010914703.0A CN111875505B (zh) 2019-12-20 2020-09-03 含氮化合物、有机电致发光器件和电子装置
CN202010914703.0 2020-09-30

Publications (1)

Publication Number Publication Date
WO2021120835A1 true WO2021120835A1 (zh) 2021-06-24

Family

ID=73199656

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2020/122846 WO2021120835A1 (zh) 2019-12-20 2020-10-22 含氮化合物、有机电致发光器件和电子装置

Country Status (4)

Country Link
US (1) US11608311B2 (zh)
KR (1) KR102442362B1 (zh)
CN (1) CN111875505B (zh)
WO (1) WO2021120835A1 (zh)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114975839A (zh) * 2022-07-26 2022-08-30 吉林奥来德光电材料股份有限公司 一种有机电致发光器件、有机电致发光装置及光电设备
WO2022223850A3 (de) * 2021-09-30 2023-01-12 Merck Patent Gmbh Verbindungen für elektronische vorrichtungen

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021170008A1 (zh) * 2020-02-28 2021-09-02 陕西莱特光电材料股份有限公司 含氮化合物、电子元件和电子装置
CN114478265A (zh) * 2020-11-13 2022-05-13 江苏三月科技股份有限公司 一种芳胺类化合物及其在有机电致发光器件的应用
CN113173858B (zh) 2021-04-21 2022-03-11 陕西莱特迈思光电材料有限公司 含氮化合物、电子元件和电子装置
CN113651703B (zh) * 2021-07-20 2024-03-19 陕西莱特迈思光电材料有限公司 有机化合物、电子元件和电子装置
CN114230473A (zh) * 2021-12-22 2022-03-25 安徽秀朗新材料科技有限公司 一种基于芘的芳香胺化合物及其制备方法和作为有机电致发光材料的应用

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101018760A (zh) * 2004-09-17 2007-08-15 出光兴产株式会社 芳胺衍生物及使用该衍生物的有机电致发光元件
CN102232068A (zh) * 2009-04-24 2011-11-02 出光兴产株式会社 芳香族胺衍生物和使用其的有机电致发光元件
KR20190118515A (ko) * 2018-04-10 2019-10-18 주식회사 엘지화학 다환 화합물 및 이를 포함하는 유기 발광 소자
WO2020080849A1 (ko) * 2018-10-17 2020-04-23 주식회사 엘지화학 화합물 및 이를 포함하는 유기 발광 소자

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8642190B2 (en) 2009-10-22 2014-02-04 Semiconductor Energy Laboratory Co., Ltd. Fluorene derivative, light-emitting element, light-emitting device, electronic device, and lighting device
KR101918953B1 (ko) * 2012-03-06 2018-11-16 삼성디스플레이 주식회사 아민계 화합물, 이를 포함한 유기 발광 소자 및 이를 포함한 유기 발광 장치
KR101917953B1 (ko) * 2016-06-02 2018-11-13 주식회사 엘지화학 화합물 및 이를 포함하는 유기 전자 소자
CN108129332B (zh) 2016-12-01 2021-12-17 北京鼎材科技有限公司 一种芴取代衍生物及其应用
US11444249B2 (en) 2017-09-07 2022-09-13 Universal Display Corporation Organic electroluminescent materials and devices
CN109651174B (zh) 2019-01-23 2022-12-06 苏州久显新材料有限公司 有机电致发光化合物、发光材料及有机电致发光器件
CN110467536B (zh) 2019-06-14 2020-06-30 陕西莱特光电材料股份有限公司 含氮化合物、有机电致发光器件和光电转化器件
CN110128279A (zh) * 2019-06-14 2019-08-16 陕西莱特光电材料股份有限公司 有机电致发光材料及包含该材料的有机电致发光器件
CN111377853B (zh) * 2019-12-27 2021-04-13 陕西莱特光电材料股份有限公司 含氮化合物、电子元件和电子装置

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101018760A (zh) * 2004-09-17 2007-08-15 出光兴产株式会社 芳胺衍生物及使用该衍生物的有机电致发光元件
CN102232068A (zh) * 2009-04-24 2011-11-02 出光兴产株式会社 芳香族胺衍生物和使用其的有机电致发光元件
KR20190118515A (ko) * 2018-04-10 2019-10-18 주식회사 엘지화학 다환 화합물 및 이를 포함하는 유기 발광 소자
WO2020080849A1 (ko) * 2018-10-17 2020-04-23 주식회사 엘지화학 화합물 및 이를 포함하는 유기 발광 소자

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022223850A3 (de) * 2021-09-30 2023-01-12 Merck Patent Gmbh Verbindungen für elektronische vorrichtungen
CN114975839A (zh) * 2022-07-26 2022-08-30 吉林奥来德光电材料股份有限公司 一种有机电致发光器件、有机电致发光装置及光电设备
CN114975839B (zh) * 2022-07-26 2022-10-28 吉林奥来德光电材料股份有限公司 一种有机电致发光器件、有机电致发光装置及光电设备

Also Published As

Publication number Publication date
KR102442362B1 (ko) 2022-09-13
CN111875505A (zh) 2020-11-03
CN111875505B (zh) 2021-10-08
US11608311B2 (en) 2023-03-21
US20220388944A1 (en) 2022-12-08
KR20220009466A (ko) 2022-01-24

Similar Documents

Publication Publication Date Title
WO2021135207A1 (zh) 含氮化合物、电子元件和电子装置
WO2021120835A1 (zh) 含氮化合物、有机电致发光器件和电子装置
WO2022089428A1 (zh) 含氮化合物、包含其的电子元件和电子装置
WO2021213109A1 (zh) 一种芳胺化合物、使用其的电子元件及电子装置
WO2021218588A1 (zh) 一种含氮化合物以及使用其的电子元件和电子装置
WO2022083598A1 (zh) 一种含氮化合物以及使用其的电子元件和电子装置
WO2022262365A1 (zh) 有机化合物及包含其的电子元件和电子装置
WO2021223688A1 (zh) 一种有机化合物和应用以及使用其的有机电致发光器件和电子装置
WO2021135183A1 (zh) 有机化合物、有机电致发光器件和电子装置
WO2022088865A1 (zh) 含氮化合物、电子元件和电子装置
WO2022199449A1 (zh) 有机化合物及包含其的电子器件和电子装置
WO2023011028A1 (zh) 有机化合物、电子元件及电子装置
WO2021135750A1 (zh) 一种有机化合物、其应用以及有机电致发光器件
JP7105388B1 (ja) 窒素含有化合物、電子部品及び電子装置
WO2022089093A1 (zh) 含氮化合物、电子元件和电子装置
WO2021136197A1 (zh) 含氮化合物、电子元件和电子装置
WO2024055658A1 (zh) 含氮化合物和电子元件及电子装置
WO2021136006A1 (zh) 含氮化合物、电子元件和电子装置
WO2021120838A1 (zh) 有机化合物、电子器件及电子装置
WO2023216669A1 (zh) 有机化合物、有机电致发光器件和电子装置
WO2023202198A1 (zh) 有机材料、电子元件和电子装置
WO2021218829A1 (zh) 有机化合物、使用其的器件和电子装置
WO2021129639A1 (zh) 一种有机化合物和应用以及使用其的有机电致发光器件
WO2021174967A1 (zh) 含氮化合物、有机电致发光器件和电子装置
CN113896720B (zh) 有机化合物、电子元件及电子装置

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20901523

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 20217042823

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 20901523

Country of ref document: EP

Kind code of ref document: A1