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WO2020088187A1 - Complexe organométallique, haut polymère le contenant, son mélange, sa composition et son dispositif électronique organique - Google Patents

Complexe organométallique, haut polymère le contenant, son mélange, sa composition et son dispositif électronique organique Download PDF

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Publication number
WO2020088187A1
WO2020088187A1 PCT/CN2019/109289 CN2019109289W WO2020088187A1 WO 2020088187 A1 WO2020088187 A1 WO 2020088187A1 CN 2019109289 W CN2019109289 W CN 2019109289W WO 2020088187 A1 WO2020088187 A1 WO 2020088187A1
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organic
atoms
organometallic complex
groups
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Chinese (zh)
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黄宏
施超
潘君友
梁志明
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Guangzhou Chinaray Optoelectronic Materials Ltd
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Guangzhou Chinaray Optoelectronic Materials Ltd
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    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K77/00—Constructional details of devices covered by this subclass and not covered by groups H10K10/80, H10K30/80, H10K50/80 or H10K59/80
    • 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
    • C07F11/00—Compounds containing elements of Groups 6 or 16 of the Periodic Table
    • 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
    • C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic Table
    • 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
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • 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
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • 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
    • 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
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • 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
    • 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

  • the present invention relates to the field of electroluminescent materials, in particular to a new type of organic ligands and organometallic complexes containing the same, as well as polymers, mixtures and compositions containing the organometallic complexes, and their use in organic electronic devices , Especially in the application of organic phosphorescent light-emitting diodes.
  • the invention also relates to an organic electronic device containing the organometallic complex of the invention and its application.
  • OLEDs organic light-emitting diodes
  • Organic light-emitting diodes using fluorescent materials have the characteristics of high reliability, but their internal electroluminescence quantum efficiency under the excitation of an electric field It is limited to 25% because the excitons produce a singlet excited state and a triplet excited state with a probability ratio of 1: 3.
  • Professor Adachi of Japan discovered the phenomenon of thermally excited delayed fluorescent luminescence.
  • the light-emitting devices including thermally excited delayed fluorescent materials have reached the requirements of phosphorescent light-emitting devices in terms of efficiency, but the device life is still short and still not good Meet the actual application needs.
  • a main objective of the present invention is to provide a new ligand and corresponding organometallic complex, in particular to provide a new high-performance phosphorescent metal complex material, used to solve the existing Phosphorescent materials have too wide emission spectrum, poor color purity and other issues, opening up new technical paths for improving device performance.
  • Another object of the present invention is to provide polymers, mixtures, compositions and organic electronic devices containing the organometallic complex.
  • L1 is a divalent anionic organic ligand, and contains the structure represented by the general formula (1):
  • Q, T, E, U are selected from C or N, and Q is different from U;
  • Ar 1 and Ar 2 are selected from substituted or unsubstituted aromatic groups with 5-25 ring atoms, heteroaromatic groups or non-aromatic ring systems with 3-25 ring atoms, Ar 1 and Ar 2 may be the same , Can also be different;
  • M is a transition metal element; the dotted line indicates the bond directly connected to the metal element M;
  • L2 is a monovalent anionic organic ligand
  • L3 is a zero-valent neutral organic ligand
  • a high polymer comprising at least one organometallic complex as described above as a repeating unit.
  • a mixture comprising the organometallic complex or polymer as described above, and at least one organic functional material the organic functional material may be selected from a hole injection material (HIM), a hole transport material (HTM), Electron transport materials (ETM), electron injection materials (EIM), electron blocking materials (EBM), hole blocking materials (HBM), luminescent materials (Emitter), host materials (Host) and organic dyes.
  • HIM hole injection material
  • HTM hole transport material
  • ETM Electron transport materials
  • EIM electron injection materials
  • EBM electron blocking materials
  • HBM hole blocking materials
  • Emitter luminescent materials
  • host materials Hos
  • organic dyes organic dyes.
  • a composition comprising an organometallic complex or polymer or mixture as described above, and at least one organic solvent.
  • An organic electronic device comprising the organometallic complex or polymer or mixture as described above.
  • the organic electronic device is selected from an organic light emitting diode (OLED), an organic photovoltaic cell (OPV), an organic light emitting cell (OLEEC), an organic field effect tube (OFET), an organic light emitting field effect tube, and an organic laser , Organic spintronic devices, organic sensors and organic plasmon emitting diodes (Organic Plasmon Emitting Diode).
  • OLED organic light emitting diode
  • OCV organic photovoltaic cell
  • OFET organic field effect tube
  • organic light emitting field effect tube organic laser
  • Organic spintronic devices organic sensors and organic plasmon emitting diodes (Organic Plasmon Emitting Diode).
  • the present invention introduces divalent anion organic ligands into organometallic complexes to form a five-membered ring with metal atoms to provide more options for phosphorescent material design; the present invention further overcomes the difficulty of synthesis of new materials and opens up new materials Synthetic path.
  • the organometallic complex of the present invention increases the luminous efficiency of the phosphorescent metal complex by introducing a new type of dianion organic ligand, increases the life of the device, and provides more material choices for efficient phosphorescent light emitting devices.
  • the present invention provides an organometallic complex and its application in an organic electroluminescent device.
  • an organic electroluminescent device In order to make the objectives, technical solutions and effects of the present invention clearer and more specific, the present invention will be described in further detail below. It should be understood that the specific embodiments described herein are only used to explain the present invention and are not intended to limit the present invention.
  • the host material, the matrix material and the Host material have the same meaning and can be interchanged.
  • metal organic complex metal organic complex
  • organic metal complex organic metal complex
  • triplet state and triplet state have the same meaning and can be interchanged.
  • substituted means that the hydrogen atom in the substituent is replaced by the substituent.
  • the "number of ring atoms" means that the structural compound obtained by atom bonding to form a ring (for example, a monocyclic compound, a fused ring compound, a cross-linked compound, a carbocyclic compound, a heterocyclic compound) constitutes the ring itself.
  • the number of atoms in the atom When the ring is substituted with a substituent, the atoms contained in the substituent are not included in the ring-forming atoms.
  • the “number of ring atoms” described below is the same unless otherwise specified.
  • the benzene ring has 6 ring atoms
  • the naphthalene ring has 10 ring atoms
  • the thienyl ring has 5 ring atoms.
  • adjacent groups means that these groups are bonded to the same carbon atom or to adjacent carbon atoms. These definitions apply correspondingly to "adjacent substituents”.
  • the energy level structure of the organic material that is, the triplet energy level T 1 , the highest occupied orbital energy level HOMO, and the lowest unoccupied orbital energy level LUMO play a key role.
  • the following is an introduction to the determination of these energy levels.
  • HOMO and LUMO energy levels can be measured by photoelectric effect, such as XPS (X-ray photoelectron spectroscopy) and UPS (ultraviolet photoelectron spectroscopy) or by cyclic voltammetry (hereinafter referred to as CV).
  • photoelectric effect such as XPS (X-ray photoelectron spectroscopy) and UPS (ultraviolet photoelectron spectroscopy) or by cyclic voltammetry (hereinafter referred to as CV).
  • CV cyclic voltammetry
  • DFT density functional theory
  • the triplet energy level E T1 of organic materials can be measured by low-temperature time-resolved luminescence spectroscopy, or by quantum simulation calculations (such as through Time-dependent DFT), such as commercial software Gaussian 09W (Gaussian Inc.), specific simulation methods See WO2011141110 or as described in the examples below.
  • the absolute values of HOMO, LUMO, and E T1 depend on the measurement method or calculation method used. Even for the same method, different evaluation methods, such as the starting point and the peak point on the CV curve, can give different HOMO / LUMO value. Therefore, a reasonable and meaningful comparison should be made with the same measurement method and the same evaluation method.
  • the values of HOMO, LUMO, and E T1 are simulations based on Time-dependent DFT, but do not affect the application of other measurement or calculation methods.
  • (HOMO-1) is defined as the second highest occupied orbital energy level
  • (HOMO-2) is the third highest occupied orbital energy level
  • (LUMO + 1) is defined as the second lowest unoccupied orbital energy level
  • (LUMO + 2) is the third lowest occupied orbital energy level, and so on.
  • the present invention provides an organometallic complex having the general formula: M (L1) (L2) (L3), L1 is a divalent anionic organic ligand, and includes the structure represented by the general formula (1):
  • Q, T, E, U are selected from C or N, and Q is different from U;
  • Ar 1 and Ar 2 are selected from substituted or unsubstituted aromatic groups with 5-25 ring atoms, heteroaromatic groups or non-aromatic ring systems with 3-25 ring atoms, Ar 1 and Ar 2 may be the same , Can also be different;
  • M is a transition metal element; the dotted line indicates the bond directly connected to the metal element M;
  • L2 is a monovalent anionic organic ligand
  • L3 is a zero-valent neutral organic ligand
  • Q and U are different, and T and E are the same; in another preferred embodiment, Q and U are different, and T and E are also different;
  • the organometallic complex according to the present invention wherein Ar 1 and Ar 2 in the general formula (1) are selected from substituted or unsubstituted having 5-20 ring atoms, preferably having 5-15 Ring atoms, more preferably 6 to 15 ring atoms, most preferably 6 to 10 ring atoms, aromatic groups or heteroaromatic groups, wherein Ar 1 and Ar 2 may be the same or different.
  • the organometallic complex according to the present invention wherein Ar 1 and Ar 2 in the general formula (1) are selected from fused ring aromatic groups or fused heterocyclic aromatic groups.
  • Aromatic group refers to a hydrocarbon group containing at least one aromatic ring.
  • Heteroaromatic group refers to an aromatic hydrocarbon group containing at least one heteroatom.
  • the heteroatom is preferably selected from Si, N, P, O, S, and / or Ge, and particularly preferably selected from Si, N, P, O, and / or S.
  • a fused ring aromatic group means that the ring of the aromatic group may have two or more rings, in which two carbon atoms are shared by two adjacent rings, that is, a fused ring.
  • a fused heterocyclic aromatic group refers to a fused ring aromatic hydrocarbon group containing at least one heteroatom.
  • aromatic groups or heteroaromatic groups include not only aromatic ring systems but also non-aromatic ring systems. Therefore, for example, pyridine, thiophene, pyrrole, pyrazole, triazole, imidazole, oxazole, oxadiazole, thiazole, tetrazole, pyrazine, pyridazine, pyrimidine, triazine, carbene and other systems, the same for the purpose of the present invention It is considered to be an aromatic group or a heterocyclic aromatic group.
  • a fused ring aromatic or fused heterocyclic aromatic ring system includes not only a system of aromatic groups or heteroaromatic groups, but also, where multiple aromatic groups or heterocyclic aromatic groups can also be short Non-aromatic unit discontinuities ( ⁇ 10% of non-H atoms, preferably less than 5% of non-H atoms, such as C, N or O atoms).
  • Non-aromatic unit discontinuities ⁇ 10% of non-H atoms, preferably less than 5% of non-H atoms, such as C, N or O atoms.
  • 9,9'-spirobifluorene, 9,9-diarylfluorene, triarylamine, diarylether and other systems are also considered to be fused ring aromatic ring systems for the purposes of the present invention.
  • fused ring aromatic group examples include naphthalene, anthracene, fluoranthene, phenanthrene, benzophenanthrene, perylene, tetracene, pyrene, benzopyrene, acenaphthene, fluorene, and derivatives thereof.
  • fused heterocyclic aromatic group examples include: benzofuran, benzothiophene, indole, carbazole, pyrroloimidazole, pyrrolopyrrole, thienopyrrole, thienothiophene, furopyrrole, furofuran , Thienofuran, benzisoxazole, benzisothiazole, benzimidazole, quinoline, isoquinoline, o-naphthyridine, quinoxaline, phenanthridine, primary pyridine, quinazoline, quinazolinone , And its derivatives.
  • the organometallic complex according to the present invention wherein Ar 1 and Ar 2 in the general formula (1) are selected from substituted or unsubstituted having 3-20 ring atoms, preferably substituted or unsubstituted Non-aromatic ring systems having 3 to 15 ring atoms, more preferably substituted or unsubstituted having 6 to 15 ring atoms, and most preferably substituted or unsubstituted having 6 to 10 ring atoms are most preferred.
  • Ar 1 and Ar 2 in the general formula (1) are selected from one of the following structural groups:
  • X When X appears multiple times, it can be independently selected from N or CR 1 ;
  • Y When Y appears multiple times, it can be independently selected from NR 2 , CR 3 R 4 , SiR 3 R 4 , O or S;
  • R 1 , R 2 , R 3 and R 4 is independently selected from H and D, linear alkyl, alkoxy or thioalkoxy groups having 1 to 20 C atoms, Or branched or cyclic alkyl, alkoxy or thioalkoxy groups with 3 to 20 C atoms or silyl groups, or substituted keto groups with 1 to 20 C atoms Group, or an alkoxycarbonyl group having 2 to 20 C atoms, or an aryloxycarbonyl group having 7 to 20 C atoms, cyano group, carbamoyl group, haloformyl group Group, formyl group, isocyano group, isocyanate group, thiocyanate group or isothiocyanate group, hydroxyl group, nitro group, CF 3 group, Cl, Br, F, a crosslinkable group or a substituted or unsubstituted aromatic or heteroaromatic group having 5 to 40 ring atoms, or an aryloxy or hetero
  • each occurrence of R 1 , R 2 , R 3 , R 4 is independently selected from H, D, linear alkyl, alkoxy or thioalkoxy having 1 to 10 C atoms Group, or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 10 C atoms or a silyl group, or a substitution having 1 to 10 C atoms Keto group, or alkoxycarbonyl group having 2 to 10 C atoms, or aryloxycarbonyl group having 7 to 10 C atoms, cyano group, carbamoyl group, halogen Formyl group, formyl group, isocyano group, isocyanate group, thiocyanate group or isothiocyanate group, hydroxyl group, nitro group, CF 3 group, Cl , Br, F, crosslinkable groups or substituted or unsubstituted aromatic or heteroaromatic groups with 5 to 20 ring atoms, or aryl
  • Ar 1 and Ar 2 in the general formula (1) are selected from one of the following structural groups:
  • R 5 when multiple occurrences, is independently selected from the group D, a linear alkyl group having 1 to 20 C atoms, alkoxy or thioalkoxy groups, or Branched or cyclic alkyl, alkoxy or thioalkoxy groups with 3 to 20 C atoms or silyl groups, or substituted keto groups with 1 to 20 C atoms Group, or an alkoxycarbonyl group having 2 to 20 C atoms, or an aryloxycarbonyl group having 7 to 20 C atoms, cyano group, carbamoyl group, haloformyl group , Formyl group, isocyano group, isocyanate group, thiocyanate group or isothiocyanate group, hydroxyl group, nitro group, CF 3 group, Cl, Br, F , A crosslinkable group or a substituted or unsubstituted aromatic or heteroaromatic group having 5 to 40 ring atoms,
  • the metal element M is selected from the transition metals molybdenum (Mo), tungsten (W), ruthenium (Ru), rhodium (Rh), nickel (Ni), gold (Au), osmium ( Os), rhenium (Re), and iridium (Ir).
  • the metal element M is selected from transition metals ruthenium (Ru), rhodium (Rh), hunger (Os), rhenium (Re) and iridium (Ir) Any of them.
  • the metal element M is selected from Ir.
  • L2 in the general formula M (L1) (L2) (L3) is selected from any one of the following general formulas:
  • L3 in the general formula M (L1) (L2) (L3) is selected from any one of the following general formulas:
  • H in the ring may be further substituted by R 5 , R 5 has the same meaning as above, and the dotted line represents the bond directly connected to the metal element M.
  • the organometallic complex of the present invention is selected from but not limited to the following general formula:
  • R 6 has the same meaning as R 1 , u is selected from any integer from 0-2, q is selected from any integer from 0-3, y is selected from any integer from 0-4, and v is selected from any integer from 0-5 An integer, z is selected from any integer from 0 to 6, and Ar 1 , Ar 2 , Q, T, E, U, M have the same meaning as above.
  • L1 is selected from the following general formulas (2-1) to (2-4):
  • X and Y are the same as above, and the dotted line represents the bond directly connected to the metal element M.
  • adjacent Xs may be independently selected from CR 1 when appearing multiple times; more preferably, adjacent R 1s in general formulas (2-1) to (2-4) may be connected to each other to form a ring .
  • L1 in the general formula (1) is preferably selected from any one of the following general formulas A1-A48:
  • organometallic complexes of the present invention
  • H in the structural formula may be further substituted arbitrarily.
  • Organic functional materials include but are not limited to: hole injection materials (HIM), hole transport materials (HTM), electron transport materials (ETM), electron injection materials (EIM), electron blocking materials (EBM), hole blocking materials ( HBM), luminous body (Emitter) and host material (Host).
  • HIM hole injection materials
  • HTM hole transport materials
  • ETM electron transport materials
  • EIM electron injection materials
  • EBM electron blocking materials
  • HBM hole blocking materials
  • luminous body Emitter
  • Hos host material
  • the organometallic complex of the present invention is a non-luminescent functional material.
  • the organometallic complex of the present invention is a light-emitting material whose emission wavelength is between 300 and 1000 nm, preferably between 350 and 900 nm, and more preferably between 400 and 800 nm.
  • Luminescence here refers to photoluminescence or electroluminescence.
  • the organometallic complex of the present invention has a photoluminescence or electroluminescence efficiency of ⁇ 30%, preferably ⁇ 40%, more preferably ⁇ 50%, and most preferably ⁇ 60%.
  • the organometallic complex of the present invention is used as a phosphorescent guest material.
  • the organometallic complex of the present invention has T 1 ⁇ 1.5 eV, preferably, T 1 ⁇ 1.8 eV, more preferably, T 1 ⁇ 2.0 eV, and most preferably, T 1 ⁇ 2.2 eV.
  • the organometallic complex of the present invention has a glass transition temperature T g ⁇ 100 ° C. In a preferred embodiment, T g ⁇ 120 ° C. In a more preferred embodiment, T g ⁇ 140 ° C. In a more preferred embodiment, T g ⁇ 160 ° C, and in a most preferred embodiment, T g ⁇ 180 ° C.
  • the organometallic complex of the present invention has HOMO ⁇ -4.9 eV, preferably, HOMO ⁇ -4.5 eV, more preferably, HOMO ⁇ -4.3 eV, most preferably, HOMO ⁇ -4.0 eV.
  • the organometallic complex of the present invention has LUMO ⁇ -3.5 eV, more preferably, LUMO ⁇ -3.3 eV, more preferably, LUMO ⁇ -3.1 eV, most preferably, LUMO ⁇ -3.0 eV .
  • the organometallic complex according to the present invention satisfies: (HOMO- (HOMO-1)) ⁇ 0.2eV, more preferably, (HOMO- (HOMO-1)) ⁇ 0.25eV, more Preferably, (HOMO- (HOMO-1)) ⁇ 0.3eV, more preferably, (HOMO- (HOMO-1)) ⁇ 0.35eV, very preferably, (HOMO- (HOMO-1)) ⁇ 0.4eV , Most preferably, (HOMO- (HOMO-1)) ⁇ 0.45 eV.
  • the organometallic complex according to the present invention satisfies: ((LUMO + 1) -LUMO) ⁇ 0.15eV, more preferably, ((LUMO + 1) -LUMO) ⁇ 0.20eV, more Preferably, ((LUMO + 1) -LUMO) ⁇ 0.25eV, more preferably, ((LUMO + 1) -LUMO) ⁇ 0.30eV, most preferably, ((LUMO + 1) -LUMO) ⁇ 0.35eV .
  • the present invention further relates to a polymer comprising at least one structural unit of the organometallic complex as a repeating unit.
  • the polymer synthesis method is selected from SUZUKI-, YAMAMOTO-, STILLE-, NIGESHI-, KUMADA-, HECK-, SONOGASHIRA-, HIYAMA-, FUKUYAMA-, HARTWIG-BUCHWALD- and ULLMAN.
  • the glass transition temperature of the polymer of the present invention T g ⁇ 100 °C, preferably, T g ⁇ 120 °C, more preferably, T g ⁇ 140 °C, still more preferably, T g ⁇ 160 ° C, most preferably, Tg ⁇ 180 ° C.
  • the molecular weight distribution (PDI) of the polymer according to the present invention preferably ranges from 1 to 5; more preferably from 1 to 4; more preferably from 1 to 3, and even more preferably from 1 to 2, most preferably 1 to 1.5.
  • the weight average molecular weight (Mw) of the polymer according to the present invention preferably ranges from 10,000 to 1 million; more preferably from 50,000 to 500,000; more preferably from 100,000 to 400,000 It is more preferably 150,000 to 300,000, and most preferably 200,000 to 250,000.
  • the polymer according to the present invention is a non-conjugated polymer, preferably, a non-conjugated structure containing a structural unit of the organometallic complex on the side chain as a repeating unit high polymer.
  • the present invention also provides a mixture comprising at least one of the above-mentioned organometallic complexes or polymers, and at least one organic functional material
  • the organic functional material may be selected from: hole injection material (HIM), Hole transport material (HTM), electron transport material (ETM), electron injection material (EIM), electron blocking material (EBM), hole blocking material (HBM), light emitting material (Emitter), host material (Host) and organic dye.
  • HIM hole injection material
  • HTM Hole transport material
  • ETM electron transport material
  • EIM electron injection material
  • EBM electron blocking material
  • Emitter hole blocking material
  • host material Host
  • organic dye organic dye
  • the content of the metal-organic complex in the mixture of the present invention is 0.01 to 30 wt%, preferably 0.5 to 20 wt%, more preferably 2 to 15 wt%, and most preferably 5 to 15 wt%.
  • the mixture according to the invention comprises the metal organic complex or polymer of the invention and a triplet host material.
  • the mixture according to the invention comprises the metal organic complex or polymer of the invention, a triplet host material and a triplet emitter.
  • the mixture according to the invention comprises the metal organic complex or polymer of the invention and a thermally activated delayed fluorescent luminescent material (TADF).
  • TADF thermally activated delayed fluorescent luminescent material
  • the mixture according to the invention comprises the metal organic complex or polymer of the invention, a triplet host material and a thermally activated delayed fluorescent luminescent material (TADF).
  • TADF thermally activated delayed fluorescent luminescent material
  • triplet host material triplet emitter and TADF material (but not limited to this).
  • Triplet host material (TripletHost):
  • triplet host materials are not particularly limited, and any metal complex or organic compound may be used as the host, as long as its triplet energy level is higher than that of the luminous body, especially the triplet luminous body or phosphorescent luminous body That's it.
  • Host triplet host
  • M is a metal
  • (Y 3 -Y 4 ) is a bidentate ligand, Y 3 and Y 4 are independently selected from C, N, O, P, and S
  • L is an auxiliary ligand
  • m is an integer, and the value of m is The maximum coordination number from 1 to M; in a preferred embodiment, the metal complex that can be used as a host material in the triplet state has the following structure:
  • (O-N) is a bidentate ligand, the metal is coordinated with O and N atoms; m is an integer, and the value of m ranges from 1 to the maximum coordination number of the metal;
  • M can be selected from Ir and Pt.
  • each Ar may be further substituted, and the substituent may be selected from hydrogen, deuterium, cyano, halogen, alkyl, alkoxy, amino, alkenyl, alkynyl, aralkyl, heteroalkyl, aryl and Heteroaryl.
  • the triplet host material may be selected from compounds containing at least one of the following groups:
  • Ar 1 to Ar 3 are selected from aromatic or heteroaromatic groups, and R can be selected from the following groups: hydrogen, deuterium, halogen atoms (F, Cl, Br, I), cyano, Alkyl, alkoxy, amino, alkenyl, alkynyl, aralkyl, heteroalkyl, aryl, and heteroaryl, n is selected from an integer of 1 to 20.
  • TDF Thermally activated delayed fluorescent luminescent material
  • Such materials generally have a small singlet-triplet energy level difference ( ⁇ Est), and triplet excitons can be converted into singlet excitons to emit light by crossing between anti-systems. This can make full use of the singlet excitons and triplet excitons formed under electrical excitation.
  • the quantum efficiency within the device can reach 100%.
  • the material structure is controllable, the properties are stable, the price is cheap and no precious metals are needed, and the application prospect in the field of OLED is broad.
  • the TADF material needs to have a small singlet-triplet energy level difference ( ⁇ Est).
  • ⁇ Est ⁇ 0.3 eV, more preferably, ⁇ Est ⁇ 0.25 eV, more preferably, ⁇ Est ⁇ 0.20 eV, most preferably, ⁇ Est ⁇ 0.1 eV.
  • the TADF material has a relatively small ⁇ Est, and in another preferred embodiment, TADF has a better fluorescence quantum efficiency.
  • TADF luminescent materials can be found in the following patent documents: CN103483332 (A), TW201309696 (A), TW201309778 (A), TW201343874 (A), TW201350558 (A), US20120217869 (A1), WO2013133359 (A1), WO2013154064 (A1 ), Adachi, et.al.Nature Photonics, 6,2012,253, Adachi, et.al.Nature, 492,2012,234, Adachi, et.al.Adv.Mater., 25,2013,3707, Adachi, et.al.Chem.Mater., 25,2013,3038, Adachi, et.al.Chem.Mater., 25,2013,3766, JYLee, et.al.Adv.Opt.Mater., 2018,1800255.
  • Triplet emitters are also called phosphorescent emitters.
  • the triplet emitter is a metal complex with the general formula M (L) n, where M is a metal atom and L is an organic ligand, which can be the same or different each time it appears, which passes a Or multiple positions are bonded or coordinated to the metal atom M, n is an integer between 1 and 6.
  • the triplet luminophore contains a chelating ligand, that is, a ligand, and the ligand is coordinated to the metal through at least two binding points.
  • the triplet luminophore contains two or three identical or different Bidentate or multidentate ligands. Chelating ligands help to improve the stability of metal complexes.
  • the metal complex that can be used as a triplet emitter has the following general formula:
  • the metal atom M is selected from transition metal elements or lanthanides or actinides, preferably selected from Ir, Pt, Pd, Au, Rh, Ru, Os, Re, Cu, Ag, Ni, Co, W or Eu, particularly preferred It is selected from Ir, Au, Pt, W or Os.
  • Ar 1 and Ar 2 are cyclic groups, which can be the same or different each time.
  • Ar 1 contains at least one donor atom, that is, an atom with a lone pair of electrons, such as nitrogen.
  • the cyclic group passes through this atom and the metal Coordinate connection;
  • Ar 2 contains at least one carbon atom through which the cyclic group is connected to the metal;
  • Ar 1 and Ar 2 are linked together by a covalent bond, Ar 1 and Ar 2 can each carry one or more Substituent groups, which can also be linked together through substituent groups;
  • L ' can be the same or different each time it appears, L' is an auxiliary ligand for bidentate chelation, preferably a monoanionic bidentate chelating ligand Q1 can be 0, 1, 2 or 3, preferably 2 or 3;
  • q2 can be 0, 1, 2 or 3, preferably 1 or 0.
  • organic ligands can be selected from phenylpyridine derivatives or 7,8-benzoquinoline derivatives. All of these organic ligands can be substituted, for example by alkyl chains or fluorine or silicon.
  • the auxiliary ligand may preferably be selected from acetone acetate or picric acid.
  • triplet emitter materials and their extremely useful applications can be found in the following patent documents and documents: WO200070655, WO200141512, WO200202714, WO200215645, WO2005033244, WO2005019373, US20050258742, US20070087219, US20070252517, US2008027220, WO2009146770, US20090061681, US20090061681, WO2009118087 , WO2010054731, WO2011157339, WO2012007087, WO201200708, WO2013107487, WO2013094620, WO2013174471, WO2014031977, WO2014112450, WO2014007565, WO2014024131, Baldo et al.
  • An object of the present invention is to provide a material solution for an evaporation type OLED.
  • the molecular weight of the organometallic complex according to the invention is ⁇ 1200 g / mol, preferably ⁇ 1100 g / mol, very preferably ⁇ 1000 g / mol, more preferably ⁇ 950 g / mol, and most preferably ⁇ 900 g / mol.
  • Another object of the invention is to provide a material solution for printed OLEDs.
  • the molecular weight of the organometallic complex according to the invention is ⁇ 800 g / mol, preferably ⁇ 900 g / mol, very preferably ⁇ 1000 g / mol, more preferably ⁇ 1100 g / mol, and most preferably ⁇ 1200 g / mol.
  • the solubility of the organometallic complex according to the invention in toluene at 25 ° C is ⁇ 2 mg / ml, preferably ⁇ 3 mg / ml, more preferably ⁇ 4 mg / ml, and most preferably ⁇ 5 mg / ml.
  • the present invention also relates to a composition
  • a composition comprising at least one organic metal complex or polymer or mixture as described above, and at least one organic solvent; the at least one organic solvent is selected from aromatic or heteroaromatic, Ester, aromatic ketone or aromatic ether, aliphatic ketone or aliphatic ether, alicyclic or olefin compound, or borate or phosphate compound, or a mixture of two or more solvents.
  • the organic solvent in the composition according to the invention is selected from aromatic or heteroaromatic based solvents.
  • Non-limiting examples of aromatic or heteroaromatic solvents suitable for the present invention are: p-diisopropylbenzene, pentylbenzene, tetrahydronaphthalene, cyclohexylbenzene, chloronaphthalene, 1,4-dimethylnaphthalene, 3 -Isopropyl biphenyl, p-methyl cumene, dipentylbenzene, tripentylbenzene, pentyltoluene, o-diethylbenzene, m-diethylbenzene, p-diethylbenzene, 1,2,3,4-tetra Toluene, 1,2,3,5-tetratoluene, 1,2,4,5-tetratoluene, butylbenzene, dodecylbenzene, dihexylbenzene, dibutylbenzene, p-diisopropylbenzene, cycl
  • Non-limiting examples of aromatic ketone-based solvents suitable for the present invention are: 1-tetralone, 2-tetralone, 2- (phenylepoxy) tetralone, 6- (methoxy) Tetralin, acetophenone, acetophenone, benzophenone, and their derivatives, such as 4-methylacetophenone, 3-methylacetophenone, 2-methylacetophenone, 4- Methyl phenyl acetone, 3-methyl phenyl acetone, 2-methyl phenyl acetone, etc.
  • Non-limiting examples of aromatic ether-based solvents suitable for the present invention are: 3-phenoxytoluene, butoxybenzene, p-anisaldehyde dimethyl acetal, tetrahydro-2-phenoxy-2H-pyridine Furan, 1,2-dimethoxy-4- (1-propenyl) benzene, 1,4-benzodioxane, 1,3-dipropylbenzene, 2,5-dimethoxytoluene, 4-ethylbenzyl ether, 1,3-dipropoxybenzene, 1,2,4-trimethoxybenzene, 4- (1-propenyl) -1,2-dimethoxybenzene, 1,3- Dimethoxybenzene, glycidyl phenyl ether, dibenzyl ether, 4-tert-butyl anisole, trans-p-propenyl anisole, 1,2-dimethoxybenzene, 1-methoxy Naphthalene, diphenyl
  • the organic solvent of the composition according to the present invention may be selected from: aliphatic ketones, for example, 2-nonanone, 3-nonanone, 5-nonanone, 2-decanone, 2,5 -Hexanedione, 2,6,8-trimethyl-4-nonanone, fenone, phorone, isophorone, di-n-amyl ketone, etc .; or aliphatic ethers, for example, pentyl ether, hexane Ether, dioctyl ether, ethylene glycol dibutyl ether, diethylene glycol diethyl ether, diethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, triethylene glycol ethyl methyl ether Ether, triethylene glycol butyl methyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, etc.
  • aliphatic ketones
  • the organic solvent of the composition according to the present invention may be selected from ester-based solvents: alkyl octoate, alkyl sebacate, alkyl stearate, alkyl benzoate, alkyl phenylacetate Ester, alkyl cinnamate, alkyl oxalate, alkyl maleate, alkanolide, alkyl oleate, etc. Particularly preferred is octyl octoate, diethyl sebacate, diallyl phthalate, and isononyl isononanoate.
  • the solvent may be used alone or as a mixture of two or more organic solvents.
  • the composition according to the invention comprises at least one organometallic complex or polymer or mixture as described above and at least one organic solvent, and may further comprise another organic solvent.
  • another organic solvent include (but are not limited to): methanol, ethanol, 2-methoxyethanol, methylene chloride, chloroform, chlorobenzene, o-dichlorobenzene, tetrahydrofuran, anisole, morpholine, Toluene, o-xylene, m-xylene, p-xylene, 1,4 dioxane, acetone, methyl ethyl ketone, 1,2 dichloroethane, 3-phenoxytoluene, 1,1 , 1-trichloroethane, 1,1,2,2-tetrachloroethane, ethyl acetate, butyl acetate, dimethylformamide, dimethylacetamide, dimethylsulfoxide, tetrahydronaphthalene
  • the solvent that is particularly suitable for the present invention is a solvent whose Hansen solubility parameter is within the following range:
  • ⁇ d (dispersion force) is in the range of 17.0 ⁇ 23.2MPa 1/2 , especially in the range of 18.5 ⁇ 21.0MPa 1/2 ;
  • ⁇ p polar forces in the range of 0.2 ⁇ 12.5MPa 1/2, especially in the 2.0 ⁇ 6.0MPa 1/2;
  • the organic solvent of the composition according to the present invention needs to consider its boiling point parameter when selecting.
  • the boiling point of the organic solvent is ⁇ 150 ° C; preferably ⁇ 180 ° C; more preferably ⁇ 200 ° C; more preferably ⁇ 250 ° C; most preferably ⁇ 275 ° C or ⁇ 300 ° C.
  • the boiling point in these ranges is beneficial to prevent nozzle clogging of the inkjet print head.
  • the organic solvent can be evaporated from the solvent system to form a thin film containing functional materials.
  • the composition according to the invention is a solution.
  • composition according to the invention is a suspension.
  • composition in the embodiment of the present invention may include 0.01 to 10 wt%, preferably 0.1 to 15 wt%, more preferably 0.2 to 5 wt%, and most preferably 0.25 to 3 wt% of the organometallic complex or polymer or mixture of the present invention.
  • the invention also relates to the use of the composition as a coating or printing ink in the preparation of organic electronic devices, especially by printing or coating.
  • suitable printing or coating technologies include (but are not limited to): inkjet printing, jet printing (Nozzle Printing), letterpress printing, screen printing, dip coating, spin coating, doctor blade coating, roller printing, twisting Roll printing, offset printing, flexographic printing, rotary printing, spraying, brushing or pad printing, slit-type extrusion coating, etc.
  • the first choice is gravure printing, jet printing and inkjet printing.
  • the solution or suspension may additionally include one or more components, such as surface-active compounds, lubricants, wetting agents, dispersing agents, hydrophobic agents, adhesives, etc., used to adjust viscosity and film-forming properties, improve adhesion, etc. .
  • the present invention also provides the application of the organic metal complexes, polymers, mixtures or compositions as described above in organic electronic devices, which can be selected from (but not limited to): organic light emitting diodes (OLED), Organic photovoltaic cell (OPV), organic light emitting cell (OLEEC), organic field effect tube (OFET), organic light emitting field effect tube, organic laser, organic spintronic device, organic sensor and organic plasmon emitting diode (Organic Plasmon Emitting Diode), etc., particularly preferably OLED.
  • OLED organic light emitting diodes
  • OOV Organic photovoltaic cell
  • OFET organic field effect tube
  • organic light emitting field effect tube organic laser
  • organic spintronic device organic spintronic device
  • organic sensor and organic plasmon emitting diode Organic Plasmon Emitting Diode
  • OLED organic Plasmon Emitting Diode
  • the invention further relates to an organic electronic device comprising at least the organometallic complex, polymer or mixture as described above.
  • an organic electronic device includes at least a cathode, an anode, and a functional layer between the cathode and the anode, wherein the functional layer includes at least one organic metal complex as described above.
  • the organic electronic device may be selected from (but not limited to): organic light emitting diode (OLED), organic photovoltaic cell (OPV), organic light emitting cell (OLEEC), organic field effect tube (OFET), organic light emitting field effect tube, organic Lasers, organic spintronic devices, organic sensors and organic plasmon emitting diodes (Organic Plasmon Emitting Diode), etc., are particularly preferably organic electroluminescent devices, such as OLED, OLEEC, organic light emitting field effect tubes.
  • the light-emitting layer of the organic electroluminescent device comprises the organometallic complex or polymer or mixture as described above.
  • the light-emitting device described above especially the OLED, includes a substrate, an anode, at least one light-emitting layer and a cathode.
  • the substrate may be opaque or transparent.
  • the transparent substrate can be used to manufacture transparent light-emitting components.
  • the substrate may be rigid or elastic.
  • the substrate may be a plastic metal semiconductor wafer or glass.
  • the substrate has a smooth surface. Substrates without surface defects are particularly ideal choices.
  • the substrate is flexible and can be selected from polymer films or plastics, and its glass transition temperature T g is above 150 ° C, preferably above 200 ° C, more preferably above 250 ° C, and most preferably above 300 ° C .
  • suitable flexible substrates are poly (ethylene terephthalate) (PET) and polyethylene glycol (2,6-naphthalene) (PEN).
  • the anode may include a conductive metal or metal oxide or a conductive polymer.
  • the anode can easily inject holes into the hole injection layer (HIL) or the hole transport layer (HTL) or the light emitting layer.
  • the absolute value of the difference between the work function of the anode and the HOMO energy level or valence band energy level of the luminous body in the light emitting layer or the p-type semiconductor material as HIL or HTL or electron blocking layer (EBL) is less than 0.5 eV, preferably less than 0.3 eV, most preferably less than 0.2 eV.
  • anode materials include, but are not limited to: Al, Cu, Au, Ag, Mg, Fe, Co, Ni, Mn, Pd, Pt, ITO, aluminum-doped zinc oxide (AZO), and the like.
  • suitable anode materials are known and can be easily selected and used by those of ordinary skill in the art.
  • the anode material can be deposited using any suitable technique, such as a suitable physical vapor deposition method, including radio frequency magnetron sputtering, vacuum thermal evaporation, e-beam, etc.
  • the anode is patterned. Patterned ITO conductive substrates are commercially available and can be used to prepare the organic electronic devices of the present invention.
  • the cathode may include a conductive metal or metal oxide.
  • the cathode can easily inject electrons into EIL or ETL or directly into the light emitting layer.
  • the absolute value of the difference in conduction band energy level is less than 0.5 eV, preferably less than 0.3 eV, and most preferably less than 0.2 eV.
  • all materials that can be used as cathodes for OLEDs are possible as cathode materials for the devices of the invention.
  • cathode materials include but are not limited to: Al, Au, Ag, Ca, Ba, Mg, LiF / Al, Mg / Ag alloy, BaF 2 / Al, Cu, Fe, Co, Ni, Mn, Pd, Pt, ITO Wait.
  • the cathode material can be deposited using any suitable technique, such as a suitable physical vapor deposition method, including radio frequency magnetron sputtering, vacuum thermal evaporation, e-beam, etc.
  • OLED can also contain other functional layers, such as hole injection layer (HIL), hole transport layer (HTL), electron blocking layer (EBL), electron injection layer (EIL), electron transport layer (ETL), hole blocking layer (HBL).
  • HIL hole injection layer
  • HTL hole transport layer
  • EBL electron blocking layer
  • EIL electron injection layer
  • ETL electron transport layer
  • HBL hole blocking layer
  • the light emitting device has a light emission wavelength between 300 and 1200 nm, preferably between 350 and 1000 nm, and more preferably between 400 and 900 nm.
  • the invention also relates to the application of the electroluminescent device according to the invention in various electronic equipment.
  • electronic devices include but are not limited to display devices, lighting devices, light sources, sensors, and so on.
  • the energy levels of the organometallic complexes M-1 to M-198 can be obtained by quantum calculations, such as TD-DFT (time-dependent density functional theory) by Gaussian09W (Gaussian Inc.), the specific simulation method can be found in WO2011141110 .
  • the HOMO and LUMO energy levels are calculated according to the following calibration formula, and S 1 and T 1 are used directly.
  • HOMO (eV) ((HOMO (Gaussian) ⁇ 27.212) -0.9899) /1.1206
  • HOMO (G) and LUMO (G) are the direct calculation results of Gaussian 09W, and the unit is Hartree. The results are shown in Table 1:
  • OLED device ITO / MoO3 (10nm) / NPB (60nm) / 10% metal complex (M-1): m-MTDATA (45nm) / Alq3 (35nm) / LiF (1nm) / Al (150nm)
  • conductive glass substrate when it is used for the first time, it can be cleaned with a variety of solvents, such as chloroform, ketone, isopropanol, and then ultraviolet ozone plasma treatment;
  • HIL 10nm
  • HTL 60nm
  • EML 45nm
  • ETL 35nm
  • HIL material is selected from MoO3
  • HTL material It is selected from NPB
  • EML material is selected from organometallic complex M-1: m-MTDATA
  • ETL material is selected from Alq3.
  • Cathode Li F / AI (1nm / 150nm) is thermally vapor deposited in high vacuum (1x10 -6 mbar);
  • Encapsulation The device is encapsulated with ultraviolet curing resin in a chlorine glove box.
  • the preparation method was the same as in Example 16, except that the complex M-1 was replaced with the compound shown in Table 1.
  • the performance of the device will be further improved, especially the efficiency, driving voltage and life.

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  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

L'invention concerne un nouveau complexe organométallique, son dispositif électronique organique et leur utilisation notamment dans des diodes organiques électrophosphorescentes. L'invention concerne aussi un dispositif électronique organique contenant le complexe organométallique et son utilisation notamment dans des diodes organiques électrophotographiques, dans des dispositifs d'affichage et dans l'ingénierie de l'éclairage. L'optimisation structurelle du dispositif modifie la concentration d'un complexe métallique dans un substrat, améliore les performances du dispositif ainsi que l'efficience, la luminosité et la stabilité d'un dispositif OLED tout en fournissant un bon matériau pour un écran couleur.
PCT/CN2019/109289 2018-11-02 2019-09-30 Complexe organométallique, haut polymère le contenant, son mélange, sa composition et son dispositif électronique organique Ceased WO2020088187A1 (fr)

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Citations (5)

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CN101040027A (zh) * 2004-08-18 2007-09-19 巴斯福股份公司 嵌入用于oled的聚合物基质中的过渡金属－碳烯配合物
CN101896493A (zh) * 2007-10-17 2010-11-24 巴斯夫欧洲公司 具有桥连碳烯配体的过渡金属配合物及其在oled中的用途
TW201527484A (zh) * 2014-01-15 2015-07-16 Nat Univ Tsing Hua 含雙唑類配基的銥金屬錯合物
WO2018108109A1 (fr) * 2016-12-13 2018-06-21 广州华睿光电材料有限公司 Complexe de métal de transition et son application, mélange et dispositif électronique organique
WO2019128848A1 (fr) * 2017-12-28 2019-07-04 广州华睿光电材料有限公司 Complexe organométallique, polymère, mélange, composition le comprenant et application de celui-ci dans un dispositif électronique

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101040027A (zh) * 2004-08-18 2007-09-19 巴斯福股份公司 嵌入用于oled的聚合物基质中的过渡金属－碳烯配合物
CN101896493A (zh) * 2007-10-17 2010-11-24 巴斯夫欧洲公司 具有桥连碳烯配体的过渡金属配合物及其在oled中的用途
TW201527484A (zh) * 2014-01-15 2015-07-16 Nat Univ Tsing Hua 含雙唑類配基的銥金屬錯合物
WO2018108109A1 (fr) * 2016-12-13 2018-06-21 广州华睿光电材料有限公司 Complexe de métal de transition et son application, mélange et dispositif électronique organique
WO2019128848A1 (fr) * 2017-12-28 2019-07-04 广州华睿光电材料有限公司 Complexe organométallique, polymère, mélange, composition le comprenant et application de celui-ci dans un dispositif électronique

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