WO2017118237A1 - 并吡咯衍生物及其在有机电子器件的应用 - Google Patents

并吡咯衍生物及其在有机电子器件的应用 Download PDF

Info

Publication number
WO2017118237A1
WO2017118237A1 PCT/CN2016/107307 CN2016107307W WO2017118237A1 WO 2017118237 A1 WO2017118237 A1 WO 2017118237A1 CN 2016107307 W CN2016107307 W CN 2016107307W WO 2017118237 A1 WO2017118237 A1 WO 2017118237A1
Authority
WO
WIPO (PCT)
Prior art keywords
organic
group
alkane
pyrrole derivative
aromatic
Prior art date
Application number
PCT/CN2016/107307
Other languages
English (en)
French (fr)
Inventor
潘君友
施超
Original Assignee
广州华睿光电材料有限公司
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 广州华睿光电材料有限公司 filed Critical 广州华睿光电材料有限公司
Priority to CN201680059920.8A priority Critical patent/CN108137604B/zh
Publication of WO2017118237A1 publication Critical patent/WO2017118237A1/zh

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-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
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic 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

Definitions

  • the present invention relates to a pyrrole derivative and its use in organic electronic devices, particularly in organic light emitting diodes.
  • the invention further relates to an organic electronic device comprising such a pyrrole derivative, in particular a light-emitting element, and its use in displays and illumination devices.
  • OLEDs Organic light-emitting diodes
  • the development of a blue fluorescent material having a narrow-band emission spectrum and good stability is advantageous for obtaining a longer-life, higher-efficiency blue light device, and on the other hand, it is advantageous for the improvement of the color gamut, thereby improving the display effect.
  • the technical solution of the present invention is: a pyrrole derivative containing a structure of the formula (I):
  • Ar 1 and Ar 2 may be the same or different selected from the group consisting of an unsubstituted or R 1 -substituted aromatic hydrocarbon or heteroaromatic cyclic hydrocarbon system;
  • R 2 In each occurrence of R 2 , the same or different is H, D, an aliphatic alkane having 1 to 10 carbon atoms, an aromatic hydrocarbon, a substituted or unsubstituted aromatic ring having 5 to 10 ring atoms. Or a heteroaromatic group.
  • the pyrrole derivative is preferably selected from the group consisting of:
  • R3 represents -H, -F, -Cl, Br, I, -D, -CN, -NO 2 , -CF 3 , B(OR 2 ) 2 , Si(R 2 ) 3 , linear alkane, alkane An ether having 1 to 10 carbon atoms of an alkane sulfide or a branched alkane or a cycloalkane, and an aryl group having 6 to 10 carbon atoms;
  • x is any one of the numbers 0-4, y is any one of the numbers 0-5, z is any one of the numbers 0-7, u is any one of the numbers 0-8, and v is the number 0-9 Any one of them, w is any one of the numbers 0-11;
  • L is a linking group and is independent of each other selected from a single bond or any one of B1 to B4:
  • R 3 to R 26 are selected from the group consisting of -H, -F, -Cl, Br, I, -D, -CN, -NO 2 , -CF 3 , B(OR 2 ) 2 , Si(R 2 ) 3 , A linear alkane, an alkane ether, an alkane thioether having 1 to 10 carbon atoms or a branched or alkane or a aryl group having 6 to 10 carbon atoms.
  • the pyrrole derivative is characterized by being selected from the group consisting of:
  • the pyrrole derivative wherein Ar 2 in the formula (I), (I-1)-(I-10) is an unsubstituted or substituted aromatic ring unit,
  • the plurality of occurrences which are independent of each other are preferably selected from any one of the general formulas C1 to C10:
  • R 27 to R 106 are selected from the group consisting of -H, -F, -Cl, Br, I, -D, -CN, -NO 2 , -CF 3 , B(OR 2 ) 2 , Si(R 2 ) 3 , A linear alkane, an alkane ether, an alkane thioether having 1 to 10 carbon atoms or a branched or alkane or a aryl group having 6 to 10 carbon atoms.
  • the pyrrole derivative is characterized in that Ar 2 in the formula (I), (I-1) to (I-10) are independently selected from the group consisting of:
  • the present invention also provides a high polymer comprising a repeating unit comprising a structural unit represented by the formula (I).
  • the invention also provides a mixture comprising a pyrrole derivative or polymer as described above and at least one organic functional material.
  • the organic functional material may be selected from the group consisting of a hole injection material (HIM), a hole transport material (HTM), an electron transport material (ETM), an electron injecting material (EIM), an electron blocking material (EBM), and a hole blocking material ( HBM), luminescent material (Emitter), host material (Host) and organic dyes.
  • the invention also provides a composition comprising a pyrrole derivative or polymer according to the invention, and at least one organic solvent.
  • the invention also provides the use of a pyrrole derivative or polymer according to the invention in an organic electronic device.
  • the invention also provides an organic electronic device comprising at least one pyrrole derivative or polymer according to the invention or a mixture thereof.
  • the organic electronic device can be selected from an organic light emitting diode (OLED), an organic photovoltaic cell (OPV), an organic light emitting cell (OLEEC), an organic field effect transistor (OFET), and an organic light emitting field effect transistor.
  • OLED organic light emitting diode
  • OLED organic photovoltaic cell
  • OFET organic field effect transistor
  • OLED organic light emitting field effect transistor
  • OLEDs organic lasers, organic spintronic devices, organic sensors and organic plasmon emitting diodes (OLEDs), especially preferred are organic light-emitting diodes (OLEDs).
  • the organic electronic device is an organic electroluminescent device comprising at least one light-emitting layer comprising a pyrrole derivative or a high polymer according to the present invention. Things.
  • the present invention provides a class of pyrrole derivatives which have good rigidity, chemical and thermal stability, and thus can effectively improve the color purity, stability, luminous efficiency and performance of the corresponding devices. Further optimization of the device structure, changes in the concentration of pyrrole derivatives in the matrix, can achieve the best device performance, achieve high efficiency, high brightness and high stability of the OLED device, providing better material options for full color display and lighting applications.
  • composition and the printing ink, or ink have the same meaning and are interchangeable.
  • the host material, the matrix material, the Host or the Matrix material have the same meaning, and In exchange.
  • metal organic complexes metal organic complexes, metal organic complexes, and organometallic complexes have the same meaning and are interchangeable.
  • the present invention relates to a pyrrole derivative represented by the following formula (I):
  • Ar 1 and Ar 2 may be the same or different selected from the group consisting of an unsubstituted or R 1 -substituted aromatic hydrocarbon or heteroaromatic cyclic hydrocarbon system;
  • R 2 In each occurrence of R 2 , the same or different is H, D, an aliphatic alkane having 1 to 10 carbon atoms, an aromatic hydrocarbon, a substituted or unsubstituted aromatic ring having 5 to 10 ring atoms. Or a heteroaromatic group.
  • the pyrrole derivative of formula (I) wherein Ar 1 , Ar 2 may be selected from unsubstituted or substituted aromatic rings or heterocycles having from 2 to 20 carbon atoms Aromatic ring.
  • the aromatic ring system contains 5 to 15 carbon atoms, more preferably 5 to 10 carbon atoms in the ring system, and the heteroaromatic ring system contains 2 to 15 carbon atoms in the ring system. It is preferably 2 to 10 carbon atoms, and at least one hetero atom, provided that the total number of carbon atoms and hetero atoms is at least 4.
  • the heteroatoms are preferably selected from the group consisting of Si, N, P, O, S and/or Ge, particularly preferably selected from the group consisting of Si, N, P, O and/or S.
  • An aromatic ring system or aromatic group refers to a hydrocarbon group containing at least one aromatic ring, including a monocyclic group and a polycyclic ring system.
  • a heteroaromatic or heteroaromatic group refers to a hydrocarbyl group (containing heteroatoms) comprising at least one heteroaromatic ring, including monocyclic groups and polycyclic ring systems. These polycyclic rings may have two or more rings in which two carbon atoms are shared by two adjacent rings, a fused ring. At least one of these rings of the polycyclic ring is aromatic or heteroaromatic.
  • aromatic or heteroaromatic ring systems include not only aromatic or heteroaromatic systems, but also multiple aryl or heteroaryl groups may also be interrupted by short non-aromatic units ( ⁇ 10%).
  • Non-H atoms preferably less than 5% of non-H atoms, such as C, N or O atoms).
  • systems such as 9,9'-spirobifluorene, 9,9-diarylfluorene, triarylamine, diaryl ether, etc., are also considered to be aromatic ring systems for the purposes of the present invention.
  • examples of the aromatic group are: benzene, naphthalene, anthracene, phenanthrene, perylene, tetracene, anthracene, benzopyrene, three Alkene, anthracene, anthracene, and derivatives thereof.
  • heteroaromatic groups are: furan, benzofuran, thiophene, benzothiophene, pyrrole, pyrazole, triazole, imidazole, oxazole, oxadiazole, thiazole, tetrazole, anthracene, anthracene Oxazole, pyrroloimidazole, pyrrolopyrrole, thienopyrrole, thienothiophene, furopyrrol, furanfuran, thienofuran, benzisoxazole, benzisothiazole, benzimidazole, pyridine, pyrazine, Pyridazine, pyrimidine, triazine, quinoline, isoquinoline, o-diazine, quinoxaline, phenanthridine, carbaidine, quinazoline, quinazolinone, and derivatives thereof.
  • the Ar 1 -Ar 2 having the formula (I) may be selected from one of the following formulae:
  • X is independently selected from CR 1 or N, and at least one is N;
  • R 1 , R 2 , R 3 are H, or D, or a linear alkyl, alkoxy or thioalkoxy group having from 1 to 10 C atoms, or A branched or cyclic alkyl, alkoxy or thioalkoxy group of 3 to 10 C atoms is either a silyl group or a substituted keto group having 1 to 10 C atoms.
  • Ar 1 and Ar 2 in formula (I) may be selected from structural units which may be further substituted:
  • Ar 1 and Ar 2 in the general formula (I) may be selected from the following structural units, which may be further substituted:
  • the pyrrole derivative according to the invention is selected from the group consisting of:
  • x is any one of the numbers 0-4, y is any one of the numbers 0-5, z is any one of the numbers 0-7, u is any one of the numbers 0-8, and v is the number 0-9 Any one of them, w is any one of the numbers 0-11;
  • L is a linking group and is independent of each other selected from a single bond or any one of B1 to B4:
  • R 3 to R 26 are selected from the group consisting of -H, -F, -Cl, Br, I, -D, -CN, -NO 2 , -CF 3 , B(OR 2 ) 2 , Si(R 2 ) 3 , A linear alkane, an alkane ether, an alkane thioether having 1 to 10 carbon atoms or a branched or alkane or a aryl group having 6 to 10 carbon atoms.
  • Ar 2 is an unsubstituted or substituted aromatic ring unit which, independently of each other, is selected from the group consisting of the formulae C1 to C10. Any one of them:
  • R 27 to R 106 are selected from the group consisting of -H, -F, -Cl, Br, I, -D, -CN, -NO 2 , -CF 3 , B(OR 2 ) 2 , Si(R 2 ) 3 , A linear alkane, an alkane ether, an alkane thioether having 1 to 10 carbon atoms or a branched or alkane or a aryl group having 6 to 10 carbon atoms.
  • the pyrrole derivative according to the present invention has an emission wavelength between 300 and 800 nm, preferably between 350 and 600 nm, more preferably between 400 and 500 nm.
  • the pyrrole derivative according to the present invention has a higher photoluminescence quantum efficiency, generally ⁇ 15%, preferably ⁇ 25%, more preferably ⁇ 35%, and most preferably ⁇ 50%.
  • the glassy temperature of the pyrrole derivative according to the present invention is ⁇ 100 ° C, preferably ⁇ 110 ° C, more preferably ⁇ 120 ° C, most preferably ⁇ 140 ° C.
  • the present invention also relates to a high polymer wherein at least one repeating unit comprises a structure as shown in the general formula (I).
  • the high polymer is a non-conjugated high polymer wherein the structural unit of formula (I) is on the side chain.
  • the high polymer is a conjugated high polymer.
  • the invention still further relates to a mixture comprising at least one pyrrole derivative or polymer according to the invention, and at least one other organic functional material.
  • Another organic functional material described herein comprising holes (also called holes) injection or transport materials (HIM/HTM), hole blocking materials (HBM), electron injecting or transporting materials (EIM/ETM), electrons Blocking material (EBM), organic matrix material (Host), singlet illuminant (fluorescent illuminant), thermally activated delayed fluorescent luminescent material (TADF), triplet illuminant (phosphorescent illuminant), especially luminescent metal organic coordination Things, and organic dyes.
  • holes also called holes injection or transport materials
  • HBM hole blocking materials
  • EIM/ETM electron injecting or transporting materials
  • EBM electrons Blocking material
  • organic matrix material Host
  • singlet illuminant fluorescent illuminant
  • TADF thermally activated delayed fluorescent luminescent material
  • phosphorescent illuminant especially luminescent metal organic coordination Things
  • organic dyes especially luminescent metal organic coordination Things, and organic dyes.
  • the organic functional material may be a small molecule or a high polymer material.
  • small molecule refers to a molecule that is not a polymer, oligomer, dendrimer, or blend. In particular, there are no repeating structures in small molecules.
  • the molecular weight of the small molecule is ⁇ 3000 g/mol, preferably ⁇ 2000 g/mol, preferably ⁇ 1500 g/mol.
  • a conjugated polymer is a high polymer whose backbone is mainly composed of sp 2 hybrid orbitals of C atoms. Famous examples are polyacetylene polyacetylene and poly(phenylene vinylene).
  • the C atom in its main chain can also be substituted by other non-C atoms, and is still considered to be a conjugated polymer when the sp 2 hybrid on the main chain is interrupted by some natural defects.
  • the conjugated high polymer further comprises an aryl amine, an aryl phosphine and other heteroarmotics, and an organometallic complexes in the main chain. )Wait.
  • the content of the pyrrole derivative in the mixture according to the invention is from 0.01 to 50% by weight, preferably from 0.1 to 40% by weight, more preferably from 0.2 to 30% by weight, most preferably 2 Up to 15% by weight.
  • the mixture according to the invention comprises a pyrrole derivative according to the invention and Another organic functional material in which the singlet energy level of the pyrrole derivative is lower than that of the other organic functional material, but the triplet level of the pyrrole derivative is higher than that of the other organic The triplet level of the functional material.
  • the mixture according to the invention comprises a pyrrole derivative or polymer according to the invention and a singlet matrix material.
  • the mixture according to the invention comprises a pyrrole derivative or polymer according to the invention, a singlet matrix material and another singlet emitter.
  • the mixture according to the invention comprises a pyrrole derivative or polymer according to the invention and a TADF material.
  • the example of the singlet matrix material is not particularly limited, and any organic compound may be used as a host as long as its singlet energy is higher than that of an illuminant, particularly a singlet illuminant or a fluorescent illuminant.
  • Examples of the organic compound used as the singlet matrix material may be selected from compounds containing a cyclic aromatic hydrocarbon such as benzene, biphenyl, triphenyl, benzo, naphthalene, anthracene, anthracene, phenanthrene, anthracene, anthracene, pyrene, fluorene, An aromatic heterocyclic compound such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, oxazole, carbazole, pyridine Anthraquinone, pyrrole dipyridine, pyrazole, imidazole, triazole, isoxazole, thiazole, oxadiazole, triazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazin
  • the singlet matrix material can be selected from compounds comprising at least one of the following groups:
  • R 1 may be independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkene, alkyne, aralkyl, heteroalkyl, aryl and heteroaryl; 1 is an aryl or heteroaryl group; n is an integer from 0 to 20; X 1 -X 8 is selected from CH or N; and X 9 and X 10 are selected from CR 1 R 2 or NR 1 .
  • R 2 may be independently selected from the following groups to: hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
  • Singlet emitters tend to have longer conjugated pi-electron systems.
  • styrylamine and its derivatives disclosed in JP 2913116 B and WO 2001021729 A1
  • indenoindenes and derivatives thereof disclosed in WO 2008/006449 and WO 2007/140847.
  • the singlet emitter can be selected from the group consisting of monostyrylamine, dibasic styrylamine, ternary styrylamine, quaternary styrylamine, styrene phosphine, styrene ether and aromatic amine.
  • a monostyrylamine refers to a compound comprising an unsubstituted or substituted styryl group and at least one amine, preferably an aromatic amine.
  • a dibasic styrylamine refers to a compound comprising two unsubstituted or substituted styryl groups and at least one amine, preferably an aromatic amine.
  • a ternary styrylamine refers to a compound comprising three unsubstituted or substituted styryl groups and at least one amine, preferably an aromatic amine.
  • a quaternary styrylamine refers to a compound comprising four unsubstituted or substituted styryl groups and at least one amine, preferably an aromatic amine.
  • An aromatic amide refers to a compound in which a diaryl arylamine group is attached directly to the oxime, preferably at the position of 9.
  • An aromatic quinone diamine refers to a compound in which two diaryl arylamine groups are attached directly to the oxime, preferably at the 9,10 position.
  • the aromatic decylamine, the aromatic guanidine diamine, the aromatic thiamine and the aromatic thiamine are similarly defined, wherein the diarylamine group is preferably bonded to the 1 or 1,6 position of the oxime.
  • Examples of singlet emitters based on vinylamines and arylamines are also preferred examples and can be found in the following patent documents: WO2006/000388, WO2006/058737, WO2006/000389, WO2007/065549, WO2007/115610, US7250532B2, DE 102005058557A1, CN1583691A, JP08053397A, US6251531B1, US2006/210830A, EP1957606A1 and US2008/0113101A1, the entire contents of each of which is hereby incorporated by reference.
  • Further preferred singlet emitters are selected from the group consisting of an indeno-amine and an indeno-diamine, as disclosed in WO2006/122630, benzoindolo-amine and benzoindeno-diamine, Dibenzoindolo-amine and dibenzoindenoindole-diamine as disclosed in WO 2008/006449, as disclosed in WO 2007/140847.
  • polycyclic aromatic hydrocarbon compounds in particular derivatives of the following compounds: for example, 9,10-bis(2-naphthoquinone), naphthalene, tetraphenyl, xanthene, phenanthrene , ⁇ (such as 2,5,8,11-tetra-t-butyl fluorene), anthracene, phenylene such as (4,4'-bis(9-ethyl-3-carbazolevinyl)-1 , 1 '-biphenyl), indenyl hydrazine, decacycloolefin, hexacene benzene, anthracene, spirobifluorene, aryl hydrazine (such as US20060222886), arylene vinyl (such as US5121029, US5130603), cyclopentane Alkene such as tetraphenylcyclopentadiene, rub
  • 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 exciton luminescence by anti-intersystem crossing. This can make full use of the singlet excitons and triplet excitons formed under electrical excitation.
  • the quantum efficiency in the device can reach 100%.
  • the TADF material needs to have a small singlet-triplet energy level difference, typically ⁇ Est ⁇ 0.3 eV, preferably ⁇ Est ⁇ 0.2 eV, more preferably ⁇ Est ⁇ 0.1 eV, and most preferably ⁇ Est ⁇ 0.05 eV.
  • TADF has better fluorescence quantum efficiency.
  • Some 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.
  • Adachi et. al. Appl. Phys. Lett., 98, 2011, 083302, Adachi, et. al. Appl. Phys. Lett ., 101, 2012, 093306, Adachi, et. al. Chem. Commun., 48, 2012, 11392, Adachi, et. al. Nature Photonics, 6, 2012, 253, Adachi, et. al.
  • TADF luminescent materials are listed in the table below:
  • Another object of the invention is to provide a material solution for printing OLEDs.
  • the pyrrole derivatives according to the invention have a molecular weight of ⁇ 700 g/mol, preferably ⁇ 800 g/mol, most preferably ⁇ 900 g/mol.
  • the pyrrole derivative according to the invention has a solubility in toluene of > 2 mg/ml, preferably > 3 mg/ml, most preferably > 5 mg/ml at 25 °C.
  • the invention further relates to a composition or ink comprising a pyrrole derivative or polymer according to the invention or a mixture as described above, and at least one organic solvent.
  • the invention further provides a film comprising a pyrrole derivative or polymer according to the invention prepared from a solution.
  • the viscosity and surface tension of the ink are important parameters when used in the printing process. Suitable surface tension parameters for the ink are suitable for the particular substrate and the particular printing method.
  • the ink according to the present invention has a surface tension at an operating temperature or at 25 ° C in the range of from about 19 dyne/cm to 50 dyne/cm; more preferably in the range of from 22 dyne/cm to 35 dyne/cm; It is in the range of 25dyne/cm to 33dyne/cm.
  • the ink according to the present invention has a viscosity at an operating temperature or 25 ° C in the range of about 1 cps to 100 cps; preferably in the range of 1 cps to 50 cps; more preferably in the range of 1.5 cps to 20 cps; Good is in the range of 4.0cps to 20cps.
  • the composition so formulated will be suitable for ink jet printing.
  • the viscosity can be adjusted by different methods, such as by selection of a suitable solvent and concentration of the functional material in the ink.
  • the ink containing the above-described pyrrole derivative or polymer according to the present invention can facilitate the adjustment of the printing ink to an appropriate range in accordance with the printing method used.
  • the composition according to the invention comprises a functional material in a weight ratio ranging from 0.3% to 30% by weight, preferably from 0.5% to 20% by weight, more preferably from 0.5% to 15% by weight, even more preferably. It is in the range of 0.5% to 10% by weight, preferably in the range of 1% to 5% by weight.
  • the at least one organic solvent is selected from the group consisting of aromatic or heteroaromatic based solvents, particularly aliphatic chain/ring substituted aromatic solvents, or aromatic ketones, in accordance with the inks of the present invention.
  • Solvent, or aromatic ether solvent is selected from the group consisting of aromatic or heteroaromatic based solvents, particularly aliphatic chain/ring substituted aromatic solvents, or aromatic ketones, in accordance with the inks of the present invention.
  • Solvent, or aromatic ether solvent is selected from the group consisting of aromatic or heteroaromatic based solvents, particularly aliphatic chain/ring substituted aromatic solvents, or aromatic ketones, in accordance with the inks of the present invention.
  • Solvent, or aromatic ether solvent is selected from the group consisting of aromatic or heteroaromatic based solvents, particularly aliphatic chain/ring substituted aromatic solvents, or aromatic ketones, in accordance with the inks of the present invention.
  • Solvent, or aromatic ether solvent is selected from the
  • solvents suitable for the present invention are, but are not limited to, aromatic or heteroaromatic based solvents: p-diisopropylbenzene, pentylbenzene, tetrahydronaphthalene, cyclohexylbenzene, chloronaphthalene, 1,4-dimethyl Naphthalene, 3-isopropylbiphenyl, p-methyl cumene, dipentylbenzene, triphenylbenzene, pentyltoluene, o-xylene, m-xylene, p-xylene, o-diethylbenzene, m-diethyl Benzene, p-diethylbenzene, 1,2,3,4-tetramethylbenzene, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, butylbenzene, dodecylbenzene, two Hexylbenzene, di
  • the at least one solvent may be selected from the group consisting of: an aliphatic ketone, for example, 2-nonanone, 3-fluorenone, 5-nonanone, 2-nonanone, 2, 5 -hexanedione, 2,6,8-trimethyl-4-indolone, phorone, di-n-pentyl ketone, etc.; or an aliphatic ether, for example, pentyl ether, hexyl ether, dioctyl ether, ethylene Dibutyl ether, diethylene glycol diethyl ether, diethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, triethylene glycol ethyl methyl ether, triethylene glycol butyl methyl ether , tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether and the like.
  • an aliphatic ketone for example, 2-nonan
  • the printing ink further comprises another organic solvent.
  • another organic solvent include, but are not limited to, methanol, ethanol, 2-methoxyethanol, dichloromethane, 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, dimethyl sulfoxide, tetrahydrogen Naphthalene, decalin, hydrazine and/or mixtures thereof.
  • the composition according to the invention is a solution.
  • composition according to the invention is a suspension.
  • the invention further relates to the use of the composition as a coating or printing ink in the preparation of an organic electronic device, particularly preferably by a printing or coating process.
  • suitable printing or coating techniques include, but are not limited to, inkjet printing, Nozzle Printing, typography, screen printing, dip coating, spin coating, blade coating, roller printing, torsion roller Printing, lithography, flexographic printing, rotary printing, spraying, brushing or pad printing, slit-type extrusion coating, etc.
  • Preferred are ink jet printing, slit type extrusion coating, jet printing and gravure printing.
  • the solution or suspension may additionally comprise one or more components such as surface active compounds, lubricated Agents, wetting agents, dispersants, hydrophobic agents, adhesives, etc., are used to adjust viscosity, film forming properties, and improve adhesion.
  • the invention also provides the use of a pyrrole derivative or polymer as described above in an organic electronic device.
  • the organic electronic device may be selected from, but not limited to, an organic light emitting diode (OLED), an organic photovoltaic cell (OPV), an organic light emitting cell (OLEEC), an organic field effect transistor (OFET), an organic light emitting field effect transistor, and an organic Lasers, organic spintronic devices, organic sensors and organic plasmon emitting diodes (Organic Plasmon Emitting Diode), especially OLEDs.
  • the pyrrole derivative is preferably used in the luminescent layer of an OLED device.
  • the invention further relates to an organic electronic device comprising at least one pyrrole derivative or polymer as described above.
  • an organic electronic device comprises at least one cathode, an anode and a functional layer between the cathode and the anode, wherein the functional layer contains at least one pyrrole derivative or polymer as described above.
  • the organic electronic device may be selected from, but not limited to, an organic light emitting diode (OLED), an organic photovoltaic cell (OPV), an organic light emitting cell (OLEEC), an organic field effect transistor (OFET), an organic light emitting field effect transistor, and an organic Lasers, 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 transistor
  • OLED organic light emitting field effect transistor
  • organic Lasers organic spintronic devices, organic sensors and organic plasmon emitting diodes (Organic Plasmon Emitting Diode).
  • the organic electronic device is an electroluminescent device, in particular an OLED, comprising a substrate, an anode, at least one luminescent layer, and a cathode.
  • the substrate can be opaque or transparent.
  • a transparent substrate can be used to make a transparent light-emitting component. See, for example, Bulovic et al. Nature 1996, 380, p29, and Gu et al, Appl. Phys. Lett. 1996, 68, p2606.
  • the substrate can be rigid or elastic.
  • the substrate can be plastic, metal, semiconductor wafer or glass.
  • the substrate has a smooth surface. Substrates without surface defects are a particularly desirable choice.
  • the substrate is flexible, optionally in the form of a polymer film or plastic, having a glass transition temperature Tg of 150 ° C or higher, preferably more than 200 ° C, more preferably more than 250 ° C, preferably More than 300 ° C. Examples of suitable flexible substrates are poly(ethylene terephthalate) (PET) and polyethylene glycol (2,6-naphthalene) (PEN).
  • PET poly(ethylene terephthalate)
  • PEN polyethylene glycol (2,6-na
  • the anode can comprise a conductive metal or metal oxide, or a conductive polymer.
  • the anode can easily inject holes into a hole injection layer (HIL) or a hole transport layer (HTL) or a light-emitting layer.
  • HIL hole injection layer
  • HTL hole transport layer
  • the absolute value of the difference between the work function of the anode and the HOMO level or the valence band level of the illuminant in the luminescent layer or the p-type semiconductor material as the HIL or HTL or electron blocking layer (EBL) is less than 0.5 eV, preferably less than 0.3 eV, and most preferably less than 0.2 eV.
  • anode material examples 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 readily selected for use by one of ordinary skill in the art.
  • the anode material can be deposited using any suitable technique, such as a suitable physical vapor deposition process, including radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), and the like.
  • the anode is patterned. Patterned ITO conductive substrates are commercially available and can be used to prepare devices in accordance with the present invention.
  • the cathode can comprise a conductive metal or metal oxide.
  • the cathode can easily inject electrons into the EIL or ETL or directly into the luminescent layer.
  • the work function of the cathode and the LUMO level of the illuminant or the n-type semiconductor material as an electron injection layer (EIL) or electron transport layer (ETL) or hole blocking layer (HBL) in the luminescent layer or
  • EIL electron injection layer
  • ETL electron transport layer
  • HBL hole blocking layer
  • the absolute value of the difference in conduction band energy levels is less than 0.5 eV, preferably less than 0.3 eV, and most preferably less than 0.2 eV.
  • all materials which can be used as cathodes for OLEDs are possible as cathode materials for the devices of the invention.
  • cathode material examples include, but are not limited to, Al, Au, Ag, Ca, Ba, Mg, LiF/Al, MgAg alloy, BaF 2 /Al, Cu, Fe, Co, Ni, Mn, Pd, Pt, ITO, and the like.
  • the cathode material can be deposited using any suitable technique, such as a suitable physical vapor deposition process, including radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), and the like.
  • the OLED may further include other functional layers such as a hole injection layer (HIL), a hole transport layer (HTL), an electron blocking layer (EBL), an electron injection layer (EIL), an electron transport layer (ETL), and a 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 layer contains the pyrrole derivative of the present invention, and is prepared by vacuum evaporation or solution processing, preferably vacuum evaporation.
  • the hole transporting layer thereof comprises the deuterated triarylamine derivative of the present invention.
  • the light-emitting layer thereof comprises the polymer of the present invention and is prepared by a solution processing method.
  • the electroluminescent device according to the invention has an emission wavelength of between 300 and 800 nm, preferably between 350 and 650 nm, more preferably between 400 and 625 nm.
  • the invention further relates to the use of an organic electronic device according to the invention in various electronic devices, including, but not limited to, display devices, illumination devices, light sources, sensors and the like.
  • the energy level of the pyrrole derivative B-1-B-7 can be obtained by quantum calculation, for example, by TD-DFT (time-dependent density functional theory) by Gaussian 03W (Gaussian Inc.), and the specific simulation method can be found in WO2011141110.
  • TD-DFT time-dependent density functional theory
  • Gaussian 03W Gaussian Inc.
  • the semi-empirical method “Ground State/Semi-empirical/Default Spin/AM1" (Charge 0/Spin Singlet) is used to optimize the molecular geometry, and then the energy structure of the organic molecule is determined by TD-DFT (time-dependent density functional theory) method.
  • TD-SCF/DFT/Default Spin/B3PW91/6-31G/d Charge 0/Spin Singlet.
  • the HOMO and LUMO levels are calculated according to the following calibration formula, and S1 and T1 are used directly.
  • HOMO(eV) ((HOMO(Gaussian) ⁇ 27.212)-0.9899)/1.1206
  • HOMO (G) and LUMO (G) are direct calculation results of Gaussian 09W, the unit is Hartree.
  • the results are shown in Table 1:
  • ADN (15 nm) / TPBi (65 nm) / LiF (1 nm) / Al (150 nm) / cathode are as follows:
  • a, cleaning of the conductive glass substrate when used for the first time, can be washed with a variety of solvents, such as chloroform, ketone, isopropyl alcohol, and then UV ozone plasma treatment;
  • HTL 60 nm
  • EML 25 nm
  • ETL 65 nm
  • hot evaporation in high vacuum (1 ⁇ 10 -6 mbar, mbar);
  • cathode LiF / Al (1nm / 150nm) in a high vacuum (1 ⁇ 10 -6 mbar) in the thermal evaporation;
  • the device is encapsulated in a nitrogen glove box with an ultraviolet curable resin.
  • the current-voltage luminance (JVL) characteristics of each OLED device are characterized by characterization equipment while recording important parameters such as efficiency and external quantum efficiency. It has been found that the maximum external quantum efficiency of OLEDx (corresponding to the pyrrole derivative B-x) is more than 4%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

本发明公开了一种并吡咯衍生物及其在有机电子器件，特别是在有机发光二极管中的应用。该并吡咯衍生物具有如通式(I)所示结构特征，这类化合物具有良好的刚性、化学及热稳定性，因此可以有效的提高化合物的色纯度、稳定性、发光效率及相应器件的性能。进一步通过器件结构优化，改变并吡咯衍生物在基质中的浓度，可达到最佳的器件性能，实现高效高亮度高稳定的OLED器件，对全彩显示和照明应用提供了较好的材料选项。

Description

并吡咯衍生物及其在有机电子器件的应用 技术领域
本发明涉及一种并吡咯衍生物，及其在有机电子器件，特别是在有机发光二极管中的应用。本发明还涉及一种包含有此类并吡咯衍生物的有机电子器件，特别是发光元件，及其在显示器及照明装置中的应用。
背景技术
由于有机半导体材料在合成上具有多样性、制造成本相对较低和优良的光学与电学性能，有机发光二极管(OLED)在光电器件(例如平板显示器和照明)的应用方面具有很大的潜力。
为了提高有机发光二极管的发光效率，各种基于荧光和磷光的发光材料体系已被开发出来，而无论是荧光材料还是磷光材料，优秀蓝光材料的开发都是一个巨大的挑战，总体而言，目前使用的蓝光荧光材料的有机发光二级管可靠性更高。尽管如此，目前大多数蓝光荧光材料的发射光谱过宽，色纯度较差，不利于高端显示，并且这类荧光材料的合成也较复杂，不利于大规模量产，同时这类蓝色荧光材料的OLED稳定性还需进一步提高。因此开发具有窄带发射光谱、稳定性好的蓝色荧光材料，一方面有利于得到更长寿命、更高效率的蓝光器件，另一方面有利于色域的提高，进而改善显示效果。
发明内容
鉴于上述现有技术的不足，本发明的目的在于提供一类并吡咯衍生物，由于这类化合物具有良好的刚性、化学及热稳定性，因此可以有效的提高化合物的色纯度、稳定性、发光效率及相应器件的性能。
本发明的技术解决方案是：一种含通式(I)结构的并吡咯衍生物：
Figure PCTCN2016107307-appb-000001
其中，Ar1，Ar2在每一次出现中，可相同或不同的选自未被取代或是R1取代的芳香烃或是杂芳香环烃体系；
R1选自H，F，Cl，Br，I，D，CN，NO2，CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，；每一个基团均可被一个或多个活性基团R2取代，且一个或多个非相邻的亚甲基可以被以下基团替换：R2C＝CR2，C＝C，Si(R2)2，Ge(R2)2，Sn(R2)2，C＝O，C＝S，C＝Se，C＝N(R2)，O，S，-COO-，或CONR2，其中一个或多个H原子可被D，F，Cl，Br，I，CN或N2所替换，或者被包含一个或多个活性基团R2、 一个芳香基团或者一个杂芳香环取代的芳香胺替换，或者被取代或未被取代的咔唑替换；
R2在每一次出现中，相同或不同的是H，D，含1～10个碳原子脂肪族烷烃，芳香碳氢化合物，含5～10个环原子的被取代或者未被取代的芳香环或杂芳香基团。
在其中一些实施例中，所述的并吡咯衍生物，优先选自如下通式：
Figure PCTCN2016107307-appb-000002
其中，R3表示-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳 基中的任一个；
x为数字0-4中的任一个，y为数字0-5中的任一个，z为数字0-7中的任一个，u为数字0-8中的任一个，v为数字0-9中的任一个，w为数字0-11中的任一个；
L为连接基团，相互独立的选自单键或B1至B4中的任一个：
Figure PCTCN2016107307-appb-000003
其中，R3至R26选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个。
在其中一些实施例中，所述的并吡咯衍生物，其特征在于，选自如下通式：
Figure PCTCN2016107307-appb-000004
在其中一些实施例中，所述的并吡咯衍生物，其中通式(I)，(I-1)-(I-10)中的Ar2为未被取代或是取代的芳香环单元，在多次出现时可相互独立的优先选自通式C1至C10中的任一个：
Figure PCTCN2016107307-appb-000005
其中，R27至R106选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个。
在其中一些实施例中，所述的并吡咯衍生物，其特征在于，通式(I)，(I-1)-(I-10)中的Ar2相互独立的选自：
Figure PCTCN2016107307-appb-000006
本发明还提供一种高聚物，包含一个重复单元，其中包含一个有如通式(I)表示的结构单元。
本发明还提供一种混合物，包含一种如上所述的并吡咯衍生物或高聚物及至少一种有机功能材料。所述有机功能材料可选自空穴注入材料(HIM)，空穴传输材料(HTM)，电子传输材料(ETM)，电子注入材料(EIM)，电子阻挡材料(EBM)，空穴阻挡材料(HBM)，发光材料(Emitter)，主体材料(Host)和有机染料等。
本发明还提供一种组合物，包含一种按照本发明的并吡咯衍生物或高聚物，及至少一种有机溶剂。
本发明还提供一种按照本发明的并吡咯衍生物或高聚物在有机电子器件中的应用。
本发明还提供一种有机电子器件，至少包含一种按照本发明的并吡咯衍生物或高聚物或其混合物。
在其中一些实施例中，所述的有机电子器件可选于有机发光二极管(OLED)、有机光伏电池(OPV)、有机发光电池(OLEEC)、有机场效应管(OFET)、有机发光场效应管、有机激光器，有机自旋电子器件，有机传感器及有机等离激元发射二极管(Organic Plasmon Emitting Diode)，特别优先的是有机发光二极管(OLED)。
优先的，在其中一些实施例中，所述的有机电子器件是一有机电致发光器件，其中至少包含有一发光层，所述的发光层包含有一种按照本发明的并吡咯衍生物或高聚物。
与现有技术相比，本发明的有益效果：
本发明的提供一类并吡咯衍生物，这类化合物具有良好的刚性、化学及热稳定性，因此可以有效的提高化合物的色纯度、稳定性、发光效率及相应器件的性能。进一步通过器件结构优化，改变并吡咯衍生物在基质中的浓度，可达到最佳的器件性能，实现高效高亮度高稳定的OLED器件，对全彩显示和照明应用提供了较好的材料选项。
具体实施方式
本发明提供一种新型的并吡咯衍生物，相应的混合物和组合物，以及在有机电子器件中的应用，为使本发明的目的、技术方案及效果更加清楚、明确，以下对本发明进一步详细说明。应当理解，此处所描述的具体实施例仅仅用以解释本发明，并不用于限定本发明。
在本发明中，组合物和印刷油墨，或油墨具有相同的含义，它们之间可以互换。
在本发明中，主体材料，基质材料，Host或Matrix材料具有相同的含义，它们之间可 以互换。
在本发明中，金属有机络合物，金属有机配合物，有机金属配合物具有相同的含义，可以互换。
本发明涉及一种如如下通式(I)表示的并吡咯衍生物：
Figure PCTCN2016107307-appb-000007
其中，Ar1，Ar2在每一次出现中，可相同或不同的选自未被取代或是R1取代的芳香烃或是杂芳香环烃体系；
R1选自H，F，Cl，Br，I，D，CN，NO2，CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，；每一个基团均可被一个或多个活性基团R2取代，且一个或多个非相邻的亚甲基(CH2)可以被以下基团替换：R2C＝CR2，C＝C，Si(R2)2，Ge(R2)2，Sn(R2)2，C＝O，C＝S，C＝Se，C＝N(R2)，O，S，-COO-，或CONR2，其中一个或多个H原子可被D，F，Cl，Br，I，CN或N2所替换，或者被包含一个或多个活性基团R2、一个芳香基团或者一个杂芳香环取代的芳香胺替换，或者被取代或未被取代的咔唑替换；
R2在每一次出现中，相同或不同的是H，D，含1～10个碳原子脂肪族烷烃，芳香碳氢化合物，含5～10个环原子的被取代或者未被取代的芳香环或杂芳香基团。
在某些优先的实施例中，按照通式(I)的并吡咯衍生物，其中Ar1，Ar2可选自未被取代或是取代的具有2～20个碳原子的芳族环或杂芳族环。
在一个优先的实施例中，芳香环系在环系中包含5～15个碳原子，更优是5～10个碳原子，杂芳香环系在环系中包含2～15个碳原子，更优是2～10个碳原子，和至少一个杂原子，条件是碳原子和杂原子的总数至少为4。杂原子优选选自Si、N、P、O、S和/或Ge，特别优选选自Si、N、P、O和/或S。
芳香环系或芳族基团指至少包含一个芳环的烃基，包括单环基团和多环的环系统。杂芳香环系或杂芳族基团指包含至少一个杂芳环的烃基(含有杂原子)，包括单环基团和多环的环系统。这些多环的环可以具有两个或多个环，其中两个碳原子被两个相邻的环共用，即稠环。多环的这些环种，至少一个是芳族的或杂芳族的。对于本发明的目的，芳香族或杂芳香族环系不仅包括芳香基或杂芳香基的体系，而且，其中多个芳基或杂芳基也可以被短的非芳族单元间断(<10％的非H原子，优选小于5％的非H原子，比如C、N或O原子)。因此，比如9,9'-螺二芴，9,9-二芳基芴，三芳胺，二芳基醚等体系，对于该发明目的同样认为是芳香族环系。
具体地，芳族基团的例子有：苯、萘、蒽、菲、二萘嵌苯、并四苯、芘、苯并芘、三 亚苯、苊、芴、及其衍生物。
具体地，杂芳族基团的例子有：呋喃、苯并呋喃、噻吩、苯并噻吩、吡咯、吡唑、三唑、咪唑、噁唑、噁二唑、噻唑、四唑、吲哚、咔唑、吡咯并咪唑、吡咯并吡咯、噻吩并吡咯、噻吩并噻吩、呋喃并吡咯、呋喃并呋喃、噻吩并呋喃、苯并异噁唑、苯并异噻唑、苯并咪唑、吡啶、吡嗪、哒嗪、嘧啶、三嗪、喹啉、异喹啉、邻二氮萘、喹喔啉、菲啶、伯啶、喹唑啉、喹唑啉酮、及其衍生物。
在一个优先的实施方案中，所述的具有通式(I)中的Ar1-Ar2可以选自如下通式中的一个：
Figure PCTCN2016107307-appb-000008
其中，X分别独立的选自CR1或N，且至少有一个是N；
Y选自CR2R3，SiR2R3，NR2，C(＝O)，S，或O；
R1，R2，R3是H，或D，或具有1至20个C原子的直链烷基、烷氧基或硫代烷氧基基团，或者具有3至20个C原子的支链或环状的烷基、烷氧基或硫代烷氧基基团或者是甲硅烷基基团，或具有1至20个C原子的取代的酮基基团，具有2至20个C原子的烷氧基羰基基团，具有7至20个C原子的芳氧基羰基基团，氰基基团(-CN)，氨基甲酰基基团(-C(＝O)NH2)，卤甲酰基基团(-C(＝O)-X其中X代表卤素原子)，甲酰基基团(-C(＝O)-H)，异氰基基团，异氰酸酯基团，硫氰酸酯基团或异硫氰酸酯基团，羟基基团，硝基基团，CF3基团，Cl，Br，F，可交联的基团或者具有5至40个环原子的取代或未取代的芳族或杂芳族环系，或具有5至40个环原子的芳氧基或杂芳氧基基团，或这些体系的组合，其中一个或多个基团R1，R2，R3可以彼此和/或与所述基团键合的环形成单环或多环的脂族或芳族环系。
在一些优选的实施例中，R1，R2，R3是H，或D，或具有1至10个C原子的直链烷基、烷氧基或硫代烷氧基基团，或者具有3至10个C原子的支链或环状的烷基、烷氧基或硫代烷氧基基团或者是甲硅烷基基团，或具有1至10个C原子的取代的酮基基团，具有2至10个C原子的烷氧基羰基基团，具有7至10个C原子的芳氧基羰基基团，氰基基团(-CN)，氨基甲酰基基团(-C(＝O)NH2)，卤甲酰基基团(-C(＝O)-X其中X代表卤素原子),甲酰基基团(-C(＝O)-H)，异氰基基团，异氰酸酯基团，硫氰酸酯基团或异硫氰酸酯基团，羟基基团，硝基基团，CF3基团，Cl，Br，F，可交联的基团或者具有5至20个环原子的取代或未取代的芳族或杂芳族环系，或具有5至20个环原子的芳氧基或杂芳氧基基团，或这些体系的组合，其中一个或多个基团R1，R2，R3可以彼此和/或与所述基团键合的环形成单环或多环的脂族或芳族环系。
在某些优先的实施例中，通式(I)中的Ar1和Ar2可选自如下结构单元，它们可进一步被取代：
Figure PCTCN2016107307-appb-000009
在另一些较为优先的实施例中，通式(I)中的Ar1和Ar2可选自如下结构单元，它们可进一步被取代：
Figure PCTCN2016107307-appb-000010
在另一些较为优先的实施例中，按照通式(I)的并吡咯衍生物，其中Ar2选自未被取代或是取代的具有5～20个环原子的芳族环，不包含杂芳族环。
在一个较为优先的实施方案中，按照本发明的并吡咯衍生物，选自如下通式：
Figure PCTCN2016107307-appb-000011
Figure PCTCN2016107307-appb-000012
其中，R3表示-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个；
x为数字0-4中的任一个，y为数字0-5中的任一个，z为数字0-7中的任一个，u为数字0-8中的任一个，v为数字0-9中的任一个，w为数字0-11中的任一个；
L为连接基团，相互独立的选自单键或B1至B4中的任一个：
Figure PCTCN2016107307-appb-000013
其中，R3至R26选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子 的芳基中的任一个。
在某些优先的实施例中，如上所述的并吡咯衍生物中，Ar2为未被取代或是取代的芳香环单元，在多次出现时可相互独立的选自通式C1至C10中的任一个：
Figure PCTCN2016107307-appb-000014
其中，R27至R106选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个。
下面给出合适的按照本发明的并吡咯衍生物的具体例子，但是不限于：
Figure PCTCN2016107307-appb-000015
Figure PCTCN2016107307-appb-000016
Figure PCTCN2016107307-appb-000017
Figure PCTCN2016107307-appb-000018
Figure PCTCN2016107307-appb-000019
Figure PCTCN2016107307-appb-000020
Figure PCTCN2016107307-appb-000021
Figure PCTCN2016107307-appb-000022
Figure PCTCN2016107307-appb-000023
Figure PCTCN2016107307-appb-000024
Figure PCTCN2016107307-appb-000025
Figure PCTCN2016107307-appb-000026
在某些实施例中，按照本发明的并吡咯衍生物，其发光波长在300到800nm之间，较好的是在350到600nm之间，更好的是在400到500nm之间。
在一些优先的实施例中，按照本发明的并吡咯衍生物具有较高的光致发光量子效率，一般≥15％，较优≥25％，更优≥35％，最优≥50％。
按照本发明的并吡咯衍生物的玻璃化温度≥100℃，较好是≥110℃，更好是≥120℃，最好是≥140℃。
本发明还涉及一种高聚物，其中至少有一个重复单元包含有如通式(I)所示的结构。在某些实施例中，所述的高聚物是非共轭高聚物，其中如通式(I)所示的结构单元在侧链上。在另一个优先的实施例中，所述的高聚物是共轭高聚物。
本发明还进一步涉及一种混合物，包含至少一种按照本发明的并吡咯衍生物或高聚物，及至少另一种的有机功能材料。
这里所述另一种的有机功能材料，包含空穴(也称电洞)注入或传输材料(HIM/HTM)，空穴阻挡材料(HBM)，电子注入或传输材料(EIM/ETM)，电子阻挡材料(EBM)，有机基质材料(Host)，单重态发光体(荧光发光体)，热激活延迟荧光发光材料(TADF)，三重态发光体(磷光发光体)，特别是发光金属有机配合物，和有机染料。例如在WO2010135519A1，US20090134784A1和WO2011110277A1中对各种有机功能材料有详细的描述，特此将此3专利文件中的全部内容并入本文作为参考。
有机功能材料可以是小分子或高聚物材料。
本文中所定义的术语“小分子”是指不是聚合物，低聚物，树枝状聚合物，或共混物的分子。特别是，小分子中没有重复结构。小分子的分子量≤3000克/摩尔，较好是≤2000克/摩尔，最好是≤1500克/摩尔。
高聚物，即Polymer，包含均聚物(homopolymer)，共聚物(copolymer)，镶嵌共聚物(block copolymer)。另外在本发明中，高聚物也包含树状物(dendrimer)，有关树状物的合成及应用请参见【Dendrimers and Dendrons,Wiley-VCH Verlag GmbH&Co.KGaA,2002,Ed.George R.Newkome,Charles N.Moorefield,Fritz Vogtle.】。
共轭高聚物(conjugated polymer)是一高聚物，它的主链(backbone)主要是由C原子的sp2杂化轨道构成，著名的例子有：聚乙炔polyacetylene和poly(phenylene vinylene)，其主链上的C原子的也可以被其他非C原子取代，而且当主链上的sp2杂化被一些自然的缺陷打断时，仍然被认为是共轭高聚物。另外在本发明中共轭高聚物也包含主链上包含有芳基胺(aryl amine)、芳基磷化氢(aryl phosphine)及其他杂环芳烃(heteroarmotics)、金属有机络合物(organometallic complexes)等。
在一某些实施例中，按照本发明的混合物中，并吡咯衍生物的含量为0.01至50wt％，较好的是0.1至40wt％，更好的是0.2至30wt％，最好的是2至15wt％。
在一个优先的实施方案中，按照本发明的混合物包含一种按照本发明的并吡咯衍生物和 另一种的有机功能材料，其中并吡咯衍生物的单线态能级低于另一种的有机功能材料的单线态能级，但并吡咯衍生物的三线态能级高于另一种的有机功能材料的三线态能级。
在一个优先的实施方案中，按照本发明的混合物包含一种按照本发明的并吡咯衍生物或高聚物和一种单线态基质材料。
在另一个优先的实施方案中，按照本发明的混合物包含一种按照本发明的并吡咯衍生物或高聚物，一种单线态基质材料和另一种的单线态发光体。
在另一个优先的实施方案中，按照本发明的混合物包含一种按照本发明的并吡咯衍生物或高聚物和一种TADF材料。
下面对单重态基质材料，单重态发光体和TADF材料作一些较详细的描述(但不限于此)。
1、单重态基质材料(Singlet Host)：
单重态基质材料的例子并不受特别的限制，任何有机化合物都可能被用作为主体，只要其单重态能量比发光体，特别是单重态发光体或荧光发光体更高。
作为单重态基质材料使用的有机化合物的例子可选自含有环芳香烃化合物，如苯、联苯、三苯基、苯并、萘、蒽、萉、菲、芴、芘、屈、苝、薁；芳香杂环化合物，如二苯并噻吩、二苯并呋喃、二苯并硒吩、呋喃、噻吩、苯并呋喃、苯并噻吩、苯并硒吩、咔唑、吲哚咔唑、吡啶吲哚、吡咯二吡啶、吡唑、咪唑、三氮唑、异恶唑、噻唑、恶二唑、恶三唑、二恶唑、噻二唑、吡啶、哒嗪、嘧啶、吡嗪、三嗪、恶嗪、恶噻嗪、恶二嗪、吲哚、苯并咪唑、吲唑、吲哚嗪、苯并恶唑、苯异恶唑、苯并噻唑、喹啉、异喹啉、噌啉、喹唑啉、喹喔啉、萘、酞、蝶啶、氧杂蒽、吖啶、吩嗪、吩噻嗪、吩恶嗪、苯并呋喃吡啶、呋喃二吡啶、苯并噻吩吡啶、噻吩二吡啶、苯并硒吩吡啶和硒吩二吡啶；包含有2至10环结构的基团，它们可以是相同或不同类型的环芳香烃基团或芳香杂环基团，并彼此直接或通过至少一个以下的基团连结在一起，如氧原子、氮原子、硫原子、硅原子、磷原子、硼原子、链结构单元和脂肪环基团。
在一个优先的实施方案中，单重态基质材料可选于包含至少一个以下基团的化合物：
Figure PCTCN2016107307-appb-000027
Figure PCTCN2016107307-appb-000028
在上述基团中，R1可相互独立地选于如下的基团：氢、烷基、烷氧基、氨基、烯、炔、芳烷基、杂烷基、芳基和杂芳基；Ar1是芳基或杂芳基；n是一个从0到20的整数；X1-X8选于CH或N；X9和X10选于CR1R2或NR1。R2可相互独立地选于如下的基团：氢、烷基、烷氧基、氨基、烯、炔、芳烷基、杂烷基、芳基和杂芳基。
在下面的表中列出一些蒽基单重态基质材料的例子：
Figure PCTCN2016107307-appb-000029
2、单重态发光体(Singlet Emitter)
单重态发光体往往有较长的共轭π电子系统。迄今，已有许多例子，例如在JP2913116B和WO2001021729A1中公开的苯乙烯胺及其衍生物，和在WO2008/006449和WO2007/140847中公开的茚并芴及其衍生物。
在一个优先的实施方案中，单重态发光体可选自一元苯乙烯胺，二元苯乙烯胺，三元苯乙烯胺，四元苯乙烯胺，苯乙烯膦，苯乙烯醚和芳胺。
一个一元苯乙烯胺是指一化合物，它包含一个无取代或取代的苯乙烯基组和至少一个胺，最好是芳香胺。一个二元苯乙烯胺是指一化合物，它包含二个无取代或取代的苯乙烯基组和至少一个胺，最好是芳香胺。一个三元苯乙烯胺是指一化合物，它包含三个无取代或取代的苯乙烯基组和至少一个胺，最好是芳香胺。一个四元苯乙烯胺是指一化合物，它包含四个无取代或取代的苯乙烯基组和至少一个胺，最好是芳香胺。一个优选的苯乙烯是二苯乙烯，其可能会进一步被取代。相应的膦类和醚类的定义与胺类相似。芳基胺或芳香胺是指一种化合物，包含三个直接联接氮的无取代或取代的芳香环或杂环系统。这些芳香族或杂环的环系统中至少有一个优先选于稠环系统，并最好有至少14个芳香环原子。其中优选的例子有芳香蒽胺，芳香蒽二胺，芳香芘胺，芳香芘二胺，芳香屈胺和芳香屈二胺。一个芳香蒽胺是指一化合物，其中一个二元芳基胺基团直接联到蒽上，最好是在9的位置上。一个芳香蒽二胺是指一化合物，其中二个二元芳基胺基团直接联到蒽上，最好是在9,10的位置上。芳香芘胺，芳香芘二胺，芳香屈胺和芳香屈二胺的定义类似，其中二元芳基胺基团最好联到芘的1或1,6位置上。
基于乙烯胺及芳胺的单重态发光体的例子，也是优选的例子，可在下述专利文件中找到：WO2006/000388，WO2006/058737，WO2006/000389，WO2007/065549，WO2007/115610，US7250532B2，DE102005058557A1，CN1583691A，JP08053397A，US6251531B1，US2006/210830A，EP1957606A1和US2008/0113101A1，特此上述列出的专利文件中的全部内容并入本文作为参考。
基于均二苯乙烯极其衍生物的单重态发光体的例子有US5121029。
进一步的优选的单重态发光体可选于茚并芴-胺和茚并芴-二胺，如WO2006/122630所公开的，苯并茚并芴-胺和苯并茚并芴-二胺，如WO2008/006449所公开的，二苯并茚并芴-胺和二苯并茚并芴-二胺，如WO2007/140847所公开的。
其他可用作单重态发光体的材料有多环芳烃化合物，特别是如下化合物的衍生物：蒽如9,10-二(2-萘并蒽)，萘,四苯，氧杂蒽，菲，芘(如2,5,8,11-四-t-丁基苝)，茚并芘，苯撑如(4,4’-双(9-乙基-3-咔唑乙烯基)-1,1’-联苯)，二茚并芘，十环烯，六苯并苯，芴，螺二芴，芳基芘(如US20060222886)，亚芳香基乙烯(如US5121029，US5130603)，环戊二烯如四苯基环戊二烯，红荧烯，香豆素，若丹明，喹吖啶酮，吡喃如4(二氰基亚甲基)-6-(4-对二甲氨基苯乙烯基-2-甲基)-4H-吡喃(DCM)，噻喃，双(吖嗪基)亚胺硼化合物(US2007/0092753A1)，双(吖嗪基)亚甲基化合物，carbostyryl化合物，噁嗪酮，苯并恶唑， 苯并噻唑，苯并咪唑及吡咯并吡咯二酮。一些单重态发光体的材料可在下述专利文件中找到：US20070252517A1，US4769292，US6020078，US2007/0252517A1，US2007/0252517A1。特此将上述列出的专利文件中的全部内容并入本文作为参考。
在下面的表中列出一些合适的单重态发光体的例子：
Figure PCTCN2016107307-appb-000030
3、热激活延迟荧光发光材料(TADF)：
传统有机荧光材料只能利用电激发形成的25％单线态激子发光，器件的内量子效率较低(最高为25％)。尽管磷光材料由于重原子中心强的自旋-轨道耦合增强了系间穿越，可以有效利用电激发形成的单线态激子和三线态激子发光，使器件的内量子效率达到100％。但磷光材料昂贵，材料稳定性差，器件效率滚降严重等问题限制了其在OLED中的应用。热激活延迟荧光发光材料是继有机荧光材料和有机磷光材料之后发展的第三代有机发光材 料。该类材料一般具有小的单线态-三线态能级差(ΔEst)，三线态激子可以通过反系间穿越转变成单线态激子发光。这可以充分利用电激发下形成的单线态激子和三线态激子。器件内量子效率可达到100％。
TADF材料需要具有较小的单线态-三线态能级差，一般是ΔEst<0.3eV，较好是ΔEst<0.2eV，更好是ΔEst<0.1eV，最好是ΔEst<0.05eV。在一个优先的实施方案中，TADF有较好的荧光量子效率。一些TADF发光的材料可在下述专利文件中找到:CN103483332(A)，TW201309696(A)，TW201309778(A)，TW201343874(A)，TW201350558(A)，US20120217869(A1)，WO2013133359(A1)，WO2013154064(A1)，Adachi,et.al.Adv.Mater.,21,2009,4802，Adachi,et.al.Appl.Phys.Lett.,98,2011,083302，Adachi,et.al.Appl.Phys.Lett.,101,2012,093306，Adachi,et.al.Chem.Commun.,48,2012,11392，Adachi,et.al.Nature Photonics,6,2012,253，Adachi,et.al.Nature,492,2012,234，Adachi,et.al.J.Am.Chem.Soc,134,2012,14706，Adachi,et.al.Angew.Chem.Int.Ed,51,2012,11311，Adachi,et.al.Chem.Commun.,48,2012,9580，Adachi,et.al.Chem.Commun.,48,2013,10385，Adachi,et.al.Adv.Mater.,25,2013,3319，Adachi,et.al.Adv.Mater.,25,2013,3707，Adachi,et.al.Chem.Mater.,25,2013,3038，Adachi,et.al.Chem.Mater.,25,2013,3766，Adachi,et.al.J.Mater.Chem.C.,1,2013,4599，Adachi,et.al.J.Phys.Chem.A.,117,2013,5607，特此将上述列出的专利或文章文件中的全部内容并入本文作为参考。
在下面的表中列出一些合适的TADF发光材料的例子:
Figure PCTCN2016107307-appb-000031
Figure PCTCN2016107307-appb-000032
Figure PCTCN2016107307-appb-000033
本发明的另一个目的是为印刷OLED提供材料解决方案。
在某些实施例中，按照本发明的并吡咯衍生物，其分子量≥700g/mol，优选≥800g/mol，最优选≥900g/mol。
在另一些实施例中，按照本发明的并吡咯衍生物，在25℃时，在甲苯中的溶解度≥2mg/ml，优选≥3mg/ml，最优选≥5mg/ml。
本发明进一步涉及一种组合物或油墨，包含一种按照本发明的并吡咯衍生物或高聚物或者如上所述的混合物，以及至少一种有机溶剂。
本发明进一步提供一种从溶液中制备包含有按照本发明的并吡咯衍生物或高聚物的薄膜。
用于印刷工艺时，油墨的粘度，表面张力是重要的参数。合适的油墨的表面张力参数适合于特定的基板和特定的印刷方法。
在一个优选的实施例中，按照本发明的油墨在工作温度或在25℃下的表面张力约在19dyne/cm到50dyne/cm范围；更好是在22dyne/cm到35dyne/cm范围；最好是在25dyne/cm到33dyne/cm范围。
在另一个优选的实施例中，按照本发明的油墨在工作温度或25℃下的粘度约在1cps到100cps范围；较好是在1cps到50cps范围；更好是在1.5cps到20cps范围；最好是在4.0cps到20cps范围。如此配制的组合物将适合于喷墨印刷。
粘度可以通过不同的方法调节，如通过合适的溶剂选取和油墨中功能材料的浓度。按照本发明的包含有所述地并吡咯衍生物或高聚物的油墨可方便人们将印刷油墨按照所用的印刷方法在适当的范围调节。一般地，按照本发明的组合物包含的功能材料的重量比为0.3％～30wt％范围，较好的为0.5％～20wt％范围，更好的为0.5％～15wt％范围，更更好的为0.5％～10wt％范围，最好的为1％～5wt％范围。
在一些实施例中，按照本发明的油墨，所述的至少一种的有机溶剂选自基于芳族或杂芳族的溶剂，特别是脂肪族链/环取代的芳族溶剂、或芳族酮溶剂，或芳族醚溶剂。
适合本发明的溶剂的例子有，但不限于：基于芳族或杂芳族的溶剂：对二异丙基苯、戊苯、四氢萘、环己基苯、氯萘、1,4-二甲基萘、3-异丙基联苯、对甲基异丙苯、二戊苯、三戊苯、戊基甲苯、邻二甲苯、间二甲苯、对二甲苯、邻二乙苯、间二乙苯、对二乙苯、1,2,3,4-四甲苯、1,2,3,5-四甲苯、1,2,4,5-四甲苯、丁苯、十二烷基苯、二己基苯、二丁基苯、对二异丙基苯、1-甲氧基萘、环己基苯、二甲基萘、3-异丙基联苯、对甲基异丙苯、1-甲基萘、1,2,4-三氯苯、1,3-二丙氧基苯、4,4-二氟二苯甲烷、1,2-二甲氧基-4-(1-丙烯基)苯、 二苯甲烷、2-苯基吡啶、3-苯基吡啶、N-甲基二苯胺、4-异丙基联苯、α,α-二氯二苯甲烷、4-(3-苯基丙基)吡啶、苯甲酸苄酯、1,1-双(3,4-二甲基苯基)乙烷、2-异丙基萘、二苄醚等；基于酮的溶剂：1-四氢萘酮，2-四氢萘酮，2-(苯基环氧)四氢萘酮，6-(甲氧基)四氢萘酮，苯乙酮、苯丙酮、二苯甲酮、及它们的衍生物，如4-甲基苯乙酮、3-甲基苯乙酮、2-甲基苯乙酮、4-甲基苯丙酮、3-甲基苯丙酮、2-甲基苯丙酮，异佛尔酮、2,6,8-三甲基-4-壬酮、葑酮、2-壬酮、3-壬酮、5-壬酮、2-癸酮、2,5-己二酮、佛尔酮、二正戊基酮；芳族醚溶剂：3-苯氧基甲苯、丁氧基苯、苄基丁基苯、对茴香醛二甲基乙缩醛、四氢-2-苯氧基-2H-吡喃、1,2-二甲氧基-4-(1-丙烯基)苯、1,4-苯并二噁烷、1,3-二丙基苯、2,5-二甲氧基甲苯、4-乙基本乙醚、1,2,4-三甲氧基苯、4-(1-丙烯基)-1,2-二甲氧基苯、1,3-二甲氧基苯、缩水甘油基苯基醚、二苄基醚、4-叔丁基茴香醚、反式-对丙烯基茴香醚、1,2-二甲氧基苯、1-甲氧基萘、二苯醚、2-苯氧基甲醚、2-苯氧基四氢呋喃、乙基-2-萘基醚、戊醚c己醚、二辛醚、乙二醇二丁醚、二乙二醇二乙醚、二乙二醇丁基甲醚、二乙二醇二丁醚、三乙二醇二甲醚、三乙二醇乙基甲醚、三乙二醇丁基甲醚、三丙二醇二甲醚、四乙二醇二甲醚；酯溶剂：辛酸烷酯、癸二酸烷酯、硬脂酸烷酯、苯甲酸烷酯、苯乙酸烷酯、肉桂酸烷酯、草酸烷酯、马来酸烷酯、烷内酯、油酸烷酯等。
进一步，按照本发明的油墨，所述的至少一种的有溶剂可选自：脂肪族酮，例如，2-壬酮、3-壬酮、5-壬酮、2-癸酮、2,5-己二酮、2,6,8-三甲基-4-壬酮、佛尔酮、二正戊基酮等；或脂肪族醚，例如，戊醚、己醚、二辛醚、乙二醇二丁醚、二乙二醇二乙醚、二乙二醇丁基甲醚、二乙二醇二丁醚、三乙二醇二甲醚、三乙二醇乙基甲醚、三乙二醇丁基甲醚、三丙二醇二甲醚、四乙二醇二甲醚等。
在另一些实施例中，所述的印刷油墨进一步包含有另一种有机溶剂。另一种有机溶剂的例子，包含(但不限于)：甲醇、乙醇、2-甲氧基乙醇、二氯甲烷、三氯甲烷、氯苯、邻二氯苯、四氢呋喃、苯甲醚、吗啉、甲苯、邻二甲苯、间二甲苯、对二甲苯、1,4二氧杂环己烷、丙酮、甲基乙基酮、1,2二氯乙烷、3-苯氧基甲苯、1,1,1-三氯乙烷、1,1,2,2-四氯乙烷、醋酸乙酯、醋酸丁酯、二甲基甲酰胺、二甲基乙酰胺、二甲基亚砜、四氢萘、萘烷、茚和/或它们的混合物。
在一个优选的实施方案中，按照本发明的组合物是一溶液。
在另一个优选的实施方案中，按照本发明的组合物是一悬浮液。
本发明还涉及所述组合物作为涂料或印刷油墨在制备有机电子器件时的用途，特别优选的是通过打印或涂布的制备方法。
其中，适合的打印或涂布技术包含(但不限于)喷墨打印，喷印(Nozzle Printing)，活版印刷，丝网印刷，浸涂，旋转涂布，刮刀涂布，辊筒印花，扭转辊印刷，平版印刷，柔版印刷，轮转印刷，喷涂，刷涂或移印，狭缝型挤压式涂布等。首选的是喷墨印刷，狭缝型挤压式涂布，喷印刷及凹版印刷。溶液或悬浮液可以另外包含一个或多个组份例如表面活性化合物，润滑 剂，润湿剂，分散剂，疏水剂，粘接剂等，用于调节粘度，成膜性能，提高附着性等。有关打印技术，及其对有关溶液的相关要求，如溶剂及浓度，粘度等，的详细信息请参见Helmut Kipphan主编的《印刷媒体手册：技术和生产方法》(Handbook of Print Media:Technologies and Production Methods),ISBN 3-540-67326-1。
本发明还提供一种如上所述的并吡咯衍生物或高聚物在有机电子器件的应用。所述的有机电子器件可选于，但不限于，有机发光二极管(OLED)，有机光伏电池(OPV)，有机发光电池(OLEEC)，有机场效应管(OFET)，有机发光场效应管，有机激光器，有机自旋电子器件，有机传感器及有机等离激元发射二极管(Organic Plasmon Emitting Diode)等，特别是OLED。本发明实施例中，优选地将所述并吡咯衍生物用于OLED器件的发光层中。
本发明进一步涉及一种有机电子器件，至少包含一种如上所述的并吡咯衍生物或高聚物。一般的，此种有机电子器件至少包含一个阴极，一个阳极及位于阴极和阳极之间的一个功能层，其中所述的功能层中至少包含一种如上所述的并吡咯衍生物或高聚物。所述的有机电子器件可选于，但不限于，有机发光二极管(OLED)，有机光伏电池(OPV)，有机发光电池(OLEEC)，有机场效应管(OFET)，有机发光场效应管，有机激光器，有机自旋电子器件，有机传感器及有机等离激元发射二极管(Organic Plasmon Emitting Diode)。
在一个特别优选的实施例中，所述的有机电子器件是电致发光器件，特别是OLED，其中包含一基片，一阳极，至少一发光层，一阴极。
基片可以是不透明或透明。一个透明的基板可以用来制造一个透明的发光元器件。例如可参见，Bulovic等Nature 1996,380,p29，和Gu等，Appl.Phys.Lett.1996,68,p2606。基片可以是刚性的或弹性的。基片可以是塑料，金属，半导体晶片或玻璃。最好是基片有一个平滑的表面。无表面缺陷的基板是特别理想的选择。在一个优选的实施例中，基片是柔性的，可选于聚合物薄膜或塑料，其玻璃化温度Tg为150℃以上，较好是超过200℃，更好是超过250℃，最好是超过300℃。合适的柔性基板的例子有聚(对苯二甲酸乙二醇酯)(PET)和聚乙二醇(2,6-萘)(PEN)。
阳极可包含一导电金属或金属氧化物，或导电聚合物。阳极可以容易地注入空穴到空穴注入层(HIL)或空穴传输层(HTL)或发光层中。在一个的实施例中，阳极的功函数和发光层中的发光体或作为HIL或HTL或电子阻挡层(EBL)的p型半导体材料的HOMO能级或价带能级的差的绝对值小于0.5eV，较好是小于0.3eV，最好是小于0.2eV。阳极材料的例子包含但不限于：Al、Cu、Au、Ag、Mg、Fe、Co、Ni、Mn、Pd、Pt、ITO、铝掺杂氧化锌(AZO)等。其他合适的阳极材料是已知的，本领域普通技术人员可容易地选择使用。阳极材料可以使用任何合适的技术沉积，如一合适的物理气相沉积法，包含射频磁控溅射，真空热蒸发，电子束(e-beam)等。在某些实施例中，阳极是图案结构化的。图案化的ITO导电基板可在市场上买到，并且可以用来制备根据本发明的器件。
阴极可包含一导电金属或金属氧化物。阴极可以容易地注入电子到EIL或ETL或直接到 发光层中。在一个的实施例中，阴极的功函数和发光层中发光体或作为电子注入层(EIL)或电子传输层(ETL)或空穴阻挡层(HBL)的n型半导体材料的LUMO能级或导带能级的差的绝对值小于0.5eV，较好是小于0.3eV，最好是小于0.2eV。原则上，所有可用作OLED的阴极的材料都可能作为本发明器件的阴极材料。阴极材料的例子包含但不限于：Al、Au、Ag、Ca、Ba、Mg、LiF/Al、MgAg合金、BaF2/Al、Cu、Fe、Co、Ni、Mn、Pd、Pt、ITO等。阴极材料可以使用任何合适的技术沉积，如一合适的物理气相沉积法，包含射频磁控溅射，真空热蒸发，电子束(e-beam)等。
OLED还可以包含其他功能层，如空穴注入层(HIL)、空穴传输层(HTL)、电子阻挡层(EBL)、电子注入层(EIL)、电子传输层(ETL)、空穴阻挡层(HBL)。
在一个优选的实施例中，按照本发明的发光器件中，其发光层包含本发明的并吡咯衍生物，并且通过真空蒸镀或溶液加工的方法制备而成，优选真空蒸镀。
在一个优选的实施例中，按照本发明的电致发光器件中，其空穴传输层包含本发明的氘代三芳胺衍生物。
在另一个优选的实施例中，按照本发明的电致发光器件中，其发光层包含本发明的高聚物，并且通过溶液加工的方法制备而成。
按照本发明的电致发光器件，其发光波长在300到800nm之间，较好的是在350到650nm之间，更好的是在400到625nm之间。
本发明还涉及按照本发明的有机电子器件在各种电子设备中的应用，包含，但不限于，显示设备，照明设备，光源，传感器等等。
下面将结合优选实施例对本发明进行了说明，但本发明并不局限于下述实施例，应当理解，所附权利要求概括了本发明的范围在本发明构思的引导下本领域的技术人员应意识到，对本发明的各实施例所进行的一定的改变，都将被本发明的权利要求书的精神和范围所覆盖。
Figure PCTCN2016107307-appb-000034
Figure PCTCN2016107307-appb-000035
1、并吡咯衍生物及其能量结构
并吡咯衍生物B-1-B-7的能级可通过量子计算得到，比如利用TD-DFT(含时密度泛函理论)通过Gaussian03W(Gaussian Inc.)，具体的模拟方法可参见WO2011141110。首先用半经验方法“Ground State/Semi-empirical/Default Spin/AM1”(Charge 0/Spin Singlet)来优化分子几何结构，然后有机分子的能量结构由TD-DFT(含时密度泛函理论)方法算得“TD-SCF/DFT/Default Spin/B3PW91/6-31G/d”(Charge 0/Spin Singlet)。HOMO和LUMO能级按照下面的校准公式计算，S1和T1直接使用。
HOMO(eV)＝((HOMO(Gaussian)×27.212)-0.9899)/1.1206
LUMO(eV)＝((LUMO(Gaussian)×27.212)-2.0041)/1.385
其中HOMO(G)和LUMO(G)是Gaussian 09W的直接计算结果，单位为Hartree。结果如表一所示：
表一
材料 HOMO[eV] LUMO[eV] T1[eV] S1[eV]
B-1 -5.06 -2.16 2.24 3.38
B-2 -5.10 -2.37 2.15 3.10
B-3 -5.06 -2.34 2.15 3.09
B-4 -5.13 -2.31 2.22 3.12
B-5 -5.13 -2.42 2.14 3.04
B-6 -5.03 -2.38 2.13 2.99
B-7 -4.99 -2.38 2.09 2.95
2、并吡咯衍生物的合成
2.1合成实施实例1：合成化合物B-1
Figure PCTCN2016107307-appb-000036
在一个干燥的双口瓶里放置苯甲醛(21.2g，200mmol)，对甲苯磺酸(6.88g，40mmol)，3-甲基苯胺(21.4g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-1(14.1g)。
2.2合成实施实例2：合成化合物B-2
Figure PCTCN2016107307-appb-000037
在一个干燥的双口瓶里放置4-联苯甲醛(36.4g，200mmol)，对甲苯磺酸(6.88g，40mmol)，苯胺(18.6g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取， 然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-2(17.8g)。
2.3合成实施实例3:合成化合物B-3
Figure PCTCN2016107307-appb-000038
在一个干燥的双口瓶里放置4-联苯甲醛(36.4g，200mmol)，对甲苯磺酸(6.88g，40mmol)，3-甲基苯胺(21.4g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-3(18.6g)。
2.4合成实施实例4：合成化合物B-4
Figure PCTCN2016107307-appb-000039
在一个干燥的双口瓶里放置苯甲醛(21.2g，200mmol)，对甲苯磺酸(6.88g，40mmol)，4-联苯胺(33.8g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-4(17.8g)。
2.5合成实施实例5：合成化合物B-5
Figure PCTCN2016107307-appb-000040
在一个干燥的双口瓶里放置4-联苯甲醛(36.4g，200mmol)，对甲苯磺酸(6.88g，40mmol)，4-联苯胺(33.8g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-5(22.38g)。
2.6合成实施实例6：
Figure PCTCN2016107307-appb-000041
合成中间体6-a：
将2-溴-9,9-二甲基芴(2.73g，10mmol)在氮气环境下加入100mL THF溶液中溶解，然后在-78℃下加入6mL正丁基锂(2M，15mmol)，保温反应1小时，然后逐滴加入干燥的DMF(2.5mL，32mmol),然后升至室温，继续搅拌反应2小时，浓缩，加水，用二氯甲烷萃取，浓缩，然后用乙酸乙酯/石油醚＝1/10过柱得到6-a(1.77g)。
合成化合物B-6：
在一个干燥的双口瓶里放置6-a(44.4g，200mmol)，对甲苯磺酸(6.88g，40mmol)，苯胺(18.6g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-6(20.22g)。
2.7合成实施实例7：合成化合物B-7
Figure PCTCN2016107307-appb-000042
在一个干燥的双口瓶里放置6-a(44.4g，200mmol)，对甲苯磺酸(6.88g，40mmol)，3-甲基苯胺(21.4g，200mmol)，然后加入700mL冰醋酸，稍加搅拌后加入2,3-丁二酮(8.6g，100mmol)，然后100℃搅拌反应3小时，冷却到室温，加水，用二氯甲烷萃取，然后干燥，浓缩，用二氯甲烷/石油醚＝1/5过柱得到B-7(21.06g)。
3、OLED器件的制备和表征：
具有ITO/NPD(60nm)/15％B-1～B-7:ADN(15nm)/TPBi(65nm)/LiF(1nm)/Al(150nm)/阴极的OLED器件的制备步骤如下:
a、导电玻璃基片的清洗:首次使用时，可用多种溶剂进行清洗，例如氯仿、酮、异丙醇进行清洗，然后进行紫外臭氧等离子处理；
b、HTL(60nm)，EML(25nm)，ETL(65nm)：在高真空(1×10-6毫巴，mbar)中热蒸镀而成；
c、阴极:LiF/Al(1nm/150nm)在高真空(1×10-6毫巴)中热蒸镀而成；
d、封装:器件在氮气手套箱中用紫外线硬化树脂封装。
各OLED器件的电流电压亮度(JVL)特性通过表征设备来表征，同时记录重要的参数如效率及外部量子效率。经检测，OLEDx(对应并吡咯衍生物B-x)的最大外部量子效率达都到4％以上。
进一步的优化，如器件结构的优化，HTM，ETM及主体材料的组合优化，将进一步提高器件的性能，特别是效率，驱动电压及寿命。
以上所述实施例的各技术特征可以进行任意的组合，为使描述简洁，未对上述实施例中的各个技术特征所有可能的组合都进行描述，然而，只要这些技术特征的组合不存在矛盾，都应当认为是本说明书记载的范围。
以上所述实施例仅表达了本发明的几种实施方式，其描述较为具体和详细，但并不能因此而理解为对发明专利范围的限制。应当指出的是，对于本领域的普通技术人员来说，在不脱离本发明构思的前提下，还可以做出若干变形和改进，这些都属于本发明的保护范围。因此，本发明专利的保护范围应以所附权利要求为准。

Claims (12)

  1. 一种如下通式(I)所示的并吡咯衍生物：
    Figure PCTCN2016107307-appb-100001
    其中，Ar1，Ar2在每一次出现中，相同或不同的选自未被取代或是R1取代的芳香烃或是杂芳香环烃体系；
    R1选自H，F，Cl，Br，I，D，CN，NO2，CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃；每一个基团均可被一个或多个活性基团R2取代，且一个或多个非相邻的亚甲基可以被以下基团替换：R2C＝CR2，C＝C，Si(R2)2，Ge(R2)2，Sn(R2)2，C＝O，C＝S，C＝Se，C＝N(R2)，O，S，-COO-或CONR2，其中一个或多个H原子可被D，F，Cl，Br，I，CN或N2所替换，或者被包含一个或多个活性基团R2、一个芳香基团或者一个杂芳香环取代的芳香胺替换，或者被取代或未被取代的咔唑替换；
    R2在每一次出现中，相同或不同的是H，D，含1～10个碳原子脂肪族烷烃，芳香碳氢化合物，含5～10个环原子的被取代或者未被取代的芳香环或杂芳香基团。
  2. 根据权利要求1所述的并吡咯衍生物，其特征在于，选自如下通式：
    Figure PCTCN2016107307-appb-100002
    Figure PCTCN2016107307-appb-100003
    其中，R3表示-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个；
    x为数字0-4中的任一个，y为数字0-5中的任一个，z为数字0-7中的任一个，u为数字0-8中的任一个，v为数字0-9中的任一个，w为数字0-11中的任一个；
    L为连接基团，相互独立的选自单键或B1至B4中的任一个：
    Figure PCTCN2016107307-appb-100004
    其中，R3至R26选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个。
  3. 根据权利要求2所述的并吡咯衍生物，其特征在于，选自如下通式：
    Figure PCTCN2016107307-appb-100005
  4. 根据权利要求1-3中任一项所述的并吡咯衍生物，其特征在于，通式(I)，(I-1)-(I-10)中的Ar2为未被取代或是取代的芳香环单元，在多次出现时相互独立的选自通式(C1)至(C10)中的任一个：
    Figure PCTCN2016107307-appb-100006
    其中，R27至R106选自-H，-F，-Cl，Br，I，-D，-CN，-NO2，-CF3，B(OR2)2，Si(R2)3，直链烷烃，烷烃醚，含1～10个碳原子烷烃硫醚或支链烷烃或环烷烃，含有6～10个碳原子的芳基中的任一个。
  5. 根据权利要求4所述的并吡咯衍生物，其特征在于，通式(I)，(I-1)-(I-10)中的Ar2相互独立的选自：
    Figure PCTCN2016107307-appb-100007
  6. 一种高聚物，其特征在于，包含一个重复单元，所述重复单元中包含一个有如通式(I)表示的结构单元。
  7. 一种混合物，其特征在于，包含一种如权利要求1至5任一项所述的并吡咯衍生物或如权利要求6所述的高聚物，及至少一种有机功能材料；所述有机功能材料可选自空穴注入材料，空穴传输材料，电子传输材料，电子注入材料，电子阻挡材料，空穴阻挡材料，发光材料，主体材料和有机染料。
  8. 一种组合物，其特征在于，包含如权利要求1至5任一项所述的并吡咯衍生物或如权利要求6所述的高聚物，及至少一种有机溶剂。
  9. 权利要求1至5任一项所述的并吡咯衍生物或如权利要求6所述的高聚物在有机电子器件中的应用。
  10. 一种有机电子器件，其特征在于，至少包含一种如权利要求1至5任一项所述的并吡咯衍生物或如权利要求6所述的高聚物或其混合物。
  11. 根据权利要求10所述的有机电子器件，其特征在于，所述有机电子器件为有机发光二极管、有机光伏电池、有机发光电池、有机场效应管、有机发光场效应管、有机激光器，有机自旋电子器件，有机传感器及有机等离激元发射二极管。
  12. 根据权利要求11或12所述的有机电子器件，其特征在于，该有机电子器件为一有机电致发光器件，至少包含有一发光层，所述的发光层包含有一种如权利要求1至5任一项所述的并吡咯衍生物或如权利要求6所述的高聚物。
PCT/CN2016/107307 2016-01-07 2016-11-25 并吡咯衍生物及其在有机电子器件的应用 WO2017118237A1 (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201680059920.8A CN108137604B (zh) 2016-01-07 2016-11-25 并吡咯衍生物及其在有机电子器件的应用

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201610013201.4 2016-01-07
CN201610013201 2016-01-07

Publications (1)

Publication Number Publication Date
WO2017118237A1 true WO2017118237A1 (zh) 2017-07-13

Family

ID=59273240

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2016/107307 WO2017118237A1 (zh) 2016-01-07 2016-11-25 并吡咯衍生物及其在有机电子器件的应用

Country Status (2)

Country Link
CN (1) CN108137604B (zh)
WO (1) WO2017118237A1 (zh)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108912125A (zh) * 2018-06-27 2018-11-30 南京邮电大学 一种基于四芳基并吡咯核非富勒烯受体材料及其应用
CN108977197A (zh) * 2018-08-21 2018-12-11 电子科技大学 有机电致发光材料及制备方法和有机电致发光器件
CN110272440A (zh) * 2018-03-15 2019-09-24 江苏三月光电科技有限公司 一种含硼六元杂环化合物及其在有机电致发光器件中的应用
CN110818727A (zh) * 2018-08-10 2020-02-21 上海和辉光电有限公司 一种热活化延迟荧光材料、其制备方法、用途及包含其的oled器件
CN114276353A (zh) * 2021-12-17 2022-04-05 江苏大学 一种以多氟取代吡咯-[3,2-b]吡咯为核心的空穴传输材料的合成方法及其应用
US11780846B2 (en) 2019-10-30 2023-10-10 Wuhan Tianma Micro-Electronics Co., Ltd. Compound, organic electroluminescent device including the same and electronic apparatus
WO2024035888A1 (en) * 2022-08-10 2024-02-15 Kennesaw State University Research And Service Foundation, Inc. Pyrrole derived compositions and sythesis methods

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010238880A (ja) * 2009-03-31 2010-10-21 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス材料、有機エレクトロルミネッセンス素子、青色燐光発光素子、表示装置及び照明装置
CN104870447A (zh) * 2012-11-05 2015-08-26 波兰科学院有机化学研究所 强荧光性杂环类和它们的合成方法
CN105038767A (zh) * 2015-06-29 2015-11-11 北京理工大学 一种检测空气中三氯甲烷的荧光试剂、制备方法及其应用
JP2016127083A (ja) * 2014-12-26 2016-07-11 出光興産株式会社 有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子及び電子機器

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010238880A (ja) * 2009-03-31 2010-10-21 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス材料、有機エレクトロルミネッセンス素子、青色燐光発光素子、表示装置及び照明装置
CN104870447A (zh) * 2012-11-05 2015-08-26 波兰科学院有机化学研究所 强荧光性杂环类和它们的合成方法
JP2016127083A (ja) * 2014-12-26 2016-07-11 出光興産株式会社 有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子及び電子機器
CN105038767A (zh) * 2015-06-29 2015-11-11 北京理工大学 一种检测空气中三氯甲烷的荧光试剂、制备方法及其应用

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
FRIESE D. H.: "Pyrrolo[3, 2-b]pyrroles-From Unprecedented Solvatofluorochromism to Two-Photon Absorption", CHEMISTRY - A EUROPEAN JOURNAL, vol. 21, no. 50, 29 October 2015 (2015-10-29) - 7 December 2015 (2015-12-07), XP055599255, ISSN: 0947-6539, DOI: 10.1002/chem.201502762 *
JANIGA A. ET AL.: "Synthesis and Optical Properties of Tetraaryl-1, 4- dihydropyrrolo-[3, 2-b]pyrroles", ASIAN JOURNAL OF ORGANIC CHEMISTRY, vol. 2, no. 5, 18 February 2013 (2013-02-18), pages 411 - 415, XP055105878, ISSN: 2193-5807, DOI: 10.1002/ajoc.201200201 *
JANIGA A.: "Diindolo[2,3-b:2',3'-f]pyrrolo[3,2-b]pyrroles as Electron- Rich, Ladder-type Fluorophores: Synthesis and Optical Properties", CHEMISTRY - AN ASIAN JOURNAL, vol. 10, no. 1, 1 October 2014 (2014-10-01) - January 2015 (2015-01-01), pages 212 - 218, XP055599227, ISSN: 1861-4728, DOI: 10.1002/asia.201402925 *
KRZESZEWSKI M. ET AL.: "x-Shaped Bis(areno)-1,4-dihydropyrrolo [3,2-b]pyrroles Generated by Oxidative Aromatic Coupling", THE JOURNAL OF ORGANIC CHEMISTRY, vol. 80, no. 5, 18 February 2015 (2015-02-18), pages 2893 - 2899, XP055599223, ISSN: 0022-3263, DOI: 10.1021/acs.joc.5b00052 *
KRZESZEWSKI M.: "Nonplanar Butterfly-shaped pi -Expanded Pyrrolopyrroles", CHEM. EUR. J., vol. 22, 23 September 2016 (2016-09-23) *
KRZESZEWSKI M.: "The Role of Steric Hindrance in the Intramolecular Oxidative Aromatic Coupling of pyrrolo[3, 2-b]pyrroles", CHEMICAL COMMUNICATIONS, vol. 52, no. 77, 24 August 2016 (2016-08-24) - 2016, pages 11539 - 11542, XP055599258, ISSN: 1359-7345, DOI: 10.1039/C6CC05904J *
ORTOWSKI R. ET AL.: "Strong Solvent Dependence of Linear and Non-linear Optical Properties of Donor-acceptor Type Pyrrolo[3, 2-b]pyrroles", PHYSICAL CHEMISTRY CHEMICAL PHYSICS, vol. 17, no. 37, 8 July 2015 (2015-07-08) - 7 October 2015 (2015-10-07), pages 23724 - 23731, XP055599246, ISSN: 1463-9076, DOI: 10.1039/C5CP03523F *
RAM KUMAR: "Quadrupolar (A- pi -D- pi -A) Tetra-aryl 1, 4-Dihydropyrrolo [3, 2- b]pyrroles as Single Molecular Resistive Memory Devices: Substituent Triggered Amphoteric Redox Performance and Electrical Bistability", J. PHYS. CHEM., vol. 120, 9 May 2016 (2016-05-09) *
TASIOR M. ET AL.: "Extension of Pyrrolopyrrole pi -System: Approach to Constructing Hexacyclic Nitrogen-containing Aromatic Systems", ORG. LETT., vol. 17, no. 24, 4 December 2015 (2015-12-04), pages 6106 - 6109, XP055599241, ISSN: 1523-7060, DOI: 10.1021/acs.orglett.5b03129 *
TASIOR M.: "Synthesis and Properties of Ladder-type BN-heteroacenes and Diazabenzoindoles Built on a Pyrrolopyrrole Scaffold", THE JOURNAL OF ORGANIC CHEMISTRY, vol. 81, no. 15, 18 July 2016 (2016-07-18), pages 6580 - 6586, XP055599262, ISSN: 0022-3263, DOI: 10.1021/acs.joc.6b01209 *
WU JIAYING ET AL.: "Pyrrolo-[3, 2-b]pyrroles for Photochromic Analysis of Halocarbons", ANALYTICAL CHEMISTRY, vol. 88, no. 2, 17 December 2015 (2015-12-17), pages 1195 - 1201, XP055599249, ISSN: 0003-2700, DOI: 10.1021/acs.analchem.5b03374 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110272440A (zh) * 2018-03-15 2019-09-24 江苏三月光电科技有限公司 一种含硼六元杂环化合物及其在有机电致发光器件中的应用
CN108912125A (zh) * 2018-06-27 2018-11-30 南京邮电大学 一种基于四芳基并吡咯核非富勒烯受体材料及其应用
CN108912125B (zh) * 2018-06-27 2021-03-02 南京邮电大学 一种基于四芳基并吡咯核非富勒烯受体材料及其应用
CN110818727A (zh) * 2018-08-10 2020-02-21 上海和辉光电有限公司 一种热活化延迟荧光材料、其制备方法、用途及包含其的oled器件
CN108977197A (zh) * 2018-08-21 2018-12-11 电子科技大学 有机电致发光材料及制备方法和有机电致发光器件
US11780846B2 (en) 2019-10-30 2023-10-10 Wuhan Tianma Micro-Electronics Co., Ltd. Compound, organic electroluminescent device including the same and electronic apparatus
CN114276353A (zh) * 2021-12-17 2022-04-05 江苏大学 一种以多氟取代吡咯-[3,2-b]吡咯为核心的空穴传输材料的合成方法及其应用
CN114276353B (zh) * 2021-12-17 2023-10-17 江苏大学 一种以多氟取代吡咯-[3,2-b]吡咯为核心的空穴传输材料的合成方法及其应用
WO2024035888A1 (en) * 2022-08-10 2024-02-15 Kennesaw State University Research And Service Foundation, Inc. Pyrrole derived compositions and sythesis methods

Also Published As

Publication number Publication date
CN108137604A (zh) 2018-06-08
CN108137604B (zh) 2020-09-15

Similar Documents

Publication Publication Date Title
CN109803957B (zh) 三嗪类稠环衍生物及其在有机电子器件中的应用
WO2017092508A1 (zh) D-a型化合物及其应用
WO2019120099A1 (zh) 有机混合物及其在有机电子器件中的应用
CN108137604B (zh) 并吡咯衍生物及其在有机电子器件的应用
WO2018095382A1 (zh) 芳香胺衍生物及其制备方法和用途
WO2018095392A1 (zh) 有机混合物、组合物以及有机电子器件
WO2019128875A1 (zh) 芳香胺衍生物及有机电子器件
WO2018103745A1 (zh) 咔唑类化合物及其应用
WO2018103744A1 (zh) 混合物、组合物及有机电子器件
WO2017118137A1 (zh) 咔唑衍生物、高聚物、混合物、组合物、有机电子器件及其应用
CN109790087B (zh) 氘代稠环化合物、高聚物、混合物、组合物以及有机电子器件
WO2018095386A1 (zh) 稠环化合物、高聚物、混合物、组合物以及有机电子器件
WO2019105326A1 (zh) 有机混合物、包含其的组合物、有机电子器件及应用
WO2018095385A1 (zh) 稠环化合物、高聚物、混合物、组合物以及有机电子器件
WO2018095393A1 (zh) 有机化合物、有机混合物、有机电子器件
WO2017118252A1 (zh) 含砜基稠杂环化合物及其应用
WO2022144018A1 (zh) 有机混合物及其在有机电子器件的应用
WO2019128599A1 (zh) 含氮杂环化合物、高聚物、混合物、组合物及其用途
WO2019120177A1 (zh) 用于制备有机电子器件的组合物、有机电子器件及应用
US11672174B2 (en) Pyrene-triazine derivative and applications thereof in organic electronic component
WO2018099432A1 (zh) 稠环化合物及制备方法和应用
WO2018095383A1 (zh) 氘代芳香胺衍生物及其制备方法和用途
WO2018103746A1 (zh) 咔唑苯类稠环衍生物、聚合物、混合物、组合物、有机电子器件及其制备方法
WO2018099433A1 (zh) 稠环化合物及其应用、混合物、有机电子器件
WO2022148464A1 (zh) 有机化合物及其在有机电子器件的应用

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: 16883363

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16883363

Country of ref document: EP

Kind code of ref document: A1