WO2018093120A2 - Composé contenant de l'azote et film de conversion de couleur comprenant celui-ci - Google Patents

Composé contenant de l'azote et film de conversion de couleur comprenant celui-ci Download PDF

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WO2018093120A2
WO2018093120A2 PCT/KR2017/012895 KR2017012895W WO2018093120A2 WO 2018093120 A2 WO2018093120 A2 WO 2018093120A2 KR 2017012895 W KR2017012895 W KR 2017012895W WO 2018093120 A2 WO2018093120 A2 WO 2018093120A2
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Prior art keywords
group
substituted
unsubstituted
compound
same
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PCT/KR2017/012895
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English (en)
Korean (ko)
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WO2018093120A3 (fr
Inventor
이미림
손선경
송철준
이호용
Original Assignee
주식회사 엘지화학
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Priority claimed from KR1020170149778A external-priority patent/KR102059242B1/ko
Application filed by 주식회사 엘지화학 filed Critical 주식회사 엘지화학
Priority to JP2019513833A priority Critical patent/JP6795089B2/ja
Priority to CN201780059238.3A priority patent/CN109790186B/zh
Priority to US16/337,816 priority patent/US10766910B2/en
Publication of WO2018093120A2 publication Critical patent/WO2018093120A2/fr
Publication of WO2018093120A3 publication Critical patent/WO2018093120A3/fr

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    • 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
    • C07F5/02—Boron compounds
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
    • H01L33/50—Wavelength conversion elements

Definitions

  • the present specification relates to a nitrogen compound, a color conversion film, a backlight unit, and a display device including the same.
  • LEDs Conventional light emitting diodes
  • LEDs are obtained by mixing a green phosphor and a red phosphor into a blue light emitting diode or by mixing a yellow phosphor and a blue-green phosphor into a UV light emitting light emitting diode.
  • this method is difficult to control the color and thus poor color rendering. Therefore, color reproduction rate falls.
  • the present specification provides a nitrogen-containing ring compound, a color conversion film, a backlight unit, and a display device including the same.
  • n is an integer from 0 to 4, when m is 2 or more, R1 is the same as or different from each other,
  • n is an integer from 0 to 5, when n is 2 or more, R2 is the same as or different from each other,
  • R 101 to R 107 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Substituted or unsubstituted alkyl group; A substituted or unsubstituted fluoroalkyl group; Substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroring group.
  • the resin matrix provides a color conversion film comprising a compound represented by the formula (1) dispersed in the resin matrix.
  • a backlight unit including the color conversion film is provided.
  • a display device including the backlight unit is provided.
  • Compound according to an exemplary embodiment of the present specification is superior in fairness and light resistance than the compound of the conventional azabodipy structure. Therefore, by using the compound described herein as a fluorescent material of the color conversion film, it is possible to provide a color conversion film excellent in brightness and color reproducibility and excellent in light resistance and heat resistance.
  • FIG. 1 is a schematic diagram applying a color conversion film according to an exemplary embodiment of the present disclosure to a backlight.
  • substituted means that a hydrogen atom bonded to a carbon atom of the compound is replaced with another substituent, and the position to be substituted is not limited to a position where the hydrogen atom is substituted, that is, a position where a substituent can be substituted, if two or more substituted , Two or more substituents may be the same or different from each other.
  • substituted or unsubstituted is deuterium; Halogen group; Cyano group; Nitro group; Carbonyl group; Carboxy group (-COOH); Ether group; Ester group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted aryl group; And it is substituted with one or two or more substituents selected from the group consisting of a substituted or unsubstituted heterocyclic group, or two or more of the substituents exemplified above are substituted with a substituent, or means that do not have any
  • a substituent to which two or more substituents are linked may be a biphenyl group. That is, the biphenyl group may be an aryl group or may be interpreted as a substituent to which two phenyl groups are linked.
  • the halogen group may be fluorine, chlorine, bromine or iodine.
  • the ether group is a linear, branched or cyclic alkyl group having 1 to 25 carbon atoms of oxygen of the ether; Or a monocyclic or polycyclic aryl group having 6 to 30 carbon atoms.
  • the ester group is a linear, branched or cyclic alkyl group having 1 to 25 carbon atoms of oxygen of the ester group; Alkenyl groups; Monocyclic or polycyclic aryl groups having 6 to 30 carbon atoms; Or a heterocyclic group having 2 to 30 carbon atoms.
  • the alkyl group may be linear or branched chain, carbon number is not particularly limited, but is preferably 1 to 30.
  • Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl , Isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n -Heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-o
  • the cycloalkyl group is not particularly limited, but preferably has 3 to 30 carbon atoms, specifically, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, and the like, but are not limited thereto. It is not.
  • the alkoxy group may be linear, branched or cyclic. Although carbon number of an alkoxy group is not specifically limited, It is preferable that it is C1-C30. Specifically, methoxy, ethoxy, n-propoxy, isopropoxy, i-propyloxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy, Isopentyloxy, n-hexyloxy, 3,3-dimethylbutyloxy, 2-ethylbutyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, benzyloxy, p-methylbenzyloxy and the like It may be, but is not limited thereto.
  • the alkenyl group may be linear or branched chain, carbon number is not particularly limited, but is preferably 2 to 30.
  • Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2- ( Naphthyl-1-yl) vinyl-1-yl, 2,2-bis (diphenyl-1-yl) vinyl-1-yl, stilbenyl group, styrenyl group, and the like, but are not limited thereto.
  • the amine group is -NH 2 ; Monoalkylamine groups; Dialkylamine groups; N-alkylarylamine group; Monoarylamine group; Diarylamine group; N-aryl heteroaryl amine group; N-alkylheteroarylamine group; It may be selected from the group consisting of a monoheteroarylamine group and a diheteroarylamine group, and the carbon number is not particularly limited, but is preferably 1 to 30.
  • amine group examples include methylamine group, dimethylamine group, ethylamine group, diethylamine group, phenylamine group, naphthylamine group, biphenylamine group, anthracenylamine group, and 9-methyl-anthracenylamine group.
  • Diphenylamine group ditolylamine group, N-phenyltolylamine group, triphenylamine group, N-phenylbiphenylamine group; N-phenylnaphthylamine group; N-biphenyl naphthylamine group; N-naphthylfluorenylamine group; N-phenylphenanthrenylamine group; N-biphenylphenanthrenylamine group; N-phenyl fluorenyl amine group; N-phenylterphenylamine group; N-phenanthrenyl fluorenyl amine group; N-biphenyl fluorenyl amine group and the like, but is not limited thereto.
  • the silyl group includes trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, and the like.
  • the present invention is not limited thereto.
  • the aryl group is not particularly limited, but preferably has 6 to 30 carbon atoms, and the aryl group may be monocyclic or polycyclic.
  • the aryl group is a monocyclic aryl group
  • carbon number is not particularly limited, but is preferably 6 to 30 carbon atoms.
  • the monocyclic aryl group may be a phenyl group, a biphenyl group, a terphenyl group, etc., but is not limited thereto.
  • the polycyclic aryl group naphthyl group, anthracenyl group, phenanthryl group, triphenyl group, pyrenyl group, perrylenyl group, chrysenyl group, fluorenyl group and dihydroanthracene ( ), Etc., but is not limited thereto.
  • the fluorenyl group may be substituted, and adjacent substituents may be bonded to each other to form a ring.
  • the fluorenyl group may be substituted, and adjacent substituents may be bonded to each other to form a ring.
  • the aryloxy group, arylthioxy group, and aryl group of the aryl sulfoxy group are the same as the examples of the aryl group described above.
  • the aryloxy group may be a phenoxy group, p-tolyloxy group, m-tolyloxy group, 3,5-dimethyl-phenoxy group, 2,4,6-trimethylphenoxy group, p-tert-butylphenoxy group, 3- Biphenyloxy group, 4-biphenyloxy group, 1-naphthyloxy group, 2-naphthyloxy group, 4-methyl-1-naphthyloxy group, 5-methyl-2-naphthyloxy group, 1-anthryloxy group , 2-anthryloxy group, 9-anthryloxy group, 1-phenanthryloxy group, 3-phenanthryloxy group, 9-phenanthryloxy group, and the like.
  • arylthioxy group examples include a phenylthioxy group and 2- The methylphenyl thioxy group, 4-tert- butylphenyl thioxy group, etc. are mentioned,
  • An aryl sulfoxy group includes a benzene sulfoxy group, p-toluene sulfoxy group, etc., but is not limited to this.
  • the heterocyclic group includes one or more atoms other than carbon and heteroatoms, and specifically, the heteroatoms may include one or more atoms selected from the group consisting of O, N, Se, and S, and the like. Although carbon number is not particularly limited, it is preferably 2 to 30 carbon atoms, the heterocyclic group may be monocyclic or polycyclic.
  • heterocyclic group examples include thiophene group, furanyl group, pyrrole group, imidazolyl group, thiazolyl group, oxazolyl group, oxadiazolyl group, pyridyl group, bipyridyl group, pyrimidyl group, triazinyl group, tria Zolyl group, acridil group, pyridazinyl group, pyrazinyl group, quinolinyl group, quinazolinyl group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group , Isoquinolinyl group, indolyl group, carbazolyl group, benzoxazolyl group, benzimidazolyl group, benzothiazolyl group, benzocarbazolyl group, benzothiophene
  • the heterocyclic group may be monocyclic or polycyclic, may be aromatic, aliphatic or a condensed ring of aromatic and aliphatic, and may be selected from examples of the heterocyclic group.
  • adjacent means a substituent substituted on an atom directly connected to an atom to which the substituent is substituted, a substituent positioned closest to the substituent, or another substituent substituted on an atom to which the substituent is substituted.
  • two substituents substituted at the ortho position in the benzene ring and two substituents substituted at the same carbon in the aliphatic ring may be interpreted as "adjacent" groups.
  • adjacent groups combine with each other to form a ring means a hydrocarbon ring substituted or unsubstituted with an adjacent group; Or it means to form a substituted or unsubstituted hetero ring.
  • Chemical Formula 1 is represented by any one of the following Chemical Formulas 2 to 7.
  • L1 is the same as defined in Formula 1,
  • L21 and L22 are the same as defined in L2 of Formula 1, wherein L21 and L22 are the same as or different from each other,
  • R11, R12, R21 and R22 are the same as the definitions of R1 and R2 of Formula 1, wherein R11 and R12 are the same as each other, and R21 and R22 are the same as each other.
  • m1 and m2 are the same as the definition of m in Formula 1, wherein m1 and m2 are the same as each other,
  • n1 and n2 are the same as the definition of n in Formula 1, wherein n1 and n2 are the same as each other,
  • X11 to X14 is the same as the definition of X1 and X2 of Formula 1, wherein X11 is the same as X14, and X12 is the same as X13.
  • R 101 to R 103 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group having 1 to 20 carbon atoms; Or a substituted or unsubstituted aryl group having 6 to 30 carbon atoms.
  • R 101 to R 103 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group having 1 to 5 carbon atoms; Or a substituted or unsubstituted aryl group having 6 to 20 carbon atoms.
  • R 101 to R 103 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Substituted or unsubstituted methyl group; Or a substituted or unsubstituted phenyl group.
  • R 101 to R 103 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Methyl group; Or a phenyl group.
  • X1 and X2 are the same as or different from each other, and each independently a halogen group; Cyano group; Ether group; Ester group; Substituted or unsubstituted alkyl group; Substituted or unsubstituted alkynyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, or X1 and X2 combine with each other to form a substituted or unsubstituted ring.
  • X1 and X2 are the same as or different from each other, and each independently a halogen group; Cyano group; Ether group; Ester group; A substituted or unsubstituted alkyl group having 1 to 20 carbon atoms; Substituted or unsubstituted C2-C20 alkynyl group; A substituted or unsubstituted alkoxy group having 1 to 20 carbon atoms; Substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms; Substituted or unsubstituted aryl group having 6 to 30 carbon atoms; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms, or X1 and X2 combine with each other to form a substituted or unsubstituted carbon ring having 3 to 30 carbon atoms.
  • X1 and X2 are the same as or different from each other, and each independently a halogen group; Cyano group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryl group; Substituted or unsubstituted alkynyl group; —OC ( ⁇ O) R 107 or —C ( ⁇ O) OR 108 , wherein R 107 and R 108 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Substituted or unsubstituted alkyl group; A substituted or unsubstituted fluoroalkyl group; Substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroring group.
  • n is 0 or 1.
  • n 0.
  • m is 0, 1 or 2.
  • m is 0, 1 or 2.
  • R 104 and R 106 are the same as or different from each other, and are each independently hydrogen or a substituted or unsubstituted alkyl group.
  • R 104 to R 106 are the same as or different from each other, and are each independently hydrogen or a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms.
  • R 104 to R 106 are the same as or different from each other, and each independently hydrogen, a substituted or unsubstituted methyl group, a substituted or unsubstituted ethyl group, a substituted or unsubstituted propyl group, or Unsubstituted or unsubstituted butyl group.
  • R 104 to R 106 are the same as or different from each other, and are each independently hydrogen, a methyl group, an ethyl group, a propyl group, or a butyl group.
  • R 104 to R 106 are the same as or different from each other, and each independently hydrogen; Profile group; Or butyl group.
  • Chemical Formula 1 is selected from the following structural formulas.
  • the compound according to an exemplary embodiment of the present application may be prepared by the manufacturing method described below.
  • the compound of Formula 1 may be prepared in the core structure as shown in Schemes 1 and 2.
  • Substituents may be combined by methods known in the art, and the type, position or number of substituents may be changed according to techniques known in the art.
  • the resin matrix provides a color conversion film comprising a compound represented by the formula (1) dispersed in the resin matrix.
  • the content of the compound represented by Chemical Formula 1 in the color conversion film may be in the range of 0.001 to 10% by weight.
  • the color conversion film may include one type of the compound represented by Formula 1, or may include two or more types.
  • the color conversion film may further include an additional fluorescent material in addition to the compound represented by Chemical Formula 1.
  • the color conversion film preferably contains both a green light emitting phosphor and a red light emitting phosphor.
  • the color conversion film may include only a red light emitting fluorescent material.
  • the present invention is not limited thereto, and in the case of using a light source that emits blue light, when laminating a separate film including a green light emitting fluorescent substance, the color conversion film may include only a red light emitting compound.
  • the color conversion film may include only a green light emitting compound.
  • the color conversion film is a resin matrix; And an additional layer including a compound dispersed in the resin matrix and emitting a light having a wavelength different from that of the compound represented by Chemical Formula 1.
  • the compound that emits light of a different wavelength from the compound represented by Formula 1 may also be a compound represented by Formula 1, or may be another known fluorescent substance.
  • the material of the said resin matrix is a thermoplastic polymer or a thermosetting polymer.
  • the material of the resin matrix is poly (meth) acrylic, polycarbonate (PC), polystyrene (PS), polyarylene (PAR), polyurethane (TPU) such as polymethyl methacrylate (PMMA) ), Styrene-acrylonitrile (SAN), polyvinylidene fluoride (PVDF), modified polyvinylidene fluoride (modified-PVDF) and the like can be used.
  • the color conversion film according to the above-described embodiment further includes light diffusing particles.
  • a resin matrix and particles having high refractive index may be used, such as TiO 2 , silica, borosilicate, alumina, sapphire, air or other gas, air- or gas-filled hollow beads or particles (eg, , Air / gas-filled glass or polymer); Polymer particles including polystyrene, polycarbonate, polymethylmethacrylate, acrylic, methyl methacrylate, styrene, melamine resin, formaldehyde resin, or melamine and formaldehyde resin, or any suitable combination thereof may be used. .
  • the particle diameter of the light diffusing particles may be in the range of 0.1 micrometers to 5 micrometers, such as in the range of 0.3 micrometers to 1 micrometer.
  • the content of the light diffusing particles may be determined as needed, and may be, for example, in the range of about 1 to 30 parts by weight based on 100 parts by weight of the resin matrix.
  • the color conversion film according to the above-described embodiment may have a thickness of 2 micrometers to 200 micrometers.
  • the color conversion film may exhibit high luminance even at a thin thickness of 2 micrometers to 20 micrometers. This is because the content of the fluorescent substance molecules contained on the unit volume is higher than that of the quantum dots.
  • the color conversion film according to the above-described embodiment may be provided with a substrate on one surface.
  • This substrate can function as a support in the production of the color conversion film. It does not specifically limit as a kind of base material, As long as it is transparent and can function as the said support body, it is not limited to the material and thickness. Transparent here means that visible light transmittance is 70% or more.
  • a PET film may be used as the substrate.
  • the above-described color conversion film may be prepared by coating and drying a resin solution in which the compound represented by Chemical Formula 1 is dissolved on a substrate and drying the film, or by extruding the compound represented by Chemical Formula 1 together with the resin to form a film.
  • the compound represented by the formula (1) Since the compound represented by the formula (1) is dissolved in the resin solution, the compound represented by the formula (1) is uniformly distributed in the solution. This is different from the manufacturing process of the quantum dot film that requires a separate dispersion process.
  • the resin solution in which the compound represented by Chemical Formula 1 is dissolved is not particularly limited as long as the compound represented by Chemical Formula 1 is dissolved in a solution.
  • the resin solution in which the compound represented by Chemical Formula 1 is dissolved may prepare a first solution by dissolving the compound represented by Chemical Formula 1 in a solvent, prepare a second solution by dissolving the resin in a solvent, and prepare the first solution. It may be prepared by a method of mixing the solution and the second solution. When mixing the first solution and the second solution, it is preferable to mix homogeneously.
  • the present invention is not limited thereto, but the method of dissolving the compound represented by the formula (1) and the resin at the same time is dissolved in the solvent, the method of dissolving the compound represented by the formula (1) in the solvent, followed by the addition of the resin to dissolve; A method of adding and dissolving a compound represented by the above may be used.
  • the above-mentioned resin matrix material a monomer curable with this resin matrix resin, or a mixture thereof can be used.
  • the monomer curable with the resin matrix resin includes a (meth) acrylic monomer, which may be formed of a resin matrix material by UV curing.
  • an initiator necessary for curing may be further added as necessary.
  • the solvent is not particularly limited and is not particularly limited as long as it can be removed by drying without adversely affecting the coating process.
  • Non-limiting examples of the solvent include toluene, xylene, acetone, chloroform, various alcohol solvents, MEK (methyl ethyl ketone), MIBK (methyl isobutyl ketone), EA (ethyl acetate), butyl acetate, DMF ( Dimethylformamide), DMAc (dimethylacetamide), DMSO (dimethylsulfoxide), NMP (N-methyl-pyrrolidone) and the like can be used, and one or two or more thereof can be used in combination.
  • the solvent contained in each of these solutions may be the same and may differ. Even when different kinds of solvents are used in the first solution and the second solution, it is preferable that these solvents have compatibility so that they can be mixed with each other.
  • the coating of the resin solution in which the compound represented by Chemical Formula 1 is dissolved on the substrate may use a roll-to-roll process.
  • the resin solution in which the compound represented by Chemical Formula 1 is dissolved may be coated on one surface of the substrate, dried, and then wound on the roll.
  • it is preferable to determine the viscosity of the said resin solution to the range in which the said process is possible, for example, it can determine within the range of 200-2,000 cps.
  • a die coater may be used, and various bar coating methods such as a comma coater and a reverse comma coater may be used.
  • the drying process can be carried out under the conditions necessary to remove the solvent.
  • the solvent is dried in a condition in which the solvent is sufficiently blown in an oven located adjacent to the coater, and the color conversion material includes a fluorescent material including a compound represented by Formula 1 of a desired thickness and concentration on the substrate.
  • a film can be obtained.
  • curing such as UV curing may be performed before or simultaneously with the drying.
  • the compound represented by Formula 1 When extruding the compound represented by Formula 1 together with the resin to form a film, extrusion methods known in the art may be used.
  • the compound represented by Formula 1 may be polycarbonate-based (PC) or poly (meth).
  • a color conversion film can be manufactured by extruding together resins, such as an acryl type and a styrene- acrylonitrile type (SAN).
  • the color conversion film may be provided with a protective film or a barrier film on at least one surface.
  • a protective film and the barrier film those known in the art may be used.
  • a backlight unit including the color conversion film described above is provided.
  • the backlight unit may have a backlight unit configuration known in the art except for including the color conversion film.
  • 1 illustrates a schematic diagram of a backlight unit structure according to an example.
  • the backlight unit according to FIG. 1 includes a side chain type light source 101, a reflection plate 102 surrounding the light source, a light guide plate 103 that emits light directly from the light source, or guides light reflected from the reflection plate, and is provided on one surface of the light guide plate.
  • a color conversion film 105 provided on a surface opposite to a surface of the light guide plate that faces the reflective layer.
  • the light dispersion pattern 106 of the light guide plate is the light dispersion pattern 106 of the light guide plate.
  • the light introduced into the light guide plate has non-uniform light distribution due to the repetition of optical processes such as reflection, total reflection, refraction, and transmission.
  • a two-dimensional light dispersion pattern may be used to guide the light to uniform brightness.
  • the scope of the present invention is not limited by FIG. 1, and the light source may be a direct chain type as well as a side chain type, and a reflecting plate or a reflective layer may be omitted or replaced with another configuration as necessary, and may be additionally added as necessary.
  • the film for example, a light diffusing film, a light collecting film, a brightness enhancement film and the like may be further provided.
  • a display device including the backlight unit is provided.
  • the display device including the backlight unit is not particularly limited and may be included in a TV, a computer monitor, a notebook computer, a mobile phone, and the like.
  • Each compound was measured at 10 -5 M concentration in toluene solvent and then measured.
  • a thin film was coated on a glass substrate and dried to prepare a color conversion film.
  • the luminance spectrum of the prepared color conversion film was measured with a spectroradiometer (SR series, TOPCON). Specifically, the manufactured color conversion film is laminated on one surface of the light guide plate of the backlight unit including the LED blue backlight (maximum light emission wavelength 450 nm) and the light guide plate, the prism sheet and the DBEF film laminated on the color conversion film and then the film
  • the initial value was set such that the brightness of the blue LED light was 600 nit.
  • Example 1 was carried out in the same manner as in Example 1, except that Compound 4 (maximum absorption wavelength 468 nm, maximum emission wavelength 535 nm, half width 80 nm) in place of Compound 2 was used.
  • Example 1 was carried out in the same manner as in Example 1 except that Compound 6 (maximum absorption wavelength in the toluene solution, 478 nm, maximum emission wavelength 538 nm, half width 71 nm) was used instead of Compound 2.
  • Compound 6 maximum absorption wavelength in the toluene solution, 478 nm, maximum emission wavelength 538 nm, half width 71 nm
  • Example 1 was carried out in the same manner as in Example 1, except that Compound 7 was used instead of Compound 2 (maximum absorption wavelength in 470 nm, maximum emission wavelength in 525 nm, full width at half maximum of 73 nm).
  • Example 1 was carried out in the same manner as in Example 1, except that Compound 8 (maximum absorption wavelength 462 nm, maximum emission wavelength 512 nm, half width 78 nm) was used instead of Compound 2.
  • Example 1 was carried out in the same manner as in Example 1 except that Compound 14 (maximum absorption wavelength 461 nm, maximum emission wavelength 512 nm, full width at half maximum 77 nm) was used instead of Compound 2.
  • Example 1 was carried out in the same manner as in Example 1, except that commercial dye Y-083 (BASF) was used instead of Compound 2.
  • BASF commercial dye Y-083
  • Example 1 was performed in the same manner as in Example 1, except that the following Comparative Compound 1 (Chem. Eur. J. 2015, 21, 12996-13003.) was used instead of Compound 2.
  • the thin film emission wavelength of Table 2 was used for SCINCO's FS-2 equipment, quantum efficiency was measured using HAMAMATSU's Quantaurus-QY equipment. Abs intensity ratio is a numerical value showing the ratio when the intensity at the maximum absorption wavelength of Comparative Example 1 as 1, and used SCINCO's MEGA-2100 equipment.

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Abstract

La présente invention concerne un composé contenant de l'azote, un film de conversion de couleur comprenant ce composé, une unité de rétroéclairage et un dispositif d'affichage.
PCT/KR2017/012895 2016-11-18 2017-11-14 Composé contenant de l'azote et film de conversion de couleur comprenant celui-ci WO2018093120A2 (fr)

Priority Applications (3)

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JP2019513833A JP6795089B2 (ja) 2016-11-18 2017-11-14 含窒素化合物およびこれを含む色変換フィルム
CN201780059238.3A CN109790186B (zh) 2016-11-18 2017-11-14 含氮化合物和包含其的色彩转换膜
US16/337,816 US10766910B2 (en) 2016-11-18 2017-11-14 Nitrogen-containing compound and color conversion film comprising same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR10-2016-0154165 2016-11-18
KR20160154165 2016-11-18
KR1020170149778A KR102059242B1 (ko) 2016-11-18 2017-11-10 함질소 화합물 및 이를 포함하는 색변환 필름
KR10-2017-0149778 2017-11-10

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WO2018093120A3 WO2018093120A3 (fr) 2018-08-09

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JP2011241160A (ja) * 2010-05-17 2011-12-01 Yamamoto Chem Inc 色変換材料、該材料を含む組成物、該組成物を使用した色変換光学部品および該色変換光学部品を使用した発光素子
CN103865290B (zh) * 2014-04-01 2016-03-30 安徽师范大学 氟硼荧光染料及其制备方法和应用
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