WO2005123634A1 - フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 - Google Patents
フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 Download PDFInfo
- Publication number
- WO2005123634A1 WO2005123634A1 PCT/JP2005/009024 JP2005009024W WO2005123634A1 WO 2005123634 A1 WO2005123634 A1 WO 2005123634A1 JP 2005009024 W JP2005009024 W JP 2005009024W WO 2005123634 A1 WO2005123634 A1 WO 2005123634A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- substituted
- prime
- substitution
- primes
- same
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/22—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system
- C07C35/37—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with a hydroxy group on a condensed system having three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/54—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
- C07C13/547—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings at least one ring not being six-membered, the other rings being at the most six-membered
- C07C13/567—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings at least one ring not being six-membered, the other rings being at the most six-membered with a fluorene or hydrogenated fluorene ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/54—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
- C07C13/605—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings with a bridged ring system
- C07C13/615—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings with a bridged ring system with an adamantane ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/62—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
- C07C13/64—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings with a bridged ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/62—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
- C07C13/66—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings the condensed ring system contains only four rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/72—Spiro hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/22—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system
- C07C35/37—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with a hydroxy group on a condensed system having three rings
- C07C35/38—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with a hydroxy group on a condensed system having three rings derived from the fluorene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/275—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings having all ether-oxygen atoms bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/18—Radicals substituted by singly bound hetero atoms other than halogen by sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-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
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/20—Acenaphthenes; Hydrogenated acenaphthenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/28—Phenalenes; Hydrogenated phenalenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
- C07C2603/42—Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
- C07C2603/50—Pyrenes; Hydrogenated pyrenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/52—Ortho- or ortho- and peri-condensed systems containing five condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/70—Ring systems containing bridged rings containing three rings containing only six-membered rings
- C07C2603/74—Adamantanes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/90—Ring systems containing bridged rings containing more than four rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/93—Spiro compounds
- C07C2603/94—Spiro compounds containing "free" spiro atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Definitions
- the present invention relates to an organic cation element and an on-conductor, and more particularly, to an octo-electron element having a high luminous efficiency and an on-conductor for realizing it.
- ct luminescence (sometimes referred to as ct luminescence) is based on the principle that a light-emitting substance emits light due to the energy of electrons injected from holes injected more than holes injected from holes. It is a photon. Children by C.W.a.
- luminescent materials are toss (8-lat) aluminium, kun, tetran, bisan and oxoazo conductors, which range from blue to red. It has been reported that light in the area of We are waiting (for example, patents ⁇ 3 etc.).
- the purpose of the present invention is to provide a semiconductor element and an on-conductor that realizes the element.
- the present invention provides an on-system conductor represented by the following ().
- X is a single bond, a substituted or substituted prime number of 5 to 5, an substituted or substituted prime number of 5 to 5, or a substituted or substituted prime number of 5 to 5. Even if X is the same or different, C is an integer of 6 to 5 substituted or substituted primes, 5 to 5 substituted or substituted primes, or 1 to 5 substituted or substituted primes. A quin or a substituted or unsubstituted aryl group having a prime number of 5 or less. C may be the same or different. However, X or is a single bond, or C represents 2 substitution or substitution, or ring 2 substitution or substitution.
- R is a hydrogen atom, a substituted or substituted prime number of 5 to 5, a substituted or substituted prime number of 5 to 5, or a substituted or substituted prime number of 5 to 5; Where e is the number of
- Q is a ring-forming group, which is a ring composed of Z, and further substituted or substituted primates with a prime number of 5 to 5, substituted or substituted primes with a prime number of 6 to 5, or substituted or substituted prime numbers Even if 5 to 5, it is fine.
- a b is a number of up to 4 each.
- the above-mentioned layer alone may be an organic conductor. It is intended to provide organic molecules that are contained in the compound.
- each is a number from to (or from 5 to 5) and satisfies. Is the number of ⁇ (mostly ⁇ 5).
- X represents a single bond, a substituted or substituted prime of 6 to 5, an substituted or substituted prime of 5 to 5, or a substituted or substituted prime of 5 to 5.
- Group. X may be the same or different.
- Tin Tin, four-methantone, four-methione, and four-tain.
- alkyne group of X examples include methine, tin, pupine, ison, tin, s-tin, isotin-methine-pentine-tin-tin-tin-tin, and cutin-tin. Cutin, 2 cutin, 2 cutin, 2 cutin, 3 ksoppin, 23 cutin, 2 cutin, 2 tinn, 2
- 0015 X includes, for example, bin
- C is an integer of 6 to 5 permuted or substituted primes, 5 to 5 substituted or commutated primes, and 5 substituted or substituted primes.
- C may be the same or different.
- Examples of the Aki group of C include meth, thi, pi, iso, thi, s, thi, meth, pliers,,,,,,,, and. Cut, 3d, 2d, 3d
- Aquine includes these divalent groups.
- Examples of 002C include, for example,
- Examples of an an include these divalent groups.
- examples of C include those having the above structure.
- One having a structure One having a structure.
- the ring is a quaki having a substituted or substituted prime number of 5 to 5, or a substituted or substituted prime number of 6 to 5, or a substituted or substituted prime number of 5 to 5.
- a substituted or substituted prime number of 5 to 5 are the respective numbers and satisfy 2.
- Examples of the ring include the same examples as those described in the above C.
- Examples of the ring include the same examples as those described in the above C.
- Examples of quake groups on the ring include cuppi, cuticle, cuppenty, ku, and 4-methic.
- Examples of the ring properties include the same examples as those described in the above C.
- Examples of the ring include, in addition to the same examples as in the above-mentioned C, the addition of saturated, tinoxy, tinsy, tintin, toti, tetradran, tetralane, tetrane, jin, Residues such as pyrazine, gin, isodine, isodine, gin, azine, rosin, rosin, and gin are listed.
- ((7), is a substituted or substituted prime of up to 5 primes, a substituted or substituted prime of 6 to 5 or a substituted or substituted prime of 5 to 5, is a substituted or substituted prime.
- prime 6 to 5 is a substituted or substituted prime of up to 5 primes, a substituted or substituted prime of 6 to 5 or a substituted or substituted prime of 5 to 5, is a substituted or substituted prime.
- Or is a substituted or substituted compound having 5 to 5 substituents.
- Examples of the body include the same examples as those described in the above C and X.
- ((9) is a substituted or substituted prime of 6-5, or a substituted or substituted prime of 5-5, is a substituted or substituted prime 8-5, a substituted or substituted prime With 8 to 5 children.)
- Examples of the group and the group include those having the group and structure of the above C.
- Examples of the group and the group include those having the group and structure of the above C.
- Examples of the group and the group include those having the group and structure of the above C.
- In (), is an on-system represented by the following shifts of (2) to (5) () to (2), or a group consisting of only these on-systems, and At this time, a plurality of () may be the same or different. 0029 4
- R is a hydrogen atom, a substituted or substituted prime number of 5 to 5, a substituted or substituted prime number of 5 to 5, or a substituted or substituted prime number of 5 to 5; Where c is the number between and
- Examples of the body include the same examples as those obtained by EC. (2) to (5) In () to (2), represents a carbon atom or a silicon atom.
- Q is a ring-forming group, a ring composed of z, and further substituted or substituted primes of up to 5 quaki or substituted. Is a prime of 6 to 5, or You may have 5 to 5 children. Examples of these bodies include the same examples as described above.
- ab is a number of up to 4, .
- it is a substituted or unsubstituted thio it has 5 to 5 primates, and if it is a substituted or substituted prime, it is 2 to 5 carbs, gens, gens, ano, tho, or radicals. When two or more are present, they may be the same or different, and those in contact with may be bonded to each other to form a structure.
- the prime of the commutation is 6-5,
- aki groups having a prime number of from 5 to 5 include meth, thi, pupi, isoppi, thi, sti, isothi, thi, pliers, thi, thi, thimeth, 2, 2, and 2 H, H, H, H, H, H, H, H, H
- the substituted or substituted prime group of R ⁇ is a group represented by O, and examples of the substituted group are the same as those of the above-mentioned group.
- aralkyl groups having a prime number of 7 to 5 are benzyl, 2 thisuppi, 2 thisuppi, and chithimethy.
- the substituted thio group having a prime number of 5 to 5 is represented by S, and the examples of 163 include the same examples as in the above-mentioned a.
- the aboradical group of ⁇ is expressed as OOZ,
- Examples thereof include the same examples as in the above-mentioned aki.
- Examples of () in the on-conductor include the same groups and specific examples as in the above (1) to (4).
- on-conductor represented by the above () is preferably represented by the following.
- F “” 004 is the same as above, and G is a structure represented by the following general formula (6) to ():
- a substituted or substituted prime 6 to 5, or a substituted or substituted 5 to 5 Is a substitution or substitution prime number of 5 to 5 or a substitution or substitution prime number of 5 to 5, is a substitution or substitution of a prime number of 8 to 5, and a substitution or substitution of a substitution number of 8 to 5. Yes, .
- the on-conductor represented by the parentheses () is preferably an organic material. .
- the above-mentioned layer has the on-conductor represented by the parentheses () alone or as a compound.
- the on-conductor represented by the general () above, and it is more preferable to have 5 to 99 as the host charge. .
- the phosphor may have phosphorescent properties.
- the light emitting element is suitable for the required light emission from anane compounds, toss (8-lat) aluminates, copper conductors, tetrane conductors, bisanthane conductors, oxoazo conductors, etc. .
- anthine-based substances furthermore, aria-based substances and / or .
- examples of the compound having 6 to 2 carbon atoms include chi, anthra, nonce, and ta.
- prime numbers 5 to 4 are, for example,
- substitutions of this group include aki having 6 to 6 carbon atoms (chi, meth, pi, pi, schi, ti, pliers,, pentchi, ku), and aki having 6 to 6 carbon atoms.
- the phosphoric acid is a substance containing at least one selected from 1, R Pd P, and se, and a small number selected from, gin, di, and Nanton.
- metal bodies are tos (2 gin) indium, tos (2 gin) alum, tos (2 gin) radium, bis (2 gin) gold, and tos (2 gin) gold.
- Examples include, but are not limited to, radium indium.
- It may contain a luminescent material, and may further contain a hole material or an electron material in order to transport holes injected from the electrode or electrons injected from the electrode to light emission. While the light emission is extremely high
- additional materials, higg materials, hole materials, and electron materials can be used as described above.
- a shift of a heavy metal body represented by phosphorescent indium can be used.
- luminescent materials, other higging materials, hole materials, and electronic materials can be used in combination.
- holes, light emission, and electrons may be formed by a layer configuration above each.
- a layer that injects holes from the electrode is called a hole
- a layer that receives holes from the hole layer and transports holes to light emission is called a hole
- a layer that receives electrons from the electron layer and transports the electrons to light emission is called an electron.
- a hole material that can be used in a luminous element it has the ability to transport holes, has an extreme result, a luminescent or excellent hole product with respect to the luminescent material, and is produced by luminescence. Prevents exciton or electron motion, .
- an conductor an conductor, a poly conductor, oxo, oxo, azo, azo, azo, zothione, pyran, pyran, tetrazo, oxo, oxoazo, Hydrazone, hydrazone, pore, stibe, tan, benzantone, stinton, diantone, etc., and their conductors, as well as zo, polan, and molecular materials of molecules However, it is not limited to these.
- Examples of conductors include ton, ton, toj, and j (3
- Examples of the conductor include Pc C Pc CoPc Pc Z Pc PdPc ePc Pc C Pc CGaPc C Pc CS Pc C SPc (O Pc (O) GaPc OPc OPc oOPc GaPc GaPc and other conductors.
- the present invention is not limited to these.
- Electron materials that can be used in the luminous element include the ability to transport electrons, the effect of the cathode and the luminescent material, and the exciton generated by luminescence. Preventing the movement of the layers, . Physically, onon, anthramethane, diquinone, thiopyrandiox, oxo, oxoazo, toazo, zo, pentetrabon, denmethane, anthraquinomethane, anthone and the like, and their conductors, are mentioned. It is not limited to. In addition, by adding an electron material to the hole material and an electron donating substance to the electron material, it is possible to improve the penetration.
- Examples of the object include 8-sodium, bis (8-nat), bis (8-nat), bis (8-nat) gangan, tos (8-nat) aum, and tos (2-meta).
- species such as a luminescent material, a hig material, a hole, and an electron material may be contained in the same layer.
- species such as a luminescent material, a hig material, a hole, and an electron material may be contained in the same layer.
- a material having a work function larger than 4e is suitable, such as carbon, aluminum, sodium, iron, iron, iron, tungsten, silver, gold, platinum, and radium. And acids such as indium used for gold, O and S, and organic conductive materials such as thiol.
- a substance having a work function higher than that of 4e is suitable, such as gallium, uranium, uranium, titanium, titanium, titanium, titanium, um, gangan, and aum. And their gold, but not limited to them.
- Representative examples of gold include, but are not limited to, gold, gallium indium, and titanium. It is controlled by the temperature, ambient temperature, and vacuum of gold, and is selected at an appropriate rate. And, if necessary, even if it is formed by the above layer configuration.
- the device it is desirable that at least one surface is clarified in the light wavelength region of the device in order to emit light efficiently. We also want it to be clear. Using the above fee, set by the method such as stuttering to ensure the predetermined property. of ,
- the lightness can be defined as: potin, tin bipolymer, tin bipolymer, poppin, postin, pomethymeact, po, pore, pola, nin, po Tetetone, Pohon, Potesone, Tetra-O-O-N-O-Cyte polymer, Polide, Tetra-O-Tin-Tin-Polymer, Tetra-O-Tin-Oxa-O-Pin Polymer, Pok Totin, povidenide, poste, ponet, potan, po, pote, po, poppin and the like can be mentioned.
- the method of moisture displacement such as drying such as vacuum evaporation, sputtering, plasming, and ion- ping of the layer of the child, digging, and tinging can be applied.
- the thickness is not particularly limited, but needs to be set to an appropriate value. If it is too high, a large pressure is required to obtain a certain level of power, and the rate will be poor. If it is too high, a light emission or the like is generated, and sufficient light emission luminance cannot be obtained even when an electric field is applied.
- the box is always suitable, but the box of O et al. 2 is more preferable.
- each layer is Tano, Kuhom, Tet It is formed by dissolving or dispersing in an appropriate solvent such as drane or xan, but it may be any other solvent.
- an appropriate solvent such as drane or xan
- Functions such as postin, pocket, point, poste, poad, button, poston, pometect, pometact, etc. And their polymers,
- Examples include photoconductive fats such as azo and polan, and fats such as potion and poppy.
- examples of the metal include UV, UV, and plastic.
- a light source such as a wall-mounted TV, a telephone, a display, a sign board, a sign of a copy, a plotter, a display, or an instrument.
- the on-conductor () represented by () was synthesized as follows.
- reaction solution was cooled to 7 C, the boiled water (o) was reduced to 7 C, and then cooled to room temperature. After further reaction 5, the reaction was carried out at room temperature. After separating the solution, it was dried with an organic saline solution and anhydrous sodium sulfate.
- the glas (5 o), the intermediate b 354 (), and the tetrakis (tin) radium () 254 (22 o 2 o) were placed in a glass and the inside of the vessel was exchanged. Further, a 2 to 22 solution of sodium (65) (3e) was added, and the mixture was heated and flowed with 9 C oil for 8 minutes. , And the deliverables were 2 Tokitan, ion and methano. The obtained body was further purified in . It was 3.37 (84). ()
- This film functions as holes.
- 4 () arrived as a host fee.
- a compound having the following group was vapor-deposited with a weight () of 34 relative to (). This film functions as light emission. An O film was formed on this. It functions as an electron.
- the contact manufactured by Getta Co., Ltd. was binary-adhered to form (O) as electrons (). A metal was attached on this to form a metal electrode, and a chip was produced.
- organic molecules were produced in the same manner except that the following compounds (2) to (4), which are the on-conductors represented by (), were used instead of ().
- Toss (2 gin) indium (Pp) 3 is described as a tip. Was added. 5 of Pp) 3 in. This film functions as light emission. On top of this, O (bis) 4 lat) bis (2 meth 8 lat) aum (bottom) was placed. This film functions as holes. Furthermore, 4 films were formed on this. This film functions as electrons. The genus Gaea was put on O.2 and then Aum was put on 5. This works as a. In this way, an organic electron was produced.
- an organic substance using an on-conductor represented by the parentheses () is useful, and has a high luminous efficiency and is useful as a practical child.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05741059A EP1780191A4 (en) | 2004-06-16 | 2005-05-18 | FLUORENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE DERIVATIVE |
JP2006519549A JPWO2005123634A1 (ja) | 2004-06-16 | 2005-05-18 | フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
US11/282,640 US7683225B2 (en) | 2004-06-16 | 2005-11-21 | Fluorene-based derivative and organic electroluminescence device employing the same |
KR1020067006217A KR101213383B1 (ko) | 2004-06-16 | 2006-03-30 | 플루오렌계 유도체 및 이를 이용한 유기 전기발광 소자 |
US12/178,807 US7781628B2 (en) | 2004-06-16 | 2008-07-24 | Fluorene-based derivative and organic electroluminescence device employing the same |
US12/838,839 US8013160B2 (en) | 2004-06-16 | 2010-07-19 | Fluorene-based derivative and organic electroluminescence device employing the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-178679 | 2004-06-16 | ||
JP2004178679 | 2004-06-16 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/282,640 Continuation US7683225B2 (en) | 2004-06-16 | 2005-11-21 | Fluorene-based derivative and organic electroluminescence device employing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005123634A1 true WO2005123634A1 (ja) | 2005-12-29 |
Family
ID=35509590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/009024 WO2005123634A1 (ja) | 2004-06-16 | 2005-05-18 | フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
Country Status (7)
Country | Link |
---|---|
US (3) | US7683225B2 (ja) |
EP (1) | EP1780191A4 (ja) |
JP (1) | JPWO2005123634A1 (ja) |
KR (1) | KR101213383B1 (ja) |
CN (1) | CN1842510A (ja) |
TW (1) | TWI395506B (ja) |
WO (1) | WO2005123634A1 (ja) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007072889A1 (en) * | 2005-12-20 | 2007-06-28 | Canon Kabushiki Kaisha | Fluorene compound and organic electroluminescence device |
JP2007208165A (ja) * | 2006-02-06 | 2007-08-16 | Toray Ind Inc | 発光素子 |
JP2007332127A (ja) * | 2005-12-20 | 2007-12-27 | Canon Inc | 化合物及び有機発光素子 |
WO2008069586A1 (en) * | 2006-12-06 | 2008-06-12 | Lg Chem, Ltd. | New fluorene derivatives and organic electronic device using the same |
JP2008162910A (ja) * | 2006-12-27 | 2008-07-17 | Canon Inc | カルバゾール化合物及びそれを用いた有機発光素子 |
EP2045231A1 (en) | 2007-10-03 | 2009-04-08 | Canon Kabushiki Kaisha | Binaphthyl compound and organic light emitting element using the same |
JP2009514812A (ja) * | 2005-10-21 | 2009-04-09 | エルジー・ケム・リミテッド | 新規のビナフタレン誘導体、その製造方法およびそれを用いた有機電子素子 |
JP2009179637A (ja) * | 2005-12-20 | 2009-08-13 | Canon Inc | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
JP2009267378A (ja) * | 2008-04-01 | 2009-11-12 | Canon Inc | 有機発光素子 |
WO2012173013A1 (ja) * | 2011-06-16 | 2012-12-20 | ユーディーシー アイルランド リミテッド | 有機電界発光素子、該素子用材料、並びに該素子を用いた発光装置、表示装置及び照明装置 |
EP2626400A1 (en) | 2012-02-10 | 2013-08-14 | Shin-Etsu Chemical Co., Ltd. | Fluorescent compound, making method, and fluorescent resin composition |
JP2020105155A (ja) * | 2018-12-28 | 2020-07-09 | 三星電子株式会社Samsung Electronics Co.,Ltd. | 化合物、組成物、液状組成物、有機エレクトロルミネッセンス素子用材料、および有機エレクトロルミネッセンス素子 |
WO2021049654A1 (ja) * | 2019-09-13 | 2021-03-18 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子及び電子機器 |
US11925106B2 (en) | 2018-12-28 | 2024-03-05 | Samsung Electronics Co., Ltd. | Condensed cyclic compound, composition including the same, and organic light-emitting device including the condensed cyclic compound |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005123634A1 (ja) * | 2004-06-16 | 2005-12-29 | Idemitsu Kosan Co., Ltd. | フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
JPWO2006001333A1 (ja) * | 2004-06-28 | 2008-04-17 | 出光興産株式会社 | 多環芳香族系化合物、発光性塗膜形成用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
US20090066227A1 (en) * | 2005-12-20 | 2009-03-12 | Canon Kabushiki Kaisha | Organic light-emitting device |
JP2008162911A (ja) * | 2006-12-27 | 2008-07-17 | Canon Inc | ジアザフルオレン化合物 |
EP2213639B1 (en) * | 2007-11-19 | 2016-04-13 | Idemitsu Kosan Co., Ltd. | Monobenzochrysene derivatives and their use in materials for organic electroluminescent devices |
KR100901887B1 (ko) * | 2008-03-14 | 2009-06-09 | (주)그라쎌 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 발광소자 |
US8841411B2 (en) * | 2008-06-23 | 2014-09-23 | Basf Se | Polymers |
KR20100000772A (ko) * | 2008-06-25 | 2010-01-06 | 다우어드밴스드디스플레이머티리얼 유한회사 | 신규한 유기 발광 화합물 및 이를 발광재료로서 채용하고있는 유기 발광 소자 |
CN102300890B (zh) | 2009-01-30 | 2014-03-26 | 惠普开发有限公司 | 嵌段共聚物和嵌段共聚物纳米粒子组合物 |
KR20110137298A (ko) | 2009-01-30 | 2011-12-22 | 휴렛-팩커드 디벨롭먼트 컴퍼니, 엘.피. | Uv 발광성 플루오렌계 공중합체 |
US8716700B2 (en) | 2009-10-29 | 2014-05-06 | E I Du Pont De Nemours And Company | Organic light-emitting diodes having white light emission |
US8716699B2 (en) * | 2009-10-29 | 2014-05-06 | E I Du Pont De Nemours And Company | Organic light-emitting diodes having white light emission |
KR101757444B1 (ko) | 2010-04-30 | 2017-07-13 | 삼성디스플레이 주식회사 | 유기 전계 발광 장치 |
CN102703058B (zh) * | 2012-05-22 | 2014-04-02 | 烟台万润精细化工股份有限公司 | 一种新型电致发光材料及其应用 |
CN103509016B (zh) * | 2012-09-24 | 2015-05-20 | Tcl集团股份有限公司 | 二吡啶芴类衍生物、其制备方法和应用及电致发光器件 |
KR102249278B1 (ko) * | 2013-04-29 | 2021-05-07 | 에스에프씨 주식회사 | 방향족 아민 유도체 및 이를 포함하는 유기전계발광소자 |
KR102445034B1 (ko) * | 2014-05-23 | 2022-09-20 | 닛산 가가쿠 가부시키가이샤 | 전하 수송성 바니시 |
US11518723B2 (en) | 2016-11-23 | 2022-12-06 | Guangzhou Chinaray Optoelectronic Materials Ltd. | Fused ring compound, high polymer, mixture, composition and organic electronic component |
KR102199112B1 (ko) * | 2018-07-31 | 2021-01-06 | 솔루스첨단소재 주식회사 | 유기 화합물 및 이를 이용한 유기 전계 발광 소자 |
CN115850256A (zh) * | 2022-11-25 | 2023-03-28 | 东莞伏安光电科技有限公司 | 一种二氮杂芴的化合物及用于有机电致发光器件的材料和有机电致发光器件 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000229893A (ja) * | 1999-02-09 | 2000-08-22 | Dainippon Ink & Chem Inc | ジアルケニル化合物 |
JP2002154993A (ja) * | 2000-08-10 | 2002-05-28 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2003064003A (ja) * | 2001-05-22 | 2003-03-05 | Korea Inst Of Science & Technology | 官能基を含有したフルオレン系化合物及びその重合体並びにそれらを利用したel素子 |
JP2003128651A (ja) * | 2001-10-16 | 2003-05-08 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2004043349A (ja) * | 2002-07-11 | 2004-02-12 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2004083481A (ja) * | 2002-08-27 | 2004-03-18 | Canon Inc | フルオレン化合物及びそれを用いた有機発光素子 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3008897A (en) * | 1959-08-07 | 1961-11-14 | Sinclair Refining Co | Hydrocarbon demetallization process |
JP2897138B2 (ja) | 1989-06-30 | 1999-05-31 | 株式会社リコー | 電界発光素子 |
JPH07138561A (ja) | 1993-11-17 | 1995-05-30 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
JP3816969B2 (ja) | 1994-04-26 | 2006-08-30 | Tdk株式会社 | 有機el素子 |
JP3724833B2 (ja) | 1995-03-06 | 2005-12-07 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JP3712760B2 (ja) | 1995-05-17 | 2005-11-02 | Tdk株式会社 | 有機el素子 |
JP3824798B2 (ja) * | 1999-01-21 | 2006-09-20 | Tdk株式会社 | 有機el素子 |
JP3539628B2 (ja) * | 1999-09-17 | 2004-07-07 | 富士写真フイルム株式会社 | 発光素子材料、それを使用した発光素子およびアミン化合物 |
JP3905265B2 (ja) | 1999-10-21 | 2007-04-18 | 富士フイルム株式会社 | 有機エレクトロルミネッセンス素子 |
JP2001160489A (ja) | 1999-12-01 | 2001-06-12 | Toyota Central Res & Dev Lab Inc | 有機電界発光素子 |
JP2001207167A (ja) | 2000-01-24 | 2001-07-31 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用発光材料およびそれを使用した有機エレクトロルミネッセンス素子 |
EP1221434B1 (en) * | 2000-08-10 | 2012-06-27 | Mitsui Chemicals, Inc. | Hydrocarbon compound, material for organic electroluminescent element and organic electroluminescent element |
JP2002063988A (ja) | 2000-08-22 | 2002-02-28 | Toray Ind Inc | 発光素子 |
JP2003086357A (ja) | 2001-09-07 | 2003-03-20 | Matsushita Electric Ind Co Ltd | 発光素子及びその製造方法 |
JP3848262B2 (ja) | 2002-03-27 | 2006-11-22 | キヤノン株式会社 | オリゴフルオレニレン化合物及び有機発光素子 |
JP4025137B2 (ja) * | 2002-08-02 | 2007-12-19 | 出光興産株式会社 | アントラセン誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
JP2004075567A (ja) * | 2002-08-12 | 2004-03-11 | Idemitsu Kosan Co Ltd | オリゴアリーレン誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
JP3848224B2 (ja) | 2002-08-27 | 2006-11-22 | キヤノン株式会社 | スピロ化合物及びそれを用いた有機発光素子 |
JP4164317B2 (ja) | 2002-08-28 | 2008-10-15 | キヤノン株式会社 | 有機発光素子 |
JP4311707B2 (ja) | 2002-08-28 | 2009-08-12 | キヤノン株式会社 | 有機発光素子 |
JP2004224766A (ja) * | 2003-01-27 | 2004-08-12 | Idemitsu Kosan Co Ltd | ビスアントラセン誘導体、それを含む発光性塗膜形成用材料及び有機エレクトロルミネッセンス素子 |
WO2005123634A1 (ja) * | 2004-06-16 | 2005-12-29 | Idemitsu Kosan Co., Ltd. | フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 |
JP2006140235A (ja) * | 2004-11-10 | 2006-06-01 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
-
2005
- 2005-05-18 WO PCT/JP2005/009024 patent/WO2005123634A1/ja not_active Application Discontinuation
- 2005-05-18 CN CNA2005800010074A patent/CN1842510A/zh active Pending
- 2005-05-18 EP EP05741059A patent/EP1780191A4/en not_active Withdrawn
- 2005-05-18 JP JP2006519549A patent/JPWO2005123634A1/ja not_active Withdrawn
- 2005-05-23 TW TW094116769A patent/TWI395506B/zh not_active IP Right Cessation
- 2005-11-21 US US11/282,640 patent/US7683225B2/en active Active
-
2006
- 2006-03-30 KR KR1020067006217A patent/KR101213383B1/ko active IP Right Grant
-
2008
- 2008-07-24 US US12/178,807 patent/US7781628B2/en active Active
-
2010
- 2010-07-19 US US12/838,839 patent/US8013160B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000229893A (ja) * | 1999-02-09 | 2000-08-22 | Dainippon Ink & Chem Inc | ジアルケニル化合物 |
JP2002154993A (ja) * | 2000-08-10 | 2002-05-28 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2003064003A (ja) * | 2001-05-22 | 2003-03-05 | Korea Inst Of Science & Technology | 官能基を含有したフルオレン系化合物及びその重合体並びにそれらを利用したel素子 |
JP2003128651A (ja) * | 2001-10-16 | 2003-05-08 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2004043349A (ja) * | 2002-07-11 | 2004-02-12 | Mitsui Chemicals Inc | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2004083481A (ja) * | 2002-08-27 | 2004-03-18 | Canon Inc | フルオレン化合物及びそれを用いた有機発光素子 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1780191A4 * |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009514812A (ja) * | 2005-10-21 | 2009-04-09 | エルジー・ケム・リミテッド | 新規のビナフタレン誘導体、その製造方法およびそれを用いた有機電子素子 |
US8674138B2 (en) | 2005-10-21 | 2014-03-18 | Lg Chem. Ltd. | Binaphthalene derivatives, preparation method thereof and organic electronic device using the same |
US8951831B2 (en) | 2005-10-21 | 2015-02-10 | Lg Chem, Ltd. | Binaphthalene derivatives, preparation method thereof and organic electronic device using the same |
WO2007072889A1 (en) * | 2005-12-20 | 2007-06-28 | Canon Kabushiki Kaisha | Fluorene compound and organic electroluminescence device |
JP2007332127A (ja) * | 2005-12-20 | 2007-12-27 | Canon Inc | 化合物及び有機発光素子 |
JP2009179637A (ja) * | 2005-12-20 | 2009-08-13 | Canon Inc | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
JP2009179636A (ja) * | 2005-12-20 | 2009-08-13 | Canon Inc | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
JP2009215308A (ja) * | 2005-12-20 | 2009-09-24 | Canon Inc | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
JP2007302650A (ja) * | 2005-12-20 | 2007-11-22 | Canon Inc | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
US8158835B2 (en) | 2005-12-20 | 2012-04-17 | Canon Kabushiki Kaisha | Fluorene compound and organic electroluminescence device |
JP2007208165A (ja) * | 2006-02-06 | 2007-08-16 | Toray Ind Inc | 発光素子 |
WO2008069586A1 (en) * | 2006-12-06 | 2008-06-12 | Lg Chem, Ltd. | New fluorene derivatives and organic electronic device using the same |
US8318948B2 (en) | 2006-12-06 | 2012-11-27 | Lg Chem, Ltd. | Fluorene derivatives and organic electronic device using the same |
JP2010511696A (ja) * | 2006-12-06 | 2010-04-15 | エルジー・ケム・リミテッド | 新規なフルオレン誘導体およびこれを用いた有機電子素子 |
JP2008162910A (ja) * | 2006-12-27 | 2008-07-17 | Canon Inc | カルバゾール化合物及びそれを用いた有機発光素子 |
EP2045231A1 (en) | 2007-10-03 | 2009-04-08 | Canon Kabushiki Kaisha | Binaphthyl compound and organic light emitting element using the same |
US8084937B2 (en) | 2007-10-03 | 2011-12-27 | Canon Kabushiki Kaisha | Binaphthyl compound and organic light emitting element using the same |
JP2009267378A (ja) * | 2008-04-01 | 2009-11-12 | Canon Inc | 有機発光素子 |
WO2012173013A1 (ja) * | 2011-06-16 | 2012-12-20 | ユーディーシー アイルランド リミテッド | 有機電界発光素子、該素子用材料、並びに該素子を用いた発光装置、表示装置及び照明装置 |
JP2013004723A (ja) * | 2011-06-16 | 2013-01-07 | Fujifilm Corp | 有機電界発光素子、該素子用材料、並びに該素子を用いた発光装置、表示装置及び照明装置 |
US11844229B2 (en) | 2011-06-16 | 2023-12-12 | Udc Ireland Limited | Electroluminescent element, and light emitting device, display device and lighting device each using organic electroluminescent element |
EP2626400A1 (en) | 2012-02-10 | 2013-08-14 | Shin-Etsu Chemical Co., Ltd. | Fluorescent compound, making method, and fluorescent resin composition |
US9062246B2 (en) | 2012-02-10 | 2015-06-23 | Shin-Etsu Chemical Co., Ltd. | Fluorescent compound, making method, and fluorescent resin composition |
JP2020105155A (ja) * | 2018-12-28 | 2020-07-09 | 三星電子株式会社Samsung Electronics Co.,Ltd. | 化合物、組成物、液状組成物、有機エレクトロルミネッセンス素子用材料、および有機エレクトロルミネッセンス素子 |
JP7329324B2 (ja) | 2018-12-28 | 2023-08-18 | 三星電子株式会社 | 化合物、組成物、液状組成物、有機エレクトロルミネッセンス素子用材料、および有機エレクトロルミネッセンス素子 |
US11925106B2 (en) | 2018-12-28 | 2024-03-05 | Samsung Electronics Co., Ltd. | Condensed cyclic compound, composition including the same, and organic light-emitting device including the condensed cyclic compound |
WO2021049654A1 (ja) * | 2019-09-13 | 2021-03-18 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子及び電子機器 |
Also Published As
Publication number | Publication date |
---|---|
US7781628B2 (en) | 2010-08-24 |
US8013160B2 (en) | 2011-09-06 |
TW200605708A (en) | 2006-02-01 |
US20080303433A1 (en) | 2008-12-11 |
US20100277063A1 (en) | 2010-11-04 |
EP1780191A1 (en) | 2007-05-02 |
CN1842510A (zh) | 2006-10-04 |
KR20070028284A (ko) | 2007-03-12 |
US7683225B2 (en) | 2010-03-23 |
KR101213383B1 (ko) | 2012-12-17 |
TWI395506B (zh) | 2013-05-01 |
US20060159956A1 (en) | 2006-07-20 |
EP1780191A4 (en) | 2008-07-02 |
JPWO2005123634A1 (ja) | 2008-04-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2005123634A1 (ja) | フルオレン系誘導体及びそれを利用した有機エレクトロルミネッセンス素子 | |
KR101324155B1 (ko) | 유기금속 착체 | |
CN103374043B (zh) | 磷光有机金属铱配合物、发光元件、发光装置、电子设备以及照明装置 | |
CN106229417B (zh) | 利用磷光发光的发光装置、电子设备及照明装置 | |
EP1550707B1 (en) | Organometallic complexes, organic el devices, and organic el displays | |
JP5165854B2 (ja) | シリル置換シクロメタル化遷移金属錯体およびこれを用いた有機電界発光素子 | |
CN104497054B (zh) | 有机金属配合物和使用它的发光元件、发光设备和电子设备 | |
US7825587B2 (en) | Charge transporting layer for organic electroluminescent device | |
JP5186085B2 (ja) | 有機金属錯体及びこれを用いた有機電界発光素子 | |
US8501328B2 (en) | Red phosphorescent compounds and organic electroluminescent devices using the same | |
WO2012077520A1 (ja) | 有機電界発光素子 | |
GB2410248A (en) | Charge transfer-promoting materials and electronic devices incorporating same | |
JP2019011362A (ja) | キノキサリン誘導体および複核錯体 | |
JP5243684B2 (ja) | 有機金属錯体、発光性固体、有機el素子及び有機elディスプレイ | |
KR20080106862A (ko) | 유기 금속 착체 및 상기 착체를 사용한 발광 소자, 발광장치 및 전자 기기 | |
CN101461075A (zh) | 具有磷光体-敏化荧光发射层的有机发光器件 | |
JP5953237B2 (ja) | 有機電界発光素子 | |
JP2008169197A (ja) | アントラセン誘導体及びこれを用いた有機電界発光素子 | |
CN1989221A (zh) | 发光电化学电池 | |
US7198730B2 (en) | Phosphorescent material | |
JP2006257024A (ja) | 有機金属錯体、発光性固体、有機el素子及び有機elディスプレイ | |
JP4880450B2 (ja) | 有機金属錯体、発光性固体、有機el素子及び有機elディスプレイ | |
JP5577122B2 (ja) | 有機電界発光素子 | |
US7279233B2 (en) | Light-emitting material and light-emitting device | |
JPWO2019039174A1 (ja) | ホスト材料、膜および有機発光素子 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200580001007.4 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 11282640 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006519549 Country of ref document: JP |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2005741059 Country of ref document: EP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1079/CHENP/2006 Country of ref document: IN Ref document number: 1020067006217 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 11282640 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: DE |
|
WWP | Wipo information: published in national office |
Ref document number: 1020067006217 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 2005741059 Country of ref document: EP |