Charge-transporting varnish

US2016248017A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016248017-A1
Application numberUS-201415026543-A
CountryUS
Kind codeA1
Filing dateSep 26, 2014
Priority dateOct 1, 2013
Publication dateAug 25, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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A charge-transporting varnish which contains a charge-transporting substance containing fluorine atoms, a charge-transporting substance containing no fluorine atoms, a dopant substance composed of a heteropolyacid, and an organic solvent. The charge-transporting substance containing fluorine atoms is a polymer which is obtained by condensing a triaryl amine compound, an arylaldehyde compound containing fluorine atoms, a fluorene derivative having a carbonyl group and a carbazole derivative having an alkyl group or an alkyl group containing an ether structure in the N-position, and which has a weight average molecular weight of 1,000-200,000. The charge-transporting substance containing no fluorine atoms is an oligoaniline compound. A thin film formed from this charge-transporting varnish is capable of providing an organic EL element having excellent luminance characteristics and durability even in cases where the thin film is used as a single layer between a positive electrode and a light emitting layer in such a manner that the thin film is in contact with the positive electrode and the light emitting layer.

First claim

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1 . A charge-transporting varnish comprising: a charge-transporting substance containing a fluorine atom; a charge-transporting substance containing no fluorine atom; a dopant substance of heteropolyacid; and an organic solvent, wherein said charge-transporting substance containing the fluorine atom is a polymer having a weight-average molecular weight of 1,000 to 200,000 which is obtained by condensation from a triarylamine compound, arylaldehyde compound containing a fluorine atom, fluorene derivative having a carbonyl group, and carbazole derivative having at the N-position an alkyl group or an alkyl group having the ether structure, said charge-transporting substance containing no fluorine atom is an oligoaniline compound. 2 . The charge-transporting varnish of claim 1 , wherein the charge-transporting substance containing the fluorine atom is a polymer which is obtained by condensation from a triarylamine compound represented by Formula (1), an arylaldehyde compound containing a fluorine atom represented by Formula (2), a fluorene derivative having a carbonyl group represented by Formula (3) or (4), and a carbazole derivative represented by Formula (5): wherein Ar 1 to Ar 3 mutually independently represent an aryl group having 6 to 20 carbon atoms with an optional substituent Z 1 , with each aryl group being composed of carbon atoms at least one of which has no substituent; Ar 4 represents an aryl group having 6 to 20 carbon atoms with at least one substituent Z 3 and an optional substituent Z 4 ; R 1 to R 8 mutually independently represent a hydrogen atom, halogen atom, nitro group, cyano group or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 2 ; R 9 and R 10 mutually independently represent a hydrogen atom or an alkyl group having 1 to 20 carbon atoms, (poly)ethyleneoxide group having 2 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 2 or alkyl group having 1 to 20 carbon atoms, a substituent of ethenyl group or ethynyl group and an optional substituent Z 2 ; R 11 represents an alkyl group having 1 to 20 carbon atoms or alkyl group having 2 to 20 carbon atoms and having the ether structure, both having an optional substituent Z 2 ; Z 1 represents a halogen atom, nitro group, or cyano group, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 2 ; Z 2 represents a halogen atom, nitro group, or cyano group; Z 3 represents a fluorine atom, fluorinated alkyl group having 1 to 20 carbon atoms, or fluorinated aryl group having 6 to 20 carbon atoms; Z 4 represents a chlorine atom, bromine atom, iodine atom, nitro group, or cyano group, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 5 ; and Z 5 represents a chlorine atom, bromine atom, iodine atom, nitro group, or cyano group. 3 . The charge-transporting varnish of claim 2 , wherein said triarylamine compound is a triphenylamine derivative represented by Formula (6): wherein R 12 to R 23 mutually independently represent a hydrogen atom, halogen atom, nitro group, or cyano group, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 2 , and Z 2 is defined as above. 4 . The charge-transporting varnish of claim 2 or 3 , wherein said arylaldehyde compound is a benzaldehyde derivative represented by Formula (7) or (8): wherein R 24 represents a fluorine atom or fluorinated alkyl group having 1 to 20 carbon atoms; R 25 to R 28 mutually independently represent a hydrogen atom, nitro group, cyano group, or an alkyl group having 1 to 20 carbon atoms optionally substituted with a nitro group or cyano group; and R 29 to R 33 mutually independently represent a fluorine atom or fluorinated alkyl group having 1 to 20 carbon atoms. 5 . The charge-transporting varnish of claim 1 , wherein said oligoaniline compound is one represented by Formula (9): wherein R 34 to R 39 mutually independently represent a hydrogen atom, halogen atom other than fluorine atom, nitro group, or cyano group, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 6 , or an aryl group having 6 to 20 carbon atoms or heteroaryl group having 2 to 20 carbon atoms, each having an optional substituent Z 7 , or —NHY 2 , —NY 3 Y 4 , —C(O)Y 5 , —OY 6 , —SY 7 , —SO 3 Y 8 , —C(O)OY 9 , —OC(O)Y 10 , —C(O)NHY 11 , or —C(O)NY 12 Y 13 group; Y 2 to Y 13 mutually independently represent an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 6 , or an aryl group having 6 to 20 carbon atoms or heteroaryl group having 2 to 20 carbon atoms, each having an optional substituent Z 7 ; X 1 represents —NY 1 —, —O—, —S—, —(CR 40 R 41 ) k —, or a single bond wherein R 40 and R 41 are identical with the R 34 mentioned above; letter k represents an integer of 1 to 20; Y 1 represents independently a hydrogen atom, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 6 , or an aryl group having 6 to 20 carbon atoms or heteroaryl group having 2 to 20 carbon atoms, each having an optional substituent Z 7 ; Z 6 represents a halogen atom other than fluorine atom, nitro group, or cyano group, or an aryl group having 6 to 20 carbon atoms or heteroaryl group having 2 to 20 carbon atoms, each having an optional substituent Z 8 ; Z 7 represents a halogen atom other than fluorine atom, nitro group, or cyano group, or an alkyl group having 1 to 20 carbon atoms, alkenyl group having 2 to 20 carbon atoms, or alkynyl group having 2 to 20 carbon atoms, each having an optional substituent Z 8 ; Z 8 represents a halogen atom other than fluorine atom, nitro group, or cyano group; and letters m and n mutually independently represent an integer of 1 to 10, with m+n≦10. 6 . The charge-transporting varnish of claim 1 , wherein said heteropolyacid is phosphotungstic acid. 7 . The charge-transporting varnish of claim 1 , further comprising a curing agent. 8 . The charge-transporting varnish of claim 7 , wherein said curing agent is a curing agent of acrylate type. 9 . A charge-transporting thin film prepared from the charge-transporting varnish of claim 1 . 10 . An electronic device having the charge-transporting thin film of claim 9 . 11 . An organic electroluminescence element having the charge-transporting thin film of claim 9 . 12 . An organic electrolumine

Assignees

Inventors

Classifications

  • comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene · CPC title

  • C09K11/06Primary

    containing organic luminescent materials · CPC title

  • Electricity · mapped topic

  • Electrically-conducting paints {(conductive materials H01B1/00)} · CPC title

  • Electricity · mapped topic

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What does patent US2016248017A1 cover?
A charge-transporting varnish which contains a charge-transporting substance containing fluorine atoms, a charge-transporting substance containing no fluorine atoms, a dopant substance composed of a heteropolyacid, and an organic solvent. The charge-transporting substance containing fluorine atoms is a polymer which is obtained by condensing a triaryl amine compound, an arylaldehyde compound co…
Who is the assignee on this patent?
Nissan Chemical Ind Ltd
What technology area does this patent fall under?
Primary CPC classification C09K11/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Aug 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).