Heterocyclic modulators of lipid synthesis
US-2024400552-A1 · Dec 5, 2024 · US
US2018102485A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018102485-A1 |
| Application number | US-201715840848-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 13, 2017 |
| Priority date | Nov 22, 2011 |
| Publication date | Apr 12, 2018 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X 1 to X 3 are a nitrogen atom or CR 1 , and A is represented by a formula (2) below. In the formula (2), L 1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y 1 is an oxygen atom, a sulfur atom or the like, and one of X 11 to X 18 is a carbon atom bonded to L 1 by a single bond and the rest of X 11 to X 18 are a nitrogen atom or CR 13 .
Opening claim text (preview).
1 . An organic electroluminescence device comprising: an anode; an emitting layer, an electron transporting zone; and a cathode in this sequence, wherein the electron transporting zone comprises an aromatic heterocyclic derivative represented by a formula (1) below, wherein: X 1 to X 3 are a nitrogen atom or CR 1 , with a proviso that at least one of X 1 to X 3 is a nitrogen atom; R 1 independently represents a hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms; A is represented by a formula (2) below, [Formula 2] (HAr) a -L 1 - (2) wherein: HAr is represented by a formula (3) below; a is an integer of 1 to 5; when a is 1, L 1 is a single bond or a divalent linking group; when a is in a range of 2 to 5, L 1 is a trivalent to hexavalent linking group and HAr is the same or different; the linking group is a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, or a divalent to hexavalent residue induced from any one of a group formed by mutually bonding two or three of the substituted or unsubstituted-aryl group having 6 to 30 ring carbon atoms and the substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms; the mutually bonded groups are the same or different, wherein: X 11 to X 18 each are independently a nitrogen atom, CR 13 or a carbon atom bonded to L 1 by a single bond; Y 1 is an oxygen atom, a sulfur atom, SiR 11 R 12 or a silicon atom bonded to each of R 11 and L 1 by a single bond; L 1 is bonded by one of a carbon atom at X 11 to X 18 and R 11 to R 12 and a silicon atom at Y 1 ; R 11 and R 12 represent the same as R 1 in the formula (1); R 11 and R 12 are the same or different; R 13 independently represents a hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms; a plurality of R 13 are mutually the same or different; adjacent R 13 optionally bond to each other to form a ring; and in the above formula (1), Ar 1 and Ar 2 each are independently represented by the formula (2), or represent a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms or a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms.
containing three or more hetero rings · CPC title
containing organic luminescent materials · CPC title
said ring comprising Si as a ring atom · CPC title
linked by a carbon chain containing aromatic rings · CPC title
containing three nitrogen atoms as heteroatoms · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.