Compounds and mixtures with antidegradant and antifatigue efficacy and compositions inluding such compounds
US-2017275239-A1 · Sep 28, 2017 · US
US9450190B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9450190-B2 |
| Application number | US-201414297585-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 5, 2014 |
| Priority date | Dec 6, 2013 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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.
A condensed cyclic compound is represented by Formula 1, and an organic light-emitting diode includes the condensed cyclic compound: wherein, in Formula 1, the descriptions of Ar 1 to Ar 4 , and R 1 to R 6 are as defined in the present specification. An organic light-emitting diode including an organic layer including the condensed cyclic compound may have a low driving voltage, a high light-emitting efficiency, and a long lifespan.
Opening claim text (preview).
What is claimed is: 1. A condensed cyclic compound represented by Formula 1: wherein, in Formula 1, Ar 1 to Ar 4 are each independently selected from a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 4 -C 30 heteroaryl group, and a substituted or unsubstituted monovalent C 6 -C 30 non-aromatic condensed polycyclic group; R 1 and R 2 are each independently selected from a substituted or unsubstituted C 1 -C 10 alkyl group, a substituted or unsubstituted C 2 -C 10 alkenyl group, a substituted or unsubstituted C 2 -C 10 alkynyl group, a substituted or unsubstituted C 1 -C 10 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 3 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 2 -C 30 heteroaryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthio group, a monovalent C 6 -C 30 non-aromatic condensed polycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), and —B(Q 4 )(Q 5 ); R 3 to R 6 are each independently selected from a hydrogen atom, a deuterium atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C 1 -C 10 alkyl group, a substituted or unsubstituted C 2 -C 10 alkenyl group, a substituted or unsubstituted C 2 -C 10 alkynyl group, a substituted or unsubstituted C 1 -C 10 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 3 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 2 -C 30 heteroaryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthio group, a monovalent C 6 -C 30 non-aromatic condensed polycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), and —B(Q 4 )(Q 5 ), wherein at least one substituent of the substituted C 1 -C 10 alkyl group, substituted C 2 -C 10 alkenyl group, substituted C 2 -C 10 alkynyl group, substituted C 1 -C 10 alkoxy group, substituted C 3 -C 10 cycloalkyl group, substituted C 3 -C 10 cycloalkenyl group, substituted C 3 -C 10 heterocycloalkyl group, substituted C 3 -C 10 heterocycloalkenyl group, substituted C 6 -C 30 aryl group, substituted C 2 -C 30 heteroaryl group, substituted C 6 -C 30 aryloxy group, and substituted C 6 -C 30 arylthio group is selected from: a deuterium atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 30 alkyl group, a C 2 -C 30 alkenyl group, a C 2 -C 30 alkynyl group, and a C 1 -C 30 alkoxy group; a C 1 -C 30 alkyl group, a C 2 -C 30 alkenyl group, a C 2 -C 30 alkynyl group, and a C 1 -C 30 alkoxy group, each substituted with at least one of a deuterium atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 3 -C 10 cycloalkyl group, a C 3 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 3 -C 10 heterocycloalkenyl group, a C 6 -C 30 aryl group, a C 2 -C 30 heteroaryl group, a C 6 -C 30 aryloxy group, a C 6 -C 30 arylthio group, a monovalent C 6 -C 30 non-aromatic condensed polycyclic group, —N(Q 11 )(Q 12 ), —Si(Q 13 )(Q 14 )(Q 15 ), and —B(Q 16 )(Q 17 ); a C 3 -C 10 cycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 3 -C 10 heterocycloalkyl group, a C 3 -C 10 heterocycloalkenyl group, a C 6 -C 30 aryl group, a C 2 -C 30 heteroaryl group, a C 6 -C 30 aryloxy group, a C 6 -C 30 arylthio group, and a monovalent C 2 -C 30 non-aromatic condensed polycyclic group; a C 3 -C 10 cycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 3 -C 10 heterocycloalkyl group, a C 3 -C 10 heterocycloalkenyl group, a C 6 -C 30 aryl group, a C 2 -C 30 heteroaryl group, a C 6 -C 30 aryloxy group, a C 6 -C 30 arylthio group, and a monovalent C 6 -C 30 non-aromatic condensed polycyclic group, each substituted with at least one of a deuterium atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 30 alkyl group, a C 2 -C 30 alkenyl group, a C 2 -C 30 alkynyl group, a C 1 -C 30 alkoxy group, a C 3 -C 10 cycloalkyl group, a C 3 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 3 -C 10 heterocycloalkenyl group, a C 6 -C 30 aryl group, a C 2 -C 30 heteroaryl group, a C 6 -C 30 aryloxy group, a C 6 -C 30 arylthio group, a monovalent C 6 -C 30 non-aromatic condensed polycyclic group, —N(Q 21 )(Q 22 ), —Si(Q 23 )(Q 24 )(Q 25 ), and —B(Q 26 )(Q 27 ); and —Si(Q 31 )(Q 32 )(Q 33 ) and —B(Q 34 )(Q 35 ); Q 1 to Q 5 , Q 11 to Q 17 , Q 21 to Q 27 , and Q 31 to Q 37 are each independently selected from a hydrogen atom, a C 1 -C 30 alkyl group, a C 2 -C 30 alkenyl group, a C 2 -C 30 alkynyl group, a C 1 -C 30 alkoxy group, a C 3 -C 10 cycloalkyl group, a C 3 -C 10 heterocycloalkyl group, a C 3 -C 10 cycloalkenyl group, a C 3 -C 10 heterocycloalkenyl group, a C 6 -C 30 aryl group, a C 2 -C 30 heteroaryl group, and a monovalent C 6 -C 30 non-aromatic condensed polycyclic group. 2. The condensed cyclic compound of claim 1 , wherein Ar 1 to Ar 4 are each independently selected from: a phenyl group, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, an indacenyl group, an acenaphthyl group, a biphenyl group, a heptalenyl group, a phenalenyl group, a fluorenyl group, a phenanthrenyl group, an anthryl group, a fluoranthenyl group, a pyrenyl group, a benzofluorenyl group, a naphthacenyl group, a chrysenyl group, a triphenylenyl group, a terphenyl group, a perylenyl group, a picenyl group, a hexacenyl group, a spiro-fluorenyl group, a pyrrolyl group, a furyl group, a pyrazolyl group, an imidazolyl group, an oxazolyl group, an isoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a pyridyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a pyranyl group, a thiophenyl group, a thiazolyl group, an isothiazolyl group, a thiopyran group, an indolyl group, an isoindolyl group, an indolizinyl group, a benzofuryl group, an isobenzofuryl group, an indazolyl group, a benzimidazolyl group, a benzoxazolyl group, a benzisoxazolyl group, an imidazopyridyl group, a purinyl group, a quinolyl group, an isoquinolyl group, a phthalazinyl group, a quinazolinyl group, a quinoxalinyl group, a naphthyridinyl group, a cinnolinyl group, a benzothiophenyl group, a benzothiazolyl group, a carbazolyl group, a benzocarbazolyl group, a pyridoindolyl group, a dibenzofuryl group, a phenanthridinyl group, a benzoquinolyl group, a phenazinyl group, a dibenzosilolyl group, a dibenzothiophenyl group, and a benzocarbazolyl group
Diphenylamines · CPC title
with at least one of the condensed ring systems formed by three or more rings · CPC title
Electricity · mapped topic
Electricity · mapped topic
Electricity · mapped topic
Related publications grouped by family.
Answers are generated from the same data shown on this page.