Condensed cyclic compound and organic light-emitting diode including the same

US9450190B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9450190-B2
Application numberUS-201414297585-A
CountryUS
Kind codeB2
Filing dateJun 5, 2014
Priority dateDec 6, 2013
Publication dateSep 20, 2016
Grant dateSep 20, 2016

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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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  7. Citations and related patents

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Abstract

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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.

First claim

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

Assignees

Inventors

Classifications

  • C07C211/55Primary

    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

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What does patent US9450190B2 cover?
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 dr…
Who is the assignee on this patent?
Samsung Display Co Ltd
What technology area does this patent fall under?
Primary CPC classification C07C211/55. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).