Luminescent material for delayed fluorescence and organic electroluminescent device comprising the same

US11800796B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11800796-B2
Application numberUS-201615738335-A
CountryUS
Kind codeB2
Filing dateJul 20, 2016
Priority dateJul 20, 2015
Publication dateOct 24, 2023
Grant dateOct 24, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to a luminescent material for delayed fluorescence and an organic electroluminescent device comprising the same. By using the luminescent material for delayed fluorescence according to the present invention, an organic electroluminescent device having long lifespan, low driving voltage, excellent color purity, and significantly improved luminous efficiency such as current efficiency is provided.

First claim

Opening claim text (preview).

The invention claimed is: 1. An organic electroluminescent device comprising a luminescent material for delayed fluorescence comprising a compound of the following formula 1 as a dopant material, and further comprising a compound of the following formula 8 as a host material: wherein R 1 represents a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted (C5-C30)aryl, a substituted or unsubstituted 5- to 30-membered heteroaryl, or CN; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, sulfur, Si, PO, SO, SO 2 , and SeO 2 ; X 1 represents —CR 3 or N; X 2 represents —CR 6 or N; R 3 and R 6 each independently represent hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted (C5-C30)aryl, a substituted or unsubstituted 5- to 30-membered heteroaryl, or CN; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, sulfur, Si, PO, SO, SO 2 , and SeO 2 ; E is represented by the following formulae 2-1 to 2-5, 2-9 to 2-13, 2-15, 2-19 to 2-28, 2-30, and 2-32 to 2-35; wherein X and Y each independently are selected from O, S, NR 4 , Si(R 4 ) 2 , C(R 4 ) 2 , PO(R 4 ) 2 , SO, SO 2 , and SeO 2 ; R 4 represents a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C5-C30)aryl, or a substituted or unsubstituted 5- to 30-membered heteroaryl; where there are two R 4 's, each of the two R 4 's may be the same or different, and the two R 4 's may be linked to each other to form a substituted or unsubstituted 11- to 60-membered polycyclic ring; and R each independently represents hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C5-C30)aryl, or a substituted or unsubstituted 5- to 30-membered heteroaryl; and * represents a bonding site between the ring comprising X 1 and X 2 , and E; independently represents N or CR 11 ; R 11 independently represents hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted (C5-C30)aryl, a substituted or unsubstituted 5- to 30-membered heteroaryl, or CN; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, sulfur, Si, PO, SO, SO 2 , and SeO 2 ; Het represents a 5- to 30-membered heteroaryl(ene); L represents hydrogen, a substituted or unsubstituted (C5-C30)aryl, or a substituted or unsubstituted 5- to 30-membered heteroaryl; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, sulfur, Si, PO, SO, SO 2 , and SeO 2 ; i represents an integer of 1 or 2; and j represents an integer of 1 to 5; where j is an integer of 2 or more, each of L may be the same or different. 2. The organic electroluminescent device comprising the luminescent material for delayed fluorescence according to claim 1 , wherein formula 1 is selected from the following formulas 1-1 to 1-16: wherein Z is selected from O, S, NR 8 , Si(R 8 ) 2 , C(R 8 ) 2 , PO(R 8 ) 2 , SO, SO 2 , and SeO 2 ; R 8 represents a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C5-C30)aryl, or a substituted or unsubstituted 5- to 30-membered heteroaryl; and Ph represents phenyl, and E is as defined in claim 1 . 3. The organic electroluminescent device comprising the luminescent material for delayed fluorescence according to claim 1 , wherein the compound represented by formula 1 is selected from the group consisting of: 4. The organic electroluminescent device according to claim 1 , wherein the compound represented by formula 8 is represented by the following formula 9: wherein X 11 independently represents N or CR 11 ; X 12 independently represents N or CR 12 ; R 11 and R 12 each independently represent hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted (C5-C30)aryl, a substituted or unsubstituted 5- to 30-membered heteroaryl, or CN; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, sulfur, Si, PO, SO, SO 2 , and SeO 2 ; and L independently represents hydrogen, a substituted or unsubstituted (C5-C30)aryl, or a substituted or unsubstituted 5- to 30-membered heteroaryl; or may be linked to an adjacent substituent to form a substituted or unsubstituted mono- or polycyclic, (C5-C30) alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one heteroatom s

Assignees

Inventors

Classifications

  • comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title

  • C07D401/04Primary

    directly linked by a ring-member-to-ring-member bond · CPC title

  • containing three or more hetero rings · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • containing three or more hetero rings · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11800796B2 cover?
The present invention relates to a luminescent material for delayed fluorescence and an organic electroluminescent device comprising the same. By using the luminescent material for delayed fluorescence according to the present invention, an organic electroluminescent device having long lifespan, low driving voltage, excellent color purity, and significantly improved luminous efficiency such as …
Who is the assignee on this patent?
Rohm & Haas Elect Materials Korea Ltd
What technology area does this patent fall under?
Primary CPC classification H10K85/6572. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Oct 24 2023 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).