University of Southern California

Universal Display Corporation

Princeton University

University of Michigan

Other

Peter I Djurovich

Mark Edward Thompson

Jason Brooks

Arnold Tamayo

Stephen R Forrest

Raymond Kwong

Bert Alleyne

Bin Ma

Marc A Baldo

Sergey Lamansky

Jui-Yi Tsai

Chun Lin

Geza Szigethy

Hsiao-Fan Chen

Jun Deng

Glenn Morello

Vadim Adamovich

Peter B MacKenzie

Chihaya Adachi

Drew Murphy

Paul E Burrows

Robert W Walters

Kenneth Hanson

Feras Abdel-Razzaq

Xiaofan Ren

Valentina Krylova

David B Knowles

Yeh-Jiun Tung

Tobias D Schmidt

Cong Trinh

Nicholas John Thompson

Michael Stewart Weaver

Peter Borden Mackenzie

Cory S Brown

Jongchan Kim

Tissa Sajoto

Carsten Borek

Rasha Hamze

Tian-Yi Li

Yiru Sun

Haiping Hong

Patrick Saris

Alberto Bossi

Matthew J Jurow

Sarah M Conron

Xiao-Chang Charles Li

Daniel Sylvinson Muthiah Ravinson

Maria Dolores Perez

Karim El Roz

Abegail Tadle

Jessica H Golden

Stuart W Sawyer

Matthew T Whited

Jian Li

Narcisse Ukwitegetse

Matthias Selke

Shuyang Shi

Moon Chul Jung

Paul A Burrows

John W Facendola

Yifei Liu

Jung Moon Chul

Brooks Jason

Mark Thompson

Stephen Forrest

Hsaio-Fan Chen

Mathew T Whited

A compound is described as having a triplet excited state and a singlet excited state; wherein the triplet excited state comprises a lowest energy triplet sublevel, a middle energy triplet sublevel, and a highest energy triplet sublevel; and wherein an energy separation between the highest energy triplet sublevel and the lowest energy triplet sublevel (ZFS) is greater than an energy separation between the singlet excited state and a the lowest energy triplet sublevel. Also described is a compound represented by the following Formula I. These compounds should find application as luminescent materials in organic light emitting diodes (OLEDs).

Fast phosphors utilizing HP2H ligands

Compounds comprising a first ligand and a second ligand; wherein the first ligand coordinates to a first metal through a first metal-carbene bond; the second ligand coordinates to a second metal through a second metal-carbene bond; the second ligand also coordinates to the first metal; the first ligand can link to the second ligand to form a multidentate ligand; and the first metal and the second metal are each independently selected from the group consisting of Au, Ag, and Cu can act as electron acceptors in tandem to increase the energy separation between the ground and excited state, which is higher than those found in analogous monometallic complexes. These compounds should find application as luminescent materials in organic light emitting diodes (OLEDs).

Tandem-carbene phosphors

Tandem carbene phosphors such as those of Formula I can act as electron acceptors in tandem to increase the energy separation between the ground and excited state, which is higher than those found in analogous monometallic complexes. These compounds should find application as luminescent materials in organic light emitting diodes (OLEDs).

Tandem carbene phosphors

Disclosed herein are organic photosensitive optoelectronic devices comprising acceptor and/or donor sensitizers to increase absorption and photoresponse of the photoactive layers of the devices. In particular, devices herein include at least one acceptor layer and at least one donor layer, wherein the acceptor layer may comprise a mixture of an acceptor material and at least one sensitizer, and the donor layer may comprise a mixture of a donor material and at least one sensitizer. Methods of fabricating the organic photosensitive optoelectronic devices are also disclosed.

Energy sensitization of acceptors and donors in organic photovoltaics

A compound selected from the group consisting of Formula I, Formula II, and Formula III,

Carbene compounds and organic electroluminescent devices

Organic light emitting devices incorporating a film of metal complex emitters that are oriented with their transition dipole moment vectors oriented parallel to the device substrate enhances the outcoupling and eliminate the need for micro-lens arrays, gratings, or other physical extraneous outcoupling methods.

Organic electroluminescent materials and devices

The present disclosure provides a compound of Formula I

The co-linear or near co-linear structure of bimetallic Janus-type two-coordinated metal complexes may allow for a large transition dipole moment that can enhance the radiative lifetime. The symmetric nature of the bimetallic Janus complexes diminishes or eliminates the polar nature of the monometallic carbene-metal-amide/arene complexes.

Luminescent janus-type, two-coordinated metal complexes

A compound of Formula X An optoelectronic device selected from the group consisting of a photovoltaic device, a photodetector device, a photosensitive device, and an OLED, the optoelectronic device including an organic layer that comprises a compound of Formula X. A consumer product that includes the optoelectronic device.

An organic light emitting device having an anode, a cathode and an organic layer disposed between the anode and the cathode is provided. In one aspect, the organic layer comprises a compound having at least one zwitterionic carbon donor ligand. In another aspect the organic layer comprises a carbene compound, including the following:

Carbene metal complexes as OLED materials

Imidazophenanthridine ligands and metal complexes are provided. The compounds exhibit improved stability through a linking substitution that links a nitrogen bonded carbon of an imidizole ring to a carbon on the adjacent fused aryl ring. The compounds may be used in OLEDs, particularly as emissive dopants in the emissive region in the OLEDs, providing devices with improved efficiency, stability, and manufacturing. In particular, the compounds provided herein may be used in blue devices having high efficiency.

The invention provides emissive materials and organic light emitting devices using the emissive materials in an emissive layer disposed between and electrically connected to an anode and a cathode. The emissive materials include compounds with the following structure: wherein at least one of Rto Ris phenyl or substituted phenyl, and/or at least two of Rto Rthat are adjacent are part of a fluorenyl group. The emissive materials have enhanced electroluminescent efficiency and improved lifetime when incorporated into light emitting devices.

Phenyl and fluorenyl substituted phenyl-pyrazole complexes of Ir

Imidazophenanthridine ligands and metal complexes are provided. The compounds exhibit improved stability through a linking substitution that links a nitrogen bonded carbon of an imidizole ring to a carbon on the adjacent fused aryl ring. The compounds may be used in organic light emitting devices, particularly as emissive dopants, providing devices with improved efficiency, stability, and manufacturing. In particular, the compounds provided herein may be used in blue devices having high efficiency.

Organic light emitting devices are described wherein the emissive layer comprises a host material containing an emissive molecule, which molecule is adapted to luminesce when a voltage is applied across the heterostructure, and the emissive molecule is selected from the group of phosphorescent organometallic complexes, including cyclometallated platinum, iridium and osmium complexes. The organic light emitting devices optionally contain an exciton blocking layer. Furthermore, improved electroluminescent efficiency in organic light emitting devices is obtained with an emitter layer comprising organometallic complexes of transition metals of formula LMX, wherein L and X are distinct bidentate ligands. Compounds of this formula can be synthesized more facilely than in previous approaches and synthetic options allow insertion of fluorescent molecules into a phosphorescent complex, ligands to fine tune the color of emission, and ligands to trap carriers.

Organometallic complexes as phosphorescent emitters in organic LEDs

Growing community of inventors

Long Beach, CA, United States of America

Peter I Djurovich