173678-11-0Relevant articles and documents
NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME
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Paragraph 0216-0221, (2021/06/01)
The present invention provides a novel compound and an organic light emitting device using the same. The compound represented by a chemical formula 1 may be used as a material for an organic layer of an organic light emitting device, and may improve efficiency, low driving voltage, and/or lifespan characteristics of the organic light emitting device.
Organic compound, and organic electroluminescent device and electronic device using same
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Paragraph 0157-0162, (2021/02/20)
The invention relates to an organic compound. The structure of the organic compound comprises a formula I. When the organic compound provided by the invention is used for a light-emitting layer of anorganic electroluminescent device, the device efficiency of the device can be effectively improved, and the service life of the organic electroluminescent device is prolonged.
AMINE COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME
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Paragraph 0397-0399; 0417-0419, (2020/02/19)
An amine compound is represented by Formula 1. An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode and including an emission
Organic glass-forming materials: 1,3,5-Tris(naphthyl)benzene derivatives
Bonvallet, Paul A.,Breitkreuz, Caroline J.,Yong, Seol Kim,Todd, Eric M.,Traynor, Katherine,Fry, Charles G.,Ediger,McMahon, Robert J.
, p. 10051 - 10057 (2008/04/05)
(Chemical Equation Presented) The organic glass-forming materials 1,3-bis(1-naphthyl)-5-(2-naphthyl)benzene (2) and its partially deuterated analogue, 1,3-bis(1-naphthyl-d7)-5-(2-naphthyl)benzene (2-d 14), have been synthesized on a gram scale using Suzuki coupling reactions. Detailed spectroscopic studies afford complete NMR assignments ( 1H, 2H, 13C) for both compounds. Modest energy barriers for the interconversion of atropisomers (ca. 15 kcal/mol) result in a propensity for these materials to form supercooled liquids and glasses, rather than undergoing crystallization. The preparation of these materials enables detailed studies of physical properties of organic glasses and molecular diffusion in condensed phases.