151391-00-3Relevant articles and documents
Synthesis and Electronic Properties of Fluoreno[2,1-a]fluorenedione and Fluoreno[1,2-a]fluorenedione
Hacker, Allison S.,Pavano, Mauricio,Wood, James E.,Immoos, Chad E.,Hashimoto, Hannah,Genis, Sam P.,Frantz, Derik K.
, p. 510 - 515 (2018)
The [2,1-a]- and [1,2-a]-isomers of fluorenofluorenedione have been synthesized via intramolecular Friedel-Crafts acylations. DFT calculations indicate that the [1,2-a]-isomer adopts a twisted, helical C2-symmetric structure and that its proton
A fluorescent naphthalene ring[3] aromatic hydrocarbon nonporous adaptive crystal and preparation method and application thereof
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Paragraph 0081-0084, (2022/01/12)
The present invention discloses a fluorescent naphthalene ring [3] aromatic hydrocarbon nonporous adaptive crystal and preparation method and application thereof. The preparation methods include: first replacing the hydroxyl group in 2,7-dihydroxynaphthal
Organic electric field light-emitting device, display device and illumination device
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Paragraph 0254-0256, (2016/10/09)
PROBLEM TO BE SOLVED: To provide an organic electroluminescent element having excellent luminous efficiency and element life.SOLUTION: In an anthracene compound where a phenyl group and a naphthyl group are bonded, respectively, to the ninth and tenth positions, a compound where a specific aryl substitutes, especially, for the seventh position of a naphthyl group (bonded to anthracene at the second position) is used as a material for the luminous layer thus manufacturing an organic electroluminescent element.