107396-48-5Relevant academic research and scientific papers
Ink Composition and Method for Manufacturing Organic Light Emitting Device
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Paragraph 0226-0227, (2021/02/19)
The present specification relates to an ink composition including: a compound represented by Formula 1; and a solvent represented by the Formula 2, and a method for manufacturing an organic light emitting device formed by using the ink composition.
CONTINUOUS PRODUCTION METHOD OF HALOARYL BASED COMPOUNDS
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Paragraph 0070-0074, (2019/04/06)
The present invention relates to a continuous production method of haloaryl based compounds. As the method quickly controls heat from a lithiation reaction, the method is capable of reducing production of a by-product and providing a continuous process wh
COMPOUND, COATING COMPOSITION COMPRISING THE SAME, ORGANIC LIGHT EMITTING DEVICE USING THE SAME AND METHOD OF MANUFACTURING THE SAME
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Paragraph 0308-0310, (2019/06/27)
The present invention relates to a compound, capable of lowering a driving voltage and improving light efficiency and lifespan characteristics of an organic light emitting device, and to a coating composition including the same, an organic light emitting
FLUORENE-BASED COMPOUND, ORGANIC LIGHT EMITTING DEVICE USING THE SAME AND METHOD OF MANUFACTURING THE SAME
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Paragraph 0288-0291, (2018/10/03)
The present invention relates to a fluorine-based compound of chemical formula 1, a coating composition including the fluorine-based compound of chemical formula 1, an organic light emitting device using the same, and a manufacturing method thereof. In chemical formula 1, L1 and L2 are identical or different and is independently a substituted or unsubstituted alkylene group; a substituted or unsubstituted cycloalkylene group; or a substituted or unsubstituted hetero arylene group; and L is a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group.COPYRIGHT KIPO 2018
COMPOSITIONS AND LIQUID CRYSTALS
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Page/Page column 57-59, (2008/06/13)
The present invention relates to compounds, compositions, and methods in the field of detection of analytes. In particular to detection of viruses, cells, bacteria, lipid-membrane containing organisms, proteins, nucleic acids, carbohydrates and other biom
SYNTHESIS, STRUCTURE AND REACTIVITIES OF PARACYCLOPHANES
Tobe, Yoshito,Ueda, Ken-ichi,Kakiuchi, Kiyomi,Odaira, Yoshinobu,Kai, Yasushi,Kasai, Nobutami
, p. 1851 - 1858 (2007/10/02)
The synthesis, structure and reactivities of paracyclophanes 2a-c, the smallest bridged paracyclophanes so far isolated, are described.The parent hydrocarbon 2a has been efficiently synthesized by oxidative decarboxylation of propellenecarboxylic acid (7) by lead tetraacetate.The 8-carbomethoxy derivative 2b has been quantitatively synthesizedby thermal valence isomerization of the propelladiene (4b) (Dewar isomer of 2b).X-Ray structure analysis of the crystalline 2c has revealed that the benzene ring of 2c is severely deformed into a boat conformation with deformation angles of α=20.5 degree and β=18.5 degree.Furthermore, the bond angles of the bridging chain (C(2), C(3), C(4) and C(5)) are considerably expanded from the normal sp3 angle.Vapor phase thermolysis of 2a gives the spiro triene 12 via homolysis at the benzyl position.Acid-catalyzed isomerization of 2a with trifluoroacetic acid takes place readily to afford the meta and ortho isomers 13a and 14a in a ratio of 1:3.UV irradiation of the ester 2b brings about valence isomerization to the Dewar isomer 4b which izomerizes slowly to the prismane derivative 15a on further irradiation.A cycloaddition of 2a with N-phenyl-1,2,4-triazoline-3,5-dione occurs at room temperature to give mainly adduct 16.Addition of bromine to 2a takes place to furnish quantitatively the unstable 1,4-addition product 18.Oxidation of 2a with mCPBA readily takes place to give the dienone dimer 20 which affords on UV irradiation the cage diketone 21 derived from intramolecular photocycloaddition.
Aryl substituted ketones
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, (2008/06/13)
Aryl substituted tertiary carbinols, useful as antiviral agents and insecticides, are prepared by reacting the Grignard reagent derived from an arylalkyl or arylalkenyl iodide with a dialkyl ketone or an alkyl alkenyl ketone; or by reacting an arylalkyl or arylalkenyl ketone with an alkyl- or alkenylmagnesium halide.
