191-07-1Relevant articles and documents
Gram scale synthesis of benzo[ghi]perylene and coronene
Van Dijk, Joost T. M.,Hartwijk, Astrid,Bleeker, Annemarie C.,Lugtenburg, Johan,Cornelisse, Jan
, p. 1136 - 1139 (1996)
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Du Vernet et al.
, p. 1629 (1975)
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Method for preparing coronene compound by using molecular sieve catalyst
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Paragraph 0065-0085, (2020/10/30)
The invention relates to a method for preparing a coronene compound by using a molecular sieve catalyst. Specifically, the method disclosed by the invention comprises the following steps of: (1) activating a molecular sieve catalyst; wherein the molecular sieve catalyst comprises an SAPO molecular sieve catalyst; and (2) carrying out contact reaction on a raw material and the molecular sieve catalyst activated in the step (1) in a reactor to obtain the coronene compound, wherein the raw material comprises an alcohol compound.
ORGANIC COMPOUND, THREE-DIMENSIONAL ORGANIC FRAMEWORK FORMED BY USING ORGANIC COMPOUND, SEPARATION SIEVE AND OPTICAL LAYER, WHICH COMPRISE ORGANIC FRAMEWORK, AND OPTICAL DEVICE COMPRISING OPTICAL LAYER AS OPTICAL AMPLIFICATION LAYER
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Paragraph 0356; 0359; 0360; 0363; 0364, (2019/02/13)
An organic compound, a three-dimensional organic structure formed by using the organic compound, a separation sieve and an optical layer having the organic structure, and an optical device having the optical layer as an optical amplification layer are provided. The organic structure includes a plurality of organic molecules self-assembled by non-covalent bonding. Each of the unit organic molecules has an aromatic ring, a first pair of substituents being connected to immediately adjacent positions of substitutable positions of the aromatic ring, and a second pair of substituents being connected to immediately adjacent positions of remaining substitutable positions of the aromatic ring. The unit organic molecules are self-assembled by van der Waals interaction, London dispersion interaction or hydrogen bonding between the first and the second pairs of the substituents and by pi-pi interactions between the aromatic rings.
1, 5, 9-trisubstituted coronene compound and synthesis method thereof
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Paragraph 0058; 0059; 0062; 0063, (2017/05/02)
The present invention relates to a 1, 5, 9-trisubstituted coronene compound and a synthesis method thereof. The structural formula of the compound is shown in img file = 'dest _ path _ image 001. TIF 'wi = '109 'he = '108', wherein R represents H, C1-C18 alkyl, phenyl, 4-methylphenyl, 4-methoxy phenyl, benzyl, cyclohexyl, 4-trifluoromethylphenyl, thiophene, furan and the like. According to the technical scheme of the invention, the easily prepared 1, 5, 9-triamido triphenylene is subjected to diazotization and halogenation reaction to obtain the tri-halogenated triphenylene. After that, the tri-halogenated triphenylene is subjected to Sonogashira reaction with various alkynes to generate atriyne-triphenylene compounds. Finally, through the metal-catalyzed reaction and the cyclization reaction under the effect of an organic base, various 1, 5, 9-trisubstituted coronene compounds, novel in structure, can be obtained. According to the technical scheme of the invention, raw materials are easy for mass preparation. Meanwhile, the synthesis step is relatively short and the operation is convenient. The obtained trisubstituted coronene compound is good in thermal stability and chemical stability, and the trisubstituted coronene emits the relatively strong fluorescence within the range of 420-550 nm according to the fluorescence emission spectrum of the trisubstituted coronene compound. Therefore, the trisubstituted coronene is an excellent fluorescent material for preparing UV ultraviolet charge-coupled devices (UV-CCD) and organic light-emitting diodes (OLEDs), and has a wide application prospect in the field of electronic materials.