Hexaarylbisimidazoles compounds, preparation method and application thereof and composition containing thereof
A technology of hexaaryldiimidazole and compound is applied in the field of compound, preparation method and application thereof, and can solve the problems of short absorption wavelength, low photosensitivity and the like
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Embodiment 1
[0130] In a 150ml flask, 3,4-dimethoxy-2'-chlorobenzil (0.05mol), 2-chloro-5-nitrobenzaldehyde (0.055mol) and ammonium acetate (0.275mol) were dissolved in In 100ml of glacial acetic acid, under the protection of nitrogen, reflux for 12 hours, pour into 1000ml of aqueous solution containing 2% sodium bisulfite after cooling, filter, and vacuum dry at 60°C for 24 hours to obtain 2-(2-chloro-5-nitro 21.8 g of phenyl)-4-(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)imidazole.
[0131] In a 250ml flask, 2-(2-chloro-5-nitrophenyl)-4-(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)imidazole (0.01mol) Dissolve in 70ml of dichloromethane, add 35ml of potassium ferricyanide (0.03mol) aqueous solution and 5ml of sodium hydroxide (0.125mol) aqueous solution, reflux for 8 hours, let stand to separate layers after cooling, separate dichloromethane phase, water phase Extracted with 35ml of dichloromethane, combined the dichloromethane phases, dried with anhydrous magnesium sulfate, concentrated, precipi...
Embodiment 2~ Embodiment 16
[0137] The synthesis method of the compounds in Example 2 to Example 16 is the same as that of Example 1.
Embodiment 2
[0139]2,2'-bis(2-chloro-5-nitrophenyl)-4,4'-bis(2-fluorophenyl)-5,5'-bis(3,4-dimethoxyphenyl) ) Diimidazole: the productive rate is 79%;
[0140] NMR (Acetone-d6, 400MHz, δ, ppm) 6.5-8.8 (20H, aromatic hydrogen), 3.4-3.9 (12H, OCH 3 );
[0141] FTIR (KBr, cm-1): 2953, 2839 (CH 3 , vC-H telescopic), 1343 (NO 2 , vN-O telescopic), 860 (NO 2 , vN-C stretching).
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