Axial substituted phthalocyanine compound, its preparation and application in optical kinetic treatment
A complex, axial technology, applied in the direction of silicon organic compounds, medical preparations with inactive ingredients, medical preparations containing active ingredients, etc., can solve the problems of high cost and complex synthesis, and achieve no isomers. , The effect of strong photosensitization ability and clear structure
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[0043] 2. The preparation method of the new axially substituted phthalocyanine complex of the present invention comprises the following major steps: (a) dichlorosilicon phthalocyanine (or a chloroaluminum phthalocyanine) and the corresponding The reactants are dispersed in a suitable solvent according to a certain molar ratio of feed; (b) in the presence of sodium hydride or potassium carbonate, reflux reaction for 1 hour to 3 days, and monitor the reaction end point by chromatography; (c) by solvent method And / or chromatography to remove excess raw materials and impurities and purify the target product. For the schematic diagram of the reaction, see Figures 19 and 20 of the description.
[0044] The corresponding reactants containing substituents described in the present invention include: sulfamic acid; Glucose; Diethylene glycol butyl ether; 4-ethyl phenol; 4-butyl phenol; 4-aminophenol; 2-ethoxy-4-formylphenol; 2-dimethylaminoethanol; 3-diethylaminophenol; pyrimidinols co...
Embodiment 1
[0048] Stir 0.1g of dichlorosilicon phthalocyanine, 0.3g of sulfamic acid, and 20mg of NaH in 10ml of toluene, reflux for 3 days, remove the solvent by rotary evaporation under reduced pressure, add 100ml of water to the solid, filter, and dissolve the filter cake with dichloromethane, Separation and purification by silica gel column chromatography, the eluent is ethanol, after vacuum drying, a dark blue bis(aminosulfonyl)silyl phthalocyanine was obtained with a yield of 38.3%.
Embodiment 2
[0050] Stir 0.1g of dichlorosilicon phthalocyanine, 10ml of diethylene glycol butyl ether, and 20mg of NaH in 10ml of toluene, reflux for 3 days, remove the solvent by rotary evaporation under reduced pressure, add 100ml of water to the solid, filter, and dissolve the filter cake with dichloromethane Afterwards, it was separated and purified by silica gel chromatography, and the eluent was chloroform. After vacuum drying, dark blue bis(2-(2-butoxyethoxy)ethoxysilylphthalocyanine was obtained with a yield of 21.2%.
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