A kind of porphyrinated polystyrene elastomer and its preparation method and application
A technology of polystyrene and elastomer, which is applied in the field of organic photoelectric conversion materials, can solve the problems of serious pollution, high energy consumption in the preparation process, and high cost of inorganic photoelectric materials, and achieve the effects of wide sources, low cost, and easy processing and molding
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[0048] Preparation of the organic photoelectric material of the present invention:
[0049] (1) Para-chloromethylation of benzene ring
[0050] The polystyrene elastomer is dissolved in chloroform solvent, and 1,4-dichloromethoxybutane is used as chloromethylation reagent. Under the catalysis of tin tetrachloride, the reaction is carried out in an ice-water bath for several hours to obtain chloromethyl. Alkylated polystyrene elastomer. The grafting rate of chloromethyl group increases with the prolongation of reaction time, and different chloromethyl grafting rates can be obtained by controlling different reaction times.
[0051] (2) Para-formylation of benzene ring
[0052] The chloromethylated polystyrene elastomer was dissolved in xylene solvent, DMSO was used as a mild oxidant, potassium iodide and sodium bicarbonate were added, and the reaction was carried out at 110 °C for 6 h to obtain the aldehyde-based polystyrene elastomer. The addition amount of the aldehyde-ylat...
Embodiment 1
[0055] Example 1 Organic optoelectronic material of the present invention
[0056] 1. Preparation of organic optoelectronic materials PPSEBS
[0057]
[0058] (1) CMSEBS was prepared by the para-chloromethylation of the benzene ring of SEBS
[0059]Dissolve 5.0 g of hydrogenated styrene butadiene block copolymer (SEBS) (molecular weight of 50,000) in 250 ml of chloroform solvent, and use 20 ml of 1,4-dichloromethoxybutane as the chloromethylation reagent. Under the catalysis of 4 ml of tin tetrachloride, in an ice-water bath for 2 h, the reaction obtains chloromethylated SEBS, which is recorded as CMSEBS.
[0060] (2) ALSEBS was prepared by the para-formylation of benzene ring
[0061] Dissolve 3.0 g of CMSEBS in 150 ml of xylene solvent, use 50 ml of DMSO as a mild oxidant, add 2.0 g of potassium iodide and 1.5 g of sodium bicarbonate, and react at 110 °C for 6 h to obtain aldehyde-based SEBS, denoted as ALSEBS.
[0062] (3) Porphyrination to prepare PPSEBS
[0063] Di...
Embodiment 2
[0078] Example 2 Organic optoelectronic material of the present invention
[0079] 1. Preparation of organic optoelectronic materials PPSEBS
[0080] (1) CMSEBS was prepared by the para-chloromethylation of the benzene ring of SEBS
[0081] Dissolve 5.0 g of hydrogenated styrene butadiene block copolymer (SEBS) (molecular weight of 50,000) in 250 ml of chloroform solvent, and use 20 ml of 1,4-dichloromethoxybutane as the chloromethylation reagent. Under the catalysis of 4 ml of tin tetrachloride, in an ice-water bath for 5 hours, the reaction obtains chloromethylated SEBS, which is recorded as CMSEBS.
[0082] (2) ALSEBS was prepared by the para-formylation of benzene ring
[0083] Dissolve 3.0g CMSEBS in 150ml xylene solvent, use 50ml DMSO as a mild oxidant, add 2.0g potassium iodide and 1.5g sodium bicarbonate, and react at 110°C for 6h to obtain aldehyde-based SEBS, denoted as ALSEBS.
[0084] (3) Porphyrination to prepare PPSEBS
[0085] Dissolve 1.0g ALSEBS in 100ml x...
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