A. M. Garamanov, R. A. Akhmedova, B. Mamedov, A. F. Mamedova, N. Gusiev, M. Gurbanov
{"title":"n -烯丙基- n -(β-氯)烯丙基乙酸的合成与聚合","authors":"A. M. Garamanov, R. A. Akhmedova, B. Mamedov, A. F. Mamedova, N. Gusiev, M. Gurbanov","doi":"10.32737/2221-8688-2021-4-250-255","DOIUrl":null,"url":null,"abstract":"The interaction of 1 mol aminoethane acid with 1 mol of allyl chloride and 1 mol of (β-chlor)allyl chloride in an aqueous solution of sodium hydroxide (pH12) leads to the synthesis of the new monomer – N-allyl-N(β-chlor)allylethanic acid (AEA) with a yield of 50%. During polymerization of AEC (T=60-70) in aqueous solution in the presence of ammonium persulfate (PA) initiator with a concentration of 4x10-4- 5x10-3 mol/L, water-soluble polymers with rather high values of reduced viscosity ([ηprid] = 0.18-0.20 dl/g) for the above mentioned amine were obtained. It was established that the polymerization proceeded on the double bonds of diallyl groups according to the cycle-linear mechanism with pyrrolidine stucture.","PeriodicalId":10015,"journal":{"name":"Chemical Problems","volume":"149 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"SYNTHESIS AND POLYMERIZATION OF N-ALLYL-N-(β-CHLOR)ALLYL ETHANIC ACID\",\"authors\":\"A. M. Garamanov, R. A. Akhmedova, B. Mamedov, A. F. Mamedova, N. Gusiev, M. Gurbanov\",\"doi\":\"10.32737/2221-8688-2021-4-250-255\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The interaction of 1 mol aminoethane acid with 1 mol of allyl chloride and 1 mol of (β-chlor)allyl chloride in an aqueous solution of sodium hydroxide (pH12) leads to the synthesis of the new monomer – N-allyl-N(β-chlor)allylethanic acid (AEA) with a yield of 50%. During polymerization of AEC (T=60-70) in aqueous solution in the presence of ammonium persulfate (PA) initiator with a concentration of 4x10-4- 5x10-3 mol/L, water-soluble polymers with rather high values of reduced viscosity ([ηprid] = 0.18-0.20 dl/g) for the above mentioned amine were obtained. It was established that the polymerization proceeded on the double bonds of diallyl groups according to the cycle-linear mechanism with pyrrolidine stucture.\",\"PeriodicalId\":10015,\"journal\":{\"name\":\"Chemical Problems\",\"volume\":\"149 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Problems\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32737/2221-8688-2021-4-250-255\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Problems","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32737/2221-8688-2021-4-250-255","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
SYNTHESIS AND POLYMERIZATION OF N-ALLYL-N-(β-CHLOR)ALLYL ETHANIC ACID
The interaction of 1 mol aminoethane acid with 1 mol of allyl chloride and 1 mol of (β-chlor)allyl chloride in an aqueous solution of sodium hydroxide (pH12) leads to the synthesis of the new monomer – N-allyl-N(β-chlor)allylethanic acid (AEA) with a yield of 50%. During polymerization of AEC (T=60-70) in aqueous solution in the presence of ammonium persulfate (PA) initiator with a concentration of 4x10-4- 5x10-3 mol/L, water-soluble polymers with rather high values of reduced viscosity ([ηprid] = 0.18-0.20 dl/g) for the above mentioned amine were obtained. It was established that the polymerization proceeded on the double bonds of diallyl groups according to the cycle-linear mechanism with pyrrolidine stucture.