{"title":"用于乌尔曼交叉偶联反应的高活性Pandanus纳米纤维素负载聚偕胺肟铜(II)配合物","authors":"C. Fui, Md. Hafizur Rahman, T. Ting, M. Sarjadi","doi":"10.3390/eccs2020-07530","DOIUrl":null,"url":null,"abstract":": The transition metal-catalyzed chemical transformation of organic electrophiles, and organometallic reagents have turned up as an exceedingly robust synthetic tool. The evolution of transition metal catalysts has attained a stage of civilization that authorizes for an extensive scope of chemical bonds formation partners to be combined efficiently. The applications of Cu-based nanoparticles have received great attention owing to the earth-abundant, low toxicity and inexpensive. Due to these characteristics, copper nanoparticles have generated a great deal of interest especially in the field of catalysis. In this study, poly(acrylonitrile) was synthesized by undergoes free-radical initiation process and followed by Beckmann rearrangement with hydroxylamine solution converted into the poly(amidoxime) ligand and anchored the copper onto poly(amidoxime). Cu(II)@PAM was characterized using different techniques such as FTIR, FESEM, EDX, TEM, TGA, DSC, ICP-OES, and XPS analyses. The Cu(II)@PAM showed high stability and high catalytic activity in a wide variety of electrophilic substituted phenols with substituted aryl/benzyl halides. 0.15 mol%, ±3 mg of Cu(II)@PAM could efficiently promote Ullmann reaction to give the corresponding coupling product up to 99 % yields. The complex was easy separated and recovered from the reaction mixture by simple filtration.","PeriodicalId":151361,"journal":{"name":"Proceedings of 1st International Electronic Conference on Catalysis Sciences","volume":"49 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly Active Pandanus Nanocellulose-Supported Poly(amidoxime) Copper (II) Complex for Ullmann Cross-Coupling Reaction\",\"authors\":\"C. Fui, Md. Hafizur Rahman, T. Ting, M. Sarjadi\",\"doi\":\"10.3390/eccs2020-07530\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": The transition metal-catalyzed chemical transformation of organic electrophiles, and organometallic reagents have turned up as an exceedingly robust synthetic tool. The evolution of transition metal catalysts has attained a stage of civilization that authorizes for an extensive scope of chemical bonds formation partners to be combined efficiently. The applications of Cu-based nanoparticles have received great attention owing to the earth-abundant, low toxicity and inexpensive. Due to these characteristics, copper nanoparticles have generated a great deal of interest especially in the field of catalysis. In this study, poly(acrylonitrile) was synthesized by undergoes free-radical initiation process and followed by Beckmann rearrangement with hydroxylamine solution converted into the poly(amidoxime) ligand and anchored the copper onto poly(amidoxime). Cu(II)@PAM was characterized using different techniques such as FTIR, FESEM, EDX, TEM, TGA, DSC, ICP-OES, and XPS analyses. The Cu(II)@PAM showed high stability and high catalytic activity in a wide variety of electrophilic substituted phenols with substituted aryl/benzyl halides. 0.15 mol%, ±3 mg of Cu(II)@PAM could efficiently promote Ullmann reaction to give the corresponding coupling product up to 99 % yields. The complex was easy separated and recovered from the reaction mixture by simple filtration.\",\"PeriodicalId\":151361,\"journal\":{\"name\":\"Proceedings of 1st International Electronic Conference on Catalysis Sciences\",\"volume\":\"49 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of 1st International Electronic Conference on Catalysis Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/eccs2020-07530\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of 1st International Electronic Conference on Catalysis Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/eccs2020-07530","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Highly Active Pandanus Nanocellulose-Supported Poly(amidoxime) Copper (II) Complex for Ullmann Cross-Coupling Reaction
: The transition metal-catalyzed chemical transformation of organic electrophiles, and organometallic reagents have turned up as an exceedingly robust synthetic tool. The evolution of transition metal catalysts has attained a stage of civilization that authorizes for an extensive scope of chemical bonds formation partners to be combined efficiently. The applications of Cu-based nanoparticles have received great attention owing to the earth-abundant, low toxicity and inexpensive. Due to these characteristics, copper nanoparticles have generated a great deal of interest especially in the field of catalysis. In this study, poly(acrylonitrile) was synthesized by undergoes free-radical initiation process and followed by Beckmann rearrangement with hydroxylamine solution converted into the poly(amidoxime) ligand and anchored the copper onto poly(amidoxime). Cu(II)@PAM was characterized using different techniques such as FTIR, FESEM, EDX, TEM, TGA, DSC, ICP-OES, and XPS analyses. The Cu(II)@PAM showed high stability and high catalytic activity in a wide variety of electrophilic substituted phenols with substituted aryl/benzyl halides. 0.15 mol%, ±3 mg of Cu(II)@PAM could efficiently promote Ullmann reaction to give the corresponding coupling product up to 99 % yields. The complex was easy separated and recovered from the reaction mixture by simple filtration.