Hwei Leong Ong, Kristina T. Constantopoulos, M. Ginic-Markovic, S. Clarke
{"title":"用点击化学方法研究了小硅烷和大硅烷在碳纳米管上的附着","authors":"Hwei Leong Ong, Kristina T. Constantopoulos, M. Ginic-Markovic, S. Clarke","doi":"10.36648/2471-9935.5.1.45","DOIUrl":null,"url":null,"abstract":"Multi-walled carbon nanotubes (MWCNTs) and other low molecular weight were functionalized with an alkyne group via an urethane bond in an attempt to attach to various azide-functionalized silanes, including polyhedral oligomeric silesquioxane (POSS), via the Cu (I)-catalysed [3+2] Huisgen cycloaddition “click” reaction. FTIR spectroscopy and NMR analysis were utilized to follow the introduction of the alkyne-and azide-groups onto their respective particles, as well as their consumption in the final POSS-MWCNT nanohybrid product. This approach provides a simple and convenient route to effectively functionalize not just silanes and POSS, but also a wide variety of nanoparticles, onto the surface of CNTs.","PeriodicalId":331662,"journal":{"name":"Polymer Sciences","volume":"48 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Study into the attachment of small and large silanes to carbon nanotube via click chemistry\",\"authors\":\"Hwei Leong Ong, Kristina T. Constantopoulos, M. Ginic-Markovic, S. Clarke\",\"doi\":\"10.36648/2471-9935.5.1.45\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Multi-walled carbon nanotubes (MWCNTs) and other low molecular weight were functionalized with an alkyne group via an urethane bond in an attempt to attach to various azide-functionalized silanes, including polyhedral oligomeric silesquioxane (POSS), via the Cu (I)-catalysed [3+2] Huisgen cycloaddition “click” reaction. FTIR spectroscopy and NMR analysis were utilized to follow the introduction of the alkyne-and azide-groups onto their respective particles, as well as their consumption in the final POSS-MWCNT nanohybrid product. This approach provides a simple and convenient route to effectively functionalize not just silanes and POSS, but also a wide variety of nanoparticles, onto the surface of CNTs.\",\"PeriodicalId\":331662,\"journal\":{\"name\":\"Polymer Sciences\",\"volume\":\"48 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36648/2471-9935.5.1.45\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36648/2471-9935.5.1.45","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Study into the attachment of small and large silanes to carbon nanotube via click chemistry
Multi-walled carbon nanotubes (MWCNTs) and other low molecular weight were functionalized with an alkyne group via an urethane bond in an attempt to attach to various azide-functionalized silanes, including polyhedral oligomeric silesquioxane (POSS), via the Cu (I)-catalysed [3+2] Huisgen cycloaddition “click” reaction. FTIR spectroscopy and NMR analysis were utilized to follow the introduction of the alkyne-and azide-groups onto their respective particles, as well as their consumption in the final POSS-MWCNT nanohybrid product. This approach provides a simple and convenient route to effectively functionalize not just silanes and POSS, but also a wide variety of nanoparticles, onto the surface of CNTs.