标题:Facile TEMPO Immobilization onto Poly(acrylic acid)-Modified Magnetic Nanoparticles: Preparation and Property
作者:Huang, Guohui; Liu, Xiaoxuan; Bei, Yiling; Ma, Huiqing
作者机构:[Huang, Guohui; Liu, Xiaoxuan] Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 510006, Guangdong, Peoples R China.; [Bei, Yiling; Ma, Huiqing] S 更多
通讯作者:Liu, XX;Bei, YL
通讯作者地址:[Liu, XX]Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 510006, Guangdong, Peoples R China;[Bei, YL]Shandong Univ, Sch Chem & Chem Engn, Jinan 25 更多
来源:INTERNATIONAL JOURNAL OF POLYMER SCIENCE
出版年:2017
DOI:10.1155/2017/9621635
摘要:Adding catalysts to magnetic polyvalent supports facilitating catalyst recycling and recovery seems feasible. Polymer-modified magnetic nanocomposites for organocatalyst immobilization are a plausible approach to this technology. Here, we present facile and efficient method for 2,2',6,6'-tetramethylpiperidinyl-1-oxy (TEMPO) immobilization onto polymer-modified magnetic nanoparticles under mild reaction conditions. Poly(acrylic acid) was chosen to graft from magnetic nanoparticle through a simple inverse emulsion polymerization technique. The resulting poly(acrylic acid) magnetic nanocomposite is an ideal material to immobilize the organocatalyst 4-hydroxy-2,2',6,6'-tetramethylpiperidinyl-1-oxy (H-TEMPO) via an esterification reaction with pendant carboxyl group on the polymer chain. Instrumental analysis confirmed that poly(acrylic acid) chain was grafted on the silica-coated magnetic particles by this simple method while maintaining their magnetic properties; elemental analysis indicated that TEMPO was efficiently immobilized onto the polymer chain. The catalysis tests under both Anelli and Minisci system showed that the nanocomposite catalyst exhibits proper selectivity and activity for the alcohol/aldehyde transformation. Recycling experiments showed that stability and reusability of the nanocomposite catalyst were satisfying.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021653712&doi=10.1155%2f2017%2f9621635&partnerID=40&md5=abdaef053e9e51bb5aa9f792e4722825
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