金丝桃素
点击化学
分子印迹聚合物
聚合
单体
聚合物
分子印迹
高分子化学
材料科学
炔烃
化学
选择性
有机化学
催化作用
医学
药理学
作者
Yuxin Pei,Fengfeng Fan,Xinxin Wang,Weiwei Feng,Yong Hou,Zhichao Pei
出处
期刊:Polymers
[MDPI AG]
日期:2017-09-24
卷期号:9 (10): 469-469
被引量:10
摘要
To fabricate molecularly imprinted polymer nanospheres via click reaction, five different clickable compounds were synthesized and two types of click reactions (azide-alkyne and thiol-yne) were explored. It was found that molecularly imprinted polymer nanospheres could be successfully synthesized via thiol-yne click reaction using 3,5-diethynyl-pyridine (1) as the monomer, tris(3-mercaptopropionate) (tri-thiol, 5) as the crosslinker, and hypericin as the template (MIP⁻NSHs). The click polymerization completed in merely 4 h to produce the desired MIP⁻NSHs, which were characterized by FTIR, SEM, DLS, and BET, respectively. The reaction conditions for adsorption capacity and selectivity towards hypericin were optimized, and the MIP⁻NSHs synthesized under the optimized conditions showed a high adsorption capacity (Q = 6.03 μmol•g-1) towards hypericin. The imprinting factors of MIP⁻NSHs towards hypericin, protohypericin, and emodin were 2.44, 2.88, and 2.10, respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI