首页> 外文会议>Symposium on Molecularly Imprinted Materials―Sensors and Other Devices, Apr 2-5, 2002, San Francisco, California >Molecularly Imprinted Polymers (MIPs) Against Uracils : Functional Monomer Design, Monomer-Template Interactions In Solution And MIP Performance In Chromatography
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Molecularly Imprinted Polymers (MIPs) Against Uracils : Functional Monomer Design, Monomer-Template Interactions In Solution And MIP Performance In Chromatography

机译:针对尿嘧啶的分子印迹聚合物(MIP):功能性单体设计,溶液中的单体模板相互作用以及色谱中的MIP性能

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摘要

The interaction of N~1-substituted uracils (cyclohexyl (1) and benzyl (2)) with three polymerisable recognition elements, the novel monomers 9-(3/4-vinylbenzyl)adenine (3) and 2, 6-diamino-9-(3/4-vinylbenzyl)purine (4) and the previously synthesised monomer 2, 6-bis(acrylamido)pyridine (5), has been studied via ~1H NMR in deuterio-chloroform solution. MIPs against (2) have been prepared using each of the monomers and tested in the chromatographic mode. The effect of the number and type of hydrogen bonds formed between the templates and the functional monomers is reflected in the values of the apparent association constants obtained from the solution study and by the performance of the subsequently prepared MIPs in the chromatographic mode.
机译:N〜1取代的尿嘧啶(环己基(1)和苄基(2))与三个可聚合识别元件,即新型单体9-(3 / 4-乙烯基苄基)腺嘌呤(3)和2,6-二氨基-9的相互作用-(3 / 4-乙烯基苄基)嘌呤(4)和先前合成的单体2,6-双(丙烯酰胺基)吡啶(5)已在氘代氯仿溶液中通过〜1H NMR进行了研究。已经使用每种单体制备了针对(2)的MIP,并在色谱模式下进行了测试。模板和功能单体之间形成的氢键数量和类型的影响反映在从溶液研究中获得的表观缔合常数的值以及随后制备的MIP在色谱模式下的性能。

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