摘要
以γ-氨丙基三乙氧基硅烷为偶联剂,三聚氯氰为反应物,采用固液表面连续反应法,依次与乙二胺、十二酰氯进行亲核取代反应,制备了一种嵌入三嗪环酰胺极性基团的新型反相色谱固定相,并采用元素分析法进行了表征。用制备的固定相装填色谱柱,以商品化C18色谱柱作为参考,对比考察了碱性化合物的分离情况。结果表明,极性三嗪环酰胺基团被成功地键合到硅胶表面,连续制备3次所得固定相的C、N、H含量的最大相对偏差均小于5%,说明制备工艺重现性良好;用制备的固定相装填的色谱柱分离5种苯胺类、4种吡啶类碱性化合物的选择性好,峰形对称。该结果为进一步推进该新型固定相的商品化提供了参考数据。
A new kind of silica-bonded reserved stationary phase with s-triazine and amide polar groups embedded for HPLC was obtained by step-wise reactions of silica gel with s-triazine,γ-aminopropyltriethoxysilane,ethanediamine and dodecanoyl chloride.The new stationary phase was characterized by elemental analysis.After that,a column packed with the new stationary phase was used to separate basic compounds.A commercial C18 column was also tested under the same chromatographic conditions for comparison.The results indicated that the ligand was successfully bonded to the surface of the silica and the maximum relative deviations of element contents were within 5% for carbon,nitrogen and hydrogen by three times.Furthermore,in the separation of five basic anilines and four basic pyridines,the excellent selectivity and symmetrical peak shapes provided a reference for advancing the commercialization of the new stationary phase.
出处
《色谱》
CAS
CSCD
北大核心
2013年第11期1035-1039,共5页
Chinese Journal of Chromatography
基金
国家重大科学仪器设备开发专项项目(2012YQ12004401
2012YQ12004403)
国家自然科学基金项目(51242001)
关键词
液相色谱固定相
三嗪环酰胺
制备
应用
碱性化合物
stationary phase for liquid chromatography
s-triazine and amide
preparation
application