Waters Corporation, 34 Maple Street, Milford, Massachusetts 01757-3696.
Anal Chem. 1999 Aug 1;71(15):2992-7. doi: 10.1021/ac9900331.
A series of HPLC bonded phases containing an internal carbamate group were studied by changing the terminal N-alkyl group from C(8)H(17) to C(18)H(37) in increments of two methylene units, i.e., C(8), C(10), C(12), C(14), C(16), and C(18). Each material was prepared via bonding of silica with the respective 3-(chlorodimethylsilyl)propyl N-alkylcarbamate silane. The materials were compared under reversed-phase conditions using a test mixture of nonpolar, polar, and basic compounds in a 65:35 (v/v) methanol/20 mM KH(2)PO(4)/K(2)HPO(4), pH 7, mobile phase. Retention factors were found to generally increase from the C(8) length to the C(12)-C(16) lengths but decreased for the C(18) length. Retention factors were also measured as a function of three ligand surface concentrations for the C(12), C(14), and C(18) materials. In this study, retention generally decreased with increasing surface concentration, especially for the C(18) chain length. Changes in particle surface area and porosity caused by bonding did not fully account for the observed changes in retention factors. Peak shapes for the basic analytes propranolol and amitriptyline were also studied as a function of N-alkylcarbamate chain length and surface concentration. Tailing factors were unaffected by chain length and only weakly dependent on surface concentration. By comparison, tailing factors decreased significantly as surface concentration increased for a set of conventional C(18) alkyl packings.
一系列含有内脂基的 HPLC 键合相,通过改变末端 N-烷基从 C(8)H(17)到 C(18)H(37),每次增加两个亚甲基单元,即 C(8)、C(10)、C(12)、C(14)、C(16)和 C(18)进行研究。每种材料都是通过与相应的 3-(氯二甲基硅基)丙基 N-烷基氨甲酸酯硅烷键合硅胶来制备的。在反相条件下,使用非极性、极性和碱性化合物的混合物在 65:35(v/v)甲醇/20 mM KH(2)PO(4)/K(2)HPO(4),pH 7 的流动相下进行了比较。保留因子通常从 C(8)长度增加到 C(12)-C(16)长度,但对于 C(18)长度则减少。还测量了保留因子作为 C(12)、C(14)和 C(18)材料的三个配体表面浓度的函数。在这项研究中,保留因子通常随表面浓度的增加而降低,特别是对于 C(18)链长。键合引起的颗粒表面积和孔隙率的变化不能完全解释观察到的保留因子的变化。作为 N-烷基氨甲酸酯链长和表面浓度的函数,还研究了碱性分析物普萘洛尔和阿米替林的峰形。拖尾因子不受链长的影响,仅受表面浓度的弱影响。相比之下,对于一组常规的 C(18)烷基填料,拖尾因子随着表面浓度的增加而显著降低。