Univ. Lille, CHU Lille, Inserm, Institut Pasteur de Lille, U1167 - Risk factors and molecular determinants of aging-related diseases, F-59000 Lille, France.
Oril industrie-Servier, 13 rue A. Desgenetais, F-76210 Bolbec, France.
J Chromatogr A. 2022 Aug 16;1677:463306. doi: 10.1016/j.chroma.2022.463306. Epub 2022 Jul 3.
Capillary electrokinetic chromatography (CEKC) and liquid chromatography (LC) methods were explored for the enantiomeric separation of six unsymmetrically disubstituted ferrocene derivatives. In normal-phase mode liquid chromatography, the use of n-heptane, ethanol or isopropanol with 1% n-butylamine as mobile phase on six polysaccharide-based columns, allowed to fully separate the enantiomers of three compounds out of the six (i.e 7-chloro-N-(2-((dimethylamino)methyl)ferrocenyl)quinolin-4-amine (ferroquine) (compound 1), 1-[(1S)-(1-Aminoethyl)]-2-(diphenylphosphino)ferrocene (compound 5) and 1-[(1R)-1-(Dicyclohexylphosphino)ethyl]-2-(diphenylphosphino)ferrocene (compound 6). Among the columns used, the Lux i-Cellulose-5 was the most effective. In capillary electrokinetic chromatography, a phosphate buffer of 25 mM concentration and pH equal to 2.5 was chosen as background electrolyte, leading to cationic ferrocene derivatives. The addition of neutral cyclodextrins was undertaken first and native β- or γ-cyclodextrins were found to resolve the enantiomers of two derivatives. Then, 15 mM of anionic cyclodextrins were added to the background electrolyte. The use of SBE-β-CD, S-β-CD or S-γ-CD have allowed the separation of the enantiomers for most of the ferrocene derivatives studied with high resolution values in short migration time. For instance, for 1-(R)-2-(Diphenylphosphino)ethyldi-tert-butylphosphine ferrocene (compound 2), the migration times were less than 2 minutes and the resolution value was equal to 3.52 in short-end mode with 15 mM S-β-CD, at 25 kV and 25°C. Finally, a dual cyclodextrins system was tested using 15 mM of S-β-CD plus 15 mM HP-γ-CD in the phosphate buffer. This system allowed the improved separation of two ferrocene derivatives with an unusual resolution value equal to 41.5 in long-end mode. Overall, CEKC showed better enantioseparating power of the six chiral ferrocenes studied than liquid chromatography.
毛细管电泳(CEKC)和液相色谱(LC)方法被探索用于分离六种不对称取代的二茂铁衍生物的对映异构体。在正相液相色谱中,使用正庚烷、乙醇或异丙醇与 1%正丁胺作为流动相,在六种基于多糖的柱上,可以完全分离出六种化合物中的三种(即 7-氯-N-(2-(二甲氨基)甲基)二茂铁基)喹啉-4-胺(ferroquine)(化合物 1)、1-[(1S)-(1-氨基乙基)]-2-(二苯基膦基)二茂铁(化合物 5)和 1-[(1R)-1-(二环己基膦基)乙基]-2-(二苯基膦基)二茂铁(化合物 6)的对映异构体。在所使用的柱中,Lux i-Cellulose-5 最为有效。在毛细管电泳中,选择 25 mM 浓度和 pH 值为 2.5 的磷酸盐缓冲液作为背景电解质,导致阳离子二茂铁衍生物。首先加入中性环糊精,发现天然β-或γ-环糊精可拆分两种衍生物的对映异构体。然后,在背景电解质中加入 15 mM 的阴离子环糊精。使用 SBE-β-CD、S-β-CD 或 S-γ-CD 允许分离大多数研究的二茂铁衍生物的对映异构体,在短迁移时间内具有高分辨率值。例如,对于 1-(R)-2-(二苯基膦基)乙基二-叔丁基膦二茂铁(化合物 2),在短端模式下,使用 15 mM 的 S-β-CD、在 25 kV 和 25°C 下,迁移时间小于 2 分钟,分辨率值为 3.52。最后,使用磷酸盐缓冲液中的 15 mM S-β-CD 加 15 mM HP-γ-CD 测试了双环糊精体系。该体系允许改进对两种具有异常分辨率值 41.5 的二茂铁衍生物的分离。总体而言,CEKC 对六种研究的手性二茂铁的对映体分离能力优于液相色谱。