4.3 Article

Comparative enantioseparation of planar chiral ferrocenes on polysaccharide-based chiral stationary phases

期刊

CHIRALITY
卷 34, 期 4, 页码 609-619

出版社

WILEY
DOI: 10.1002/chir.23417

关键词

electrostatic potential; enantioseparation; ferrocenes; planar chirality; polysaccharide-based chiral stationary phases

资金

  1. European Social Fund [BEFPI/2021/073]
  2. Generalitat Valenciana [ACIF/2019/158]
  3. Centre national de la recherche scientifique
  4. University of Strasbourg
  5. Consiglio Nazionale delle Ricerche

向作者/读者索取更多资源

Planar chiral ferrocenes have various applications in synthesis, catalysis, material science, and medicinal chemistry. This study investigated the enantioseparation of ten planar chiral 1,2- and 1,3-disubstituted ferrocenes using polysaccharide-based chiral stationary phases (CSPs) under multimodal elution conditions. Baseline enantioseparations were achieved for nine analytes, demonstrating the potential of polysaccharide-based CSPs for efficient separation of planar chiral ferrocenes.
Planar chiral ferrocenes are well-known compounds that have attracted interest for application in synthesis, catalysis, material science, and medicinal chemistry for several decades. In spite of the fact that asymmetric synthesis procedures for obtaining enantiomerically enriched ferrocenes are available, sometimes, the accessible enantiomeric excess of the chiral products is unsatisfactory. In such cases and for resolution of racemic planar chiral ferrocenes, enantioselective high-performance liquid chromatography (HPLC) on polysaccharide-based chiral stationary phases (CSPs) has been used in quite a few literature articles. However, although moderate/high enantioselectivities have been obtained for planar chiral ferrocenes bearing polar substituents, the enantioseparation of derivatives containing halogens, or exclusively alkyl groups, remains rather challenging. In this study, the enantioseparation of ten planar chiral 1,2- and 1,3-disubstituted ferrocenes was explored by using five polysaccharide-based CSPs under multimodal elution conditions. Baseline enantioseparations were achieved for nine analytes with separation factors (alpha) ranging from 1.20 to 2.92. The presence of pi-extended systems in the analyte structure was shown to impact affinity of the most retained enantiomer toward amylose-based selectors, observing retention times higher than 80 min with methanol-containing mobile phases (MPs). Electrostatic potential (V) analysis and molecular dynamics (MD) simulations were used in order to study interaction modes at the molecular level.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据