• Issue

    Chirality: Volume 37, Issue 8

    August 2025

ISSUE INFORMATION

Free Access

Issue Information

  • First Published: 17 July 2025

RESEARCH ARTICLE

Chiral Post-Modification of UiO-66-NH2 on Gas Chromatography Chiral Separation

  • First Published: 17 July 2025
Chiral Post-Modification of UiO-66-NH2 on Gas Chromatography Chiral Separation

A particular type of zirconium metal–organic framework (MOF) called chiral UiO-66 was created to serve as a stationary phase in gas chromatography. It successfully achieved high-resolution separation of enantiomers, such as linalool and α-pinene, as well as positional isomers. This MOFs is effective for chiral analysis in the chemical and pharmaceutical industries.

Chiral Separation and Molecular Simulation of Five Quinolones on a Bonded Amylose[(S)-α-Methylbenzyl Carbamate] Column (CHIRALPAK IH) and the Elucidation of Its Recognition Mechanism

  • First Published: 17 July 2025
Chiral Separation and Molecular Simulation of Five Quinolones on a Bonded Amylose[(S)-α-Methylbenzyl Carbamate] Column (CHIRALPAK IH) and the Elucidation of Its Recognition Mechanism

This study revealed that hydrogen bonding, π–π stacking, and hydrophobic interactions are the key interacting forces driving the enantioseparation.

Variations in the Optical Activity of L-Arginine in Electrolyte and Nonelectrolyte Solutions

  • First Published: 22 July 2025
Variations in the Optical Activity of L-Arginine in Electrolyte and Nonelectrolyte Solutions

The specific rotation of L-arginine depends on the solution that the amino acid is dissolved in. The variations in the optical activity arise from changes in the zwitterionic structure upon protonation and/or complex formation with a metal cation.