Chiral recognition mechanism and enantioseparation conditions of tryptophan enantiomers using ligand exchange chromatography are reported here. The effect of different kinds and concentration of ligands, bivalent copper ion, organic modifier, pH of mobile phase, and temperature on enantioseparation has been evaluated. The results show that the enantioselectivity is strongly affected by the pH a...

A new chromatographic procedure was proposed for the separation of propranolol (PRN) enantiomers based upon enantioselective chiral ligand-exchange chromatography. The separation was carried out on a short C8 column leading to considerably short separation time. L-alanine and Cu2+ were applied as chiral selector and central bivalent complexing ion, respectively. It was found that the kind of co...

Naringenin and eriodictyol are chiral flavanones widely present in citrus fruits and herbal products. Pharmacological interest in the two flavanones is well known. Due to the chiral carbon atom, the compounds always exist in the racemic form. The present study reported a stereospecific HPLC method for the enantioseparation of naringenin and eriodictyol, which was performed on an amylase-based c...

A new chromatographic procedure was proposed for the separation of propranolol (PRN) enantiomers based upon enantioselective chiral ligand-exchange chromatography. The separation was carried out on a short C8 column leading to considerably short separation time. L-alanine and Cu2+ were applied as chiral selector and central bivalent complexing ion, respectively. It was found that the kind of co...

Defect-free one-handed contracted helical tubular ladder polymers with a π-electron-rich cylindrical cavity were synthesized by alkyne benzannulations of the random-coil precursor containing 6,6′-linked-1,1′-spirobiindane-7,7′-diol-based chiral monomer units. The resulting tightly-twisted showed remarkably high enantioseparation abilities toward variety hydrophobic aromatics point, axial, and p...

Fast and reliable separation of enantiomers of chiral nanoparticles requires elimination of all the forces that are independent of the nanoparticle handedness and creation of a sufficiently strong force that either pushes different enantiomers in opposite directions or delays the diffusion of one of them with respect to the other. Here we show how to construct such a completely chiral optical f...

Homochiral metal-organic frameworks with fine-tuned pore sizes/walls and large surface areas are promising porous materials for enantioseparation considering the traditional zeolite molecular sieves have no chirality. Using enantiopure pyridyl-functionalized salen [(N-(4-Pyridylmethyl)-L-leucine·HBr)] as a starting material, we have prepared a noninterpenetrated three-dimensional homochiral met...

We apply matched molecular pair (MMP) analysis to data from ChirBase, which contains literature reports of chromatographic enantioseparations. For the 19 chiral stationary phases we examined, we were able to identify 289 sets of pairs where there is a statistically significant and consistent difference in enantioseparation due to a small chemical change. In many cases these changes highlight en...

Herein is presented a strategy for the enantioseparation of amino acids enantiomers using β-CD functionalized Fe(3)O(4) nanospheres, in which β-CD provides the ability to chirally discriminate amino acids enantiomers, while the Fe(3)O(4) nanoparticles serve as magnetic separators.