Chiral self-recognition, the ability of a molecule to distinguish between a copy and a mirror
copy of itself via intermolecular interactions, is demonstrated for dimers of glycidol …

Photoionization of the chiral molecule glycidol has been investigated in the valence region.
Photoelectron circular dichroism (PECD) curves have been obtained at various photon …

Rotational spectra were recorded in natural abundance for the 13C isotopomers of two
conformers of glycidol. Moments of inertia from the 13C isotopomers were used to calculate …

Catalytic transformation of glycidol while maintaining its epoxide moiety intact is challenging
because the terminal epoxide that interacts with the hydroxyl group via a hydrogen bond is …

Molecular Recognition of Chiral Conformers: A Rotational Study of the Dimers of Glycidol |
Journal of the American Chemical Society ACS ACS Publications C&EN CAS Find my institution …

Chirality recognition in the hydrogen‐bonded glycidol⋅⋅⋅ propylene oxide complex has
been studied by using rotational spectroscopy and ab initio calculations. An extensive …

The noncovalent interactions between glycidol molecules in the CDCl3 solvent have been
studied by means of vibrational absorption (VA), vibrational circular dichroism (VCD), optical …

Supersonic jet FTIR spectra of the OH-stretching bands of glycidol monomers and clusters
are presented. Chiral discrimination leads to marked differences in the absorption patterns …

Rotational constants were determined for 18O-substituted isotopologues of the lower energy
conformer of glycidol, which has an intramolecular inner hydrogen bond from the hydroxyl …

Copolymerization of established epoxide monomers with glycidol (G) is a key reaction to
prepare branched or hyperbranched polyethers. The kinetics of the multibranching anionic …