Category: CHROMATOGRAPHY

[NEW] E. Kanao, T. Kubo, K. Otsuka, Bull. Chem. Soc. Jpn. 2020, 93, 482-489: Carbon-Based Nanomaterials for Separation Media.

[NEW] E. Kanao, T. Kubo, K. Otsuka et al., Chem. Sci. 2020, 11, 409-418: Separation of halogenated benzenes enabled by investigation of halogen–π interactions with carbon materials.

T. Shibata, K. Ueda, Cellulose Commun., 2012, 19 (4), 171-175: Molecular Recognition of Polysaccharide Derivetives.

T. Shibata, Kobunsi, 2010, 59 (6), 1-2: Polysaccharide as Chiral Stationary Phase.

L. S. Birchall et al., Chem. Sci. 2011, 2, 1349-1355: Exploiting CH/pi interactions in supramolecular hydrogels of aromatic carbohydrate amphiphiles.

H. Kawaki, Chem. Pharm. Bull. 2008, 56, 323-327: Properties of the Solute-Stationary Liquid Interactions in Gas Liquid Chromatography.

T. Ueno et al., Carbohydr. Res. 2007, 342, 954-960: Conformational changes in in single carboxymethylcellulose chains on a highly oriented pyrolitic graphite surface under different salt conditions.

S. Yokota et al., Carbohydr. Res. 2007, 342, 2593-2598: Molecular imaging of single cellulose chains aligned on a highly oriented pyrolytic graphite surface.

C. Roussel et al., Biomed. Chromatogr. (Special Issue: Chiral separations) 2005, 19, 434-438: Enantiorecognition on solid chiral selectors using microbatch technology: an example of limitation in case of strong association in the racemate.

M. TakafujI et al., J. Chromatogr. A 2005, 1074, 223-228: Dioctadecyl L-glutamide-derived lipid-grafted silica as a novel organic stationary phase for RP-HPLC.

C. Roussel et al., J. Chromatogr. A 2004, 1037, 311-328: Chiral liquid chromatography contribution to the determination of the absolute configuration of enantiomers. [Review]

Y. Goto et al., Chromatographia 2002, 56, 19-23.

Y. Abe et al., Chem. Pharm. Bull. 1996, 44, 1250-1251: Enantioselective distribution behavior of DL-pindolol in a liquid-liquid two-phase system containing optically active diol and boric acid.

Y. Sasaki et al., Chem. Pharm. Bull. 1990, 38, 721-723: On the solute-stationary phase interaction in gas-liquid chromatography. Evaluation on the relative retention values for mono- and polyalkyl-substituted benzene derivatives.

T. Endo et al., Chem. Commun. 1983, 1430-1432: Gas-liquid partition chromatographic evidence that alkyl-phenyl interactions are specific for the shape of the alkyl group.