The direct separation of โค-aminoester enantiomers by HPLC on synthetic chiral stationary phases based on aacidic derivative of trans 1,2-diaminocyclohexane as selector is described. The application of different columns containing the stationary phase with opposite configurations and in the racemic f
HPLC separation of fullerenes on two charge-transfer stationary phases
โ Scribed by Qiong-Wei Yu; Zhi-Guo Shi; Bo Lin; Yan Wu; Yu-Qi Feng
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 533 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1615-9306
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โฆ Synopsis
Abstract
Two chargeโtransfer stationary phases were prepared by immobilizing pโnitrobenzoic acid and naphthyl acetic acid onto silica. The nitrophenyl moiety and the naphthyl moiety were grafted to silica gel through the spacer of aminoalkyl silanes. The HPLC separation of C~60~, C~70~, and higher fullerenes on the new stationary phases was also studied. The influence of mobile phase and column temperature on the separation of C~60~ and C~70~ was examined, respectively. The retentions of C~60~ and C~70~ on the two stationary phases increased with decreasing toluene content in the mobile phase or with increasing column temperature. Higher fullerenes can be separated well using toluene as the mobile phase on the stationary phase of pโnitrobenzoic acidโbonded silica.
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