## Abstract The 4‐__tert__‐butylphenylcarbamates of cellulose and amylose bearing a small amount of 3‐(triethoxysilyl)propyl residues were synthesized by a one‐pot process and efficiently immobilized onto a silica gel through intermolecular polycondensation of the triethoxysilyl groups. The obtaine
Preparation and chiral recognition in HPLC of cellulose 3,5-dichlorophenylcarbamates immobilized onto silica gel
✍ Scribed by Hai-tao Qu; Jun-qing Li; Guang-shun Wu; Jun Shen; Xian-de Shen; Yoshio Okamoto
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 176 KB
- Volume
- 34
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
Abstract
The 3,5‐dichlorophenylcarbamates (2) of cellulose bearing a small amount of 3‐(triethoxysilyl)propyl residues were synthesized by a one‐pot process and immobilized onto a silica gel through intermolecular polycondensation of the triethoxysilyl groups. The obtained cellulose derivatives were characterized by ^1^H NMR and elemental analysis (EA), and their recognition abilities were evaluated by high‐performance liquid chromatography (HPLC). The cellulose derivatives containing about 1–5% of the 3‐(triethoxysilyl)propyl residue were efficiently immobilized with a high chiral recognition ability. The immobilized chiral packing materials (CPMs) could be used with the eluents containing chloroform and tetrahydrofuran (THF), which cannot be used with the conventional coated‐type chiral packing materials. By using these eluents, the chiral recognition for many racemates was improved.
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