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Enantioseparation Using Cellulose Tris(35-dimethylphenylcarbamate) as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose

机译:使用纤维素三(35-二甲基苯基氨基甲酸酯)手性固定相进行HPLC的对映体分离:纤维素分子量的影响

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摘要

The cellulose oligomers with different degrees of polymerization (DP), 7, 11, 18, 24, 26, 40 and 52, were prepared by hydrolysis of microcrystalline cellulose with phosphoric acid. These oligomers including the starting microcrystalline cellulose (DP 124) were converted to tris(3,5-dimethylphenylcarbamate) (CDMPC) derivatives by the reaction with an excess of 3,5-dimethylphenyl isocyanate to be used as the chiral stationary phase (CSP) in high-performance liquid chromatography (HPLC). The structures of the CDMPC derivatives were investigated by infrared spectroscopy (IR), 1H-NMR, circular dichroism (CD) and size exclusion chromatography (SEC), and the DPs of the derivatives estimated by SEC agreed with those estimated by 1H-NMR. After coating the derivatives on silica gel, their chiral recognition abilities were evaluated using eight racemates under a normal phase condition with a hexane-2-propanol (99/1) mixture as an eluent. The chiral recognition abilities of 7- and 11-mers, particularly the former, were lower than those of the higher oligomers from DP 18 to 52, which had rather similar abilities to that of 124-mer, although the abilities depended on the racemates. DP 18 seems to be sufficient for CDMPC to exhibit chiral recognition similar to that of the CDMPC with larger DPs.
机译:通过用磷酸水解微晶纤维素来制备具有不同聚合度(DP)7、11、18、24、26、40和52的纤维素低聚物。通过与过量的3,5-二甲基苯基异氰酸酯反应,将包括起始微晶纤维素(DP 124)在内的这些低聚物转化为三(3,5-二甲基苯基氨基甲酸酯)(CDMPC)衍生物,用作手性固定相(CSP)在高效液相色谱(HPLC)中进行分析。用红外光谱(IR), 1 H-NMR,圆二色性(CD)和尺寸排阻色谱法(SEC)研究了CDMPC衍生物的结构,并通过SEC估算了衍生物的DP。用 1 H-NMR估算的那些将衍生物包被在硅胶上后,使用八种外消旋体在正相条件下,使用己烷-2-丙醇(99/1)混合物作为洗脱液,评估其手性识别能力。 7聚体和11聚体的手性识别能力,特别是前者,比DP 18至52的高级低聚体的手性识别能力低,后者的能力与124聚体的手性相当,尽管该能力取决于外消旋体。 DP 18似乎足以使CDMPC表现出与较大DPs相似的手性识别能力。

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