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Amylose tris(3,5-dimethylphenylcarbamate) (ADMPC) coated on a kind of small particle silica gel was prepared. On this ADMPC chiral stationary phase (CSP), the direct enantiomeric separation of six novel chiral transition metal tetrahedral clusters has firstly been achieved using n-hexane as the mobile phase containing various alcohols as modifiers. The effect of mobile phase modifiers and the structural variation of the solutes on their retention factors (k‘) and resolutions (Rs) were investigated. The result suggests that not only the structure and concentration of alcohol in mobile phase, but also the structural differences in racemates can have a pronounced effect on enantiomeric separation. ADMPC-CSP is a suitable CSP for the optical resolution of chiral tetrahedral cluster by HPLC. 相似文献
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In the present work, an amylose tris(3,5-dimethylphenylcarbamate) (ADMPC) chiral stationary phase (CSP) was prepared by coating ADMPC on small-particle silica gel. This ADMPC-CSP was for the first time successfully applied to separate a series of novel chiral metal tetrahedrane-type clusters. Furthermore, the influence of a mobile-phase modifier (various alcohols added in the mobile phase), including its concentration and structure, and the structures of the clusters on the chiral separation and retention was investigated. The results suggest that not only the structure and concentration of alcohol in the mobile phase, but also the subtle structural differences in racemate can have a pronounced effect on the enantiomeric separation and retention. 相似文献
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用两种相似多糖类手性固定相拆分阿托品外消旋对映体的比较 总被引:1,自引:0,他引:1
分别涂敷纤维素-三(3,5-二甲基苯基氨基甲酸酯)(CDMPC)与直链淀粉-三(3,5-二甲基苯基氰基甲酸酯)(ADMPC)于自制的球形氨丙基硅胶上,制备了两种多糖类手性崮定相。用高效液相色谱法(HPLC)在正相条件下,用两种固定相直接拆分了阿托品(atmpine)外消旋体、在正己烷中加入了不同的醇类改性剂对阿托品进行拆分,并优化了流动相中醇类改性剂的比例:结果发现,阿托品在CDMPC固定相上可以得到基线拆分,而在ADMPC固定相上只能得到部分拆分。 相似文献
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A series of novel chiral triazole compounds were synthesized. They were separated into enantiomers by liquid chromatography on an amylose tris(3,5-dimethylphenylcarbamate) (ADMPC) chiral stationary phase (CSP). The absolute configuration of each enantiomer of the investigated compounds was established by combined use of chemical correlation, chiral HPLC and circular dichroism (CD) spectra analysis methods. The influence of the mobile-phase modifiers and the structure of chiral triazole compounds on the chiral separation and retention were investigated. Reversal of the elution order of some enantiomeric pairs upon using different mobile-phase modifier was observed. The temperature effect on the chiral separation and the thermodynamic properties including enthalpy and entropy change of binding to the ADMPC-CSP were also investigated. 相似文献
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选用不同的醇改性剂,在自制的直链淀粉-三(3,5-二甲基苯基氨基甲酸酯)(ADMPC)手性固定相上,对2种吲哚环衍生物对映体进行了手性拆分研究,并考察了样品的保留时间和立体选择性. 相似文献
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流动相组成对外消旋阿苯达唑亚砜对映体拆分的影响 总被引:2,自引:0,他引:2
涂敷直链淀粉-三(3,5-二甲基苯基氨基甲酸酯)(ADMPC)于自制的球形氨丙基硅胶上,制备了一种手性固定相。采用高效液相色谱法(HPLC),在正相条件下用该固定相直接拆分了广谱驱虫药物阿苯达唑的代谢产物阿苯达唑亚砜(albendazole sulfoxide, ABZSO)的外消旋对映体。系统地选用了多种二元及三元流动相体系对样品进行拆分,结果表明,流动相中不同种类的醇改性剂及其含量的不同对样品的保留时间和立体选择性有不同程度的影响,甲醇、乙醇等作改性剂用于拆分样品的效果较好;采用三元流动相体系正己烷- 相似文献
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流动相对百树菊酯高效液相色谱手性分离的影响 总被引:6,自引:0,他引:6
在一种由N-3,5二硝基苯甲酸苯基甘氨酸衍生而成的Pirkle1-A型手性固定相上分离百树菊酯的8个立体异构体,通过选用不同的醇作为流动相的强溶剂,研究二元体系中流动相组分对保留值和选择性的影响。结果表明:对同一种组分的流动相,增加流动相的强度会缩短溶质的保留时间,且对非对映体的选择性影响比较大,而对对映体的选择性影响却不大,作为强溶剂的醇的结构不同会对异构体的分高度及峰形产生影响,二级醇或三级醇作强溶剂时的分高度好于一级醇,小分子醇作强溶剂时的峰形好于较大分子醇。 相似文献
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将纤维素-三(3,5-二甲基苯基氨基甲酸酯)(CDMPC)涂敷于自制的球形氨丙基硅胶上,制备成了纤维素-三(3,5-二甲基苯基氨基甲酸酯)手性固定相(CDMPC-CSP)。利用正相高效液相色谱,在该固定相上对新合成的4种吲哚类衍生物对映体进行了手性拆分。通过选择不同结构和浓度的醇类改性剂,优化了色谱分离条件,同时探讨了醇的结构和浓度对于对映体拆分和保留的影响。结果表明,适合Ⅱ~Ⅳ号样品拆分的醇类改性剂分别为正丁醇、乙醇和乙醇,而适合Ⅰ号样品的醇类改性剂为乙醇和正丙醇组成的混合体系。在优化的各流动相体系下,4种吲哚类衍生物的对映体都得到了很好的分离。在此基础上计算了它们的对映体过量值(e.e.值)。实验结果令人满意,表明高效液相色谱手性固定相法是拆分这类化合物的一种理想方法。 相似文献
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手性配位体交换流动相添加剂法拆分对映体 总被引:7,自引:0,他引:7
综述了手性配合基交换色谱法通常采用三种手性相系统中的流动相添加剂方法。主要内容有:(A)手性配合基交换机制,给出了描述对映体对在色谱系统中的保留时间和分离选择性的公式,包括手性选择剂在固定相和流动相中的各种不同情况。公式表明整个色谱往系统的对映体选择性不同于溶液中所存在的选择剂与被选择物作用的情况;(B)影响配合交换的参数,讨论了金属离子、金属离子/配位体比率、金属离子络合物浓度、固定相、流动相pH、洗脱顺序、有机调节剂、离子对试剂、流动相离子强度、温度、立体选择性和手性交互识别;(C)应用。 相似文献
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用大环抗生素替考拉宁手性固定相(TE CSP)分别与3,5-二甲基苯基异氰酸酯和苯基异氰酸酯反应得到了两种新型的高效液相色谱手性固定相----3,5-二甲基苯基异氰酸酯替考拉宁手性固定相(DMP-TE CSP)和苯基异氰酸酯替考拉宁手性固定相(Ph-TE CSP)。用十八个手性化合物在反相及极性流动相模式对这两种CSP的对映体分离能力进行了评价和比较。在反相流动相中,十二个化合物(包括八个氨基酸和四个非氨基酸化合物----对羟基苯甘氨酸,拉米夫定,醇酸和去甲羟安定)的对映体在这两种手性固定相上都获得了分离,大部分的溶质在DMP-TE上获得了更强的保留和稍好的手性分离效果。在极性流动相中,六个氨基醇类化合物在DMP-TE上获得了更强的保留,但它们在两种CSP上的选择因子几乎没有区别。对自制的替考拉宁衍生物手性固定相进行评价和比较,将有助于大环糖肽类抗生素手性固定相手性识别机理的研究。 相似文献
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HPLC enantiomeric separations of 8 α‐amino acids were achieved using two self‐made chiral stationary phases (CSP)–phenyl isocyanate teicoplanin (Phe‐TE) and 3,5‐dimethylphenyl isocyanate teicoplanin (DMP‐TE), using reversed phase mobile phases. The Phe‐TE or the DMP‐TE CSP was prepared from the TE using derivative agents, phenyl isocyanate or 3,5‐dimethylphenyl isocyanate, respectively. The chromatographic results were given as the retention, selectivity, resolution factor and the enantioselective free energy difference corresponding to the separation of the two enantiomers. The effect of pH, organic modifier type and amount were discussed, and the stereoselectivities for two TE‐based CSPs were compared. The chiral selectivity factor for six α‐amino acids on DMP‐TE is somewhat bigger than that on Phe‐TE CSP under reversed phase (RP) mode. Comparison of the enantiomeric separations using self‐made Phe‐TE and DMP‐TE was conducted to gain a better understanding of the chiral recognition mechanism of the macrocyclic glycopeptide CSP. 相似文献
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S. Ma S. ShenH. Lee M. ErikssonX. Zeng J. XuK. Fandrick N. YeeC. Senanayake N. Grinberg 《Journal of chromatography. A》2009,1216(18):3784-3793
Enantiomeric separation of two aromatic α-substituted alanine esters was achieved on two commercially available polysaccharide-based chiral stationary phases (CSPs): amylose tris(3,5-dimethylphenylcarbamate) (ADMPC) and cellulose tris(3,5-dimethylphenylcarbamate) (CDMPC). The interactions between enantiomeric analytes and the CSPs were investigated using chromatographic methods and vibration circular dichroism (VCD). The two analytes differ on the aromatic portion of the molecules where one analyte has a π-acceptor aromatic ring (1) while the other has a π-donor aromatic ring (2). When an ADMPC CSP was employed, an increase in the polarity of the mobile phase leads to a reversal of the elution order for the two enantiomers of 1. The elution order of compound 2 was not affected by the polarity of the mobile phase. In order to gain an understanding of these phenomena, the enantiomeric separation of 1 and 2 was also performed on the CDMPC CSP. Interestingly, no reversal of elution order was observed upon the chromatographic separation of both pairs of enantiomers of compounds 1 and 2 upon increasing the solvent polarity when a CDMPC CSP was utilized. To understand the underlying mechanism governing these chiral separations, VCD was applied to study the structure of the ADMPC and CDMPC polymers and their conformational behaviors under chromatographic conditions. For the first time the conformations of the side chains of both polymers were revealed based on the VCD spectra along with DFT calculations. Furthermore, the interactions between the two analytes and the two CSPs were directly probed by VCD. By comparing the spectral differences of the two CSPs in the presence of the two analytes, the detailed interactions involving different functional groups associated with the chiral recognition were elucidated and thus explained the unusual reversal of elution order associated with increasing solvent polarity. 相似文献
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Basma Saleh Tongyan Ding Yuwei Wang Xiantong Zheng Rong Liu Limin He 《Molecules (Basel, Switzerland)》2021,26(23)
Closantel is an antiparasitic drug marketed in a racemic form with one chiral center. It is meaningful to develop a method for separating and analyzing the closantel enantiomers. In this work, two enantiomeric separation methods of closantel were explored by normal-phase high-performance liquid chromatography. The influences of the chiral stationary phase (CSP) structure, the mobile phase composition, the nature and proportion of different mobile phase modifiers (alcohols and acids), and the column temperature on the enantiomeric separation of closantel were investigated in detail. The two enantiomers were successfully separated on the novel CSP of isopropyl derivatives of cyclofructan 6 and n-hexane-isopropanol-trifluoroacetic acid (97:3:0.1, v/v/v) as a mobile phase with a resolution (Rs) of about 2.48. The enantiomers were also well separated on the CSP of tris-carbamates of amylose with a higher Rs (about 3.79) when a mixture of n-hexane-isopropanol-trifluoroacetic acid (55:45:0.1, v/v/v) was used as mobile phase. Thus, the proposed separation methods can facilitate molecular pharmacological and biological research on closantel and its enantiomers. 相似文献
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以自制1-萘万古霉素(Na-VAN)为手性固定相(CSP),D-酒石酸(D-Tar)、L-酒石酸二乙酯(L-TADE)、D-酒石酸二乙酯(D-TADE)分别为手性流动相添加剂(CMPA),建立了西那卡塞原料1-(1-萘基)乙胺(化合物1)及西那卡塞中间体(化合物2)的高效液相色谱手性拆分方法。考察了流动相中醇类改性剂、CMPA对对映体分离的影响,初步探讨了手性识别机理。以Na-VAN为CSP,正相模式下,添加不同种类的CMPA,化合物1、化合物2均可获得一定程度的分离,其中以D-TADE为CMPA时,化合物1、化合物2获得最佳分离。结果表明,醇的分子体积、CMPA的立体构型均对手性分离有影响。 相似文献
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脲衍生物型手性固定相拆分噻利洛尔对映体 总被引:4,自引:0,他引:4
用脲衍生物型手性固定相直接拆分了药物对映体噻利洛尔。优化的正相色谱流动相的组成为正己烷/1,2-二氯乙烷/乙醇(77∶21∶2,V/V/V)。实验表明,流动相中乙醇含量的改变对分离度产生了较大的影响;不同极性调节剂的使用表现出了不同的拆分效果。最后讨论了异构体的出峰次序,认为异构体与固定相的手性中心之一的氢键作用力是造成异构体分离的主要因素。 相似文献