Akbay Cevdet, Shamsi Shahab A
Department of Chemistry, Center of Biotechnology and Drug Design, Georgia State University, Atlanta 30303, USA.
Electrophoresis. 2004 Feb;25(4-5):622-34. doi: 10.1002/elps.200305763.
The influence of surfactant hydrocarbon tail on the solute/pseudostationary phase interactions was examined. Four anionic sulfated surfactants with 8-, 9-, 10-, and 11-carbon chains having a polymerizable double bond at the end of the hydrocarbon chain were synthesized and characterized before and after polymerization. The critical micelle concentration (CMC), polarity, and aggregation number of the four sodium alkenyl sulfate (SAIS) surfactants were determined using fluorescence spectroscopy. The partial specific volume of the polymeric SAIS (poly-SAIS) surfactants was estimated by density measurements and capillary electrophoresis (CE) was employed for determination of methylene selectivity as well as for elution window. The CMC of the monomers of SAIS surfactants decrease with increase in chain length and correlated well when fluorescence method was compared to CE. The physicochemical properties (partial specific volume, methylene selectivity, electrophoretic mobility, and elution window) increased with an increase in chain length. However, no direct relationship was found between the aggregation number and the length of hydrophobic tail of poly-SAIS surfactants. These polymeric surfactants were then used as pseudostationary phases in micellar electrokinetic chromatography (MEKC) to study the retention behavior and selectivity factor of 36 benzene derivatives with different chemical characteristics. Although variation in chain length of the polymeric surfactants significantly affects the retention of nonhydrogen bonding (NHB) benzene derivatives, these effects were less pronounced for hydrogen bond acceptor (HBA) and hydrogen bond donor (HBD) benzene derivatives. Therefore, hydrophobicity of poly-SAIS surfactants was found to be a major driving force for retention of NHB derivatives. However, for several benzene derivatives (NHB, HBA, and HBD) significantly higher selectivity factor was observed with longest chain polymeric surfactant (e.g., poly(sodium 10-undecenyl sulfate), poly-SUS) compared to shorter chain polymeric surfactant (e.g., poly(sodium 7-octenyl sulfate), poly-SOcS). In addition, the effect of the surfactant hydrophobic chain was also found to have some impact on migration order of NHB, HBA, and HBD benzene derivatives.
研究了表面活性剂碳氢链对溶质/准固定相相互作用的影响。合成了四种碳链长度分别为8、9、10和11个碳原子且在碳氢链末端带有可聚合双键的阴离子硫酸化表面活性剂,并对其聚合前后进行了表征。使用荧光光谱法测定了四种链烯基硫酸钠(SAIS)表面活性剂的临界胶束浓度(CMC)、极性和聚集数。通过密度测量估算了聚合SAIS(聚-SAIS)表面活性剂的偏比容,并采用毛细管电泳(CE)测定亚甲基选择性以及洗脱窗口。SAIS表面活性剂单体的CMC随链长增加而降低,荧光法与CE法比较时相关性良好。物理化学性质(偏比容、亚甲基选择性、电泳迁移率和洗脱窗口)随链长增加而增加。然而,未发现聚-SAIS表面活性剂的聚集数与疏水链长度之间存在直接关系。然后将这些聚合表面活性剂用作胶束电动色谱(MEKC)中的准固定相,以研究36种具有不同化学特性的苯衍生物的保留行为和选择性因子。尽管聚合表面活性剂链长的变化显著影响非氢键(NHB)苯衍生物的保留,但这些影响对氢键受体(HBA)和氢键供体(HBD)苯衍生物不太明显。因此,发现聚-SAIS表面活性剂的疏水性是保留NHB衍生物的主要驱动力。然而,对于几种苯衍生物(NHB、HBA和HBD),与较短链的聚合表面活性剂(例如聚(7-辛烯基硫酸钠),聚-SOcS)相比, 最长链聚合表面活性剂(例如聚(10-十一碳烯基硫酸钠),聚-SUS)观察到显著更高的选择性因子。此外,还发现表面活性剂疏水链的影响对NHB、HBA和HBD苯衍生物的迁移顺序也有一定影响。