Infrared Spectroscopy of Anionic, Cationic, and Zwitterionic Surfactants

R. Viana, A. D. Silva, A. S. Pimentel
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引用次数: 237

Abstract

This paper describes the ordering degree of anionic, cationic, and zwitterionic surfactants with the increase of their packing density on Ge substrate by using Fourier transform infrared-attenuated total reflection (FTIR-ATR) spectroscopy. This work shows new insights on the conformational order of sodium dodecyl sulfate (SDS), N-hexadecyl-N-N-dimethyl-3-ammonio-1-propane-sulfonate (HPS), hexadecyl-trimethylammonium bromide (CTAB), and dodecyl trimethylammonium bromide (DTAB). DFT and semiempirical calculations are also performed in order to evaluate the effect of headgroup hydration and counterion. The CH2 asymmetric and symmetric stretching bands for the SDS molecule show a shift of 1.7 and 0.9 cm−1 to higher frequencies as the packing density increases, while it is observed a shift of 2.6 and 2.7 cm−1 for the HPS molecule, respectively. The DTAB molecule shows a shift of 4.5 cm−1 to lower frequencies for both CH2 asymmetric and symmetric stretching bands as the packing density increases, indicating the decrease of gauche conformations and the increase of all-trans conformations over the aliphatic chain.
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阴离子、阳离子和两性离子表面活性剂的红外光谱
本文利用傅里叶变换红外衰减全反射(FTIR-ATR)光谱研究了阴离子、阳离子和两性离子表面活性剂随其在Ge衬底上堆积密度的增加而产生的有序度。这项工作对十二烷基硫酸钠(SDS)、n -十六烷基- n - n -二甲基-3-氨-1-丙烷磺酸盐(HPS)、十六烷基-三甲基溴化铵(CTAB)和十二烷基三甲基溴化铵(DTAB)的构象顺序有了新的认识。为了评价头基水化和反离子的效果,还进行了DFT和半经验计算。SDS分子的CH2不对称和对称拉伸带随着填充密度的增加而向更高频率移动1.7和0.9 cm−1,而HPS分子的CH2不对称和对称拉伸带分别为2.6和2.7 cm−1。DTAB分子的CH2不对称和对称伸展带随着填充密度的增加向更低频率移动4.5 cm−1,表明脂肪链上的间扭构象减少,全反式构象增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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