TY - JOUR
T1 - Probing the alkyl chain length effects on molecular packing characteristics of mixed ion pair amphiphile/double-chained cationic surfactant vesicular bilayers with the Langmuir monolayer approach
AU - Kuo, An Tsung
AU - Li, Wei Ta
AU - Tseng, Chia Yao
AU - Hsiao, Fang Wei
AU - Chang, Chien-Hsiang
PY - 2014/7/20
Y1 - 2014/7/20
N2 - Alkyl chain length effects of added double-chained cationic surfactants, dialkyldimethylammonium bromides (DXDABs), including ditetradecyldimethylammonium bromide (DTDAB), dihexadecyldimethylammonium bromide (DHDAB), and dioctadecyldimethylammonium bromide (DODAB), on the Langmuir monolayer behavior of a pseudodouble-chained ion pair amphiphile, hexadecyltrimethylammonium-dodecylsulfate (HTMA-DS), were analyzed with the Langmuir monolayer technique, infrared reflection-absorption spectroscopy, and Brewster angle microscopy. It was found that DXDA+ of DXDAB could displace HTMA+ from HTMA-DS and the displaced HTMA+ might desorb into the aqueous subphase, with the extent depending on the alkyl chain length of DXDAB. In the mixed HTMA-DS/DODAB monolayer, DODAB possessing long alkyl chains was capable of restraining HTMA+ from desorption with enhanced intermolecular interaction reflected by the favorable molecule aggregation. As for the mixed monolayers of HTMA-DS and DTDAB with short alkyl chains, incomplete displacement of HTMA+ from HTMA-DS by DTDA+ was detected and ascribed to weak intermolecular attraction exhibited by the fractal-like domain formation. Among the three DXDABs, DHDAB with the best molecular structure match to HTMA-DS in terms of alkyl chain length could form well-packed monolayer structures with HTMA-DS. The finding has the implication on the surface characteristic control of catanionic vesicles composed of ion pair amphiphile with double-chained cationic surfactant.
AB - Alkyl chain length effects of added double-chained cationic surfactants, dialkyldimethylammonium bromides (DXDABs), including ditetradecyldimethylammonium bromide (DTDAB), dihexadecyldimethylammonium bromide (DHDAB), and dioctadecyldimethylammonium bromide (DODAB), on the Langmuir monolayer behavior of a pseudodouble-chained ion pair amphiphile, hexadecyltrimethylammonium-dodecylsulfate (HTMA-DS), were analyzed with the Langmuir monolayer technique, infrared reflection-absorption spectroscopy, and Brewster angle microscopy. It was found that DXDA+ of DXDAB could displace HTMA+ from HTMA-DS and the displaced HTMA+ might desorb into the aqueous subphase, with the extent depending on the alkyl chain length of DXDAB. In the mixed HTMA-DS/DODAB monolayer, DODAB possessing long alkyl chains was capable of restraining HTMA+ from desorption with enhanced intermolecular interaction reflected by the favorable molecule aggregation. As for the mixed monolayers of HTMA-DS and DTDAB with short alkyl chains, incomplete displacement of HTMA+ from HTMA-DS by DTDA+ was detected and ascribed to weak intermolecular attraction exhibited by the fractal-like domain formation. Among the three DXDABs, DHDAB with the best molecular structure match to HTMA-DS in terms of alkyl chain length could form well-packed monolayer structures with HTMA-DS. The finding has the implication on the surface characteristic control of catanionic vesicles composed of ion pair amphiphile with double-chained cationic surfactant.
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U2 - 10.1016/j.colsurfa.2014.04.013
DO - 10.1016/j.colsurfa.2014.04.013
M3 - Article
AN - SCOPUS:84899073235
VL - 454
SP - 23
EP - 31
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
SN - 0927-7757
IS - 1
ER -