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Surfactant and Water Ordering in Triacontanol Monolayers at the Water−Hexane Interface
Our view of molecular ordering in Langmuir monolayers at the water−vapor interface influences our understanding of molecular ordering at other interfaces, including liquid−liquid interfaces for which structural information is scarce. We present a comparative study of a monolayer of a long-chain alka...
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Published in: | The journal of physical chemistry. B 2003-04, Vol.107 (15), p.3344-3347 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Our view of molecular ordering in Langmuir monolayers at the water−vapor interface influences our understanding of molecular ordering at other interfaces, including liquid−liquid interfaces for which structural information is scarce. We present a comparative study of a monolayer of a long-chain alkanol at the water−vapor and water−hexane interfaces using X-ray reflectivity to highlight significant differences between these two interfaces. The molecules in the Langmuir monolayer form an ordered phase of nearly rigid rods. In contrast, at the water−hexane interface, the triacontanol molecules form a condensed phase with progressive disordering of the chain from the −CH2OH to the −CH3 group. Surprisingly, at the water−hexane interface, the density in the headgroup region is 10−15% greater than either bulk water or the ordered headgroup region found at the water−vapor interface. It is conjectured that this higher density is a result of water penetration into the headgroup region of the disordered monolayer. |
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ISSN: | 1520-6106 1520-5207 |
DOI: | 10.1021/jp0271817 |