| Home > Publications database > Hexagonal and Lamellar Superstructure in DSPE-PEG1000 Monolayers at the Air/Water Interface |
| Journal Article | PUBDB-2026-00227 |
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2025
ACS Publ.
Washington, DC
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Please use a persistent id in citations: doi:10.1021/acs.langmuir.5c03900 doi:10.3204/PUBDB-2026-00227
Abstract: Inspired by diblock copolymer self-assembly, we study lipopolymer monolayers at the air/water interface. We investigated DSPE-PEG1000 (DSPE-EO22) monolayers with alkyl chains in the liquid-condensed phase in dependence of the molecular area. Due to its conformational entropy, the moderately hydrophilic PEG has a larger area requirement than the alkyl chains in all-trans conformation. Small-angle grazing incidence X-ray diffraction (GID) measurements identified a hexagonal superstructure. The ordered alkyl chains form hydrophobic domains that are embedded in dissolved PEG. These domains consist of the alkyl chains of ≈200 PEGylated lipid molecules. During monolayer compression, the number of alkyl chains in a domain remains constant, while their area fraction increases. At an area fraction of 50%, a transition to a lamellar superstructure occurs. During this transition, the alkyl chain domains merge. This transition is attributed to the entropy loss of the laterally compressed PEG chains. Wide-angle GID reveals that the alkyl chains in the liquid-condensed phase possess the same small cross-sectional area (19.75 Å2) as those in DSPE monolayers, indicating that PEG has little influence on the liquid-condensed phase. The hexagonal superstructure was confirmed with AFM images.
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