Journal Article PUBDB-2026-00227

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Hexagonal and Lamellar Superstructure in DSPE-PEG1000 Monolayers at the Air/Water Interface

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2025
ACS Publ. Washington, DC

Langmuir 41(50), 33838 - 33847 () [10.1021/acs.langmuir.5c03900]
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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.

Classification:

Contributing Institute(s):
  1. DOOR-User (DOOR ; HAS-User)
Research Program(s):
  1. 899 - ohne Topic (POF4-899) (POF4-899)
  2. SFB 1270 A04 - Elektrisch leitfähige Multischichten für Implantatoberflächen (A04) (384293903) (384293903)
Experiment(s):
  1. DORIS Beamline BW1 (DORIS III)

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 Record created 2026-01-13, last modified 2026-03-24


Published on 2025-12-09. Available in OpenAccess from 2026-12-09.:
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