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Telechelic poly(ethylene glycol)-POSS amphiphiles at the air/water interface

  • Woojin Lee
  • , Suolong Ni
  • , Jianjun Deng
  • , Byoung Suhk Kim
  • , Sushil K. Satija
  • , Patrick T. Mather
  • , Alan R. Esker*
  • *Corresponding author for this work
  • Virginia Polytechnic Institute and State University
  • Intel
  • University of Connecticut
  • National Institute of Standards and Technology
  • Case Western Reserve University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Combining two non-surface-active building blocks, oligomeric poly(ethylene glycol) (PEG) and a completely hydrophobic polyhedral oligomeric silsesquioxane (POSS) cage, creates amphiphilic telechelic polymers (POSS-PEG-POSS), which exhibit surface activity at the air/water (A/W) interface. POSS moieties serve as the hydrophobic groups for hydrophilic PEG chains of different number-average molar mass (1, 2, 3.4, 8, and 10 kg mol-1)- For short PEG chains (1, 2, and 3.4 kg mol-1), insoluble monolayers form, whereas POSS end groups were not sufficiently hydrophobic to keep higher molar mass hydrophilic PEG blocks (8 and 10 kg mol-1) at the A/W interface. Thermodynamic analyses of the 1, 2, and 3.4 kg mol-1 POSS-PEG-POSS via surface pressure-area per monomer isotherms indicate that the POSS end groups reside at the A/W interface and that the PEG chains are squeezed into the subphase with increasing surface pressure. This conclusion is supported by X-ray reflectivity studies on Y-type Langmuir-Blodgett multilayer films which reveal a double-layer structure with a double-layer spacing of about 3.52 nm. These findings provide a strategy for producing new surface active species from non-surface-active precursors.

Original languageEnglish
Pages (from-to)682-688
Number of pages7
JournalMacromolecules
Volume40
Issue number3
DOIs
StatePublished - 2007.02.6

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