Journal
MACROMOLECULES
Volume 42, Issue 15, Pages 5761-5765Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ma900497j
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Funding
- Army Research Office at Department of Defense [W911NF-07-1-0653]
- Division of Material Research, National Science Foundation(NSF-DMR) [0805301]
- Direct For Mathematical & Physical Scien
- Division Of Materials Research [0805301] Funding Source: National Science Foundation
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We report a simple route to generate nonequilibrium nanostructures combining two known block copolymer (BCP) morphologies by first templating the spatial arrangement of BCP in thin films using a supramolecule. The BCP subsequently assembles within the morphological framework established by the supramolecule, leading to a templated, nonequilibrium nanostructures not accessible by the BCP alone. Thin Films with hexagonally packed cylindrical domains oriented normal to the surface were formed initially by the self-assembly of the diblock copolymer-based supramolecules, comprised of symmetric polystyrene-b-poly-(4-vinylpyridine) (PS-b-P4VP) with 3-pentadecylphenol (PDP) hydrogen-bonded to the 4VP. After selective removal of similar to 90% of the PDP and a brief solvent annealing in a chloroform atmosphere, symmetric PS-b-P4VP, containing a trace amount of PDP, self-assembled forming polygonal (dominantly hexagonal) microdomains oriented normal to the surface. This process reported should c applicable to the large library of copolymer-based supramolecules and enables the generation of novel nonequilibrium nanostructured morphologies. It also provides a new platform to study the pathway-dependent self-assembly in polymer thin films.
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