Surface-initiated, ring-opening metathesis polymerization: Formation of diblock copolymer brushes and solvent-dependent morphological changes

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In this article, we report the formation of diblock copolymer brushes on a gold surface by surface-initiated, ring-opening metathesis polymerization (SI-ROMP) with the newly developed ruthenium catalyst [(H(2)IMes)(3-Br-py)(2)(Cl)(2)RuCHPh]. Taking advantage of the highly improved activity of the ruthenium catalyst and the rapid initiation step of ROMP, we successfully formed thin films of well-defined block copolymers with 5-norbornene-2-endo,3-endo-dimethanol and norbornene carboxylic acid methyl esters (44:56 endo/exo). The catalyst was found to be active enough to polymerize endo isomers of norbonene derivatives from the surface as well as to form diblock copolymer brushes. SI-ROMP of diblock copolymers from the surface was confirmed by ellipsometry, infrared spectroscopy, and X-ray photoelectron spectroscopy. After the formation, the polymer-grafted substrates were immersed in various solvents, and the selective swelling characteristics of polymer brushes were investigated by atomic force microscopy.
Publisher
AMER CHEMICAL SOC
Issue Date
2007-06
Language
English
Article Type
Article
Keywords

TRANSFER RADICAL POLYMERIZATION; SELF-ASSEMBLED MONOLAYERS; AMPHIPHILIC BLOCK-COPOLYMERS; CONJUGATED POLYMERS; N-CARBOXYANHYDRIDE; CROSS-METATHESIS; SILICON SURFACES; THIN-FILMS; STYRENE; GROWTH

Citation

LANGMUIR, v.23, no.12, pp.6761 - 6765

ISSN
0743-7463
DOI
10.1021/la700568j
URI
http://hdl.handle.net/10203/12151
Appears in Collection
CH-Journal Papers(저널논문)
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