LIQUID-CRYSTALLINE, SEMIFLUORINATED SIDE-GROUP BLOCK-COPOLYMERS WITH STABLE LOW-ENERGY SURFACES - SYNTHESIS, LIQUID-CRYSTALLINE STRUCTURE, AND CRITICAL SURFACE-TENSION

Citation
Jg. Wang et al., LIQUID-CRYSTALLINE, SEMIFLUORINATED SIDE-GROUP BLOCK-COPOLYMERS WITH STABLE LOW-ENERGY SURFACES - SYNTHESIS, LIQUID-CRYSTALLINE STRUCTURE, AND CRITICAL SURFACE-TENSION, Macromolecules, 30(7), 1997, pp. 1906-1914
Citations number
28
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00249297
Volume
30
Issue
7
Year of publication
1997
Pages
1906 - 1914
Database
ISI
SICI code
0024-9297(1997)30:7<1906:LSSBWS>2.0.ZU;2-8
Abstract
Monodisperse poly(styrene-b-semifluorinated side chain) block copolyme rs were synthesized by anionic polymerization of poly(styrene-b-1,2/3, 4-isoprene) followed by the corresponding polymer analogous reactions. By controlling the block copolymer composition and the relative lengt hs of the fluorocarbon and hydrocarbon units in the side group, the ef fect of chemical structure on surface properties and the influence of liquid crystalline structure of the semifluorinated side chain on the surface behavior were evaluated. The composition of side groups does n ot greatly affect the as-prepared sample surface tension, but influenc es instead the transition temperatures of the room temperature liquid crystal phase. It was observed that the shorter fluorocarbon units (si x -CF2- units) form a smectic A phase at room temperature. The critica l surface tension of the SA phase is 10.8 mN/m, and the polymer surfac e undergoes significant reconstruction when immersed in water. However , when the fluorocarbon side chain contains more than eight -CF2- unit s, the resulting surface possesses a lower critical surface tension (c a. 8 mN/ m) and exhibits negligible surface reconstruction. We believe the stability results from the highly ordered packing of the room tem perature smectic B phase. This mesophase resists the reconstruction of the surface, since to do so would require loss of the enthalpies of t ransition. The estimated activation energy to destroy the smectic B ph ase is about 3-10 times higher than that of smectic A phase. This phas e forms a uniform, hexagonally packed -CF3 terminated surface with a l ow critical surface tension similar to that of fluorocarbon-based Lang muir-Blodgett films. The self-assembly of these liquid crystalline blo ck copolymers at both the molecular and microstructural level provides a valuable approach to creating stable, low surface energy materials.