Structure and self-assembling effects over photoinduced anisotropy in do13-modified block copolymers

SÁIZ LUCIANA; ZUCCHI ILEANA; OYANGUREN PATRICIA; GALANTE M. JOSÉ

Praga

Conferencia; 7th International Conference on Nanostructured Polymers and Nanocomposites; 2012

European Centre for Nanostructured Polymers

Azopolymers have more stable thermal and mechanical properties than their respective monomers. They have been used among other applications to produce optical, artificial taste, and ph sensors. However their main characteristic is the capacity of displaying reversible cis-trans isomerization with very useful applications in optical information storage, light switching devices, surface relief gratings, holograms, and induction of liquid-crystals alignment. To overcome the problems of the initially used guest-host systems, the active molecules have been covalently linked to the polymer backbone as either pendant group or a comonomer. Such covalently functionalized polymers can contain a large response to optical fields. Moreover, the induced anisotropy in such systems can be highly stable. Also, studies on photo-orientation processes in amorphous polymers have addressed the role of glass transition temperature (Tg) and polymer structural effects over the photo-induced anisotropy. Recently, the development of block copolymers (BC) covalently functionalized with azobenzene units has gained importance since the confinement of photo-responsive units in nanosized block copolymer domains gives these materials unique properties. BC nanostructuration eliminated the scattering of visible light, and at the same time reduced azo aggregation.