Block copolymers for stimuli responsive nanometric systems

Abad Andrés, Miriam
Oriol Langa, Luis Teodoro (dir.) ; Piñol Lacambra, Milagros (dir.)

Universidad de Zaragoza, CIEN, 2016
Departamento de Química Orgánica, Área de Química Orgánica

Máster Universitario en Materiales Nanoestructurados para Aplicaciones Nanotecnológicas (Nanostructured Materials for Nanotechnology Applications)

Resumen: Amphiphilic block copolymers are able to self-assemble and form polymeric micelles able to encapsulate hydrophobic molecules, or vesicles able to encapsulate both hydrophobic and hydrophilic molecules. By using stimuli responsive polymers, the encapsulated molecules can be controlled release. Light is one of the most investigated stimuli because it can be remotely and locally applied. Photoresponsive polymers are composed by moieties that react or isomerize when they are irradiated with light of a particular wavelength. Azobenzene is one of these functional molecules whose light activity is due to its reversible photoisomerization trans-cis-trans. Azobenzene can be covalently bound to polymeric chains, which is the most frequent situation, or can be bound using the principles of Supramolecular Chemistry, which constitutes a far less explored approach. The aims of this project were: The synthesis and characterization of amphiphilic supramolecular block copolymers containing units of 2.6-diacylaminopiridine (DAP, analog to adenine) capable of binding, via hydrogen bonds, azobenzenes having thymine terminal groups, including the - study of association constants in supramolecular amphiphilic block copolymers. - study of aggregation of amphiphilic supramolecular block copolymers in aqueous solutions by microfluidics to check a fast and reproducible methodology of preparing polymeric nanoparticles. According to these objectives, amphiphilic block copolymers containing DAP units and poly (ethylene glycol) were first synthesized by controlled RAFT polymerization. Azobenzenes having thymine terminal groups are linked through a triple hydrogen bond to the DAP units to give amphiphilic supramolecular block copolymers. All copolymers were characterized by spectroscopic techniques. Association constant (Ka) for H-bond complex was calculated by 1H-NMR titrations. It has a lower value (4 M-1) in THF than in chloroform (42 M-1) thus H-bonds are weakened due to a solvation effect. Reproducible polymeric aggregates from both block copolymers and supramolecular block copolymers were obtained by microfluidics in THF/water systems. In chloroform/water systems no reproducible results were obtained, so further studies are required.

Tipo de Trabajo Académico: Trabajo Fin de Master