Sonochemical Synthesis of Optically Tuneable Conjugated Polymer Nanoparticles

The development of novel and simple methodologies for the obtaining of semiconductive polymer nanoparticles with fine-tuned optical properties represents nowadays a challenging research area as it involves a simultaneous chemical modification and nanostructuration of the polymer. Here, starting from...

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Detalles Bibliográficos
Autores: Bellacanzone, Christian|||0000-0002-1986-6440, Roscini, Claudio|||0000-0002-0157-8934, Ruiz Delgado, María del Carmen, Ponce Ortiz, Rocío, Ruiz-Molina, Daniel|||0000-0002-6844-8421
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:220665
Acceso en línea:https://ddd.uab.cat/record/220665
https://dx.doi.org/urn:doi:10.1002/ppsc.201700322
Access Level:acceso abierto
Palabra clave:Fluorescent nanoparticles
MEH-PPV
Nanoemulsions
Semiconducting polymers
Sonochemistry
Descripción
Sumario:The development of novel and simple methodologies for the obtaining of semiconductive polymer nanoparticles with fine-tuned optical properties represents nowadays a challenging research area as it involves a simultaneous chemical modification and nanostructuration of the polymer. Here, starting from poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene], this objective is achieved with the one-pot synthesis of oligomers with tunable conjugation length and their nanostructuration, employing a miniemulsion method. Ultrasound irradiation of heterogeneous mixtures leads to the formation of hypochlorous acid that disrupts the electronic conjugation through polymer chain cleavage. Moreover, control over the degree of the electronic conjugation of the oligomers, and therefore of the optical properties, is achieved simply by varying the polymer concentration of the initial solution. Finally, the presence of surfactants during the sonication allows for the formation of nanoparticles with progressive spectral shift of the main absorption (from λ = 476 to 306 nm) and emission bands (from λ = 597 to 481 nm). The integration of conducting polymer nanoparticles into polymeric matrices yields self-standing and flexible fluorescent films.