Organic–Inorganic Hybrid Nanoparticles via Photoinduced Micellation and Siloxane Core Cross-Linking of Stimuli-Responsive Copolymers

Photoacid-induced siloxane cross-linking of stimuli-responsive copolymer micelles allows the synthesis of well-defined organic–inorganic hybrid nanoparticles. Two conceptually different synthetic approaches are presented, both via photoinduced cross-linking of poly(4-hydroxystyrene-block-styrene) mi...

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Veröffentlicht in:ACS macro letters 2013-02, Vol.2 (2), p.121-124
Hauptverfasser: Anger, Christian, Deubel, Frank, Salzinger, Stephan, Stohrer, Jürgen, Halbach, Tobias, Jordan, Rainer, Veinot, Jonathan G. C, Rieger, Bernhard
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container_end_page 124
container_issue 2
container_start_page 121
container_title ACS macro letters
container_volume 2
creator Anger, Christian
Deubel, Frank
Salzinger, Stephan
Stohrer, Jürgen
Halbach, Tobias
Jordan, Rainer
Veinot, Jonathan G. C
Rieger, Bernhard
description Photoacid-induced siloxane cross-linking of stimuli-responsive copolymer micelles allows the synthesis of well-defined organic–inorganic hybrid nanoparticles. Two conceptually different synthetic approaches are presented, both via photoinduced cross-linking of poly(4-hydroxystyrene-block-styrene) micelles and via one-pot photoacid-catalyzed micelle formation and siloxane cross-linking of poly(4-tert-butoxystyrene-block-styrene). The multistep synthetic route showed intermicellar cross-linking leading to agglomerates. In contrast to this, the formation of the nanoparticles via the one-pot synthesis yielded well-defined structures. The use of different siloxane cross-linking agents and their effects on the properties of the cross-linked micellar structures have been evaluated. Scanning electron microscopy and differential scanning calorimetry indicate rigid core cross-linked nanoparticles. Their size, molar mass, and swelling behavior were analyzed by dynamic and static light scattering. Cyclic siloxane cross-linking agents lead to residual CC double bonds within the nanoparticle core that allow postsynthetic modification by, e.g., thiol–ene click reactions.
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