Suspension Photopolymerization of Methyl Methacrylate and ATRP Grafting of Thermo‐Responsive Polymers Using a Perylediimide Derivative Photoinitiator

Author:

Diacon Aurel12,Rizea Florica2,Mocanu Alexandra2,Dinescu Adrian3,Stavarache Cristina45,Jinga Luiza Izabela6,Mihăilescu Cristian N.6,Rusen Edina2ORCID

Affiliation:

1. Military Technical Academy “Ferdinand I” 39–49 George Coșbuc Boulevard Bucharest 050141 Romania

2. Faculty of Chemical Engineering and Biotechnologies University Politehnica of Bucharest 1‐ 7 Gh. Polizu Street Bucharest 011061 Romania

3. National Institute for Research and Development in Microtechnologies (IMT‐Bucharest) 126 A Erou Iancu Nicolae Street, P.O. Box 38–160 Bucharest 023573 Romania

4. Advanced Polymer Materials Group University Politehnica of Bucharest 1–7 Gh. Polizu Street Bucharest 011061 Romania

5. “C. D. Nenitzescu” Institute of Organic and Supramolecular Chemistry 202‐B Spl. Independentei Bucharest 060023 Romania

6. National Institute for Laser, Plasma and Radiation Physics Măgurele RO‐077125 Romania

Abstract

AbstractThe first aim of this study is to develop a photo‐ATRP process using methyl methacrylate (MMA) by employing a novel perylenediimide derivative (PDI) as photoinitiator. The analysis of the MMA photopolymerization process kinetics is performed in solution and in bulk, demonstrating control over the reaction progress even if the polymerizations display a slow initiation step. The photo‐ATRP process for MMA in suspension is also developed and the obtained PMMA particles are further used to reinitiate the ATRP polymerization of thermoresponsive polymers (different molecular weights poly(ethylene glycol) methyl ether methacrylate and poly(N‐isopropylacrylamide)) (PNIPAM) in solution and surface‐initiated processes. The synthesized polymers by surface‐initiated process display a bimodal molecular weight distribution with a clear modification of the signal areas ratio depending on the grafted monomer and on the reaction conditions. The grafting process can take place on the surface of the polymer particles (Mn2), or it can also involve polymer chains located further at the interior of the polymer particles (Mn1). The lower critical solution temperature (LCST) transition is demonstrated for the PNIPAM functionalized polymer particles.

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Organic Chemistry,General Chemical Engineering

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