Networks Based on "Core‐First" Star Polymers End‐Linked Using a Degradable Ketal Cross‐Linker: Synthesis, Characterization, and Cleavage. Issue 1 (11th December 2017)

• Record Type: Journal Article
• Authors: Kepola, Eleni J.; Patrickios, Costas S.
• Other Names: Frey Holger guestEditor.; Ishizone Takashi guestEditor.
• Is Part Of: Macromolecular chemistry and physics. Volume 219:Issue 1(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-12-11
• Subjects: anionic polymerization -- crosslinking -- degradation -- group transfer polymerization -- networks -- star polymers; Polymers -- Periodicals; Polymerization -- Periodicals; Synthetic products -- Periodicals; Macromolecules -- Periodicals; 547.7
• DOI: 10.1002/macp.201700404
• Languages: English
• ISSNs: 1022-1352

Abstract

Abstract: Sequential group transfer polymerization of cross‐linker, monomer (methyl methacrylate), and cross‐linker again is used to prepare cleavable polymer networks based on interconnected "core‐first" star polymers. By employing a degradable and a nondegradable cross‐linker, four networks are prepared. While cleavage of the degradable cross‐linker residues leads to complete polymer network dissolution, the degradation products do not always display the expected molecular weight features. These products are the expected in the case of the network prepared using only the degradable cross‐linker (monomodal size distribution with expected low molecular weight) and also in the case of the network prepared using first the degradable and then the nondegradable cross‐linker (bimodal size distribution including high molecular weight star polymers), but not so in the case of the network prepared using first the nondegradable and then the degradable cross‐linker, where the expected high molecular weight star polymer component is missing due to star recombination after hydrolysis. Abstract : Group transfer polymerization is employed for the facile preparation of degradable polymer networks comprising interconnected "core‐first" star polymers. The polymerization involves the one‐pot, sequential addition of cross‐linker, monomer, and cross‐linker again. The combination of a degradable and nondegradable cross‐linker enables the preparation of isomeric networks with different properties.