Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5209579 | Reactive and Functional Polymers | 2016 | 8 Pages |
Abstract
We report a ring expansion vinyl polymerization producing cyclic polymers using a tetra(oxyethylene) (TOE)-tethered cyclic initiator for the nitroxide-mediated controlled radical polymerization (NMP). Styrene (St) was polymerized with the cyclic NMP initiator 1 in the bulk to produce polymer 2. Structural analyses of 2 were performed by a size exclusion chromatograph equipped with a multiangle laser light scattering (SEC-MALS) detector, focusing on the relationships between the z-averaged root-mean-square radii of gyration (ãS2ãz1/2) versus the molecular weights. The results proved that 2 would consist of ring components as a result of the ring expansion polymerizations and radical ring crossover reactions together with ring-opened linear components, in which the amount of ring components increased with the increasing molecular weights. The data also enabled the quantification that approximately 13-40 wt% of the final polymer 2 could be identified as the ring species in the Mw range of 1 Ã 105-5 Ã 105 g molâ 1.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Atsushi Narumi, Shuhei Hasegawa, Ryo Yanagisawa, Miho Tomiyama, Masatsugu Yamada, Wolfgang H. Binder, Moriya Kikuchi, Seigou Kawaguchi,