Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81321
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dc.contributor.authorXiao, Longqiangen
dc.contributor.authorSakakibara, Keitaen
dc.contributor.authorTsujii, Yoshinobuen
dc.contributor.authorGoto, Atsushien
dc.date.accessioned2017-07-26T09:25:56Zen
dc.date.accessioned2019-12-06T14:28:23Z-
dc.date.available2017-07-26T09:25:56Zen
dc.date.available2019-12-06T14:28:23Z-
dc.date.issued2017en
dc.identifier.citationXiao, L., Sakakibara, K., Tsujii, Y., & Goto, A. (2017). Organocatalyzed Living Radical Polymerization via in Situ Halogen Exchange of Alkyl Bromides to Alkyl Iodides. Macromolecules, 50(5), 1882-1891.en
dc.identifier.issn0024-9297en
dc.identifier.urihttps://hdl.handle.net/10356/81321-
dc.description.abstractHalogen exchange of alkyl bromide (R–Br) with sodium iodide (NaI) was used for the transformation of R–Br to alkyl iodide (R–I) in situ in organocatalyzed living radical polymerization (LRP). R–Br was employed as a starting compound (precursor), and the R–I formed in situ was employed as an initiating dormant species for the polymerization. The efficiency of the transformation significantly depends on the R group of R–Br. By the rational selection of the R group and reaction temperature along with the use of tetrabutylammonium iodide (Bu4NI) as a catalyst, low-polydispersity (Mw/Mn = 1.1–1.4) polymers were obtained with high conversions (e.g., 70–90%) in reasonably short periods of time (typically 3–10 h) in the polymerizations of methyl methacrylate, butyl acrylate, styrene, acrylonitrile, and functional methacrylates. Well-defined diblock and triblock copolymers and a chain-end functional polymer were also obtained. R–Br is generally much more stable than R–I upon storage. Various R–Br are commercially available. The use of simple, stable, and inexpensive R–Br as precursors of the dormant species is an attractive feature of this system. The high monomer versatility and the accessibility to a wide range of polymer structural designs demonstrated in this work show the capability of this system for use in a range of applications.en
dc.format.extent30 p.en
dc.language.isoenen
dc.relation.ispartofseriesMacromoleculesen
dc.rights© 2017 American Chemical Society (ACS). This is the author created version of a work that has been peer reviewed and accepted for publication by Macromolecules, American Chemical Society (ACS). It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/acs.macromol.6b02813].en
dc.subjectHalogen exchangeen
dc.subjectAlkyl bromidesen
dc.titleOrganocatalyzed Living Radical Polymerization via in Situ Halogen Exchange of Alkyl Bromides to Alkyl Iodidesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1021/acs.macromol.6b02813en
dc.description.versionAccepted versionen
item.fulltextWith Fulltext-
item.grantfulltextopen-
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