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HERO ID
6622998
Reference Type
Journal Article
Title
Alkyl Bromide as Precursor of Initiating Dormant Species in Organocatalyzed Living Radical Polymerization
Author(s)
Li, F; Xiao, L; Goto, A; ,
Year
2018
Publisher
AMER CHEMICAL SOC
Location
WASHINGTON
Book Title
ACS Symposium Series
Volume
1284
Page Numbers
365-378
Language
English
DOI
10.1021/bk-2018-1284.ch018
Web of Science Id
WOS:000456766500018
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052804036&doi=10.1021%2fbk-2018-1284.ch018&partnerID=40&md5=6b8aad45c4464d2bd2e56943893bd796
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Abstract
Alkyl bromide (R-Br) was transformed to alkyl iodide (R-I) in the presence of tributylamine and molecular iodine (I-2). This transformation was conducted in situ in organocatalyzed living radical polymerization; R-Br was used as a starting compound (precursor), and the R-I formed in situ was employed as an initiating dormant species for the polymerization. The polymer molecular weight (M-n being up to 31,000) and its distribution (M-w/M-n = 1.2-1.4) were well controlled up to high conversions (e.g., 80%) in the polymerizations of methyl methacrylate. The monomer scope encompassed functional methacrylates and styrene. Well-defined diblock copolymers were also obtained. R-Br is generally much more stable than R-I upon storage. The use of simple, stable, and inexpensive R-Br as precursors of the dormant species is an attractive feature of this system.
Editor(s)
Matyjaszewski, K; Gao, H; Sumerlin, BS; Tsarevsky, NV;
ISBN
978-0-8412-3323-2
Conference Name
American-Chemical-Society Symposium on Controlled Radical Polymerization / 254th ACS National Meeting
Conference Location
Washington, DC
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