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Thorpe-Ingold Effect on the ATRP-Induced Cyclopolymerization of Bismethacrylate Tethered by a Substituted Silylene Moiety

✍ Scribed by Ziqiang Hu; Yong-Ping Xu; Di Wu; Bin Li; Yen-Chin Huang; Jian-Xiong Jiang; Guo-Qiao Lai; Tien-Yau Luh


Book ID
102942014
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
582 KB
Volume
213
Category
Article
ISSN
1022-1352

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✦ Synopsis


Abstract

ATRP‐induced cyclopolymerization of dialkylsilylene‐tethered bismethacrylates leads to the corresponding polymethacrylate having fourteen‐membered cyclic pendants. The presence of bulky substituents on silicon is essential to facilitate the overall cyclopolymerization process in 3. Simple methacrylate derivatives do not undergo polymerization under these conditions. This observation can be understood within the framework of the Thorpe‐Ingold effect in organosilicon chemistry. The high rr stereoselectivity suggests that the cyclization step may selectively lead to the r diastereomer. Density functional theory calculations also show that r selectivity might be slightly favored.