期刊
MACROMOLECULES
卷 51, 期 17, 页码 6859-6864出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.8b01707
关键词
-
资金
- Alfred P. Sloan Foundation
- American Academy of Arts and Sciences
- Johns Hopkins University
A new synthetic platform accessing stereoregular polar polyolefins is introduced. We showcase the stability of aromatic azaborine derivatives by demonstrating the syndioselective polymerization of BN 2-vinylnaphthalene (BN2VN) by a monocyclopentadienyl titanium complex. Homogeneous early transition metal catalysts are well-established systems for the synthesis of highly stereoregular syndiotactic polystyrene (sPS), but the oxophilic nature of these complexes results in catalyst decomposition with polar monomers. BN2VN's compatibility with coordination polymerization, and its ability to intercept the mechanism of styrene polymerization, is attributed to its aromaticity. Stereoretentive postpolymerization oxidation of the organoborane side chain generates syndiotactic poly(vinyl alcohol) (sPVA), an example of PBN2VN's potential for diverse postfunctionalization.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据