Controlled ring-opening polymerization of ε-caprolactone promoted by "in situ" formed yttrium alkoxides

被引:137
作者
Martin, E
Dubois, P
Jérôme, R
机构
[1] Univ Liege, Ctr Educ & Res Macromol, B-4000 Liege, Belgium
[2] Univ Mons, Lab Polymer & Composite Mat, B-7000 Mons, Belgium
关键词
D O I
10.1021/ma991045r
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The ring-opening polymerization of epsilon-caprolactone has been initiated by [tris(hexamethyl-disilyl)amide]yttrium in the presence of an excess of 2-propanol. This initiating system is very active even at high alcohol-to-Ti molar ratio. Polymers with controlled molecular parameters (M-n, end groups) and low dispersity are formed as result of fast alkoxide/alcohol exchange. At molar excess of 2-propanol higher than 100, this exchange is no longer quantitative. The in situ formed active species involved in this new initiating system are different from those ones present in the commercial yttrium oxo-isopropoxide Y-5(mu-O)((OPT)-P-i)(13) cluster. Evidence is provided by H-1 NMR spectroscopy.
引用
收藏
页码:1530 / 1535
页数:6
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