Ring-Opening Bulk Polymerization of Five- and Six-Membered Cyclic Phosphonates Using Maghnite, a Nontoxic Proton Exchanged Montmorillonite Clay

被引:14
|
作者
Oussadi, Karima [1 ,2 ,3 ]
Montembault, Veronique [1 ]
Belbachir, Mohamed [2 ]
Fontaine, Laurent [1 ]
机构
[1] Univ Maine, UMR CNRS 6011, UCO2M, LCOM Chim Polymeres, F-72085 Le Mans 9, France
[2] Univ Oran Es Senia, Lab Chim Polymeres, Oran 31000, Algeria
[3] Univ Sci & Technol Mohamed Boudiaf, Oran El Mnaouar 31000, Algeria
关键词
cationic polymerization; ring-opening polymerization; cyclic phosphonate; clay; poly(alkylene H-phosphonate); PHARMACOLOGICALLY ACTIVE AMINES; POLY(ALKYLENE PHOSPHATES); CATIONIC-POLYMERIZATION; SIDE-CHAIN; POLYPHOSPHONATES; ESTERS; POLY(EPSILON-CAPROLACTONE); STABILITY; MICELLES; FIXATION;
D O I
10.1002/app.34193
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new method of preparation of poly(alkylene H-phosphonate)s by ring-opening bulk polymerization of the five- and six-membered cyclic phosphonates monomers using the nontoxic Maghnite-H+ as the initiator is described. Cyclic phosphonate monomers have been first synthesized. In particular, a new one-step synthesis of 2-hydro-2-oxo-1,3,2-dioxaphospholane is reported with a yield of 70%. The efficiency of the montmorillonite sheet silicate clay which exchanged with protons, called Maghnite-H+, as cationic initiator has been proved and the resulting biomimetic poly(alkylene H-phosphonate) s have been characterized. The Maghnite-H+ regenerated after one turn-over has showed to be still efficient as initiator for the ring-opening polymerization. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 122: 891-897, 2011
引用
收藏
页码:891 / 897
页数:7
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