1,3-Dioxepane was polymerized with triflic acid as an initiator in the presence of acetic acid (AA) and hexane diacid. The structure of the poly(1,3-dioxepane) (polyDOP) obtained was characterized by 1 H NMR spectra and gel permeation chromatography. The molecular weights (MWs) were determined by va
Study on cationic ring-opening polymerization of 1,3-dioxepane with oxocarbenium salt as initiator
โ Scribed by Yijin Xu; Caiyuan Pan
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 173 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
Poly (1,3-dioxepane) [PDOP] triol was prepared by cationic ring-opening polymerization with [C 2 H 5 C(CH 2 OCH 2 CH 2 CO ฯฉ ClO 4 ฯช ) 3 ], trioxocarbenium perchlorate, as an initiator. The structures of the PDOP triols obtained were verified by 1 H-NMR, FTIR, and GPC results. Initiation, propagation, and termination mechanisms were discussed based on the structural analysis of the polyacetal polyols. The results of GPC, NMR, and IR measurements showed that the PDOP triols obtained had similar branch chain lengths. Number-average molecular weights were determined by vapor pressure osmometry (VPO), end group titration and 1 H-NMR.
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