## Abstract 2,3‐Bis(methoxymethyl)‐7‐oxanorbornene was polymerised in water plus at least 9gdm^−3^ Synperonic F127 by ring‐opening metathesis polymerisation (ROMP) initiated by commercial ruthenium trichloride. Stable dispersions with particle radii 0.03 μn or less were formed. Polymer molecular we
Aqueous ring-opening metathesis polymerisation of 7-oxanorbornene derivatives with oxygen-containing functionalities
✍ Scribed by Shui-Yu Lu; Judith M. Amass; Nazia Majid; Dermott Glennon; Andrew Byerley; Frank Heatley; Peter Quayle; Colin Booth; Stephen G. Yeates; John C. Padget
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 671 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
A number of 7‐oxanorbornene derivatives with hydroxymethyl, methoxymethyl and acetoxymethyl functionalities were synthesised and investigated as monomers in ring‐opening metathesis polymerisation (ROMP) catalysed by commercial ruthenium trichloride in aqueous ethanolic solvents. Comparison was made with related polymerisations of 7‐oxanorbornene derivatives with anhydride, methoxymethyl and carboxylic acid functionalities. The structures of the polymers were investigated by ^1^H and ^13^C NMR and their molar masses and molar mass distributions by gel‐permeation chromatography.
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## Abstract Ring‐opening metathesis polymerization of dicyclopentadiene catalyzed by TiCl~4~ · 2L/CH~3~Li system [where L is tetrahydropyran (1), dioxane, 2,5‐dimethylfuran, or tetrahydrofurfyl alcohol] is reported. The obtained polymer was characterized by IR and ^1^H‐NMR. These catalytic systems
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