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Well phase separated segmented copolymers via acyclic diene metathesis (ADMET) polymerization

✍ Scribed by K. B. Wagener; K. Brzezinska; J. D. Anderson; S. Dilocker


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
199 KB
Volume
35
Category
Article
ISSN
0887-624X

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✦ Synopsis


Segmented oligomers consisting of polyoctenylene hard segments and unsaturated polytetrahydrofuran soft segments were prepared using acyclic diene metathesis (ADMET) copolymerization techniques. These are the first such segmented materials prepared via metathesis chemistry. Two different molecular weight a,v-poly(tetrahy-

(1) were synthesized by the cationic living polymerization of tetrahydrofuran (THF). Trifluoromethanesulfonic anhydride, (CF 3 SO 2 ) 2 O (triflic anhydride) (2), was employed as the initiator, followed by in situ bis-functionalization with 5-hexen-1-ol, [CH 2 |CH(CH 2 ) 4 OH] ( 3), to yield soft segment dienes with vinyl end groups. The functionality of these soft segment monomers was approximately 1.9. These telechelic monomers possessed sufficient functionality to be homopolymerized or copolymerized with 1,9-decadiene (4) to generate well phase separated, segmented oligomers exhibiting hard segment/soft segment thermal behavior. The segmented copolymers were characterized by 1 H-NMR, 13 C-NMR, and IR spectroscopy, elemental analysis, and TGA and DSC analysis. Average molecular weights were determined by gel permeation chromatography (GPC) and end-group analysis.


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Acyclic diene metathesis (ADMET) polymer
✍ Krystyna Brzezinska; Patrick S. Wolfe; Mark D. Watson; Kenneth B. Wagener 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 422 KB

## Abstract A series of α,ω‐dienes have been exposed to Ru(Cl~2~)(CHPh)(PCy~3~)~2~, [Ru] 3, metathesis catalyst under acyclic diene metathesis (ADMET) conditions, and the products were compared with those obtained previously using Schrock's well defined Mo and W alkylidenes. High molecular weight