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Dielectric relaxation spectroscopy of amorphous and liquid-crystalline side-chain polycarbonates

✍ Scribed by Michael Wübbenhorst; Ernout M. Van Koten; John C. Jansen; Wim Mijs; Jan van Turnhout


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
437 KB
Volume
18
Category
Article
ISSN
1022-1336

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✦ Synopsis


Abstract

The molecular dynamics of amorphous and liquid‐crystalline (LC) side‐chain polycarbonates was studied by dielectric spectroscopy at frequencies from 10^−2^ to 10^6^ Hz and at temperatures from −160 to 180°C. ‘Model’ compounds containing no mesogenic side‐groups showed two relaxations, which originate from the carbonate group (α, β~m~‐relaxation). By contrast, in LC‐polycarbonates bearing a mesogenic nitrostilbene side group around and above the glass transition temperature T~g~ up to three relaxation modes were distinguished (α‐, λ~1~‐, λ~2~‐process); below T~g~ four secondary relaxations (γ‐, β~m~‐, β~s~‐, β~sc~‐relaxation) were observed. The γ‐relaxation was found only in compounds possessing an aliphatic spacer linked to the backbone by an ether bond. Apart from β~m~‐, two additional β‐processes were identified as relaxations associated with the mesogenic unit in the glassy (β~s~) or in the crystalline state (β~sc~).


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Dielectric Relaxation of Side-Chain Liqu
✍ Natalia A. Nikonorova; Evgeny B. Barmatov; Dimitry A. Pebalk; Ricardo Diaz-Calle 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 248 KB

## Abstract **Summary:** Two sets of side‐chain, liquid‐crystalline ionomers based on copolymers of butyl acrylate and 4‐{[6‐(acryloyloxy)hexyl]oxy}benzoic acid containing 2.5–20 mol‐% of lithium or rubidium ions were studied. As the content of ions of alkali metals increases, segmental mobility ma