Reference : Restriction of mobility in model liquid crystalline ionomers
Scientific journals : Article
Engineering, computing & technology : Materials science & engineering
Physical, chemical, mathematical & earth Sciences : Chemistry
http://hdl.handle.net/2268/15109
Restriction of mobility in model liquid crystalline ionomers
English
Gohy, Jean-François [University of Liège (ULg) > Department of Chemistry > Center for Education and Research on Macromolecules (CERM) > >]
Jérôme, Robert mailto [University of Liège (ULg) > Department of Chemistry > Center for Education and Research on Macromolecules (CERM) > >]
Van den Bossche, Guy [University of Liège (ULg) > Department of Physics > Unité de Cristallographie > >]
Sobry, Roger [Universisty of Liège (ULg) > Department of Physics > Laboratoire de Physique Expérimentale > >]
Oct-1998
Macromolecular Chemistry and Physics
Wiley-V C H Verlag Gmbh
199
10
2205-2210
Yes (verified by ORBi)
International
1022-1352
Weinheim
[en] halatotelechelic polymer
[en] Model liquid crystalline ionomers have been analyzed by SAXS both in bulk and in toluene solution. These compounds are referred to as liquid crystalline halatosemitelechelic polystyrenes (LC HSTP's) and consist of low molecular weight polystyrene chains end-capped at one end by a sulfonate group associated to a mesogenic counterion. The results are in agreement with a microphase separation between the polymer chain and the mesogenic counterion. The main characteristic feature of the SAXS profile for the bulk material is the so-called ionic peak, whose position obeys a general law which is in favor of a rod-like organization of the multiplets and which shows that the polymer chains are stretched in the very close vicinity of the mesogenic core, in agreement with the Eisenberg, Hird and Moore model for ionomers. The thickness of this region of restricted mobility has been estimated to 1 nm, which is the order of magnitude of the persistence length of polystyrene. This very local restriction in mobility persists in toluene solution, in contrast to what is observed for the ω-Li-sulfonato-polystyrene precursors. The results also agree with an isotropic distribution of the multiplets in toluene.
Center for Education and Research on Macromolecules (CERM)
Politique Scientifique Fédérale (Belgique) = Belgian Federal Science Policy ; Fonds de la Recherche Scientifique (Communauté française de Belgique) - F.R.S.-FNRS ; The “Ministère de l’Enseignement Supérieur et de la Recherche de la Communauté Française de Belgique”
Researchers
http://hdl.handle.net/2268/15109
10.1002/(SICI)1521-3935(19981001)199:10<2205::AID-MACP2205>3.0.CO;2-D
http://www3.interscience.wiley.com/cgi-bin/fulltext/10003805/PDFSTART

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