@misc{RozanskiKremerKoeberleetal.1995,
  author    = {Rozanski, Stanislaw A. and Kremer, Friedrich and K{\"o}berle, Peter and Laschewsky, Andr{\´e}},
  title     = {Relaxation and charge transport in mixtures of zwitterionic polymers and inorganic salts},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17438},
  year      = {1995},
  abstract  = {Dielectric spectroscopy is employed to analyze the molecular dynamics and the charge transport in mixtures of zwitterionic polymers of the type poly{3 [N(-methacryloyloxyalkyl)] N, [N-dimethylammonio propanesulfonate] with sodium iodide in the frequency range of 10²Hz-10(up)7 Hz and in the temperature range of 110 K-400 K. The amount of inorganic salt added varies from 0-200 mol-\% relative to the number of zwitterionic groups present in the polymer, contributing strongly to the conductivity. One relaxation process is observed whose relaxation rate depends strongly on the length of the aliphatic spacer between the polymethacrylate main chain and the zwitterionic group. Exhibiting an Arrhenius-like temperature depence with activation energy EA = 47 KJ/mol, this relaxation process is assigned to fluctuation of the quaternary ammonium groups in the side chains. At higher temperatures, the dielectric properties and the conductivity are primarily dominated by the mobile inorganic ions: conductivity strongly depends on the salt concentration, showing a pronounced electrode polarization effect. The frequency and salt concentration, dependences of the conductivity can be quantitatively described as hopping of charge carriers being subject to spatially randomly varying energy barriers. For the low-frequency regime and for the critical frequency marking the onset of the conductivity's dispersion, the Barton-Nakajima-Namikawa (BNN) relationship is fulfilled.},
  language  = {en}
}
@misc{Laschewsky1995,
  author    = {Laschewsky, Andr{\´e}},
  title     = {Molecular concepts, self-organisation and properties of polysoaps},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-26895},
  year      = {1995},
  abstract  = {The article reviews water-soluble polymers characterized by surfactant side chains, and related amphiphilic polymers. Various synthetic approaches are presented, and rules for useful molecular architectures are given. Models for the self-organization of such polymers in water are presented comparing them with the micellization of low molecular weight surfactants. Highlighting key properties of aqueous polysoap solutions such as viscosity, surface tension and solubilization power, some structure-property relationships are established. Further, the formation of mesophases and of superstructures in bulk is addressed. Finally, the functionalization of polysoaps, and potential applications are discussed.},
  language  = {en}
}
@misc{CochinHendlingerLaschewsky1995,
  author    = {Cochin, Didier and Hendlinger, P. and Laschewsky, Andr{\´e}},
  title     = {Polysoaps with fluorocarbon hydrophobic chains},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17347},
  year      = {1995},
  abstract  = {A series of amphiphilic copolymers is prepared by copolymerization of choline methacrylate with 1,1,2,2-tetrahydroperfluorooctyl methacrylate in varying amounts. The copolymers bearing fluorocarbon chains are studied concerning their effects on viscosity, solubilization and surface activity in aqueous solution, exhibiting a general behavior characteristic for polysoaps. The results are compared with the ones obtained for an analogous series of amphiphilic copolymers bearing hydrocarbon chains.},
  language  = {en}
}
@misc{AntonLaschewskyWard1995,
  author    = {Anton, Peter and Laschewsky, Andr{\´e} and Ward, M. D.},
  title     = {Solubilization control by redox-switching of polysoaps},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17336},
  year      = {1995},
  abstract  = {Reversible changes in the self-organization of polysoaps may be induced by controlling their charge numbers via covalently bound redox moieties. This is illustrated with two viologen polysoaps, which in response to an electrochemical stimulus, change their solubility and aggregation in water, leading from homogeneously dissolved and aggregated molecules to collapsed ones and vice verse. Using the electrochemical quartz crystal microbalance (EQCM), it could be shown that the reversibility of this process is better than 95\% in 16 cycles.},
  language  = {en}
}