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@ARTICLE{Uchman:279324,
      author       = {Uchman, Mariusz and Hajduová, Jana and Vlassi, Eleni and
                      Pispas, Stergios and Appavou, Marie-Sousai and Štěpánek,
                      Miroslav},
      title        = {{S}elf- and co-assembly of amphiphilic gradient
                      polyelectrolyte in aqueous solution: {I}nteraction with
                      oppositely charged ionic surfactant},
      journal      = {European polymer journal},
      volume       = {73},
      issn         = {0014-3057},
      address      = {New York, NY [u.a.]},
      publisher    = {Elsevier},
      reportid     = {FZJ-2015-07339},
      pages        = {212 - 221},
      year         = {2015},
      note         = {"final draft post referee" kann nicht beigebracht werden},
      abstract     = {Association behavior of the biocompatible amphiphilic
                      cationic gradient polyelectrolyte
                      poly[(2-methyl-2-oxazoline)-grad-(2-phenyl-2-oxazoline)-mod-(ethylene
                      imine)] (HPPhMeOx) prepared by partial hydrolysis of the
                      gradient copolymer
                      poly[(2-methyl-2-oxazoline)-grad-(2-phenyl-2-oxazoline)] and
                      the interaction of HPPhMeOx with the anionic surfactant
                      sodium dodecyl sulfate (SDS) in aqueous solutions were
                      investigated by scattering techniques (SANS, DLS) and by
                      atomic force microscopy. SANS measurements revealed that
                      large particles with the hydrodynamic radius of ca. 500 nm
                      observed in HPPhMeOx aqueous solutions by DLS are formed by
                      a network of physically crosslinked compact hydrophobic
                      domains with the mean radius of ca. 10 nm. Upon addition of
                      sodium dodecyl sulfate (SDS), the size of the domains
                      increases at low amounts of the added SDS due to hydrophobic
                      interaction of the single surfactant ions with the
                      aggregates. Further addition of SDS leads to the formation
                      of the co-assembled polyelectrolyte–surfactant complex
                      manifested in SANS by the presence of the correlation peak
                      from the densely packed SDS micelles as well as by partial
                      disruption of the domains.},
      cin          = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
                      (München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1},
      ddc          = {670},
      cid          = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
                      I:(DE-Juel1)JCNS-1-20110106},
      pnm          = {6G15 - FRM II / MLZ (POF3-6G15) / 6G4 - Jülich Centre for
                      Neutron Research (JCNS) (POF3-623)},
      pid          = {G:(DE-HGF)POF3-6G15 / G:(DE-HGF)POF3-6G4},
      experiment   = {EXP:(DE-MLZ)KWS2-20140101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000366536900019},
      doi          = {10.1016/j.eurpolymj.2015.10.015},
      url          = {https://juser.fz-juelich.de/record/279324},
}