% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Shi:580332,
      author       = {Shi, Li and Carn, Florent and Goukassov, Arsen and Buhler,
                      Eric and Boue, Francois},
      title        = {{S}elf-{I}nduced {C}rystallization in {C}harged {G}old
                      {N}anoparticle-{S}emiflexible {B}iopolyelectrolyte
                      {C}omplexes},
      journal      = {Langmuir},
      volume       = {36},
      number       = {27},
      issn         = {0743-7463},
      address      = {Washington, DC},
      publisher    = {ACS Publ.},
      reportid     = {PUBDB-2023-01200},
      pages        = {7925 - 7932},
      year         = {2020},
      note         = {Waiting for fulltext},
      abstract     = {Mixing negatively charged polyelectrolyte (PEL) with
                      positively charged gold nanoparticles (Au NPs) in aqueous
                      solution results in electrostatics complexes of different
                      shapes and compactness. Here, when complexing with a
                      semirigid PEL hyaluronic acid (HA), we obtain crystals made
                      of nanoparticles in a new region of the phase diagram, as
                      evidenced by small-angle X-ray scattering (SAXS). The Au NPs
                      were initially well dispersed in solution; their size
                      distribution is well controlled but does not need to be
                      extremely narrow. The bacterial hyaluronic acid,
                      polydispersed, is commercially available. Such rather simple
                      materials and mixing preparation produce a highly ordered
                      crystalline phase of electrostatic complexes. The details of
                      the interactions between spherical nanoparticles and linear
                      polymer chains remain to be investigated. In practice, it
                      opens a completely new and unexpected method of
                      complexation. It has high potential, in particular because
                      one can take advantage of the versatility of Au NPs
                      associated with the specificity of biopolymers, varied due
                      to natural biodiversity.},
      cin          = {DOOR ; HAS-User},
      ddc          = {540},
      cid          = {I:(DE-H253)HAS-User-20120731},
      pnm          = {899 - ohne Topic (POF4-899)},
      pid          = {G:(DE-HGF)POF4-899},
      experiment   = {EXP:(DE-H253)D-A2-20150101},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {32539413},
      UT           = {WOS:000576704700021},
      doi          = {10.1021/acs.langmuir.0c01064},
      url          = {https://bib-pubdb1.desy.de/record/580332},
}