@misc{Laschewsky2014,
  author    = {Laschewsky, Andr{\´e}},
  title     = {Structures and synthesis of zwitterionic polymers},
  series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  journal   = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  number    = {1043},
  issn      = {1866-8372},
  doi       = {10.25932/publishup-47616},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-476167},
  pages     = {60},
  year      = {2014},
  abstract  = {The structures and synthesis of polyzwitterions ("polybetaines") are reviewed, emphasizing the literature of the past decade. Particular attention is given to the general challenges faced, and to successful strategies to obtain polymers with a true balance of permanent cationic and anionic groups, thus resulting in an overall zero charge. Also, the progress due to applying new methodologies from general polymer synthesis, such as controlled polymerization methods or the use of "click" chemical reactions is presented. Furthermore, the emerging topic of responsive ("smart") polyzwitterions is addressed. The considerations and critical discussions are illustrated by typical examples.},
  language  = {en}
}
@misc{Laschewsky2014,
  author    = {Laschewsky, Andr{\´e}},
  title     = {Structures and synthesis of zwitterionic polymers},
  series = {Polymers},
  volume    = {6},
  journal   = {Polymers},
  number    = {5},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {2073-4360},
  doi       = {10.3390/polym6051544},
  pages     = {1544 -- 1601},
  year      = {2014},
  abstract  = {The structures and synthesis of polyzwitterions ("polybetaines") are reviewed, emphasizing the literature of the past decade. Particular attention is given to the general challenges faced, and to successful strategies to obtain polymers with a true balance of permanent cationic and anionic groups, thus resulting in an overall zero charge. Also, the progress due to applying new methodologies from general polymer synthesis, such as controlled polymerization methods or the use of "click" chemical reactions is presented. Furthermore, the emerging topic of responsive ("smart") polyzwitterions is addressed. The considerations and critical discussions are illustrated by typical examples.},
  language  = {en}
}
@article{HildebrandLaschewskyZehm2014,
  author    = {Hildebrand, Viet and Laschewsky, Andr{\´e} and Zehm, Daniel},
  title     = {On the hydrophilicity of polyzwitterion poly (N, N-dimethyl-N(3-(methacrylamido)propyl)ammoniopropane sulfonate) in water, deuterated water, and aqueous salt solutions},
  series = {Journal of biomaterials science : Polymer edition},
  volume    = {25},
  journal   = {Journal of biomaterials science : Polymer edition},
  number    = {14-15},
  publisher = {Routledge, Taylor \& Francis Group},
  address   = {Abingdon},
  issn      = {0920-5063},
  doi       = {10.1080/09205063.2014.939918},
  pages     = {1602 -- 1618},
  year      = {2014},
  language  = {en}
}
@article{HerfurthVollBulleretal.2012,
  author    = {Herfurth, Christoph and Voll, Dominik and Buller, Jens and Weiss, Jan and Barner-Kowollik, Christopher and Laschewsky, Andr{\´e}},
  title     = {Radical addition fragmentation chain transfer (RAFT) polymerization of ferrocenyl (meth)acrylates},
  series = {Journal of polymer science : A, Polymer chemistry},
  volume    = {50},
  journal   = {Journal of polymer science : A, Polymer chemistry},
  number    = {1},
  publisher = {Wiley-Blackwell},
  address   = {Malden},
  issn      = {0887-624X},
  doi       = {10.1002/pola.24994},
  pages     = {108 -- 118},
  year      = {2012},
  abstract  = {We report on the controlled free radical homopolymerization of 1-ferrocenylethyl acrylate as well as of three new ferrocene bearing monomers, namely 4-ferrocenylbutyl acrylate, 2-ferrocenylamido-2-methylpropyl acrylate, and 4-ferrocenylbutyl methacrylate, by the RAFT technique. For comparison, the latter monomer was polymerized using ATRP, too. The ferrocene containing monomers were found to be less reactive than their analogues free of ferrocene. The reasons for the low polymerizability are not entirely clear. As the addition of free ferrocene to the reaction mixture did not notably affect the polymerizations, sterical hindrance by the bulky ferrocene moiety fixed on the monomers seems to be the most probable explanation. Molar masses found for 1-ferrocenylethyl acrylate did not exceed 10,000 g mol(-1), while for 4-ferrocenylbutyl (meth) acrylate molar masses of 15,000 g mol(-1) could be obtained. With PDIs as low as 1.3 in RAFT polymerization of the monomers, good control over the polymerization was achieved.},
  language  = {en}
}