@article{22210,
  abstract     = {We disclose a method for the synthesis of chiral colloids from spontaneously formed hollow sugar-surfactant microtubes with internally confined mobile colloidal spheres. Key feature of our approach is the grafting of colloid surfaces with photoresponsive coumarin moieties, which allow for UV-induced, covalent clicking of colloids into permanent chains, with morphologies set by the colloid-to-tube diameter ratio. Subsequent dissolution of tube confinement yields aqueous suspensions that comprise bulk quantities of a variety of linear chains, including single helical chains of polystyrene colloids. These colloidal equivalents of chiral (DNA) molecules are intended for microscopic study of chiral dynamics on a single-particle level.},
  author       = {Ouhajji, Samia and van Ravensteijn, Bas G. P. and Fernández-Rico, Carla and Lacina, Kanvaly S. and Philipse, Albert P. and Petukhov, Andrei V.},
  issn         = {1936-086X},
  journal      = {ACS Nano},
  number       = {12},
  pages        = {12089--12095},
  publisher    = {American Chemical Society},
  title        = {{Wet-chemical synthesis of chiral colloids}},
  doi          = {10.1021/acsnano.8b05065},
  volume       = {12},
  year         = {2018},
}

