TY - JOUR
T1 - Surface-Reactive Patchy Nanoparticles and Nanodiscs Prepared by Tandem Nanoprecipitation and Internal Phase Separation
AU - Varadharajan, Divya
AU - Turgut, Hatice
AU - Lahann, Joerg
AU - Yabu, Hiroshi
AU - Delaittre, Guillaume
N1 - Funding Information:
The authors would like to thank the German Federal Ministry of Education and Research (BMBF) for the current funding in the frame of Molecular Interaction Engineering program (Biotechnologie 2020+, Grant No. 031A095C). D.V. and H.Y. are grateful to Minori Suzuki for providing training and assistance with TEM. The authors are also thankful to the “Michigan Center for Materials Characterization” and its staff assistance (Bobby Kerns, Kai Sun, and Haiping Sun) for the use of JEOL 2100-F STEM. D.V. also thanks Linda Barthel and UMICH Microscopy and Image Analysis for the STED microscopy measurements. H.Y. would like to thank KAKENHI (Nos. 17H01223 and 16K14071), Japan for financial support, respectively. Finally, Prof. Barner-Kowollik (QUT and ITCP, KIT) is thanked for his constant support.
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/9/26
Y1 - 2018/9/26
N2 - Nanoparticles with structural or chemical anisotropy are promising materials in domains as diverse as cellular delivery, photonic materials, or interfacial engineering. The surface chemistry may play a major role in some of these contexts. Introducing reactivity into such polymeric nanomaterials is thus of great potential, yet is still a concept in its infancy. In the current contribution, a simple nanoprecipitation technique leads to nanoparticles with diameters as low as 150 nm and well-defined reactive surface patches of less than 30 nm in width, as well as surface-reactive flat, disc-like nanoparticles with corresponding dimensions, via an additional crosslinking/delamination sequence. To this aim, chemically doped block copolymers (BCPs) are employed. Control over morphology is attained by tuning preparation conditions, such as polymer concentration, solvent mixture composition, and blending with non-functional BCP. Surface reactivity is demonstrated using a modular ligation method for the site-selective immobilization of thiol molecules. The current approach constitutes a straightforward methodology requiring minimal engineering to produce nanoparticles with confined surface reactivity and/or shape anisotropy.
AB - Nanoparticles with structural or chemical anisotropy are promising materials in domains as diverse as cellular delivery, photonic materials, or interfacial engineering. The surface chemistry may play a major role in some of these contexts. Introducing reactivity into such polymeric nanomaterials is thus of great potential, yet is still a concept in its infancy. In the current contribution, a simple nanoprecipitation technique leads to nanoparticles with diameters as low as 150 nm and well-defined reactive surface patches of less than 30 nm in width, as well as surface-reactive flat, disc-like nanoparticles with corresponding dimensions, via an additional crosslinking/delamination sequence. To this aim, chemically doped block copolymers (BCPs) are employed. Control over morphology is attained by tuning preparation conditions, such as polymer concentration, solvent mixture composition, and blending with non-functional BCP. Surface reactivity is demonstrated using a modular ligation method for the site-selective immobilization of thiol molecules. The current approach constitutes a straightforward methodology requiring minimal engineering to produce nanoparticles with confined surface reactivity and/or shape anisotropy.
KW - functional block copolymers
KW - morphology control
KW - nanodiscs
KW - nanoparticles
KW - para-fluoro–thiol reaction
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U2 - 10.1002/adfm.201800846
DO - 10.1002/adfm.201800846
M3 - Article
AN - SCOPUS:85052665824
SN - 1616-301X
VL - 28
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 39
M1 - 1800846
ER -