Reconfigurable hybrid nanoparticles made by decorating flexible polymer shells on rigid inorganic nanoparticle cores can provide a unique means to build stimuli‐responsive functional materials. The polymer shell reconfiguration has been expected to depend on the local core shape details, but limited systematic investigations have been undertaken. Here, two literature methods are adapted to coat either thiol‐terminated polystyrene (PS) or polystyrene‐poly(acrylic acid) (PS‐
Polylysine-grafted Au 144 nanoclusters: birth and growth of a healthy surface-plasmon-resonance-like band
Poly(amino acid)-coated gold nanoparticles hold promise in biomedical applications, particularly because they combine the unique physicochemical properties of the gold core, excellent biocompatibility, and easy functionalization of the poly(amino acid)-capping shell. Here we report a novel method for the preparation of robust hybrid core–shell nanosystems consisting of a Au 144 cluster and a densely grafted polylysine layer. Linear polylysine chains were grown by direct N -carboxyanhydride (NCA) polymerization onto ligands capping the gold nanocluster. The density of the polylysine chains and the thickness of the polymer layer strongly depend on the amount and concentration of the NCA monomer and the initiator. The optical spectra of the so-obtained core–shell nanosystems show a strong surface plasmon resonance (SPR)-like band at 531 nm. In fact, despite maintenance of the gold cluster size and the absence of interparticle aggregation, the polylysine-capped clusters behave as if they have a diameter nearly 4 times larger. To the best of our knowledge, this is the first observation of the growth of a fully developed, very stable SPR-like band for a gold nanocluster of such dimensions. The robust polylysine protective shell makes the nanoparticles very stable under conditions of chemical etching, in the presence of glutathione, and at different pH values, without gold core deshielding or alteration of the SPR-like band. This polymerization method can conceivably be extended to prepare core–shell nanosystems based on other mono- or co-poly(amino acids).
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- Award ID(s):
- 1605971
- PAR ID:
- 10296933
- Date Published:
- Journal Name:
- Chemical Science
- Volume:
- 8
- Issue:
- 4
- ISSN:
- 2041-6520
- Page Range / eLocation ID:
- 3228 to 3238
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/c6sc05187a
