Peptide-mediated
routes to the synthesis of plasmonic nanoparticles
have been drawing increasing attention for the development of chiroptically
active nanoscale architectures. However, designing a multifunctional
peptide able to drive the formation of structurally defined nanomaterials
endowed with specific functionalities is still challenging. In this
work, iodination has been devised as a strategy to strengthen Au-reduction
capability of the amyloidogenic peptide DFNKF and combine it with
its distinctive self-assembly features. Thanks to the Au-mediated
C—I activation on the phenylalanine iodobenzenes, the peptides
yield efficient Au-reduction ability promoting the synthesis of Au
nanoparticles, and simultaneously working as templates for their spontaneous
self-assembly into spherical superstructures endowed with chiroptical
activities. The reaction occurs
in situ
through a
one-pot process in aqueous media. The generality of this approach
has been demonstrated using an iodinated derivative of the peptide
KLVFF, which also showed reducing and templating abilities forming
chiroptically active helical superstructures decorated with Au nanoparticles.
The synthesis and self-assembly capabilities of a new halogen-bond donor ligand, 2,3,5,6-tetrafluoro-4-iodophenyl 5-(1,2-dithiolan-3-yl)pentanoate (1), are reported. The crystal structure of ligand (1) and the formation of a cocrystal with 1,2-di(4-pyridyl)ethylene, (1)·(2), both show halogen bonds involving the 4-iodotetrafluorobenzene moiety. Ligand (1), being a self-complementary unit, forms an infinite halogen-bonded chain driven by the S...I synthon, while the cocrystal (1)·(2) self-assembles into a discrete trimeric entity driven by the N...I synthon. Ligand (1) was also successfully used to functionalize the surface of gold nanoparticles, AuNP-(1). Experiments on the dispersibility profile of AuNP-(1) demonstrated the potential of halogen bonding in facilitating the dispersion of modified NPs with halogen-bond donors in pyridine.
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