The
chirality of nanostructured systems has gained growing attention
in catalysis, biotechnology, and optoelectronics owing to their exotic
enantio-/spin-selective interactions and intriguing chiroptical features.
However, large-scale fabrication of chiral inorganic nanostructures
still remains a challenge. Herein, we report a simple but generalized
route for the synthesis of diverse chiral inorganic nanoparticles
(NPs) such as Au, Ag, PdO, and TiO2 NPs using block copolymer
(BCP) templates. The self-assembled BCP inverse micelles offered a
specific environment, wherein dl-alanine induced left-handedness
via hydrogen bonding with the pyridines of polystyrene-block-poly(4-vinyl pyridine), for the evolution of chirality. The BCPs
were then used as a chiral host to transfer their handedness to the
anchored inorganic NPs, resulting in an anisotropy factor of −8.6
× 10–4 for the BCP/Au NP hybrid. Our design
concept pinpoints the steps required to construct an extended library
of viable chiral nanostructures and will aid in the development of
artificial chiral materials.