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Ultrathin inorganic nanowires are an emerging class of building blocks for creating functional materials and devices, but there remains challenging to fine‐tune the structure and property of the nanowires at the molecular level. Here, this work shows that ultrathin polymer‐grafted gold nanowires (PG‐AuNWs) can exhibit bottlebrush polymer‐like physical behaviors and macroscopic properties. The hybrid PG‐AuNWs in solutions show polymer‐like viscoelasticity which can be finely regulated by controlling the structural parameters (e.g., length of the AuNWs, molecular weight of grafted polymers) of the PG‐AuNWs, the environmental conditions (e.g., temperature, solvent compositions), and the aging time. Furthermore, this work unravels at the molecular level that the conformational properties (e.g., contour length, persistence length, and mean‐squared radius of gyration) of the PG‐AuNWs can be correlated to their structural parameters following similar power‐law relations as molecular bottlebrush polymers. This work bridges the fundamental gap between polymer‐like inorganic nanowires and bottlebrush polymers, thus accelerating the development of new nanowire‐based functional hybrid materials and devices. [ABSTRACT FROM AUTHOR]

Ultrasmall silica‐based nanoparticles (SNPs) are attractive for application in many fields, but existing synthetic approaches show limited control over the size and morphology of these SNPs. This study describes a general single copolymer chain‐mediated strategy for the scalable synthesis of highly monodispersed symmetric and asymmetric SNPs with sub‐50 nm diameter. Random copolymers of poly(acrylic acid‐r‐styrene) intramolecularly collapse into ultrasmall single‐chain nanoparticles and serve as seeds to template the hydrolysis of silica precursors to produce uniform SNPs. It is shown in experiments and simulations that the composition and random architecture of the copolymers are crucial to the formation of ultrasmall seeds and the uniform deposition of silica. Furthermore, tailoring the architecture of copolymers can be used to produce ultrasmall asymmetric Janus‐like and dumbbell‐like SNPs with well‐defined polymer and silica domains. This study paves a new route to the scalable production of ultrasmall SNPs with tailored morphologies. [ABSTRACT FROM AUTHOR]