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DNA secondary structures, such as dimers and hairpins, are important for the synthesis of DNA templateembedded silver nanoclusters (DNA/AgNCs). However, the arrangement of AgNCs within a given DNA template and how the AgNC influences the secondary structure of the DNA template are still unclear. Here, we introduce a noncanonical head-to-head hairpin DNA nanostructure that is driven by orange-emissive AgNCs. Through detailed in-gel analysis, sugar backbone switching, inductively coupled plasma mass spectrometry, small-angle X-ray scattering, and small angle neutron scattering, we show that the orange-emissive AgNCs mediate cytosine-Ag-cytosine bridging between two six-cytosine loop (6C-loop) hairpin DNA templates. Unlike green, red, or far-red emissive AgNCs, which are embedded inside a hairpin and duplex DNA template, the orange-emissive AgNCs are localized on the interface between the two 6C-loop hairpin DNA templates, thereby linking them. Moreover, we found that deoxyribose in the backbone of the 6C-loop at the third and fourth cytosines is crucial for the formation of the orange-emissive AgNCs and the head-to-head hairpin DNA structure. Taken together, we suggest that the specific wavelength of AgNCs fluorescence is determined by the mutual interaction between the secondary or tertiary structures of DNA-and AgNC-mediated intermolecular DNA cross-linking.

Boron nitride nanotubes (BNNTs) have attracted significant interest because of the remarkable difference in their physical properties compared with carbon nanotubes and their far-reaching potential applications, including electrical insulators; thermally conducting, catalytic, and piezoelectric materials; and neutron absorbers. Despite their unique physical properties, the bundling and insolubility of BNNTs in water because of its substantial van der Waals attraction and hydrophobicity, respectively, give rise to many limitations in practical applications. Here, we present a new way to produce a highly stable BNNT dispersion by the noncovalent functionalization of the BNNT surface in water. The noncovalently functionalized BNNTs (p-BNNTs) have been found to be highly stable in water for a long time (>1 year) and easily water-redispersible by mild vortex mixing for a few minutes even after freeze-drying at −45 °C. The p-BNNTs were cylindrically encapsulated with polymerizable surfactants (BNNT diameter = ca. 3 nm and surfactant thickness = 0.8 nm).

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