Programming nanoparticle valence bonds with single-stranded DNA encodersYao, G., Li, J., Li, Q., Chen, X., Liu, X., Wang, F., Qu, Z., Ge, Z., Narayanan, R. P., Williams, D., Pei, H., Zuo, X., Wang, L., Yan, H., Feringa, B. L. & Fan, C., Jul-2020, In : Nature Materials. 19, 7, p. 781-+ 10 p.
Research output: Contribution to journal › Article › Academic › peer-review
Nature has evolved strategies to encode information within a single biopolymer to program biomolecular interactions with characteristic stoichiometry, orthogonality and reconfigurability. Nevertheless, synthetic approaches for programming molecular reactions or assembly generally rely on the use of multiple polymer chains (for example, patchy particles). Here we demonstrate a method for patterning colloidal gold nanoparticles with valence bond analogues using single-stranded DNA encoders containing polyadenine (polyA). By programming the order, length and sequence of each encoder with alternating polyA/non-polyA domains, we synthesize programmable atom-like nanoparticles (PANs) with n-valence that can be used to assemble a spectrum of low-coordination colloidal molecules with different composition, size, chirality and linearity. Moreover, by exploiting the reconfigurability of PANs, we demonstrate dynamic colloidal bond-breaking and bond-formation reactions, structural rearrangement and even the implementation of Boolean logic operations. This approach may be useful for generating responsive functional materials for distinct technological applications.
Single-stranded DNA encoders containing polyadenine domains endow colloidal gold nanoparticles with programmable bond valence, orthogonality and reconfigurability, thus achieving post-synthetic control over colloidal structures.
|Number of pages||10|
|Publication status||Published - Jul-2020|
- PLASMONIC NANOSTRUCTURES, ASYMMETRIC FUNCTIONALIZATION, GOLD NANOPARTICLES, PATCHY PARTICLES, QUANTUM DOTS, FORCE-FIELDS, OLIGONUCLEOTIDE, SUPERLATTICES