DNA crystallization;
hydrophobic interactions;
amphiphilic molecules;
self-assembly;
single crystals;
DNA nanotechnology;
NUCLEIC-ACID JUNCTIONS;
NANOSTRUCTURED MATERIALS;
ENERGY-CONVERSION;
BLOCK-COPOLYMERS;
PHASE-BEHAVIOR;
CRYSTAL;
POLYMER;
NANOSTARS;
HYDROGEL;
STORAGE;
D O I:
10.1021/acs.nanolett.7b00980
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Many emerging technologies require materials with well-defined three-dimensional nanoscale architectures. Production of these structures is currently underpinned by self-assembling amphiphilic macromolecules or engineered all-DNA building blocks. Both of these approaches produce restricted ranges of crystal geometries due to synthetic amphiphiles simple shape and limited specificity, or the technical difficulties in designing space-filling DNA motifs with targeted shapes. We have overcome these limitations with amphiphilic DNA nanostructures, or C-Stars, that combine the design freedom and facile functionalization of DNA-based materials with robust hydrophobic interactions. C-Stars self-assemble into single crystals exceeding 40 mu m in size with lattice parameters exceeding 20 nm.