Programming Dimensional Transitions in DNA Brick Crystals via Interfacial Connectivity
ABSTRACT The precise control of assembly dimensionality and macroscopic structural parameters remains a fundamental challenge in molecular self‐assembly. Here, we introduce a programmable strategy to govern the 1D‐to‐2D dimensional transition and structural width of DNA brick crystals by engineering their connecting interfaces. Using the number of interface connecting strands ( N x ) as a quantitative design parameter, we discover a sharp dimensional threshold that is preserved across both honeycomb and square lattices. At N x ≤ 8, the assembly is strictly confined to one‐dimensional nanoribbons; whereas at N x ≥ 12, lateral coupling activates extended two‐dimensional arrays whose structural width increases monotonically with N x . Thermal and thermodynamic analyses reveal that this sharp threshold behavior is lattice‐independent and originates from the size‐dependent thermal stability of the laterally connected domains. Our work establishes interfacial connectivity as a predictive handle for the on‐demand engineering of self‐assembled nanostructures with programmable dimensionality and prescribed widths.
Authors
- Chunhai Fan (ORCID: https://orcid.org/0000-0002-7171-7338)
- Xin Huang (ORCID: https://orcid.org/0000-0002-4063-5292)
- L C WANG
- Sisi Jia (ORCID: https://orcid.org/0000-0002-5877-5138)
- Yi‐Cheng Lin (ORCID: https://orcid.org/0000-0002-5130-5280)
- Jiang Li (ORCID: https://orcid.org/0000-0003-2372-6624)
- Wenhe Ma
- B U.K. Li
- Yue Wang
- Xiaoguo Liu
Institutions
- Macau University of Science and Technology (MO)
- University of Macau (MO)
- Shanghai Innovative Research Center of Traditional Chinese Medicine (CN)
- Shanghai Institute of Materia Medica (CN)
- Shanghai Zhangjiang Laboratory (CN)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2026-06-18
- DOI
- https://doi.org/10.1002/ange.2278382
- Primary Topic
- Surface Chemistry and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00