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Updated: Oct 16, 2025

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Manifold dynamic non-covalent interactions for steering molecular assembly and cyclization.
Shaotang Song1, Lulu Wang1, Jie Su1
1Department of Chemistry, National University of Singapore 3 Science Drive 3 Singapore 117543 chmwmw@nus.edu.sg.
Researchers used advanced microscopy to reveal weak molecular interactions in clusters. These interactions control molecular assembly and chemical reactions, enabling new ways to build complex nanostructures.
Area of Science:
- Chemical Physics
- Surface Science
- Supramolecular Chemistry
Background:
- Non-covalent interactions are vital for molecular design and function.
- Characterizing weak interactions at the single-bond level in complex systems is challenging.
Purpose of the Study:
- To elucidate the multiple non-covalent interactions governing molecular clustering.
- To understand how these interactions control chemical reactions on surfaces.
Main Methods:
- Bond-resolved scanning probe microscopy (SPM).
- Exhaustive structural search algorithms.
- Quantum chemistry calculations.
Main Results:
- Identified diverse non-covalent interactions (hydrogen, halogen, C-H⋯π, lone pair⋯π) in dimer and trimer clusters.
- Observed dynamic transformation of dimers to trimers with increasing molecular density.
- Demonstrated that trimer formation facilitates Ullmann coupling, while dimer disassembly favors cyclization.
Conclusions:
- Weak interactions play a critical role in controlling molecular assembly and on-surface synthesis.
- This approach offers new possibilities for designing complex molecular architectures and quantum nanostructures.
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