Related Experiment Video
Updated: Jan 5, 2026

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species
Published on: August 16, 2018
Surface-assisted Ullmann coupling
1Deutsches Museum, Museumsinsel 1, 80538 München, Germany.
Surface-assisted Ullmann coupling enables on-surface synthesis of organic nanostructures. This review details its reliability, control, and applications in reticular synthesis, while exploring complexities like defects and side reactions.
Area of Science:
- Materials Science
- Organic Chemistry
- Surface Chemistry
Background:
- Surface-assisted Ullmann coupling is a key method for on-surface synthesis.
- It involves dehalogenation of precursors on metal surfaces to form C-C bonds.
- This reaction is crucial for creating novel organic nanostructures.
Purpose of the Study:
- To review published work on surface-assisted Ullmann coupling.
- To highlight its reliability, controllability, and applications.
- To discuss complexities and current trends in the field.
Main Methods:
- Deposition of halogenated precursors onto coinage metal surfaces.
- Surface-induced dehalogenation to form reactive species.
- Recombination of species to form C-C bonds and covalent nanostructures.
Main Results:
- Ullmann coupling is a reliable and controllable method for on-surface synthesis.
- Precursor halogenation patterns dictate nanostructure dimensionality and topology.
- Complexities include topological defects and competing C-H activation.
Conclusions:
- Surface-assisted Ullmann coupling is a powerful tool for reticular synthesis of organic nanostructures.
- Understanding reaction complexities is vital for fundamental research and advanced applications.
- The field continues to evolve with ongoing research into trends and challenges.
More Related Videos
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
08:24Optimization of the Ugi Reaction Using Parallel Synthesis and Automated Liquid Handling
Published on: November 10, 2008
Related Concept Videos
¹H NMR: Long-Range Coupling
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
Spin–Spin Coupling: One-Bond Coupling
NMR Spectroscopy: Spin–Spin Coupling
Cycloaddition Reactions: MO Requirements for Thermal Activation