Constructing covalent organic nanoarchitectures molecule by molecule via scanning probe manipulation

Constructing low-dimensional covalent assemblies with tailored size and connectivity is challenging yet often key for applications in molecular electronics where optical and electronic properties of the quantum materials are highly structure dependent. We present a versatile approach for building such structures block by block on bilayer sodium chloride (NaCl) films on Cu(111) with the tip of an atomic force microscope, while tracking the structural changes with single-bond resolution. Covalent homo-dimers in cis and trans configurations and homo-/hetero-trimers were selectively synthesized by a sequence of dehalogenation, translational manipulation and intermolecular coupling of halogenated precursors. Further demonstrations of structural build-up include complex bonding motifs, like carbon-iodine-carbon bonds and fused carbon pentagons. This work paves the way for synthesizing elusive covalent nanoarchitectures, studying structural modifications and revealing pathways of intermolecular reactions. Tailoring the size and connectivity of organic nanostructures is challenging but is often key in molecular electronics for tuning the properties of the quantum materials. Now an approach has been developed for building low-dimensional covalent architectures block by block on a surface by highly selective tip-induced intermolecular reactions.

Automated summary

Constructing low-dimensional covalent assemblies with tailored size and connectivity is challenging but important in molecular electronics for tuning the properties of quantum materials. A versatile approach has been developed for building such structures block by block on a surface through highly selective tip-induced intermolecular reactions.