Structural characterisation of molecular conformation and the incorporation of adatoms in an on-surface Ullmann-type reaction.

ABSTRACT: The on-surface synthesis of covalently bonded materials differs from solution-phase synthesis in several respects. The transition from a three-dimensional reaction volume to quasi-two-dimensional confinement, as is the case for on-surface synthesis, has the potential to facilitate alternative reaction pathways to those available in solution. Ullmann-type reactions, where the surface plays a role in the coupling of aryl-halide functionalised species, has been shown to facilitate extended one- and two-dimensional structures. Here we employ a combination of scanning tunnelling microscopy (STM), X-ray photoelectron spectroscopy (XPS) and X-ray standing wave (XSW) analysis to perform a chemical and structural characterisation of the Ullmann-type coupling of two iodine functionalised species on

SUBMITTER: Judd CJ 

PROVIDER: S-EPMC9814584 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature