Steering Effect of Bromine on Intermolecular Dehydrogenation Coupling of Poly(p-phenylene) on Cu(111)

Among the multitudinous methodologies to steer on-surface reactions, less attention has been paid to the effect of externally introduced halogen atoms. Herein, highly selective trans-dehydrogenation coupling at the specific meta-C–H site of two poly(p-phenylene) molecules, p-quaterphenyl (Ph4) and p-quinquephenyl (Ph5), is achieved on Cu(111) by externally introduced bromine atoms. Scanning tunneling microscopy/spectroscopy experiments reveal that the formed molecular assembly structure at a stoichiometric ratio of 4:1 for Br to Ph4or 5:1 for Br to Ph5can efficiently promote the reactive collision probability to trigger the trans-coupling reaction at the meta-C–H site between two neighboring Ph4or Ph5molecules, leading to an increase in the coupling selectivity. Such Br atoms can also affect the electronic structure and adsorption stability of the reacting molecules. It is conceptually demonstrated that externally introduced halogen atoms, which can provide an adjustable halogen-to-precursor stoichiometry, can be employed to efficiently steer on-surface reactions.