Lucas Carreras, Marta Serrano-Torné, Piet W. N. M. van Leeuwen and Anton Vidal-Ferran
Chem. Sci., 2018,9, 3644-3648
DOI:
10.1039/C8SC00233A,
Edge Article
The use of halogen bonding as a tool to construct a catalyst backbone is reported. Specifically, pyridyl- and iodotetrafluoroaryl-substituted phosphines were assembled in the presence of a rhodium(I) precursor to form the corresponding halogen-bonded complex XBphos-Rh. The presence of fluorine substituents at the iodo-containing supramolecular motif was not necessary for halogen bonding to occur due to the template effect exerted by the rhodium center during formation of the halogen-bonded complex. The halogen-bonded supramolecular complexes were successfully tested in the catalytic hydroboration of terminal alkynes.