“…This is in agreement with the results recently published by Abram and co-workers, who observed that the number of NHCs introduced in a series of oxorhenium complexes depends on the electron-donating nature of the carbene, the more electron-donating the carbene, the higher the number of ligands [13]. In this sense, 4,5-dimethyl substituted NHCs always provide complexes with general formula [ReOCl-(NHC) 4 ] 2+ [4,15] (complexes with less than four carbenes could not be obtained), while non-substituted and triazolylidene NHCs provide ReOCl 3 (NHC) 2 [5] and [ReO(OMe)-Cl 2 (NHC)(PPh 3 )], respectively.…”