Hi,
I am studying pi-arene ligands and there bonding to transition metals (in this case ruthenium)
I have been studying the "piano stool" structure of the compound (η6-p-cymene)RuCl2(PPh3) and was wondering the reasons why the Ru-C bonds are longer than in e.g. [(η6-p-cymene)RuCl2]2.
I'm sure it has something to do with the PPh3 ligand but I am unable to justify this.
Any help on this would be greatly appreciated.
J