“…For instance, in {[Ti](m-h 1 :h 2 -C^CFc) 2 }Pt(PPh 3 ) (Fc ¼ Fe(h 5 -C 5 H 5 )(h 5 -C 5 H 4 )) the ferrocenyl moieties are oriented below the [Ti](C^CFc) 2 Pt plane with the PPh 3 ligand lying above, as a result of steric constraints [17]. Alkynyl migration is observed in {[Ti](C^CSiMe 3 ) 2 }M(PPh 3 ) (M ¼ Ni, Pt) complexes due to the steric interaction between the bulky groups M(PPh 3 ) and Me 3 Si, thus forming type E molecules [2f, 15,18,19]. Compounds 5e8 represent one of the few samples of heterobimetallic doubly alkynyl-bridged transition metal species [2,3], featuring a group-IV and a group VI metal atom.…”