“…In the reported complexes, the ferrocenedicarboxylate moieties usually exist as bi-(OOCFcCOO) coordination mode such as in complexes [Cu 2 {Fc(COOH) 2 } 2 (py) 2 -(DMF) 2 (H 2 O) 2 ], [Zn{Fc(COOH) 2 }(1-methylimidazole) 2 ] 2 , and [M 2 (O 2 CFcCO 2 ) 2 (2,2 0 -bpy) 2 (l 2 -OH 2 ) 2 ] (M = Co, Ni) [3e,3f], tri-(g 2 -OOCFcCOO) mode such as in complexes Ni 2 {Fc(COOH) 2 } 2 (py) 4 (H 2 O) and [M 2 (g 2 -O 2 CFcCO 2 ) 2 (2,2 0 -bpy) 2 (H 2 O) 2 ] (M = Zn, Cd) [3b,3f], tetra-(g 2 -OOCFc COO-g 2 ) mode such as in complex {[Cd(O 2 CFcCO 2 )(H 2 O) 3 ] AE 4H 2 O} n [8]. In complexes {[M(O 2 CFcCO 2 ) 1.5 (H 2 O) 2 ] AE mH 2 O} n (M = Tb 3+ , or Eu 3+ , or Y 3+ ; m = 1 or 2), ferrocenedicarboxylate groups coordinate to metal ions as tetra-(g 2 -OOCFcCOO-g 2 ) and hexa-(l 2 -g 2 -OOCFcCOOg 2 -l 2 ) modes simultaneously [8].…”