The reaction of ligands based on 3,6-diIJ2-pyridyl)pyridazine with symmetrical carbocyclic rings fused to the pyridazine ring; 7,10-diIJ2-pyridyl)-8,9-diazafluoranthene (L 1 ), 1,4-diIJ2-pyridyl)-6,7,8,9-tetrahydro-5H-with silver salts gave a series of complexes (1-7). Characterisation of these using single crystal X-ray structure determination clearly showed that the steric bulk of the carbocycle affects the degree to which pyridine groups remain co-planar with pyridizine, and hence their ability to chelate. The more hindered ligands L 1 -L 3 form a mixture of bischelating and tetrabridging, while the least hindered (L 4 ) was able to chelate exclusively. In the case of L 4 , the nature of the anion and solvent were also able to affect the outcome of the reaction, with tetrafluoroborate giving the first example of a 4,5-substituted 3,6-diIJ2-pyridyl)pyridazine ring forming a [2 × 2]-grid.