“…However the solvated acacH molecule exists in the keto form in crystal 1, whereas both acacH molecules in crystal 2 exist in the enol tautomeric form ( Figure 1). N1,C(1-8), N3,C(9-16), N5,C (17)(18)(19)(20)(21)(22)(23)(24) and N7,C(25-32) are inclined to the N 4 -isoindole plane defined by the N1, N3, N5 and N7 atoms by 8.8(1), 15.4(1), 13.2(1) and 13.4(1)°, respectively, in crystal 1 and by 11.2(1), 6.0(1), 15.9(1) and 8.0(1)°, respectively, in crystal 2. The respective dihedral angles that describe the distortion of the antiprism polyhedron around the Hf cation differ slightly from the expected value of 45°that is expected for an ideal antiprism.…”