Formation of Ruthenium(II) Complexes with Unsymmetrical Terdentate Ligands
journal contributionposted on 02.07.1997 by Yurngdong Jahng, Randolph P. Thummel, Simon G. Bott
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Three unsymmetrical terdentate ligands, 2-(2‘-quinolyl)-1,10-phenanthroline (4), 2-(1‘-isoquinolyl)-1,10-phenanthroline (5), and 3,3‘-dimethylene-2-(2‘-quinolyl)-1,10-phenanthroline (6), have been prepared by application of the Friedländer condensation. Ligand 4 forms predominantly a pentaaza-coordinated (N5) complex with Ru(II), [Ru(4-N,N‘,N‘‘)(4-N,N‘)Cl](PF6), whose structure was determined by X-ray analysis (C42H26ClF6N6PRu: monoclinic, C2/c, a = 29.308(3) Å, b = 15.205(2) Å, c = 19.505(2) Å, β = 107.312(8)°, V = 8298(1) Å3, Z = 8). Ligand 5 forms predominantly a hexaaza-coordinated (N6) complex, [Ru(5-N,N‘,N‘‘)2](PF6)2. The bridged species 6 shows intermediate behavior, and the rate for interconversion of the N5 to N6 complex has been measured. The stereochemical features of these two binding modes are examined, and both π-stacking and steric effects are invoked to explain the observed behavior, leading to the proposal of a backside displacement mechanism for their interconversion.