Incorporation of Ru2(O2C(CH2)6CH3)4 into Extended Chains: Interaction of Ru2(O2C(CH2)6CH3)4 with Pyrazine, 4-Cyanopyridine, TCNE, and p-Benzoquinone
journal contributionposted on 16.07.1997, 00:00 by Jodi L. Wesemann, Malcolm H. Chisholm
In attempts to form extended chains Ru2(O2C(CH2)6CH3)4 (1) was reacted with both simple coordination and redox-active bridging ligands. The simple coordination ligands, pyrazine (pz) and 4-cyanopyridine (4-cp), coordinated in the axial sites of the diruthenium complex. With the symmetric ligand pyrazine, the polymer [1(pz)]n was isolated. With the asymmetric ligand 4-cp, the pyridine nitrogen coordinated preferentially and the bis-adduct 1(4-cp)2 was isolated. Solution UV/visible and NMR studies indicated that π-interactions between the Ru−Ru π* and ligand π orbitals were occurring in both cases. Mole ratio and continuous variation studies of 1 with pyrazine and 4-cp indicated that these axial ligands were labile and that a number of solution species existed. When 1 was reacted with TCNE, redox reactions occurred. Solid-state IR and solution NMR studies also showed that both 1(TCNE) (2) and 2TCNE (3) contained diruthenium carboxylate cores which no longer possessed the D4h paddle-wheel geometry. With p-benzoquinone, redox reactions occurred upon coordination to give [1+][SQ-•] (4), which contained an undisrupted oxidized diruthenium tetracarboxylate core. Formation of 4 was reversible in solution, with 1 and p-benzoquinone being favored at higher temperatures.