Example of Highly Stereoregulated Ruthenium Amidine Complex Formation: Synthesis, Crystal Structures, and Spectral and Redox Properties of the Complexes [Ru<sup>II</sup>(trpy){NC<sub>5</sub>H<sub>4</sub>CHNN(C<sub>6</sub>H<sub>5</sub>)C(CH<sub>3</sub>)NH}](ClO<sub>4</sub>)<sub>2</sub> (<b>1</b>) and [Ru<sup>II</sup>(trpy)(NC<sub>5</sub>H<sub>4</sub>CHNNHC<sub>6</sub>H<sub>5</sub>)Cl]ClO<sub>4</sub> (<b>2</b>) (trpy = 2,2‘:6‘,2‘ ‘-Terpyridine)
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The reaction of Ru(trpy)Cl3 (trpy = 2,2‘:6‘,2‘ ‘-terpyridine) with the pyridine-based imine function NpC5H4−CHNi-NH−C6H5 (L), incorporating an NH spacer between the imine nitrogen (Ni) and the pendant phenyl ring, in ethanol medium followed by chromatographic work up on a neutral alumina column using CH3CN/CH2Cl2 (1:4) as eluent, results in complexes of the types [Ru(trpy)(L‘)](ClO4)2 (1) and [Ru(trpy)(L)Cl]ClO4 (2). Although the identity of the free ligand (L) has been retained in complex 2, the preformed imine-based potentially bidentate ligand (L) has been selectively transformed into a new class of unusual imine−amidine-based tridentate ligand, NpC5H4CHNiN(C6H5)C(CH3)NaH (L‘), in 1. The single-crystal X-ray structures of the free ligand (L) and both complexes 1 and 2 have been determined. In 2, the sixth coordination site, that is, the Cl- function, is cis to the pyridine nitrogen (Np) of L which in turn places the NH spacer away from the RuCl bond, whereas, in 1, the corresponding sixth position, that is, the RuNa (amidine) bond, is trans to the pyridine nitrogen (Np) of L‘. The trans configuration of Na with respect to the Np of L‘ in 1 provides the basis for the selective L → L‘ transformation in 1. The complexes exhibit strong Ru(II) → π* (trpy) MLCT transitions in the visible region and intraligand transitions in the UV region. The lowest energy MLCT band at 510 nm for 2 has been substantially blue-shifted to 478 nm in the case of 1. The reversible Ru(III)−Ru(II) couples for 1 and 2 have been observed at 0.80 and 0.59 V versus SCE, respectively. The complexes are weakly luminescent at 77 K, exhibiting emissions at λmax, 598 nm [quantum yield (Φ) = 0.43 × 10-2 ] and 574 nm (Φ = 0.28 × 10-2 ) for 1 and 2, respectively.



