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Diruthenium dithiolato cyanides: Basic reactivity studies and a post hoc examination of nature's choice of Fe versus Ru for hydrogenogenesis

The reaction of Ru2(S2C3H 6)(CO)6 (1) with 2 equiv of Et4NCN yielded (Et4N)2[Ru2(S2C3H 6)(CN)2(CO)4], (Et4N) 2[3], which was shown crystallographically to consist of a face-sharing bioctahedron with the cyanide ligands in the axial positions, trans to the Ru-Ru bond. Competition experiments showed that 1 underwent cyanation >100x more rapidly than the analogous Fe2(S2C 3H6)(CO)6. Furthermore, Ru2(S 2C3H6)(CO)6 underwent dicyanation faster than [Ru2(S2C3H6)(CN)(CO) 5]-, implicating a highly electrophilic intermediate [Ru2(S2C3H6)(μ-CO)(CN)(CO) 5]-. Ru2(S2C3H 6)(CO)6 (1) is noticeably more basic than the diiron compound, as demonstrated by the generation of [Ru2(S 2C3H6)(μ-H)(CO)6]+, [1H]+. In contrast to 1, the complex [1H]+ is unstable in MeCN solution and converts to [Ru2(S2C3H 6)(μ-H)(CO)5(MeCN)]+. (Et4N) 2[3] was shown to protonate with HOAc (pKa = 22.3, MeCN) and, slowly, with MeOH and H2O. Dicyanide [3]2- is stable toward excess acid, unlike the diiron complex; it slowly forms the coordination polymer [Ru2(S2C3H6)(μ-H)(CN) (CNH)(CO)4]n, which can be deprotonated with Et 3N to regenerate [H3]-. Electrochemical experiments demonstrate that [3H]- catalyzes proton reduction at -1.8 V vs Ag/AgCl. In contrast to [3]2-, the CO ligands in [3H]- undergo displacement. For example, PMe3 and [3H]- react to produce [Ru2(S2C3H6)(μ-H)(CN) 2(CO)3(PMe3)]-. Oxidation of (Et4N)2[3] with 1 equiv of Cp2Fe+ gave a mixture of [Ru2(S2C3H 6)(μ-CO)(CN)3(CO)3]- and [Ru 2(S2C3H6)(CN)(CO)5] -, via a proposed [Ru2]2(μ-CN) intermediate. Overall, the ruthenium analogues of the diiron dithiolates exhibit reactivity highly reminiscent of the diiron species, but the products are more robust and the catalytic properties appear to be less promising.