640727-53-3Relevant academic research and scientific papers
Nitrido-ruthenium(VI) and -osmium(VI) complexes of multianionic chelating (N, O) ligands. Reactions with nucleophiles, electrophiles and oxidizing agents
Yip, Ka-Lai,Yu, Wing-Yiu,Chan, Pui-Ming,Zhu, Nian-Yong,Che, Chi-Ming
, p. 3556 - 3566 (2003)
This account presents the diverse reactivity of nitridoruthenium(VI) complexes with nucleophilic, electrophilic and oxidizing agents. [Ru VI(N)(L1)Cl] (1) [H2L1 = 2,6-bis(2,2-diphenyl-2-hydroxyethyl)pyridine] reacted with excess phosphines such as PPh3, PPhMe2 and dppe to give [Ru III(HL1)(PPh3)Cl2] (2a), [Ru III(L1)(PPhMe2)2Cl] (2b) and [RuIII(L1)(dppe)Cl] (2c), respectively. In the presence of py or Hpz, 1 was converted to LRuIII(L1)(py) 2Cl] (3a) and [RuIII(L1)(Hpz)3]Cl (3b), respectively. A dinuclear μ-nitridoruthenium complex, [Ru IV(L1)Cl2(μ-N)RuVI(L 1)(C8H10N)Cl] (4), was obtained by treating 1 with 2,6-dimethylaniline, Based on X-ray crystallographic study, the compound is characterized by an unsymmetrical Ru-Nequiv;Ru moiety with the measured Ru-N distances being 1.661(5) and 1.837(5) A. Complex 1 reacted with dmf to give [RuIII(HL1)(dmf)Cl2] (5) in 17% yield. Excess (Me3O)BF4 reacted with 1 to give a dinuclear μ-OH ruthenium complex, [Ru2(N)2(L1) 2(OH)]PF6 (6). The measured Ru-O(OH) distance is 1.984(3) A and the average Ru-O-Ru angle was found to be 100.4(2)°. Other nitrido-metal complexes, [n-Bu4N][MVI(N)(L)] [L = L2 and L3; M = Os and Ru; H4L2 = 1,2-dichloro-4,5-bis(2-hydroxybenzamido)benzene, H4L3 = 1,2-bis(2-hydroxybenzamido)benzene], underwent ligand protonation to form [MVI(N)(HL)] complexes, which have been characterized by X-ray crystallography. Oxidation of [n-Bu4N][OsVI(N)(L 2)] by PhI(OAc)2 produced [n-Bu4N][Os VI(N)(L2O2)] (8) in 10% yield. X-ray structure analysis of 8 showed that the coordinated phenoxy moiety was converted to a benzoquinone moiety while the Os≡N group remained intact.
