Heterobimetallic nitrido porphyrin complexes with the [(L)(por)M-N-M'(L)Cl] formula {por = 5,10,15,20-tetraphenylporphyrin (TPP) or 5,10,15,20-tetra(p-tolyl)porphyrin (TTP) dianion; L = [Co(η-CH){P(O)(OEt)}]; M = Fe, Ru, or Os; M' = Ru or Os; L = HO or pyridine} have been synthesized, and their electrochemistry has been studied. Treatment of trans-[Fe(TPP)(py)] (py = pyridine) with Ru(VI) nitride [Ru(L)(N)Cl] (1) afforded Fe/Ru μ-nitrido complex [(py)(TPP)Fe(μ-N)Ru(L)Cl] (2). Similarly, Fe/Os analogue [(py)(TPP)Fe(μ-N)Os(L)Cl] (3) was obtained from trans-[Fe(TPP)(py)] and [Os(L)(N)Cl]. However, no reaction was found between trans-[Fe(TPP)(py)] and [Re(L)(N)Cl(PPh)]. Treatment of trans-[M(TPP)(CO)(EtOH)] with 1 afforded μ-nitrido complexes [(HO)(TPP)M(μ-N)Ru(L)Cl] [M = Ru (4a) or Os (5)]. TTP analogue [(HO)(TTP)Ru(μ-N)Ru(L)Cl] (4b) was prepared similarly from trans-[Ru(TTP)(CO)(EtOH)] and 1. Reaction of [(HO)(por)M(μ-N)M(L)Cl] with pyridine gave adducts [(py)(por)M(μ-N)Ru(L)Cl] [por = TTP, and M = Ru (6); por = TPP, and M = Os (7)]. The diamagnetism and short (por)M-N(nitride) distances in 2 [Fe-N, 1.683(3) Å] and 4b [Ru-N, 1.743(3) Å] are indicative of the M═N═M' bonding description. The cyclic voltammograms of the Fe/Ru (2) and Ru/Ru (4b) complexes in CHCl displayed oxidation couples at approximately +0.29 and +0.35 V versus Fc (Fc = ferrocene) that are tentatively ascribed to the oxidation of the {LRu} and {Ru(TTP)} moieties, respectively, whereas the Fe/Os (3) and Os/Ru (5) complexes exhibited Os-centered oxidation at approximately -0.06 and +0.05 V versus Fc, respectively. The crystal structures of 2 and 4b have been determined.
Treatment of Ru(dCHPh)Cl 2 (PCy 3 ) 2 (Cy = cyclohexyl) with K[N(i-Pr 2 PS) 2 ] afforded a mixture of Ru-(dCHPh)[N(i-Pr 2 PS) 2 ](PCy 3 )Cl (1) and Ru(dCHPh)-[N(i-Pr 2 PS) 2 ] 2 (2). Reaction of 1 with TlOPh gave Ru-(dCHPh)[N(i-Pr 2 PS) 2 ](PCy 3 )(OPh) (3), whereas that with NaOMe yielded the Ru(II) hydride compound Ru(H) [N(i-Pr 2 PS) 2 ][PCy 2 (η 2 -C 6 H 9 )] ( 4), in which the dicyclohexyl(cyclohex-3-enyl)phosphine ligand binds to Ru via the phosphorus atom and the CdC bond of the cyclohex-3-enyl ring. The structures of complexes 3 and 4 have been established by X-ray crystallography.
Iridium porphyrin complexes containing μ-nitrido, hydroxo, hydrosulfido, and alkynyl ligands have been synthesized and structurally characterized, and their oxidation has been studied.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.