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The trans-labilization of nitric oxide in Ru-II complexes by C-bound imidazoles

机译:C结合的咪唑使Ru-II络合物中的一氧化氮反式转移

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The synthesis, characterization and reactivity of trans-[NO(L)(NH3)(4)Ru]Cl-3 (L = imidazole, theophylline and caffeine) are presented. H-1 NMR spectroscopy indicates that the imidazole ligands are coordinated to the Ru-II through a carbon atom (im kappa (2) 1,3Me(2)Xan kappa (8) and 1,3,7Me(3)Xan kappa (8)). The nitrosyl stretching frequencies (v(NO) congruent to 1913 cm(-1)) suggest the coordinated nitrosyl has substantial NO+ character. The complexes undergo a single-electron reduction (E-degrees congruent to - 0.50 V versus Ag/AgCl), which involves the coordinated nitrosyl. Dissociation of NO. in the reduced species is facilitated by the trans-imidazolylidene ligand. The lower than expected reduction potentials of these complexes may account for their inactivity in evoking neuronal firing in the hippocampus by releasing NO following reduction. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 30]
机译:介绍了反式[NO(L)(NH3)(4)Ru] Cl-3(L =咪唑,茶碱和咖啡因)的合成,表征和反应性。 H-1 NMR光谱表明咪唑配体通过碳原子与Ru-II配位(im kappa(2)1,3Me(2)Xan kappa(8)和1,3,7Me(3)Xan kappa( 8))。亚硝酰基的拉伸频率(v(NO)等于1913 cm(-1))表明配位的亚硝酰基具有明显的NO +特性。配合物经历单电子还原(E-度相当于-0.50 V对Ag / AgCl),其中包括配位的亚硝酰基。 NO解离反式咪唑基亚配体促进了还原物种中的α-内酰胺。这些复合物的还原电位低于预期,可能是由于它们在还原后释放NO而无法激发海马神经元放电。 (C)2001 Elsevier Science B.V.保留所有权利。 [参考:30]

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