Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Modena e Reggio Emilia, via G. Campi 103, 41125 Modena, Italy.
Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy.
Int J Mol Sci. 2020 Oct 23;21(21):7882. doi: 10.3390/ijms21217882.
The reactivity of the shortened salen-type ligands Hsalmp, Hsalmen and Hsal(-X)ben with variable -substituent on the central aromatic ring (X = Bu, Me, H, F, Cl, CF, NO) towards the trivalent metal ions manganese(III) and iron(III) is presented. The selective formation of the dinuclear complexes [M(μ-salmp)], M = Mn (), Fe (), [M(μ-salmen)(μ-OR))], R = Et, Me, H and M = Mn (-) or Fe (-), and (M(μ-sal[-X]ben)(μ-OMe)), X = Bu, Me, H, F, Cl, CF, NO and M = Mn (-) or Fe (-), could be identified by reaction of the Schiff bases with metal salts and the base NEt, and their characterization through elemental analysis, infrared spectroscopy, mass spectrometry and single-crystal X-ray diffraction of ·2AcOEt, ·2CHCN and ·2DMF was performed. In the case of iron(III) and Hsalmp, when using NaOH as a base instead of NEt, the dinuclear complexes [Fe(μ-salmp)(μ-OR)(salim)], R = Me, H (,) could be isolated and spectroscopically characterized, including the crystal structure of ·1.5HO, which showed that rupture of one salmp to two coordinated salim ligands and release of one salH molecule occurred. The same hydrolytic tendency could be identified with sal(-X)ben ligands in the case of iron(III) also by using NEt or upon standing in solution, while manganese(III) did not promote such a C-N bond breakage. Cyclic voltammetry studies were performed for , , and , revealing that the iron(III) complexes can be irreversibly reduced to the mixed-valence FeFe and Fe dinuclear species, while the manganese(III) derivatives can be reversibly oxidized to either the mixed-valence MnMn or to the Mn dinuclear species. The super-exchange interaction between the metal centers, mediated by the bridging ligands, resulted in being antiferromagnetic (AFM) for the selected dinuclear compounds , , , , and . The coupling constants (-2 formalism) had values around -13 cm for manganese(III) compounds, among the largest AFM coupling constants reported so far for dinuclear Mn derivatives, while values between -3 and -10 cm were obtained for iron(III) compounds.
缩短的 salen 型配体 Hsalmp、Hsalmen 和 Hsal(-X)ben 与中央芳环上可变取代基(X = Bu、Me、H、F、Cl、CF、NO)与三价金属离子锰(III)和铁(III)的反应性。通过反应希夫碱与金属盐和碱 NEt,可以鉴定出选择性地形成双核配合物 [M(μ-salmp)],M = Mn (),Fe (),[M(μ-salmen)(μ-OR))],R = Et,Me,H 和 M = Mn (-)或 Fe (-),和 (M(μ-sal[-X]ben)(μ-OMe)),X = Bu、Me、H、F、Cl、CF、NO 和 M = Mn (-)或 Fe (-),并通过元素分析、红外光谱、质谱和单晶 X 射线衍射对 ·2AcOEt、·2CHCN 和 ·2DMF 进行了表征。在铁(III)和 Hsalmp 的情况下,当使用 NaOH 作为碱而不是 NEt 时,可以分离并光谱表征双核配合物 [Fe(μ-salmp)(μ-OR)(salim)],R = Me,H (,),包括 ·1.5HO 的晶体结构,表明一个 salmp 断裂为两个配位的 salim 配体并释放一个 salH 分子。同样的水解倾向也可以在铁(III)的情况下识别出 sal(-X)ben 配体,也可以通过使用 NEt 或在溶液中放置来识别,而锰(III)则不会促进这种 C-N 键断裂。进行了循环伏安研究,对于 、 、 和 ,表明铁(III)配合物可以不可逆地还原为混合价态的 FeFe 和 Fe 双核物种,而锰(III)衍生物可以可逆地氧化为混合价态的 MnMn 或 Mn 双核物种。金属中心之间的超交换相互作用,由桥联配体介导,导致所选双核化合物 、 、 、 、 和 的反铁磁(AFM)性质。耦合常数 (-2 形式)对于锰(III)化合物的值约为-13 cm,是迄今为止报道的双核 Mn 衍生物中最大的 AFM 耦合常数之一,而对于铁(III)化合物的值在-3 到-10 cm 之间。