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五核双(三联吡啶)锰配合物中的多可逆氧化还原过程,其特征为一个以氧为中心的三角形{Mn(II)2Mn(III)(μ3-O)}5+或{Mn(II)Mn(III)2(μ3-O)}6+核,被两个{Mn(II)2(bpp)3}-所包裹。

Multireversible redox processes in pentanuclear bis(triple-helical) manganese complexes featuring an oxo-centered triangular {Mn(II)2Mn(III)(μ3-O)}5+ or {Mn(II)Mn(III)2(μ3-O)}6+ core wrapped by two {Mn(II)2(bpp)3}-.

机构信息

Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, E-43007 Tarragona, Spain.

出版信息

Inorg Chem. 2011 Sep 5;50(17):8427-36. doi: 10.1021/ic201009z. Epub 2011 Aug 3.

Abstract

A new pentanuclear bis(triple-helical) manganese complex has been isolated and characterized by X-ray diffraction in two oxidation states: {Mn(II)(μ-bpp)(3)}(2)Mn(II)(2)Mn(III)(μ-O) (1(3+)) and {Mn(II)(μ-bpp)(3)}(2)Mn(II)Mn(III)(2)(μ-O) (1(4+)). The structure consists of a central {Mn(3)(μ(3)-O)} core of Mn(II)(2)Mn(III) (1(3+)) or Mn(II)Mn(III)(2) ions (1(4+)) which is connected to two apical Mn(II) ions through six bpp(-) ligands. Both cations have a triple-stranded helicate configuration, and a pair of enantiomers is present in each crystal. The redox properties of 1(3+) have been investigated in CH(3)CN. A series of five distinct and reversible one-electron waves is observed in the -1.0 and +1.50 V potential range, assigned to the Mn(II)(4)Mn(III)/Mn(II)(5), Mn(II)(3)Mn(III)(2)/Mn(II)(4)Mn(III), Mn(II)(2)Mn(III)(3)/Mn(II)(3)Mn(III)(2), Mn(II)Mn(III)(4)/Mn(II)(2)Mn(III)(3), and Mn(III)(5)/Mn(II)Mn(III)(4) redox couples. The two first oxidation processes leading to Mn(II)(3)Mn(III)(2) (1(4+)) and Mn(II)(2)Mn(III)(3) (1(5+)) are related to the oxidation of the Mn(II) ions of the central core and the two higher oxidation waves, close in potential, are thus assigned to the oxidation of the two apical Mn(II) ions. The 1(4+) and 1(5+) oxidized species and the reduced Mn(4)(II) (1(2+)) species are quantitatively generated by bulk electrolyses demonstrating the high stability of the pentanuclear structure in four oxidation states (1(2+) to 1(5+)). The spectroscopic characteristics (X-band electron paramagnetic resonance, EPR, and UV-visible) of these species are also described as well as the magnetic properties of 1(3+) and 1(4+) in solid state. The powder X- and Q-band EPR signature of 1(3+) corresponds to an S = 5/2 spin state characterized by a small zero-field splitting parameter (|D| = 0.071 cm(-1)) attributed to the two apical Mn(II) ions. At 40 K, the magnetic behavior is consistent for 1(3+) with two apical S = 5/2 {Mn(II)(bpp)(3)}(-) and one S = 2 noninteracting spins (11.75 cm(3) K mol(-1)), and for 1(4+) with three S = 5/2 noninteracting spins (13.125 cm(3) K mol(-1)) suggesting that the {Mn(II)(2)Mn(III)(μ(3)-O)}(5+) and {Mn(II)Mn(III)(2)(μ(3)-O)}(6+) cores behave at low temperature like S = 2 and S = 5/2 spin centers, respectively. The thermal behavior below 40 K highlights the presence of intracomplex magnetic interactions between the two apical spins and the central core, which is antiferromagnetic for 1(3+) leading to an S(T) = 3 and ferromagnetic for 1(4+) giving thus an S(T) = 15/2 ground state.

摘要

一种新的五核双(三螺旋)锰配合物已通过 X 射线衍射在两个氧化态下被分离和表征:{Mn(II)(μ-bpp)(3)}(2)Mn(II)(2)Mn(III)(μ-O)(1(3+))和{Mn(II)(μ-bpp)(3)}(2)Mn(II)Mn(III)(2)(μ-O)(1(4+))。该结构由一个中心{Mn(3)(μ(3)-O)}核组成,其中包含 Mn(II)(2)Mn(III)(1(3+))或 Mn(II)Mn(III)(2)离子(1(4+)),这些离子通过六个 bpp(-)配体与两个顶点 Mn(II)离子相连。两种阳离子都具有三重螺旋螺旋构象,每个晶体中都存在一对对映异构体。1(3+)的氧化还原性质已在 CH(3)CN 中进行了研究。在-1.0 和+1.50 V 的电位范围内观察到一系列五个明显且可逆的单电子波,归因于 Mn(II)(4)Mn(III)/Mn(II)(5)、Mn(II)(3)Mn(III)(2)/Mn(II)(4)Mn(III)、Mn(II)(2)Mn(III)(3)/Mn(II)(3)Mn(III)(2)、Mn(II)Mn(III)(4)/Mn(II)(2)Mn(III)(3)和 Mn(III)(5)/Mn(II)Mn(III)(4)氧化还原对。导致 Mn(II)(3)Mn(III)(2)(1(4+))和 Mn(II)(2)Mn(III)(3)(1(5+))的前两个氧化过程与中心核的 Mn(II)离子的氧化以及两个电位相近的更高氧化波有关,因此被分配给两个顶点 Mn(II)离子的氧化。1(4+)和 1(5+)氧化物种以及还原的 Mn(4)(II)(1(2+))物种通过大量电解定量生成,证明了五核结构在四个氧化态(1(2+)至 1(5+))下的高稳定性。还描述了这些物种的光谱特性(X 波段电子顺磁共振、EPR 和紫外可见)以及 1(3+)和 1(4+)在固态中的磁性。1(3+)的粉末 X-和 Q-波段 EPR 特征对应于 S = 5/2 自旋态,其特征为小的零场分裂参数(|D| = 0.071 cm(-1))归因于两个顶点 Mn(II)离子。在 40 K 时,1(3+)的磁性行为与两个顶点 S = 5/2 {Mn(II)(bpp)(3)}(-)和一个 S = 2 非相互作用自旋(11.75 cm(3) K mol(-1))一致,与 1(4+)与三个 S = 5/2 非相互作用自旋(13.125 cm(3) K mol(-1))一致,表明 {Mn(II)(2)Mn(III)(μ(3)-O)}(5+)和 {Mn(II)Mn(III)(2)(μ(3)-O)}(6+)核在低温下分别表现为 S = 2 和 S = 5/2 自旋中心的行为。低于 40 K 的热行为突出了两个顶点自旋和中心核之间的内配合物相互作用的存在,对于 1(3+)为反铁磁,导致 S(T) = 3,对于 1(4+)为铁磁,从而给出 S(T) = 15/2 的基态。

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