Sirenko Valerii Y, Kucheriv Olesia I, Shova Sergiu, Shylin Sergii I, Ksenofontov Vadim, Fritsky Igor O, Tremel Wolfgang, Gural'skiy Il'ya A
Department of Chemistry, Taras Shevchenko National University of Kyiv, 64 Volodymyrska St., 01601 Kyiv, Ukraine.
Department of Inorganic Polymers, "Petru Poni" Institute of Macromolecular Chemistry, 41A Aleea Gr. Ghica Voda, 700487 Iasi, Romania.
Dalton Trans. 2024 Feb 27;53(9):4251-4259. doi: 10.1039/d3dt04372j.
Chemical composition is leading among the numerous factors that determine the spin transition properties of coordination compounds. Classic dicyanometallic bridges {M(CN)} are commonly used to build Hofmann-like spin-crossover frameworks, but some extended bridges are also synthetically available. In this paper, we describe a successful synthesis of two very similar spin-crossover frameworks that differ in the cyanometallic bridges involved, namely [Fe(etpz){Ag(CN)}] (1) and {Fe(etpz)[Ag(CN)][Ag(CN)]} (2) (where etpz = 2-ethylpyrazine). Magnetic and Mössbauer studies demonstrated the occurrence of abrupt one-step high-spin (HS) ↔ low-spin (LS) transitions for both complexes. The spin transition temperatures are ↓ = 233 K and ↑ = 243 K for 1 and ↓ = 188 K and ↑ = 191 K for 2 with thermal hysteresis loops of 10 K for 1 and 3 K for 2. The bridging mononuclear [Ag(CN)] units and Fe cations assemble to form infinite 2D layers in the structure of 1. Interestingly, compound 2 forms 2D layers of Fe cations bridged by both binuclear [Ag(CN)] and mononuclear [Ag(CN)] units. The structures of 1 and 2 comprise different types of intermolecular interactions including Ag⋯Ag and Ag⋯N, which induce the creation of supramolecular 3D frameworks. The synergy between metallophilic interactions and the spin transition is also confirmed by the variation of Ag⋯Ag distances during spin crossover. The characterization of such analogues allowed us to analyze in detail the effect of the cyanometallic bridge on the structure of new frameworks and on the bistability in Hofmann-like complexes.
在决定配位化合物自旋转变性质的众多因素中,化学成分起着主导作用。经典的二氰基金属桥{M(CN)}通常用于构建类霍夫曼自旋交叉框架,但一些扩展桥也可通过合成获得。在本文中,我们描述了两种非常相似的自旋交叉框架的成功合成,它们在所涉及的氰基金属桥上有所不同,即[Fe(etpz){Ag(CN)}] (1) 和{Fe(etpz)[Ag(CN)][Ag(CN)]} (2)(其中etpz = 2 - 乙基吡嗪)。磁性和穆斯堡尔研究表明,这两种配合物都发生了突然的一步高自旋(HS)↔ 低自旋(LS)转变。配合物1的自旋转变温度为↓ = 233 K,↑ = 243 K,配合物2的自旋转变温度为↓ = 188 K,↑ = 191 K,配合物1的热滞回环为10 K,配合物2的热滞回环为3 K。桥连单核[Ag(CN)]单元和Fe阳离子在1的结构中组装形成无限二维层。有趣的是,化合物2形成了由双核[Ag(CN)]和单核[Ag(CN)]单元桥连的Fe阳离子二维层。1和2的结构包含不同类型的分子间相互作用,包括Ag⋯Ag和Ag⋯N,这导致了超分子三维框架的形成。自旋交叉过程中Ag⋯Ag距离的变化也证实了亲金属相互作用与自旋转变之间的协同作用。对这些类似物的表征使我们能够详细分析氰基金属桥对新框架结构以及类霍夫曼配合物双稳性的影响。