BCMaterials, Basque Center for Materials, Applications and Nanostructures , UPV/EHU Science Park , 48940 Leioa , Spain.
Departamento de Química Inorgánica, Facultad de Ciencia y Tecnología , Universidad del País Vasco UPV/EHU , P.O. Box 644, 48080 Bilbao , Spain.
Inorg Chem. 2019 Apr 1;58(7):4365-4375. doi: 10.1021/acs.inorgchem.8b03471. Epub 2019 Mar 14.
A series of 14 isostructural [Cu(cyclam)][{Cu(cyclam)}{(α-GeWO)Ln(HO)(OAc)}]·18HO (1-Ln, where Ln = La-Lu; cyclam = 1,4,8,11-tetraazacyclotetradecane) polyoxometalate-based hybrids reported herein represent (i) the first example of a two-dimensional covalent hybrid lattice involving the [{(α-XWO)Ln(HO)(OAc)}] archetype and (ii) the first structural characterization of such a dimeric polyoxotungste for Ln = La and Pr as well as for the combination of X = Ge and Ln = Ce, Nd, Sm, or Lu. Compounds 1-Ln have been characterized by elemental analyses, infrared spectroscopy, and thermogravimetric analysis, and their thermostructural behavior has been monitored by powder and single-crystal X-ray diffraction. The title compounds undergo two single-crystal-to-single-crystal transformations triggered by thermal dehydration leading to the [{Cu(cyclam)}{(α-GeWO)Ln(HO)(OAc)}]·4HO intermediate (2-Ln, where Ln = Eu or Er) and [Cu(cyclam)][{Cu(cyclam)}{(α-GeWO)Ln(OAc)}] (3-Ln, where Ln = Ce or Eu) final anhydrous phases, the latter evidencing a coordinatively unsaturated derivative of the dimeric archetype for the first time. These transitions involve formation and disruption of Cu-O bonds that result in different {Cu(cyclam)} moieties grafting onto and being released from Keggin surfaces, which reduces the dimensionality of 1-Ln to one-dimensional covalent assemblies for 2-Ln and 3-Ln. While all 3-Ln phases rehydrate fully upon exposure to air for 24 h, the kinetics governing the crystal transitions back toward 1-Ln through 2-Ln depend on the nature of Ln. Under ambient moisture, the anhydrous structures fully revert back to the parent framework for Ln = La-Sm, while the samples containing Eu to Lu afford mixtures of 1-Ln and 2-Ln and require immersion in water for the structural reversion to reach completion. Single-crystal X-ray diffraction analyses of the rehydrated 1R-Ln samples (Ln = Ce, Eu, and Er) support these observations.
本文报道了一系列 14 个同构的[Cu(cyclam)][{Cu(cyclam)}{(α-GeWO)Ln(HO)(OAc)}]·18HO(1-Ln,其中 Ln = La-Lu;cyclam = 1,4,8,11-四氮杂环十四烷)多金属氧酸盐基杂化物,它们代表了 (i) 第一个涉及[{(α-XWO)Ln(HO)(OAc)}] 原型的二维共价杂化晶格的例子,以及 (ii) 作为 Ln = La 和 Pr 以及 X = Ge 和 Ln = Ce、Nd、Sm 或 Lu 的这种二聚多钨酸盐的第一个结构特征。通过元素分析、红外光谱和热重分析对化合物 1-Ln 进行了表征,并通过粉末和单晶 X 射线衍射监测了它们的热结构行为。标题化合物经历了两个由热脱水触发的单晶到单晶的转变,导致形成[{Cu(cyclam)}{(α-GeWO)Ln(HO)(OAc)}]·4HO 中间体(2-Ln,其中 Ln = Eu 或 Er)和[Cu(cyclam)][{Cu(cyclam)}{(α-GeWO)Ln(OAc)}](3-Ln,其中 Ln = Ce 或 Eu)最终无水相,后者首次证明了二聚原型的配位不饱和衍生物。这些转变涉及 Cu-O 键的形成和破坏,导致不同的{Cu(cyclam)}部分接枝到和从 Keggin 表面释放,从而将 1-Ln 的维度降低到 2-Ln 和 3-Ln 的一维共价组装。虽然所有的 3-Ln 相在暴露于空气 24 小时后都完全重新水合,但控制晶体通过 2-Ln 向 1-Ln 转变的动力学取决于 Ln 的性质。在环境湿度下,无水结构完全恢复到 La-Sm 的母体框架,而含有 Eu 到 Lu 的样品则得到 1-Ln 和 2-Ln 的混合物,需要浸入水中才能完成结构反转。重新水合的 1R-Ln 样品(Ln = Ce、Eu 和 Er)的单晶 X 射线衍射分析支持这些观察结果。