Pérez-Aguirre Rubén, Beobide Garikoitz, Castillo Oscar, de Pedro Imanol, Luque Antonio, Pérez-Yáñez Sonia, Rodríguez Fernández Jesús, Román Pascual
Departamento de Química Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco , UPV/EHU, Apartado 644, E-48080 Bilbao, Spain.
CITIMAC, Facultad de Ciencias, Universidad de Cantabria , E-39005 Santander, Spain.
Inorg Chem. 2016 Aug 1;55(15):7755-63. doi: 10.1021/acs.inorgchem.6b01231. Epub 2016 Jul 13.
The present work provides two new examples of supramolecular metal-organic frameworks consisting of three-dimensional extended noncovalent assemblies of wheel-shaped heptanuclear Cu7(μ-H2O)6(μ3-OH)6(μ-adeninato-κN3:κN9)6 entities. The heptanuclear entity consists of a central Cu(OH)6 core connected to six additional copper(II) metal centers in a radial and planar arrangement through the hydroxides. It generates a wheel-shaped entity in which water molecules and μ-κN3:κN9 adeninato ligands bridge the peripheral copper atoms. The magnetic characterization indicates the central copper(II) center is anti-ferromagnetically coupled to external copper(II) centers, which are ferromagnetically coupled among them leading to an S = 5/2 ground state. The packing of these entities is sustained by π-π stacking interactions between the adenine nucleobases and by hydrogen bonds established among the hydroxide ligands, sulfate anions, and adenine nucleobases. The sum of both types of supramolecular interactions creates a rigid synthon that in combination with the rigidity of the heptameric entity generates an open supramolecular structure (40-50% of available space) in which additional sulfate and triethylammonium ions are located altogether with solvent molecules. These compounds represent an interesting example of materials combining both porosity and magnetic relevant features.
本工作提供了两个超分子金属有机框架的新例子,其由轮状七核Cu7(μ-H2O)6(μ3-OH)6(μ-腺嘌呤-N3: N9)6实体的三维扩展非共价组装组成。七核实体由一个中心Cu(OH)6核心组成,该核心通过氢氧化物以径向和平面对称排列连接到另外六个铜(II)金属中心。它形成了一个轮状实体,其中水分子和μ-κN3:κN9腺嘌呤配体桥接外围铜原子。磁性表征表明,中心铜(II)中心与外部铜(II)中心反铁磁耦合,而外部铜(II)中心之间铁磁耦合,导致基态S = 5/2。这些实体的堆积通过腺嘌呤核碱基之间的π-π堆积相互作用以及氢氧化物配体、硫酸根阴离子和腺嘌呤核碱基之间形成的氢键得以维持。这两种超分子相互作用的总和形成了一个刚性合成子,该合成子与七聚体实体的刚性相结合,产生了一个开放的超分子结构(可用空间占比40 - 50%),其中额外的硫酸根和三乙铵离子与溶剂分子一起位于其中。这些化合物代表了一种兼具孔隙率和磁性相关特性的有趣材料实例。