State Key Laboratory of Coordination Chemistry, Coordination Chemistry Institute, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210093, PR China.
Dalton Trans. 2011 Feb 14;40(6):1307-12. doi: 10.1039/c0dt01019g. Epub 2011 Jan 5.
Two isostructural metal phosphonates M₃(2-cpp)₂(H₂O)₃·H₂O [M(II) = Co (1), Zn (2), 2-cppH₃ = 2-carboxyphenylphosphonic acid] are synthesized and structurally characterized. Both exhibit layer structures in which -Co-O- "columns" are connected by the {PO₃C} linkages. The "column" consists of triangular shaped {M₃O₃} trimers, inter-linked through either corner- or edge-sharing of the {MO₆} octahedra. The phenyl groups are grafted on the two sides of the inorganic layer. Thermal analyses suggest that the layer structures of 1 and 2 are stable after removal of the lattice and coordination water. The dehydrated sample can be rehydrated reversibly in the case of compound 1. Magnetic studies reveal that antiferromagnetic interactions dominate in both 1 and 1-de, resulting in ferrimagnetic layers in both cases. The large inter-layer distance in 1 favors a ferromagnetic interaction between the layers. Hence ferrimagnetism is observed in both cases at low temperature. For 1-de, slow magnetization relaxation is also observed below ca. 2.8 K.
两种同构的金属膦酸盐 M₃(2-cpp)₂(H₂O)₃·H₂O [M(II) = Co (1), Zn (2), 2-cppH₃ = 2-羧苯基膦酸] 被合成并进行了结构表征。两者都表现出层状结构,其中 -Co-O- "柱子" 通过 {PO₃C} 连接体连接。"柱子"由通过 {MO₆} 八面体的角共享或边共享相互连接的三角形 {M₃O₃} 三聚体组成。苯基基团接枝在无机层的两侧。热分析表明,1 和 2 的层状结构在去除晶格和配位水后是稳定的。在化合物 1 的情况下,脱水样品可以可逆地再水合。磁性研究表明,在 1 和 1-de 中,反铁磁相互作用占主导地位,导致两种情况下都出现亚铁磁层。1 中的大层间距离有利于层间的铁磁相互作用。因此,在低温下两种情况下都观察到亚铁磁性。对于 1-de,在大约 2.8 K 以下也观察到缓慢的磁化弛豫。