【摘 要】
:
稀土金属的配位化合物不仅具有特殊的拓扑结构,还在气体吸附、光学、磁性、催化等功能材料领域有潜在的应用价值,因而备受关注[1].吡啶羧酸类配体因其含有吡啶环N原子和
【机 构】
:
福建师范大学化学与材料学院,福州,350007
论文部分内容阅读
稀土金属的配位化合物不仅具有特殊的拓扑结构,还在气体吸附、光学、磁性、催化等功能材料领域有潜在的应用价值,因而备受关注[1].吡啶羧酸类配体因其含有吡啶环N原子和羧基O原子,所以具有丰富多样的配位方式和较强的配位性能而被广泛应用于配位聚合物的合成当中.本文以5-(吡啶基-3-甲氧基)-间苯二甲羧酸(H2L)为有机配体,引入Sm3+为金属源在水热条件下反应得到了一个2D层状配位聚合物{[Sm2L3(H2O)4]·(4,4-bpy)·3H2O}n.化合物中Sm3+离子采取Sm(O9)单盖帽的四方反棱柱和Sm(O8)四方反棱柱两种不同的配位几何构型.两个相邻的Sm1离子之间和相邻Sm2离子之间均通过L2-配体上的1个羧基基团桥连形成双核单元.2个晶体学独立的L2-配体将这些相邻的{Sm2}单元连接形成1D链状结构.这些1D链之间进一步通过另一晶体学独立的L2-配体连接成二维层状结构,如图2所示.
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