Pinar A B, McCusker L B, Baerlocher C, Schmidt J, Hwang S-J, Davis M E, Zones S I
Laboratory of Crystallography, ETH Zurich, Zurich, Switzerland.
Dalton Trans. 2015 Apr 7;44(13):6288-95. doi: 10.1039/c4dt03831b.
The germanosilicate ITQ-24 (IWR framework type) was synthesized in fluoride medium using 1,3,5-tris(1,2-dimethylimidazolium) benzene as the structure directing agent (SDA). A structure analysis of the as-synthesized ITQ-24 material using synchrotron powder diffraction data and difference electron density calculations have allowed the fluoride ions and the germanium atoms to be located and the conformation of the SDA to be determined. The benzyl ring is perpendicular to the b axis with the three imidazolium moieties forming a "T-shaped" arrangement. Ge atoms replace some of the Si in the double-4-ring (d4r) and in one of the single-4-rings (s4r). The other s4r contains only Si. Fluoride ions are in the d4r units. Initially, the space group Cmmm (highest possible symmetry) was assumed, but the framework geometry was strained. An independent evaluation of the symmetry using the powder charge flipping algorithm in Superflip led to a successful refinement with reasonable geometry and a refined composition of |[(C6H3)(C7H10N2)3]2F2|[Si(40.2)Ge(15.8)O112] in the space group Pban.
锗硅酸盐ITQ - 24(IWR骨架类型)是在氟化物介质中以1,3,5 - 三(1,2 - 二甲基咪唑鎓)苯作为结构导向剂(SDA)合成的。利用同步加速器粉末衍射数据和差分电子密度计算对合成后的ITQ - 24材料进行结构分析,确定了氟离子和锗原子的位置以及SDA的构象。苄基环垂直于b轴,三个咪唑鎓部分形成“T形”排列。锗原子取代了双4环(d4r)和其中一个单4环(s4r)中的一些硅原子。另一个s4r只含有硅原子。氟离子存在于d4r单元中。最初假设空间群为Cmmm(可能的最高对称性),但骨架几何结构存在应变。使用Superflip中的粉末电荷翻转算法对对称性进行独立评估,成功地进行了精修,得到了合理的几何结构和精修后的化学式|[(C6H3)(C7H10N2)3]2F2|[Si(40.2)Ge(15.8)O112],空间群为Pban。