Structure-directing role of immobilized polyoxometalates in the synthesis of porphyrinic Zr-based metal-organic frameworks

被引:17
|
作者
Duguet, Mathis [1 ,2 ]
Lemarchand, Alex [2 ]
Benseghir, Youven [1 ,2 ]
Mialane, Pierre [1 ]
Gomez-Mingot, Maria [2 ]
Roch-Marchal, Catherine [1 ]
Haouas, Mohamed [1 ]
Fontecave, Marc [2 ]
Mellot-Draznieks, Caroline [2 ]
Sassoye, Capucine [3 ]
Dolbecq, Anne [1 ]
机构
[1] Univ Paris Saclay, UVSQ, CNRS, UMR 8180,Inst Lavoisier Versailles, F-78035 Versailles, France
[2] Sorbonne Univ, Lab Chim Proc Biol, UMR CNRS 8229, Coll France,PSL Res Univ, 11 Pl Marcelin Berthelot, F-75231 Paris 05, France
[3] Sorbonne Univ, UMR 7574, Coll France, Lab Chim Matiere Condensie Paris, 4 Pl Jussieu, F-75252 Paris 05, France
关键词
DIFFRACTION;
D O I
10.1039/d0cc04283h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We evidence the structure-directing role of the PW(12)O(40)(3-)polyoxometalate in porphyrinic MOF synthesis whereby it promotes the formation of the kinetic topology. Its immobilization into the MOF is successfully achieved at a high temperature yielding the kinetic MOF-525/PCN-224 phases, while prohibiting the formation of the thermodynamic MOF-545 product. A combined experimental/theoretical approach uses differential PDF and DFT calculations along with solid-state NMR to show the structural integrity of the POM and its location next to the Zr-based nodes.
引用
收藏
页码:10143 / 10146
页数:4
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