摘要
Two porous coordination polymers, Co-Py2PO and Co-Py2PO', have been obtained via reactions of in situ oxidized terpyridyl phosphines and cobalt(II) nitrate. Single-crystal structure analysis reveals that Co-Py2PO' has a three-dimensional (3D) structure with (8.10(2))(8(3)) net topology, while the structural analysis of Co-Py2PO reveals a 2D polycatenated framework consisting of two sets of parallel 2D networks of (6(3)) net topology. For Co-Py2PO', guest CHCl3 molecules are locked in the channels along the b axis by P(O)Ph-2 phenyl rings and coordinated nitrate ions, and cannot be released out of the host framework. In contrast, the as-synthesized 2D framework Co-Py2PO readily loses its solvated guest molecules to give an activated amorphous material for sorption. Activated Co-Py2PO has a flexible structure and shows dynamic adsorption behaviours towards various guests (N-2 and benzene). The flexibility may arise from the combination of layer-layer motion and the local flexibility of the P-C bond of -P(O) Ph-2 groups.
- 出版日期2015
- 单位中山大学