A\} novel two-dimensional coordination polymer Zn 3(PTC) 2(H 2O) 8·4H 2O was formed by \{Zn(CH 3COO) 2·\}2H 2O and 2-pyridine-1,3,5-tricarboxylate(H 3PTC) under the hydrothermal condition at 417 K and characterized by fluorescence. The crystal structure of the compound was determined by single-crystal X-ray diffraction analyses. The six-coordinated Zinc(Ⅱ) center displays an octahedral geometry . The crystal is monoclinic and space group is P2(1)/c with a=0.722 70(14) nm, b= 1.866 7(4) nm , \{c=\}1.072 6(3) nm, α=90°, β=103.198(19)°, γ=90°, V=1.408 7(6) nm 3, Z=4, D c= 2.474 Mg/m 3, M r=828.536, μ=3.099 mm -1 , F(000)=1 060, GOF=0.892, R=0.061 3, wR= 0.133 9 .
Silica mesoporous material MCFs with 16.0 nm pore sizes was prepared by using non-ionic block copolymers and the swelling agents, and was used as the support for the immobilization of enzyme. Penicillin G acylase, an enzyme, was assembled in the channel of MCFs by immersion method. The activity and stability of immobilized penicillin G acylase were studied. It was found that the activity and stability of the immobilized penicillin G acylase increased significantly compared to those of free enzyme. The optimum reaction temperature is 60 ℃. After incubation at 60 ℃ for 1 h, the activity of these immobilized penicillin G acylase remains 69%. These results showed that thermostability and durability on heating of the immobilized penicillin G acylase in MCFs was improved remarkably. The silica mesoporous material MCFs with 3-dimensional channel structure is a good support for the immobilization of enzyme.
The title compound [Zn3（BTC）2（H2O）3]n（BTC=1,3,5-benzenetricarboxylic acid） was synthesized under mild conditions and its crystal structure was determined by single crystal X-ray diffraction. The compound crystallizes in the cubic system and belongs to space group Fm-3m with a=2.662 6（3） nm ,V=18.877（4） nm 3,Z=16,Dc=1.51 g/cm 3,Mr=664.4,μ=0.198 mm -1 , F（000）=852 ,R=0.062 5,wR=0.129 4. Its structure reveals that the title polymer is composed of dimeric zinc tetracarboxylate units,with a short Zn-Zn internuclear separation of 0.295 0（4） nm. The coordination of BTC ligands with Zn ions forms a 3D infinite framework with about 1.117 4 nm×1.327 4 nm pores along the [001],[100] and [010] direction. [WT5HZ]
A 3-D inorganic-organic hybrid framework microporous material [Co 3(BDC) 3(EG) 4]·2DMF was synthesized under mild conditions and its crystal structure was determined by using single crystal X-ray diffraction. The crystal structure was solved by a direct method and refined by full-matrix least-square method. The crystal is the triclinic system and belongs to space group P-1 with a=9.978(2) nm, b=11.223(2) nm, c=11.283(2) nm, α=102.26(3)°, β=113.52(3)°, γ=92.73(3)°, V=6.329(2) nm 3, Z=1, D c=1.565 Mg/m 3, M r=1 063.59, μ=1.183 mm -1, F(000)=541, GOF=1.024, R=0.044 2, wR=0.124 9.
