Nano-composite of hydroxyapatite/lysozyme with a size of 100 nm was synthesized in situ by chemical wet method,and characterized by nitrongen gas adsorption method,IR,SEM and UV-Vis spectroscopic techniques.In comparison with that synthesized by the dipping adsorbing method,the composite synthesized by wet method has much more content and activity of lysozyme.These results suggest the composite can be used as a controlling carrier of releasing lysozyme.
Compound [Co 3(BTC)(HBTC)(H 2BTC)(C 2H 4O 2) 3]·3(DMF)·6(H 3O) was synthesized under mild conditions and its crystal structure was determined by using single crystal X-ray diffraction. The crystal structure was solved by direct method and refined by full-matrix least-square method. The crystal is monoclinic and belongs to space group Cc with a=2.645 3(5) nm, b= 1.670 4(3) nm, c=1\^821 6(4) nm, β=128.16(3) °, V=6.329(2) nm 3, Z=2 , D c=20.200 Mg/m 3, M r= 1 314.744, μ=10.274 mm -1, F(000) =38 226, GOF=0.99, R=0.094 1, ωR=0.257 3.
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 .
The title compound Mn 3(BTC) 2(bpy)(EG)(DMF)·(DMF)·1/3(C 2H 5OH)(BTC=1,3,5-benzenetricarboxylic acid, bpy=4,4′-bipyridine, EG=ethylene glycol, DMF=dimethylformamide) was synthesized under mild conditions and its crystal structure was determined by single crystal X-ray diffraction. The compound crystallizes in the monoclinic system and belongs to space group P2 1/n with a= 1.637 2(3) nm, b=1.481 4(3) nm, c=1.838 4(4) nm, β=113.70(3)°, V=4.082 5(14) nm 3, Z=4, D c=1.508 Mg/m 3, M r=958.85, μ=1.001 mm -1, F(000)=1 920. R 1=0.098 5, wR 2= 0.218 3. Its structure reveals that Mn(Ⅱ) centers and the carboxylate groups of BTC construct 1D O—C—O—Mn chains. Then, adjacent chains are interlinked by benzene rings of BTC to form a novel 3D architecture. It contains eight-membered rings channels that are about 0.8 nm×0.8 nm viewed along the (101) direction. In addition, it is believed that the bpy acts as both an organic ligand and a structure-directing agent in the synthesis of the title compound.
The title compound [Zn(Py) 2L] n(L=1,2′-ferrocenedicarboxylate) was synthesized under mild conditions and its crystal structure was characterized. It crystallizes in a monoclinic system, space group C2/c with the cell parameters a=1.683 0(5) nm, b=1.380 4(3) nm, c=1.746 2(3) nm, β=108.78(2)°, V=3.840 8(15) nm 3, Z=8, M r=485.52, T=293(2) K, D c=3.359 Mg/m 3, μ= 4.073 mm -1, F(000)=3 872, R 1=0.040 1, wR 2=0.113 2. The compound exhibits an unusual one-dimensional chain consisting of two zigzag chains.
Organic templates of as-synthesized siliceous,MCM-41 and SBA-15 can be effectively removed by oxidation treatment.The highly ordered mesostructures and surface properties of inorganic frameworks were retained after the template being removed.MCM-41 and SBA-15 obtained after oxidation treatment showed larger pores and richer silanol groups compared with those obtained by conventional calcinations at 550 ℃ in air.The removing ratios of templates of MCM-41 and SBA-15 were respectively 88% and 98%.
