A novel 3 D compound, [H 0.5 CoP 0.5 O 2.5 ], was hydrothermally synthesized and structurally characterized by singly crystal X ray diffraction, ICP, elemental analysis and IR spectra. The compound crystallizes in orthorhombic system, space group Pnnm with a =0.805 1(2) nm, b =0.838 09(13) nm, \{ c =\}0.595 0(2) nm, V =0.401(2) nm 3, Z=1, D =1.669 Mg/cm 3, R=0.049 1, wR =0.153 2.
The title compound [Co(en) 2(H 2O) 2] 2· [Mo Ⅴ 4Mo Ⅵ 4V Ⅳ 8O 40 (AsO 4)] was synthesized by hydrothermal method and its structure was determined with single crystal X ray analysis. The cluster anion is a tetracapped Keggin polyanion, which contains different coordinated cations. The crystal is monoclinic, space group C2/c with a =1.458 3(2) nm, b =2.174 07(13) nm, c =1.893 2(2) nm, β =91.532°, V =6.000 2(10) nm 3, Z =2, D c=1.452 g/cm 3, R =0.035 9, R w=0.079 8, S =1.092.
A new Co 2(HPO 4) 2·H 2O has been hydrothermally synthesized firstly. Single crystal X-ray analysis indicates that this compound crystallizes in a hexagonal system, space group P6 5 with a=1.048 31(15) nm, b=1.048 31(15) nm, c=1.496 3(3) nm, α=90°, β=90°, γ=120°, V= 1.424 1(4) nm 3, μ=3.849 mm -1, Z=6, F(000)=960, D c=2.294 g/cm 3, R=0.072 1, wR= 0.212 1, S=1.182, Δρ max=1.671×10 3 e·nm -3 and (Δρ) min=-1.210×10 3 e·nm -3. Co 2(HPO 4) 2·H 2O is characterized by 1D 12-ring helical channels. Tetrahedral primary structure-building units of CoO 4 and PO 4 indicates the title compound has a zeotype framework.
A Hydrothermal reaction of MoO 3, NiCl 2·6H 2O, WO 3 and H 2O with a molar ratio of 1∶0.6∶1∶83.3 gives a rhombic-shaped black crystal [NiMo 12O 40H 10{Ni(H 2O) 3} 4]. It crystallizes in a tetragonal system with space group I4 1/amd and unit cell parameters a=b=1.518 4(2) nm, c=3.082 9(6) nm, Z=4, V=7.108(2) nm 3, R=0.067 1, wR=0.217 8. The compound possesses a four-capped Keggin structure. The structure of the Keggin- [NiMo 12O 40H 10] 8- consists of twelve MoO 6 octahedrons and a NiO 4 tetrahedron on the center. Four [Ni(H 2O) 3] 2+ at the cap positions are linked to Keggin-structure by three μ 3-O, respectively. The calculation of bond valence shows that the oxidation state of Mo in the compound is +5.
A new complex [Ni（en）3]4[HVⅣ12VⅤ6O42（PO4）] has been hydrothermally synthesize d and characterized by X-Ray diffraction,IR and Elemental analysis.Single crystal X-ray analysis indicates that this compoud cry stallizes in cubic system,space group Im3m with a=17.4081（2）*!,V=5275.38（10）*! 3 ,R=0.0420,w R=0.1055,Z =2,D c =1.663g·cm -3 ,μ=2.297mm -1 ,F（000）=2636.The crystal structure consis ts of[Ni （en） 3 ] 2+ cations and{HV 18 O 42 （PO 4 ）} 8- cluster anion which construct from 18{VO 5 }.square pyramids.The VO 5 pyramids joined each other to form a {V 18 O 42 }cage hosting a tetrahedral{PO 4 } 3- moiety with disordered oxygen atoms .CCDC:185574.
A new complex[Ni(en) 2V 6O 14] n was hydrothermally synthesized and characterized by 2-dimensional vanadium oxide framework pillared by Ni(en) 2 group. Single crystal X-ray analysis indicates that this compound crystallizes in monoclinic system, space group P2 1/c with a= 0.892 17(18) nm, b= 1.711 1(3) nm, c=0.662 73(13) nm, β=111.58(3)°, V=0.940 8(3) nm 3, Z=2, D c= 2.501 g/cm 3, R=0.042 3, wR=0.060 9, S=1.006.
Mortierella isabellina was found to accumulate lipid with 2% hexadecanol and 1% yeast extract as the growth substrates. The amount of lipid reached 64.5% of dry mycelia, and unsaturated acids accounted for 97.05% of the total fatty acids. Mean while, 75% of hexadecanol in medium was converted to lipid. The biosynthetic route from hexadecanol to linoleic acid was presumed as follows: HexadecanolC18∶0（Steric acid）C18∶1（Oleic acid）C18∶2（Linoleic
