Hydrothermal Synthesis, Crystal Structure and Thermal Analysis of a Dinuclear Complex Cd2（3,5-Dinitrobenzoate）4（pyridine）4

A dinuclear complex Cd2(dnba)4(pyridine)4 (dnba = 3,5-dinitrobenzoate) has been synthesized by hydrothermal method and characterized by X-ray single-crystal diffraction, elemen- tal analysis, FT-IR spectroscopy, DSC and TG-DTG techniques. The complex with empirical formula C48H32Cd2N12O24 (Mr = 692.83) crystallizes in monoclinic, space group P21/n with a = 12.0344(14), b = 10.5752(13), c = 21.578(3) (A), β = 104.150(2)o, V = 2662.8(6) (A)3, Z = 2, Dc = 1.728 g/cm3, μ(MoKα) = 0.897 mm-1, F(000) = 1384, S = 1.016 and (Δ/σ)max = 0.001. R = 0.0638 and wR = 0.0737 for all data; the final R = 0.0337 and wR = 0.0644. In this complex, four carboxylates are bidentate- or chelate-coordinated with the Cd(Ⅱ) centers to give the dinuclear structure. The other coordination positions of Cd(Ⅱ) are occupied by the lone pair electrons from N of four pyridines. Thermal analyses DSC and TG-DTG have been used to determine the thermal decomposition mechanism of the title complex.     

Hydrothermal Synthesis,Crystal Structure and Thermal Stability of a Binuclear Copper（Ⅱ） Complex with 3-（Pyridin-2-yl）-1,2,4-triazole

One novel binuclear copper(Ⅱ) complex [Cu 2 (Hpt) 2 (CO 3) 2 (H 2 O) 2 ]·H 2 O with copper carbonate and 3-(pyridin-2-yl)-1,2,4-triazole (Hpt) was hydrothermally synthesized and characterized by IR and X-ray diffraction analysis.The complex crystallizes in triclinic,space group P2 1 /n with a=0.6862(1),b=0.7805(1),c=1.1983(2) nm,α=72.03(2),β=107.72(3),γ=75.28(2)o,V=0.5884 nm 3,D c=2.105 g/cm 3,Z=1,F(000)=357,GOOF=1.041,the final R=0.01859 and wR=0.04348.The whole molecule is composed of two cooper ions,two Hpt molecules,two carbonate and three water molecules,forming a binuclear structure.The crystal structure shows that the cooper ion is coordinated with three nitrogen atoms from two Hpt molecules,two oxygen atoms from one carbonic acid and one water molecule,forming a distorted square pyramidal geometry.The TG analysis result shows that the title complex is stable under 131.0 ℃.     

Synthesis and Crystal Structure of 3,5-Diphenyl- 1,2- di（4- chlorophenyl）pyrrole

1 INTRODUCTION The pyrrole ring constitutes a basic heteroaro- matic structure. It is a vital building block for the construction of porphyrins and alkloids[1]. Several substituted pyrroles have potential applications as fungicides and bactericides and as active compo- nents of nonsteroidal anti-inflammatory drugs inhi- biting human cyclooxygenase[2, 3]. Besides the clas- sical Knorr’s method, there are a number of poten- tially useful methods for the synthesis of pyrrole he- terocyclic …     

Synthesis, Crystal Structure,and Antioxidant and Antibacterial Activities of 3,5-Dihydroxy-N＇-（4-nitrobenzylidene）benzohydrazide

A new compound, 3,5-dihydroxy-N＇-（4-nitrobenzylidene）benzohydrazide （I）, has been synthesized and characterized by single-crystal X-ray diffraction. The title compound crystallizes in the monoclinic system, space group P21/c with a = 9.632（12）, b = 12.256（15）, c = 11.425（14） A, β = 105.306（11）°, Z = 4, V = 1301（3） A3, Dc = 1.538 g/cm3, F（000） = 704,μ = 0.276 and S = 1.011. The final R = 0.0444 and wR = 0.1186 for 3808 observed reflections with I〉 20（I）. We used methods such as ABTS, DPPH assays and in vitro hydroxyl radical scavenging experiment to assess the in vitro antioxidant activity of the new compound, and found that its IC50 value was 48.59 μg/mL for scavenging ABTS radicals, 48.04 μg/mL for scavenging DPPH radicals, and 1.03 mg/mL for scavenging hydroxyl radicals, indicating that it had a good in vitro antioxidant activity. We also test the antibacterial activities of this compound against three bacteria, and it showed considerable antibacterial activity against S.aureus. The MIC values of S.aureus, K.pneumoniae and P. aeruginosa are respectively 0.156, 0.625 and 1.25 mg/mL.     

Synthesis,Crystal Structure and Recognition Properties of 2-（5-（4-Chlorophenyl）-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl）pyridine

The title compound 2-(5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)- pyridine(C20H16ClN3, Mr = 333.81) has been synthesized and its crystal structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/n with a = 10.9925(12), b = 11.0378(12), c = 14.2751(18) , β = 98.074(11)°, V = 1714.9(3)3, Z = 4, Dc = 1.293 g/cm3, μ(MoKα) = 0.228 mm-1, F(000) = 696, the final R = 0.0521 and wR = 0.1349 for 3495 observed reflections with I 2σ(I). Intermolecular C–H...π interactions and π-π stacking interactions stabilize the crystal structure. The binding study by fluorescence spectroscope titration showed that the title compound can selectively recognize Fe3+ in THF solution with fluorescence quenching.     

Synthesis, Crystal Structure and Antibacterial Activity of 1-（（2-Chloroquinolin-3-yl）-methyl）-pyridin-2（1H）-one

On the basis of the interesting structures and biological activities exhibited by several heterocyclic systems possessing the pyridone nucleus such as mappcine and camptothecin, we have planed to design the synthesis, crystal studies and antibacterial activity of the new 1-((2- chloroquinolin-3yl)-methyl)-pyridine-2(1H)-one building block. An X-ray analysis has provided valuable insight into the effect of steric factors on the three-dimensional shape of this compound which serves as a useful advanced intermediate in the synthesis of these biologically active molecules. A multistep synthesis of camptothecin (5) has been designed by retrosynthetic analysis as part of an ongoing program on lead anticancer drug.     

Synthesis and Crystal Structure of Gd3（BSiO6）（SiO4）

1INTRODUCTIONRareearthborosilicateshaverarelybeenreportedinthepastdecade.LnBMO5(M=Ge,Si)(l,z,31exhibitsthestillwellitestructureonlyforlargerlanthanide,initsstructure,twoBO'tetrahedraandoneSiO'tetrahedronareconnectedbycorner-sharedeachothertoformsix-memberringthatconstructinfinitehelicalchainsparal-lelto3lscrewaxis-Serhanetal(43synthesizedNd,BM2O,,(M=Si Ge)whosestructurecontainstri-coordinatedboronatoms.Recently,wehavesynthesizedSm3BSi2O1,andEu,BSi,O,,t"6),herewerffportthesynthes…     

Synthesis and Crystal Structure of a Novel Heterometallic Complex with 1,2,4,5-Benzenetetracarboxylic Acid and 1,3,5-Tris（imidazol-1-ylmethyl）-2,4,6-trimethylbenzene

A novel heterometallic complex,[Zn4Ni(OH)2(btec)2(titb)2(H2O)2]·2H2O(1)(H4btec=1,2,4,5-benzenetetracarboxylic acid,titb=1,3,5-tris(imidazol-1-ylmethyl)-2,4,6-trime-thylbenzene),has been hydrothermally prepared and characterized by IR spectroscopy,elemental analysis and single-crystal X-ray diffraction.The crystal is of triclinic system,space group P1 with a=10.817(10),b=11.878(11),c=14.569(14),α=71.762(12),β=76.122(13),γ=71.493(13)°,V=1665(3)3,C62H62N12O22Zn4Ni,Mr=1647.43,Dc=1.643 g/cm3,F(000)=842,μ=1.784 mm-1 and Z=1.The final R=0.0531 and wR=0.0890 for 3545 observed reflections(Ⅰ 2σ(Ⅰ)).In the title complex,the btec ligand acts as a five-dentate bridging ligand to link up zinc and nickel atoms into a lamellar framework,which are further interlinked into a 3-D framework via the titb ligands.     

Synthesis,Characterization and Crystal Structure of Some Novel 1‐(3,5‐Dimethyl‐1H‐pyrazol‐1‐yl)‐3‐(substituted anilino)propan‐1‐ones

Michael addition of some substituted anilines to methyl acrylate in acidic medium afforded the methyl 3-(substituted anilino)propionates (1a—1i), which on treatment with hydrazine hydrate in methanol were converted into corresponding 3-(substituted anilino) propionohydrazides (2a—2i) in good yields. Microwave irradiation of the latter with pentane-2,4-dione afforded 1-(3,5-dimethyl-1H-pyrazol-1-yl)-3-(substituted anilino)propan-1-ones (3a—3i) under solventless conditions. The structures were confirmed by spectroscopic data, elemental analyses and in case of the 3h by single crystal X-ray diffraction data.     

Synthesis, Crystal Structure Analysis and DFT Calculation of 1-Benzoyl-3,6-diphenyl-1,4-dihydro-1,2,4,5-tetrazine

The new title compound, 1-benzoyl-3,6-diphenyl-1,4-dihydro-1,2,4,5-tetrazine (C21H16N4O, Mr = 340.38), has been prepared and its crystal structure can not be confirmed by the results of MS, elemental analysis, IR spectrum and 1H NMR spectrum, but determined by X-ray diffraction. The title compound crystallizes in an orthorhombic space group P212121 with a = 7.1100(19), b = 12.115(3), c = 19.884(6), V = 1712.7(8)3, Z = 4, Dc = 1.320 g/cm3, F(000) = 712, μ = 0.085 mm-1, MoKa radiation (λ = 0.71073), R = 0.0334 and wR = 0.0845 for 2254 observed reflections with I 2σ(I). X-ray diffraction analysis reveals that the central tetrazine adopts an unsymmetrical boat conformation. According to the bond lengths of tetrazine ring, the molecule should be 1,4-dihydro-1,2,4,5-tetrazine, rather than 1,2-dihydro-1,2,4,5-tetrazine. The crystal structure is stabilized mainly by intermolecular N–H···O hydrogen bonds.     

3-硝基胍-6-(3,5-二甲基吡唑)-1,2,4,5-四嗪的晶体结构及热行为

合成了3-硝基胍-6-(3,5-二甲基吡唑)-1,2,4,5-四嗪(NDT),在二甲基甲酰胺(DMF)中培养出NDT的单晶(NDT·DMF),该晶体属于三斜晶系,P-1空间群,晶胞参数为a=0.7070(4) nm,b=0.8468(6) nm,c=1.4123(9) nm,α=73.281(8)°,β=80.423(11)°,γ=81.740(9)°,Z=2。 利用DSC和TG-DTG研究了NDT的热分解行为,其放热过程的表观活化能和指前因子分别为288.245 kJ/mol和10^29.04 s^-1。 对NDT的热安全性进行了研究,获得NDT的自加速分解温度T_SADT为212.19 ℃,热点火温度T_be为213.52 ℃,热爆炸临界温度T_bp为214.95 ℃,绝热至爆时间范围在5.43~6.26 s。     

3,5-二羟基-2,4,6-三硝基苯酚氨基脲铵盐半水合物的合成、晶体结构和热分解特性

A new compound, semicarbazidium 3,5-dihydroxy-2,4,6-trinitrophenolate hemihydrate （SCDHTNP·0.5H2P）, was synthesized by the reaction of the aqueous solutions of semicarbazide with trinitrophloroglucinol. Its structure was determined by single-crystal X-ray diffraction analysis and characterized by elemental analysis, FTIR, DSC and TG-DTG techniques. The crystal is monoclinic with space group P21/n and the empirical formula C7H9N6O10.50. The unit cell parameters are： a= 1.3791（3） nm, b=0.9256（2） nm, c=2.0468（4） nm,β= 106.93（3）°, V=2.4995（9）nm^3, Z=8, Dc= 1.835 g/cm^3, Mr=345.20, F（000）= 1416, s=0.945,μ（Mo Ka）=0.174 mm^-1. The final R and wR are 0.0401 and 0.0896. Its structure consists of two semicarbazidium cations, two 3,5-dihydroxy-2,4,6-trinitrophenolate anions and one crystal water molecule, which are interconnected by electrostatic forces and hydrogen bonds into layer structure, making the title compound very stable. Under a linear heating rate, the thermal decomposition processes of SCDHTNP·0.5H2O have one endothermal dehydration stage and two intensive exothermic decomposition stages at 178-241℃ to evolve abundant gas products.     

新型N-（4，6-双取代嘧啶-2-基）-N’-（三氟甲基苯基）胍的合成，结构及生物活性研究

设计,合成了10种新型的胍衍生物,结构经FTIR, MS, 1H NMR 和元素分析确证,并且采用X-射线衍射分析方法确证了具有较好生物活性的化合物11a的结构。并且对这些化合物进行了除草活性测试,结果表明化合物11a,11b,11c在100µg·mL-1 对油菜具有较好的抑制作用,初步的KARI活性结果表明这些化合物对KARI的活性很弱。     

Li3AlB2O6： Synthesis, Crystal Structure, and Its Luminescence Property Compared with LiSrBO3

The synthesis and crystal structure of Li3AlB2O6 with different cell parameters are reported and these cells are transformed each other from the confirmation of crystallographic structural analyses. The absorption spectrum, luminescence and lifetimes of the Li3AlB2O6 and LiSrBO3 solid compounds are measured and the comparisons are made between them. It is shown that the absorption edges are at about 400 nm (or band gap 3.1 eV) and there is one of absorption peaks at about 350 nm for the Li3AlB2O6 and LiSrBO3. The emission band (530 nm) makes a red shift and fluorescence decay time (24.39 ns) of the Li3AlB2O6 becomes smaller compared with the emission band (480 nm) and lifetime (93.16 ns) of the LiSrBO3 at the visible region. The transition energies and oscillator strengths of the clusters (Li3AlB2O6)2 and (LiSrBO3)2 lying at low excited states are calculated by the time-dependent Hartree-Fock method. The obtained results are used to model the photophysical properties and discuss the origin of spectral bands of the Li3AlB2O6 and LiSrBO3.     

Crystallographic report: Crystal structure of 1‐bromo‐1′‐[(2S)‐N‐(1‐hydroxy‐3‐methylbutane‐2‐yl)]‐ferroceneamide

For the unsymmetrical title compound, 1‐bromo‐1′‐[(2S)‐N‐(1‐hydroxy‐3‐methylbutane‐2‐yl)]‐ferroceneamide, two independent molecules were found in the asymmetric unit. Copyright © 2003 John Wiley & Sons, Ltd.     

Synthesis, Reactivity and Crystal Structure of β—Diketiminate Ytterbium Chlorides

Reaction of anhydrous YbCl3 with 1 equiv, of LLi [L=p-ClPhNC(Me)CH(Me)N(C6H3-2,6-i-Pr2)] in THF at room temperature gave the β-diketiminate lanthanide dichloride LYbCl2(THF)2 (1) in good isolated yield. Similarly reaction of anhydrous YbCl3 with 1 equiv, of LLi, then with 1 equiv, of t-BuCpNa in THF yielded the expected mixed-ligand β-diketiminate ytterbium chloride (t-BuCp)YbL(μ-Cl)2Li(THF)2 (2). Both 1 and 2 were well characterized by elemental analysis, IR spectra, ^1H NMR spectra, and X-ray diffraction analysis.     

Synthesis,Crystal Structure and Thermal Behavior of 4,5‐Diacetoxyl‐2‐(dinitromethylene)‐imidazolidine

A new energetic material, 4,5‐diacetoxyl‐2‐(dinitromethylene)‐imidazolidine (DADNI), was synthesized by the reaction of 4,5‐dihydroxyl‐2‐(dinitromethylene)‐imidazolidine (DDNI) and acetic anhydride, and characterized by single crystal X‐ray diffraction. Crystal data for DADNI are monoclinic, space group C2/c, a=15.9167(3) Å, b=8.6816(4) Å, c=8.5209(3) Å, β=103.294(9)°, V=1145.9(3) ų, Z=4, µ=0.150 mm⁻¹, F(000)=600, D_c=1.682 g·cm⁻³, R₁=0.0565 and wR₂=0.1649. Thermal decomposition behavior of DADNI was studied and an intensely exothermic process was observed. The kinetic equation of the decomposition reaction is: dα/dT=(10^16.64/β)×4α^3/4exp(−1.582×10⁵/RT). The critical temperature of thermal explosion is 163.76°C. The specific heat capacity of DADNI was studied with micro‐DSC method and theoretical calculation method. The molar heat capacity is 343.30 J·mol⁻¹·K⁻¹ at 298.15 K. The adiabatic time‐to‐explosion of DADNI was calculated to be 87.7 s.     

3，5-二羟基-2，4，6-三硝基苯酚铷的晶体结构和热行为

0IntroductionSom e nitrogen鄄rich alkaline and alkali鄄earth m et鄄als com pounds of polynitro hydroxybenzenes can beused environm entally friendly prim ary explosives[1￣5].2,4,6鄄Trinitro鄄1,3,5鄄trihydroxybenzene(trinitrophloroglu鄄cinol,TNPG)belongs to a polynitro hydroxybenzeneand has been used in chem icalindustry as an ingredi鄄entfor prim ing com position,percussion caps and deto鄄nator form ulations[6].Therefore,in recent years,ithasbeen exploited to prepare a num ber of salts of ba…