规整Cu-Zn-Mg-Al类水滑石的合成及其结构分析

以CuCl2·2H2O、ZnCl2·6H2O、MgCl2·6H2O、AlCl3·6H2O、Na2CO3为原料,采用丙三醇-水热法组装了优质铜-锌-镁-铝类水滑石.样品采用XRD、SEM、TEM、TG-DAT、N2吸附-解吸的分析方法进行了物相、粒度、晶体形貌结构、热分析和比表面分析.分析了不同介质条件对Cu-Zn-Mg-Al-HTlc类水滑石样品特征的影响.结果发现,在水热反应体系中加入体积分数为15;的丙三醇,反应温度为180 ℃,反应时间为18 h时可获得晶形好、板层结构显著、规整性好、分散性好的优质铜锌铁镁铝水滑石,估算薄层厚度约在36 nm左右.     

Synthesis and Structural Analysis of a Semi-Rigid Cd(II) Coordination Polymer

Crystallography Reports - A semi-rigid chiral coordination polymer, {Cd3(4-cpta)2(dpp)2(H2O)}n (1), was synthesized solvothermally with 4-H3cpta (4-H3cpta = 3-(4'-carboxyphenoxy)phthalic acid),...     

室温核辐射探测材料碘化铟多晶合成及结构分析

以高纯I2(5N)和In(7N)为原料,采用两温区气相输运法制备了InI多晶料,研究了高纯InI多晶合成工艺.用X射线粉末衍射(XRD)方法对合成的InI多晶进行结构测定,用扫描电子显微镜-X射线能量色散谱仪(SEM-EDS)对其成分进行分析,用等离子体原子发射光谱仪(ICP-AES)对其组成的元素进行痕量测定.研究结果表明:合成的InI多晶料晶格结构完整,纯度高,晶格参数为a=0.476 nm,b=1.278 nm,c =0.491 nm,且碘和铟比例接近1∶1.     

Synthesis and Structural Characterisation of 2-Aminoacetophenonesalicylaldazine Complexes of Some Bivalent Transition Metal Ions

Metal(II) complexes M(aas)₂ [M = Mn. Co, Ni, Cu and Zn, Haas = 2-aminoacetophenonesalicylaldazine] have been prepared and characterized. Magnetic and spectral data such as electronic, ESR, and IR are used to establish the stereochemistry and mode of bonding of azine in the complexes. X-ray diffraction study suggests orthorhombic unit lattice for Co(aas)₂, Ni(aas)₂, Cu(aas)₂ and Zn(aas)₂ complexes.     

Structural Analysis of the Layered Compounds Cu x TiS2

Abstract

A structural analysis of single crystals of the layered compounds Cu _x TiS₂ (x=0. 0.21 and 0.38), which were prepared by the iodine transport and the electrochemical methods, has been performed by X-ray diffraction. The displacement parameters of Ti and S atoms along the c axis are larger than those along the a axis. It is understood that the intra-layer bonding between Ti-Ti and S-S atoms is stronger than the inter-layer bonding between Ti-and S-layers. Both distances between Ti-and S-layers and between Cu-and S-layers are enlarged without changing the structure of the mother phase after intercalating Cu atoms.     

Bis[(2,3,4-Trimethoxy-Benzylidenepropylideneamino)Phenyl]Ether: Synthesis,Characterization and Crystal Structure

Abstract  

New Schiff base compound bis[(2,3,4-trimethoxy-benzylidenepropylideneamino)phenyl]-ether (1) was synthesized and characterized by elemental analyses (CHN), FT-IR and ¹H-NMR spectroscopy and single-crystal X-ray diffraction. The title compound 1 crystallizes in triclinic system, space group P-1, with a = 6.8255(4) Å, b = 10.4346(4) Å, c = 19.4166(8) Å, α = 86.588(3)°, β = 85.019(4)°, γ = 89.042(4)°, V = 1375.12(11) Å³ and Z = 2. It displays a trans configuration about the C=N double bonds.     

Synthesis and Crystal Structure Analysis of Methyl 2-Hydroxyimino-3-phenyl-propionate

Abstract  

As precursors of α-amino acids, methyl 2-hydroxyimino-3-phenyl-propionate (F.W. 193.20) was synthesized, characterized by ¹H NMR, IR, element analysis and confirmed by X-ray crystal structure analysis. This compound crystallizes in monoclinic class under the space group P2₁/c with cell parameters, a = 8.6435(17) Å, b = 5.4957(11) Å, c = 21.146(4) Å; β = 97.12(3)°, and Z = 4. The structure exhibits inter-molecular hydrogen bonds of the type O–H···N, O–H···O, C–H···O.     

钙钛矿型层状化合物K2Pr2Ti3O10的合成及XRD研究

在K2CO3-镧系元素氧化物(Pr2O3)-TiO2三元体系中,用固相反应法合成K2Pr2Ti3O10,利用X射线粉晶衍射仪对K2Pr2Ti3O10进行扫描测定,获得X射线衍射数据,进行指标化,得到其晶胞参数。XRD分析结果表明,K2Pr2Ti3O10为四方晶系,空间群I4/mmm。     

Alternative Synthesis and Structural Analysis of the Antioxidant and Antitumor Agent 2-(3,5-Dimethoxyphenyl)-2,3-Dihydroquinolin-4(1H)-One

Journal of Chemical Crystallography - Herein we present the synthesis, structure and NMR and mass spectroscopic analyses of the antioxidant 2-(3,5-dimethoxyphenyl)-2,3-dihydroquinolin-4(1H)-one...     

Structural and spectroscopic properties of 2-thiophenecarboxaldehyde 2-thienylhydrazone

In this paper the crystal and molecular structure of the title compound is reported. The crystals are monoclinic, P2₁/c,Z=4,a=13.406(4),b=5.367(1),c=15.545(6)Å,=110.00(5)°. The structure was solved by direct and Fourier methods and refined by full-matrix least squares toR=0.0497 andRw=0.0537 for 1094 unique reflections. The molecule shows an E-conflguration with respect to the C=N double bond. Mass and IR spectra are also discussed.     

Synthesis and Structural Proof of a Potent 5-Lipoxygenase Inhibitor

Abstract  

5-Lipoxygenase inhibitor 3-O-acetyl-9,11-dehydro-β-boswellic acid was detected in the extract of Boswellia serrata gum resulting from unstable 11-hydroxy precursor. It was reported more potent than other Boswellic acids in its inhibition of 5-Lipoxygenase. Here, we report the method of conversion of 3-acetoxy-β-boswellic acid to 3-O-acetyl-9,11-dehydro-β-boswellic acid, and the crystal structure of later. This compound crystallizes in orthorhombic space group P2₁2₁2₁ with cell parameters of a = 12.726(1) ?, b = 16.597(1) ?, c = 27.332(2) ?, α = β = γ = 90°, V = 5772.7(5) ?³, D _c = 1.143 Mg/m³, and Z = 8. The X-ray structure investigation indicates that the rings A, B, D and E are exhibit chair and the ring C adopts a distorted half chair conformation. The conformational difference of the two structures in the arrangement is due to crystal packing of 3-O-acetyl-9,11-dehydro-β-boswellic acid. The molecular packing is stabilized by C–H···O and O–H···O types of hydrogen bonding interactions.     

CdSiP2多晶杂相分析与合成工艺改进

以高纯(6N) Cd、Si、P单质为原料,按CdSiP2化学计量比并适当富磷配料,采用传统气相输运法合成出CdSiP2多晶.X射线衍射(XRD)分析及Rietveld全谱拟合精修结果表明合成产物中含有微量SiP和CdP2杂相,分析了杂相产生的原因.针对存在的问题改进合成工艺,引入高温熔体机械和温度振荡以及分步控温冷却等新工艺,获得了外观完整、内部致密均匀的CdSiP2多晶.XRD及能量色散谱仪(EDS)分析结果表明,合成产物为高纯单相CdSiP2多晶,为高质量单晶体的生长奠定了可靠基础.以改进工艺获得的CdSiP2多晶为原料生长出质量较好的单晶体,厚度为2mm的晶片样品在1500 ～ 7000 cm-1范围内的红外透过率在45;以上,计算出晶体的禁带宽度为2.09 eV.     

气相输运合成PbI2多晶的热力学研究

本文对PbI2合成反应体系的反应焓变,反应熵增,Gibbs自由能变化和反应平衡常数进行了理论计算,从热力学角度论证了选取PbI2熔点(678K)以上的723K作为体系合成反应控制温度的可行性.在723K的控温工艺下,采用两温区气相输运方法合成出高纯、单相的PbI2多晶材料,XRD分析结果表明符合热力学计算结果的控温工艺能有效地应用于PbI2多晶合成.     

Synthesis and Structural Studies of Novel Taxoids Derived from 1-DeoxybaccatinVI

Abstract  

Three novel taxoids were synthesized from 1-deoxybaccatinVI and their crystal structures were determined by X-ray crystallographic techniques. The influence of C(7), C(10) and C(4) substituents of the tetracyclic moiety on molecular conformations were investigated. The result shows that 4-acetyl moiety plays an important role in the conformation of the diterpenoid core. All of these 1-deoxybaccatinVI derivatives crystallize in orthorhombic system, space group P2₁2₁2₁. In the structures, the six-membered A ring exhibits the 1,4-di-planar conformation, the eight-membered B ring adopts boat–chair conformation and the six-membered C ring exhibits slightly distorted half-chair conformation.     

Synthesis and X-Ray Crystallographic Analysis of 2-(2, 4-Dimethyl Pyrrolyl) Benzothiazole

Abstract  

Synthesis of 2- (2, 4-dimethyl pyrrolyl) benzothiazole by chemical means and molecular structure by X-ray crystallographic techniques is reported. The compound crystallizes in the orthorhombic crystal system with space group Pbca and unit cell parameters: a = 12.161(9), b = 0.787(1), c = 16.792(2) Ǻ, V = 2202.8(4) Ǻ³ and Z = 8. The final reliability index is 0.073 for 7,959 observed reflections. The benzothiazole and pyrrole rings exist in planar conformations. The dihedral angle between the least-squares planes of both these moieties is 13.31°. There exists an isolated C4–H4···N1 intermolecular interaction, besides two C–H···S and C–H···N intermolecular interactions. The presence of C–H···S and C–H···N intramolecular interactions make the present molecule look like a virtual two-six-membered and three-five-membered ring structure.