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1 INTRODUCTION -Thiocarbonylthioformamide synthesized in 1980[1, 2] is a class of stable and almost unexplored compounds[3]. We have reported the reaction of - thiocarbonylthioformamides in our previous paper[4]. Here, we will report a novel synthesis of 2 by the reaction of 1 and trimethyl phosphite in refluxing xylene. In order to determine the structure of 2, X- ray crystallographic study was carried out. 2 EXPERIMENTAL 2. 1 Preparation of the title compound Trimethyl phosph…  相似文献   

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1 INTRODUCTION Imidazole which is a part of histidine, plays an important role as a ligand in bioinorganic chemistry. Up to now, a variety of coordination compounds with imidazole ligands have been synthesized and characterized[1]. Its complexes have a…  相似文献   

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The title complex bis(2-acetylpyridine thiosemicarbazonato)-indium(iii) perchlo-rate hydrate has been synthesized by the reaction of 2-acetylpyridine thiosemicarbazide(L) with indium(iii) perchlorate,and its structure was characterized by elemental analysis,IR and single-crystal X-ray diffraction.The crystal of the title compound([In(C8H9N4S)2]ClO4·H2O) belongs to monoclinic,space group P21/c with a = 12.6438(18),b = 12.6259(18),c = 15.116(2) nm,β = 105.800(2)°,Z = 4,V = 2321.9(6) nm3,Mr = 618.79,Dc = 1.770 g/cm3,μ = 1.359 mm-1,F(000) = 1240,R = 0.0265 and wR = 0.0675.X-ray analysis indicates that various intriguing hydrogen patterns involving both the solvent intermedia and polyatomic counterions play crucial roles in the self-assembly of functional supramolecules.  相似文献   

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蔡群  杨亲万  张建明 《结构化学》2014,33(5):785-789
A novel [2+4+2]-macrocyclic compound 3(C52H69N16O12, Mr = 1109.53) con- taining bis(ethoxycarbonyl)glycoluril groups was synthesized via the Mannich three-component reaction in one pot and its structure was characterized by single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 10.077(3), b = 10.642(3), c = 15.324(5) , α = 96.704(5), β = 102.304(5), γ = 104.546(5)°, Z = 2, V = 1528.7(8)3, Dc = 1.283 g/cm3, μ = 0.097 mm-1, F(000) = 628, R = 0.0818 and wR(I 2σ(I)) = 0.2346 for 3034 observed reflections.  相似文献   

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3,4-二氨基呋咱基氧化呋咱的合成及其晶体结构   总被引:5,自引:2,他引:3  
通过3-氨基-4-氯肟基呋咱在稀碱作用下发生脱HC l,1,3-偶极反应制备了新型呋咱(氧化呋咱)类含能化合物3,4-二氨基呋咱基氧化呋咱(DAFF),产率70%。其结构经NMR,IR,四圆单晶X-射线衍射仪和元素分析表征。DAFF晶体属单斜晶系,空间群P21/c,a=0.8255(3)nm,b=0.9731(3)nm,c=1.1958(4)nm,β=91.93(3)°,Z=4,Dc=1.745 g.cm-3。DAFF分子不共面,三个环面扭曲。晶体中存在分子内和分子间氢键。  相似文献   

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3,4-二氨基呋咱基氧化呋咱的制备及晶体结构研究   总被引:9,自引:0,他引:9  
首次通过3-氨基-4-氯肟基呋咱在热作用下脱HCl、[4 2]关环反应制备了新型呋咱(氧化呋咱)类含能化合物3,4-二氨基呋咱基氧化呋咱(DAFF),并培养出了DAFF单晶.用X射线单晶衍射、元素分析和红外光谱对其分子结构进行了表征.测试结果表明:DAFF晶体属三斜晶系,空间群P1,a=0.6400(4)nm,b=1.0609(8)nm,c=1.4634(7)nm,α=83.53(5)°,β=87.27(4)°,γ=77.74(5)°,V=0.9645(11)nm3,Z=4,Dc=1.737g?cm-3,F(000)=512,μ(MoKα)=0.149mm-1;R1=0.0568,wR2=0.1137.DAFF分子不共面,三环面扭曲,面间夹角为27.18(1.99)°和30.48(2.07)°,晶体中存在分子内和分子间氢键.  相似文献   

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The complex [Ag(L)]NO3 (1) [L=1,5-bis(imidazol-1-yl)pentane] was synthesized in ethanol and water, and characterized by elemental analysis and X-ray crystal structural analysis. The result shows that the complex crystallizes in monoclinic, space group P21/c with a=0.695 7(4) nm, b=0.988 7(4) nm, c=1.974 8(7) nm, β=91.934(19)°, V=1.357 5(10) nm3, Z=4, Dcalc=1.831 g·cm-3, F(000)=752, μ=1.50 cm-1, the final R=0.036 6, wR=0.091 0. The coordination environment of Ag(Ⅰ) is nearly linear with two N atoms, and each L ligand links two Ag(Ⅰ) atoms using its two imidazolyl N atoms to generate an infinite one-dimensional (1D) chain structure. The 1D chains are further connected by C-H…O hydrogen bonds to give a three-dimensional structure. CCDC: 609514.  相似文献   

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以丙二腈为原料,用一锅法合成了呋咱类含能化合物3-氨基-4-氨基肟基呋咱(AAOF),收率72.4%。用1H NMR,13C NMR,IR,MS,元素分析和四圆单晶X-射线衍射仪对其分子和晶体结构进行了表征。结果表明:AAOF晶体属单斜晶系,空间群P21/c。主要晶体结构参数为:a=0.7651(3)nm,b=1.1702(3)nm,c=1.9216(10)nm,β=96.47(4)°,V=1.7095(12)nm3,Z=12,Dc=1.668 g.cm-3,F(000)=888。AAOF分子共面性较好,晶体中存在分子内和分子间氢键。  相似文献   

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The title compound [In(H2ip)(pdc)(H2O)] (H3ip = 5-hydroxyisophthalic acid, H2pdc = pyridine-2,6-dicarboxylic acid) has been synthesized and characterized by single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group P21/c with a = 13.830(8), b = 6.488(4), c = 17.632(10) , β = 92.510(10)°, C15H10InNO10, Mr = 479.06, V = 1580.6(15) 3, Z = 4, Dc = 2.013 g/cm3, F(000) = 944, μ = 1.557 mm-1, the final R = 0.0413 and wR = 0.0793 for 2950 observed reflections with I > 2σ(I). The In(III) ion is seven-coordinated in a slightly distorted penta-bipyramidal geometry. The mixed ligands connect the In(III) ions into 21 helical chains along the [010] direction, and the hydrogen bonds assemble the chains into a three-dimensional supramolecular network.  相似文献   

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1INTRODUCTION The macrocyclic compounds play an important ro-le in life science and materials science[1].In recent years,teta has gained extensive attention as a raw material of crystal engineering,and its coordination behavior with metallic ion has been …  相似文献   

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N-(m-ferrocenylphenyl)-formamide has been synthesized by the reaction of m-ferrocenyl-aniline with DMF, and characterized by elements analysis, IR, 1H NMR, and X-ray structure determination. The crystallized was in the monoclinic, P21/c space group, with a=0.140 94(3) nm, b=0.102 87(2) nm, c=0.100 26(2) nm, β=104.85(3)° and final R indices [I>2σ(I)] R1=0.072 7, wR2=0.184 5. An infinite one-dimensional chain is formed by intermolecular hydrogen bonding N-H…O. Cyclic voltammetry was studied comparing with the parent compound (m-ferrocenylaniline). CCDC: 243511.  相似文献   

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1 INTRODUCTION Palladium compounds have attracted much attention as a consequence of their application in homogeneous and heterogeneous catalyses[1]. For instance, palladium compounds are the most active catalysts for the carbonylation, such as palladium-catalyzed carbonylation of nitroarenes, aryl halides, alkyne and so on[2~4]. Some dramatic results in the homogeneous catalysis of the reactions of organic compounds, particularly the successful commercial exploitation of the Wacker on…  相似文献   

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0IntroductionThestudyofcopper?complexesisinvestigatedinmanylaboratories.Amongthereasonsforcarryingouttheinvestigationofsuchspeciesaretheirstructuralfeatures犤1犦,theusefulnessofcopper?compoundsinorganicsyntheses犤2犦andthewell-documentedimpor-tanceofcopper?centersattheactivesitesofanumberofprotein犤3犦.Concerningcopper?carboxy-latesafurtherinterestexists,stemmingfromtheiruseinhomogeheouscatalysedhydrogenation犤4犦.Thecopper?bis(triphenylphosphine)cationisasoft,butflexi-bleacceptorionthatcanacc…  相似文献   

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