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961.
SynthesisandStructureof(NH4)2[V2O4(OCH2COO)2]ZHOUZhao-hui,WANGJinzhi,WANHui-linandTSAlKhi-rui(DepartmentofChemistry,XiamenUni... 相似文献
962.
A. Kh. Khanamiryan A. L. Gyulbudagyan P. S. Vartanyan M. Kh. Dzhafarov Yu. T. Struchkov 《Russian Chemical Bulletin》1993,42(3):496-499
A series of new 1,2,4-substituted hexahydropyridazines was prepared in order to evaluate qualitatively and quantitatively the role and influence of substituents on the biological activity of this system. An X-ray structural investigation of 4-hydroxyimino-2-methyl-1-phenethylhexahydropyridazine was performed. The compounds considered exhibit moderate local anesthetic, antihistaminic, and anticonvulsive activity.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 539–541, March, 1993. 相似文献
963.
Robin L. Garrell John C. Smyth Frank R. Fronczek Richard D. Gandour 《Journal of inclusion phenomena and macrocyclic chemistry》1988,6(1):73-78
Single crystal X-ray analysis of the 2:1 acetonitrile complex of 18-crown-6 is reported. Crystals of the complex are monoclinic,P21/n, witha=9.123(3),b=8.524(3),c=13.676(4) Å, =104.68(3)°, andD
c
=1.118 g cm–3 forZ=2. The complex lies on a center of symmetry, with the crown in theD
3d conformation. Methyl groups of the acetonitrile molecules have weak interactions with the crown oxygen atoms, and are tilted 31.7° from the host's threefold axis. Methyl hydrogen atoms are rotationally disordered about the acetonitrile axis.
Supplementary Data relating to this article are deposited with the British Library as Supplementary Publication No. SUP 82057 (12 pages). 相似文献
964.
α-异丙基、β-异丁基丙烯酸希土配合物的合成和配位性质研究 总被引:3,自引:0,他引:3
本文制备了α-异丙基、β-异丁基丙烯酸的15种希土配合物RE(C9H17COO)3,用X射线多晶粉末衍射、电子光谱、红外光谱和热重差热分析方法研究了配合物中RE-O键的成键性能以及羧基的配位性质.配合物中存在两种不同的羧基配位形式,轻中希土配合物(La,Ce,Pr,Nd,Sm,Eu)中羧基具有不对称桥式双齿配位形式,而重希土配合物(Gd,Tb,Dy,Ho,Er,Tm,Yb,Lu,Y)中羧基具有对称螯合双齿配位形式,配位形式的不同使得希土配合物呈现两种不同的多晶衍射图和热分解过程. 相似文献
965.
Inrecentyears,thenewsedricrystallinepolymersyndiotacticp0lystyrene(sPS)hasat-ITactedmuchattentionduetoitsg0odchendcalresistanceandenhancedmechanicalperformanceatelevatedtemPeratUre.'H0wever,itexhibitshighbrittlenessandpoorimPact-resistanceandtCar-resistance.2Therefore,itisnecessarytomodifyitwithtougheningpolyIners.AsimPlemeth0dto0verc0methedriscibilityofatwo-phaseblendofsPSandatougheningpolymristotwrovetheinterfacialaffmity,wheretheadditionofablockcoP0lymerisconsideredtobemosteffective.3… 相似文献
966.
A.A. FilaretovM.G. Zhizhin L.N. KomissarovaV.P. Danilov V.V. ChernyshevB.I. Lazoryak 《Journal of solid state chemistry》2002,166(2):362-368
A new ammonium indium phosphate (NH4)In(OH)PO4 was prepared by hydrothermal reaction in the In2O3-NH4H2PO4-NH3/OH system (T=200°C, autogenous pressure, 7 days). The formula (NH4)In(OH)PO4 was determined on the basis of chemical and thermal analysis (TG/DSC), X-ray powder diffraction and IR-spectroscopy. (NH4)In(OH)PO4 crystallizes in the tetragonal system with space group P43212 (No. 96); a=9.4232(1) Å, c=11.1766(1) Å, V=992.45(2) Å3; Z=8. The crystal structure was refined by the Rietveld method (Rw=6.35%, Rp=5.10%). The second-harmonic generation study confirmed that structure of (NH4)In(OH)PO4 does not have a center of symmetry. The cis-InO4(OH)2 octahedra form helical chains, parallel to the c-axis. The In-O-In bonds are nearly equidistant. The chains are interconnected by phosphate tetrahedra and create tunnels containing the NH4+ ions along the c-axis. (NH4)In(OH)PO4 is isostructural with RbIn(OH)PO4. 相似文献
967.
René Rojas 《Journal of organometallic chemistry》2004,689(13):2268-2272
Reaction of CrCl3 with LiCpSiMe3 in THF leads to the formation of a solvated intermediate, [(η5-Me3SiCp)CrCl2(THF)], which in turn reacts with diphenyl-2-pyridylphosphine to yield the complex [(C6H5)2PC5H4NH][(η5-Me3SiCp)CrCl3] (1) in 66% yield. As a secondary product was isolated the neutral complex [(η5-Me3SiCp)CrCl2{(C6H5)2PC5H4N}] (2) in 5% yield. The structure of complex 1 has been determined by single crystal X-ray diffraction. In the anion the metal centre shows a pseudo-octahedral geometry with the centroid of the trimethylsilylcyclopentadienyl ligand occupying the centre of three octahedral sites, and three chloride atoms completing the co-ordination sphere. Complex 1 in the presence of MAO leads to the formation of an active catalyst for the polymerization of ethylene. 相似文献
968.
标题化合物(C24H22Fe2HgO2)3是由2 氯汞基 1 乙酰基二茂铁与乙二胺反应得到的,其结构通过单晶X 射线衍射法确定。其晶体属三斜晶系,P 1空间群,Mr=1964 12,a=10 193(2),b=11 504(2),c=14 413(3) ,α=92 21(3),β=104 12(3),γ=102 67(3)°,V=1591 55(5) 3,Z=1,Dc=2 049mg/cm3,μ=8 583mm-1,F(000)=942,最终偏离因子为R=0 0859,wR=0 2617。该晶体中同时含有meso型及dl型分子,各分子中Hg原子的配位情况不一样。meso分子中的两个二茂铁是相互平行的,而另两分子dl型的二茂铁是相互垂直的。Hg原子以桥联形式连接两个二茂铁部分。meso型与dl型分子通过Hg O弱配位作用相连。 相似文献
969.
O. N. Leonidova V. I. Voronin I. A. Leonidov R. F. Samigullina B. V. Slobodin 《Journal of Structural Chemistry》2003,44(2):243-247
The crystal structures of vanadates Li1-2xCo1+xVO4 with x = 0 and 0.25 have been studied by a full pattern analysis. It has been shown that in cubic spinel LiCoVO4 (space group Fd3m), the 8a tetrahedral sites contain a majority of vanadium and a small amount of lithium; all cobalt, lithium, and a small amount of vanadium occupy the 16d octahedral sites. Li0.5Co1.25VO4 crystals belong to the rhombic system (Imma space group) with unit cell parameters a = 5.939(1), b = 5.810(1), and c = 8.303(1). On substitution of lithium by cobalt according to the scheme 2Li+ Co2+ + , half of the lithium and 70% of the vacancies formed are in the 4a octahedral sites, and onethird of lithium and most of cobalt occupy the 4d octahedral sites. The 4e tetrahedral sites are completely occupied by vanadium and lithium in a ratio of 0.92/0.08. The interatomic distances in LiCoVO4 and Li0.5Co1.25VO4 are calculated, and the sizes of lithium ion transport channels are evaluated. 相似文献
970.
Tsuneo Okubo 《Colloid and polymer science》2006,284(12):1395-1401
Sedimentation and drying dissipative structural patterns formed in the course of drying colloidal silica spheres (1.2 μm in diameter) in aqueous suspension have been studied in a glass dish and a polystyrene dish. The broad ring patterns are formed within a short time in suspension state by the convection flow of water and colloidal spheres. The broad ring patterns are not formed when a dish is covered with a cap, which demonstrates the important role of the convectional flow of silica spheres and water accompanied with the evaporation of water on the air-suspension interface. The sedimentary spheres always move by the convectional flow of water, and the broad ring patterns became sharp with time. Broad ring and microscopic fine structures are formed in the solidification processes on the bases of the convectional and sedimentation patterns. Drying patterns of the colloidal suspensions containing sodium chloride are star-like ones, which strongly supports the synchronous cooperative interactions between the salt and colloidal spheres. 相似文献