Coordination compounds of norbornadiene with silver tetrafluoroborate

1968 ◽  
Vol 46 (2) ◽  
pp. 117-124 ◽  
Author(s):  
Harold W. Quinn
Keyword(s):  
Aqueous Solution ◽  
Aqueous Solutions ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrated Complexes ◽  
Crystalline Complexes Of

Crystalline complexes of norbornadiene with silver tetrafluoroborate have been obtained both from anhydrous and aqueous solution. While both solutions yield complexes of stoichiometry AgBF4•C7H8 and 2AgBF4•3C7H8, those from the aqueous solutions also contain water of crystallization. The infrared spectra show that norbornadiene is similarly complexed in both the anhydrous and hydrated complexes but that the coordination in the 1:1 complex is different from that in the 2:3 complex. The anhydrous and hydrated 1:1 complexes have the same X-ray diffraction powder patterns while those of 2:3 complexes are different.

Structure characterization of the non-crystalline complexes of copper salts with native cyclodextrins

2016 ◽  
Vol 45 (26) ◽  
pp. 10696-10707 ◽  
Author(s):  
Manuel I. Velasco ◽  
Claudio R. Krapacher ◽  
Rita H. de Rossi ◽  
Laura I. Rossi
Keyword(s):  
Physicochemical Properties ◽  
Coordination Compounds ◽  
Simple Procedure ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
Copper Salts ◽  
X Ray ◽  
Ft Ir ◽  
Crystalline Complexes Of

The characterization of non-crystalline complexes is very difficult when techniques like X-ray diffraction or NMR are not available. We propose a simple procedure to characterize the physicochemical properties of amorphous new coordination compounds between cyclodextrins (CD) and Cu2+ salts, by several techniques as TGA, FT-IR, EPR.

Interaction of the methylmercury cation with glycine and alanine: a vibrational and X-ray diffraction study

1986 ◽  
Vol 64 (9) ◽  
pp. 1876-1884 ◽  
Author(s):  
Marie-Claude Corbeil ◽  
André L. Beauchamp ◽  
Serge Alex ◽  
Rodrigue Savoie
Keyword(s):  
Aqueous Solutions ◽  
Diffraction Study ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Carboxylate Oxygen

The complexes (CH3Hg)Gly, (CH3Hg)(L-Ala), and (CH3Hg)(DL-Ala) were prepared by reacting CH3HgOH with glycine (HGly) and alanine (HAla). Crystals of (CH3Hg)(DL-Ala) are monoclinic, space group P21/c, a = 9.460(2), b = 8.794(2), c = 8.723(2) Å, β = 97.49(2)°, Z = 4. The structure was refined on 935 MoKα reflections to R = 0.042. The complex results from displacement of an alanine NH3+ proton by the CH3Hg+ ion, which is linearly bonded to the —NH2 group. An intramolecular Hg … O contact of 2.63 Å is also formed with a carboxylate oxygen. The Raman and infrared spectra of solid (CH3Hg)Gly and (CH3Hg)(L-Ala) are compared with those of the ligands. Raman spectra of aqueous solutions at different pH indicate that the NH2-bonded structure is retained in solution, although no complexation via the carboxylate occurs.

Structural Study of a new Compound Based on Acid 1,4-Cyclohexanedicarboxylic (1,4-CDC)

2010 ◽  
Vol 6 (1) ◽  
pp. 891-896
Author(s):  
Manel Halouani ◽  
M. Dammak ◽  
N. Audebrand ◽  
L. Ktari
Keyword(s):  
Aqueous Solution ◽  
Water Molecules ◽  
Carboxyl Group ◽  
X Ray Diffraction ◽  
Compound I ◽  
Unit Cell Parameters ◽  
Monoclinic System ◽  
X Ray ◽  
Cell Parameters ◽  
Cyclohexanedicarboxylic Acid

One nickel 1,4-cyclohexanedicarboxylate coordination polymers, Ni2 [(O10C6H4)(COO)2].2H2O  (I), was hydrothermally synthesized from an aqueous solution of Ni (NO3)2.6H2O, (1,4-CDC) (1,4-CDC = 1,4-cyclohexanedicarboxylic acid) and tetramethylammonium nitrate. Compound (I) crystallizes in the monoclinic system with the C2/m space group. The unit cell parameters are a = 20.1160 (16) Å, b = 9.9387 (10) Å, c = 6.3672 (6) Å, β = 97.007 (3) (°), V= 1263.5 (2) (Å3) and Dx= 1.751g/cm3. The refinement converged into R= 0.036 and RW = 0.092. The structure, determined by single crystal X-ray diffraction, consists of two nickel atoms Ni (1) and Ni (2). Lots of ways of which is surrounded by six oxygen atoms, a carboxyl group and two water molecules.

Infrared spectroscopic study of the YPO4-YCrO4 system

1985 ◽  
Vol 50 (10) ◽  
pp. 2139-2145
Author(s):  
Alexander Muck ◽  
Eva Šantavá ◽  
Bohumil Hájek
Keyword(s):  
Spectroscopic Study ◽  
Infrared Spectra ◽  
Point Of View ◽  
Mixed Crystals ◽  
Crystal Symmetry ◽  
Infrared Spectroscopic Study ◽  
X Ray Diffraction ◽  
X Ray ◽  
Infrared Spectroscopic ◽  
Diffraction Patterns

The infrared spectra and powder X-ray diffraction patterns of polycrystalline YPO4-YCrO4 samples are studied from the point of view of their crystal symmetry. Mixed crystals of the D4h19 symmetry are formed over the region of 0-30 mol.% YPO4 in YCrO4. The Td → D2d → D2 or C2v(GS eff) correlation is appropriate for both PO43- and CrO43- anions.

scholarly journals Leaching Titaniferous Magnetite Concentrate by Alkaline Aqueous Solution

2021 ◽  
Author(s):  
Ke Guo ◽  
Shaoyan Wang ◽  
Renfeng Song ◽  
Zhiqiang Zhang
Keyword(s):  
Aqueous Solution ◽  
Alkali Concentration ◽  
Water Usage ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Iron Concentrate ◽  
Titaniferous Magnetite ◽  
Magnetite Concentrate ◽  
Kinetics Of

AbstractLeaching titaniferous magnetite concentrate with alkali solution of high concentration under high temperature and high pressure was utilized to improve the grade of iron in iron concentrate and the grade of TiO2 in titanium tailings. The titaniferous magnetite concentrate in use contained 12.67% TiO2 and 54.01% Fe. The thermodynamics of the possible reactions and the kinetics of leaching process were analyzed. It was found that decomposing FeTiO3 with NaOH aqueous solution could be carried out spontaneously and the reaction rate was mainly controlled by internal diffusion. The effects of water usage, alkali concentration, reaction time, and temperature on the leaching procedure were inspected, and the products were characterized by X-ray diffraction, scanning electron microscope, and energy dispersive spectroscopy, respectively. After NaOH leaching and magnetic separation, the concentrate, with Fe purity of 65.98% and Fe recovery of 82.46%, and the tailings, with TiO2 purity of 32.09% and TiO2 recovery of 80.79%, were obtained, respectively.

Removal of Heavy Metals from Aqueous Solution by Hydroxyapatite/Chitosan Composite

2013 ◽  
Vol 789 ◽  
pp. 176-179 ◽  
Author(s):  
Eny Kusrini ◽  
Nofrijon Sofyan ◽  
Dwi Marta Nurjaya ◽  
Santoso Santoso ◽  
Dewi Tristantini
Keyword(s):  
Heavy Metals ◽  
Aqueous Solution ◽  
Metal Ions ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Removal Of Heavy Metals ◽  
Sem Micrograph ◽  
Pseudo Second Order ◽  
Chitosan Composite

Hydroxyapatite/chitosan (HApC) composite has been prepared by precipitation method and used for removal of heavy metals (Cr6+, Zn2+and Cd2+) from aqueous solution. The HAp and 3H7C composite with HAp:chitosan ratio of 3:7 (wt%) were characterized by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy-energy dispersive X-ray spectroscopy. The SEM results showed that HAp is spherical-shaped and crystalline, while chitosan has a flat structure. SEM micrograph of 3H7C composite reveals crystalline of HAp uniformly spread over the surface of chitosan. The crystal structure of HAp is maintained in 3H7C composite. Chitosan affects the adsorption capacity of HAp for heavy metal ions; it binds the metal ions as well as HAp. The kinetic data was best described by the pseudo-second order. Surface adsorption and intraparticle diffusion take place in the mechanism of adsorption process. The binding of HAp powder with chitosan made the capability of composite to removal of Cr6+, Zn2+and Cd2+from aqueous solution effective. The order of removal efficiency (Cr6+> Cd2+> Zn2+) was observed.

Syntheses, Crystal Structures and Thermal Stability of Co(II) and Zn(II) Complexes with Ethyl Carbazate

2005 ◽  
Vol 60 (5) ◽  
pp. 505-510 ◽  
Author(s):  
Tong-Lai Zhang ◽  
Jiang-Chuang Song ◽  
Jian-Guo Zhang ◽  
Gui-Xia Ma ◽  
Kai-Bei Yu
Keyword(s):  
Thermal Stability ◽  
Aqueous Solutions ◽  
Diffraction Analysis ◽  
Single Crystals ◽  
Slow Evaporation ◽  
X Ray Diffraction ◽  
Element Analysis ◽  
Thermal Stabilities ◽  
X Ray ◽  
Thermal Stability Of

Cobalt(II) and zinc(II) complexes of ethyl carbazate (ECZ), [Co(ECZ)3](NO3)2 and [Zn(ECZ)3] (NO3)2, were synthesized. Single crystals of these two compounds were grown from aqueous solutions using a slow evaporation method. Their structures have been determined by X-ray diffraction analysis. Both of them are monoclinic with space group P21/n. The complexes are further characterized by element analysis and IR measurements. Their thermal stabilities are studied by using TG-DTG, DSC techniques. When heated to 350 °C, only metal oxide was left for both complexes.

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