scholarly journals Synthesis, Structural Characterization, and Antibacterial Activity of Novel Erbium(III) Complex Containing Antimony

2018 ◽  
Vol 2018 ◽  
pp. 1-9
Author(s):  
Ting Liu ◽  
Rong-Gui Yang ◽  
Guo-Qing Zhong
Keyword(s):  
Ethylenediaminetetraacetic Acid ◽  
Antimicrobial Activities ◽  
Diffusion Method ◽  
Water Molecules ◽  
Equatorial Position ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
Adjacent Layer ◽  
X Ray ◽  
Oxygen Atoms

The novel 3D edta-linked heterometallic complex [Sb2Er(edta)2(H2O)4]NO3·4H2O (H4edta = ethylenediaminetetraacetic acid) was synthesized and characterized by elemental analyses, single-crystal X-ray diffraction, powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and thermal analysis. The complex crystallizes in the monoclinic system with space group Pm. In the complex, each erbium(III) ion is connected with antimony(III) ions bridging by four carboxylic oxygen atoms, and in each [Sb(edta)]− anion, the antimony(III) ion is hexacoordinated by two nitrogen atoms and four oxygen atoms from the edta4− ions, together with a lone electron pair at the equatorial position. The erbium(III) ion is octacoordinated by four oxygen atoms from four different edta4− ions and four oxygen atoms from the coordinated water molecules. The carboxylate bridges between antimony and erbium atoms form a planar array, parallel to the (1 0 0) plane. There is an obvious weak interaction between antimony atom and oxygen atom of the carboxyl group from the adjacent layer. The degradation of the complex proceeds in several steps and the water molecules and ligands are successively emitted, and the residues of the thermal decomposition are antimonous oxide and erbium(III) oxide. The complex was evaluated for its antimicrobial activities by agar diffusion method, and it has good activities against the test bacterial organisms.

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.

scholarly journals Synthesis and Complexation Properties of 2-Hydroxy-5-methoxyphenylphosphonic Acid (H3L1). Crystal Structure of the [Cu(H2L1)2(Н2О)2] Complex

2021 ◽  
Vol 91 (11) ◽  
pp. 2176-2186
Author(s):  
G. S. Tsebrikova ◽  
Yu. I. Rogacheva ◽  
I. S. Ivanova ◽  
A. B. Ilyukhin ◽  
V. P. Soloviev ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Methoxy Group ◽  
Protonation Constants ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Stability ◽  
Intramolecular Hydrogen ◽  
Oxygen Atoms

Abstract 2-Hydroxy-5-methoxyphenylphosphonic acid (H3L1) and the complex [Cu(H2L1)2(H2O)2] were synthesized and characterized by IR spectroscopy, thermogravimetry, and X-ray diffraction analysis. The polyhedron of the copper atom is an axially elongated square bipyramid with oxygen atoms of phenolic and of monodeprotonated phosphonic groups at the base and oxygen atoms of water molecules at the vertices. The protonation constants of the H3L1 acid and the stability constants of its Cu2+ complexes in water were determined by potentiometric titration. The protonation constants of the acid in water are significantly influenced by the intramolecular hydrogen bond and the methoxy group. The H3L1 acid forms complexes CuL‒ and CuL24‒ with Cu2+ in water.

Synthesis, crystal structure, and vibrational spectra of the complex maleic acid•2H2O•18-crown-6

1990 ◽  
Vol 68 (12) ◽  
pp. 2183-2189 ◽  
Author(s):  
Pierre Audet ◽  
Rodrigue Savoie ◽  
Michel Simard
Keyword(s):  
Crystal Structure ◽  
Water Molecule ◽  
Maleic Acid ◽  
Water Molecules ◽  
Infrared And Raman Spectra ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
X Ray ◽  
O 18 ◽  
Stoichiometric Complex

A stoichiometric complex of formula maleic acid•2H2O•18-crown-6 has been obtained from maleic acid and the macrocyclic polyether 18-crown-6. Crystals of this complex have been shown by X-ray diffraction crystallography to belong to the Cc space group of the monoclinic system. The acid molecules in the adduct are linked to each other through a water molecule, giving infinite [-acid-H2O-]n chains. They are also linked to the crown ether via water molecules. The infrared and Raman spectra of the complex are presented and compared to those of crystalline maleic acid. Keywords: maleic acid/18-crown-6, structure, X-ray, spectra.

Dodecamethyl Bisimidotriphosphoramide (TRIPA), Part III [1, 2] The Crystal and Molecular Structure of TRIPA · H2O

1980 ◽  
Vol 35 (10) ◽  
pp. 1203-1206 ◽  
Author(s):  
Johannes C. P. M. Lapidaire ◽  
Anthoni J. De Kok
Keyword(s):  
Molecular Structure ◽  
Single Crystal ◽  
Crystal And Molecular Structure ◽  
Van Der Waals ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
Space Group ◽  
X Ray

Abstract The crystal and molecular structure of dodecamethyl bisimidotriphosphoramide mono-hydrate (TRIPA • H2O, C12H38N7O4P3) has been determined by single crystal X-ray diffraction techniques. The compound crystallises in the monoclinic system, space group P2i/n with a = 9.236(3), b = 14.016(4), c = 17.534(5) A, β = 97.32(4)°, Z = 4. The building units are dimers of TRIPA • H2O. These units are separated by normal van der Waals distances. The two molecules in the dimer are connected by four hydrogen bridges involving two water molecules. The nitrogen atoms display a nearly planar hybridisation.

scholarly journals X-ray structure of 1D-coordination polymer of copperII bearing 1,4-pyrazine-2,3-dicarboxylic acid and 2-aminopyrimidine

2012 ◽  
Vol 77 (1) ◽  
pp. 67-73 ◽  
Author(s):  
Masoud Mirzaei ◽  
Hossein Eshtiagh-Hosseini ◽  
Azam Hassanpoor ◽  
Victor Barba
Keyword(s):  
Coordination Polymer ◽  
Dicarboxylic Acid ◽  
Supramolecular Assembly ◽  
Axial Position ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Double Chain ◽  
X Ray ◽  
1D Coordination Polymer ◽  
Oxygen Atoms

The new 1D-coordination polymer of CuII ion, {(2- apymH)2[Cu(pyzdc)2] .6H2O}n, (2-apym = 2-aminopyrimidine, pyzdcH2 = 1,4- pyrazine-2,3-dicarboxylic acid), was synthesized based on proton transfer mechanism and characterized by elemental analysis, infrared spectroscopy, and single crystal X-ray diffraction. The coordination polymer consists of infinite anionic chains of [Cu(pyzdc)2]2- anion bridged crossing double chain running along a-axis and discrete (2-apymH)+ fragment. The CuII ion is located on inversion centre in the basal plane of an elongated octahedron and two oxygen atoms from adjacent (pyzdc)2-ligands occupy axial position. The interaction between oxygen atoms of water molecules along with the dicarboxylic acid play an important role in the overall supramolecular assembly.

The crystal structures of sjögrenite and pyroaurite

1967 ◽  
Vol 36 (280) ◽  
pp. 465-479 ◽  
Author(s):  
L. Ingram ◽  
H. F. W. Taylor
Keyword(s):  
Crystal Structures ◽  
Three Dimensional ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Approximate Composition ◽  
Oxygen Atoms

SummaryThe crystal structures of sjögrenite and pyroaurite, two stacking modifications of approximate composition Mg6Fe2(OH)16(CO3).4H2O, have been determined by X-ray diffraction using three-dimensional methods. Sjögrenite is hexagonal, with a 3·13, c 15·66 Å, space group P63/mmc , Z = ¼; pyroaurite is rhombohedral, with aH 3·13, cH 23·49 Å, space group R3̄m or R3m, Z = ⅜. Both structures are based on brucite-like layers, with magnesium and iron distributed among the octahedral positions. The cations appear to be largely disordered, although ordered regions may occur in some crystals. Between the brucite-like layers are the water molecules and carbonate groups. These are statistically arranged, with their oxygen atoms distributed among a larger number of possible sites.

scholarly journals SYNTHESIS, CHARACTERIZATION OF ANTIMICROBIAL ACTIVITY OF 22’DICHLOROHYDROBENZOIN

2018 ◽  
Vol 11 (12) ◽  
pp. 334
Author(s):  
Thanuja B ◽  
Charles Kanagam
Keyword(s):  
Antimicrobial Activity ◽  
Antimicrobial Activities ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
Vis Spectroscopy ◽  
Optical Behavior ◽  
Thermal Stability Of

Objective: The objective of this work to evaluate the antimicrobial activities of synthesized 22’dichlorohydrobenzoin (22’CD) a new organic crystal.Methods: 22’CD a new organic crystal was grown by vapor diffusion method. Single crystals of 22’CD have been subjected to X-ray diffraction analysis to estimate the lattice parameters and the space group. The molecular structure was confirmed using Fourier transform infrared and nuclear magnetic resonance (NMR) spectral analyses. Optical behavior and thermal stability of the crystal were determined using UV-Vis spectroscopy and thermogravimetry-differential thermal analysis curves. In the present study, antimicrobial activity of 22’CD was evaluated against Escherichia coli and Bacillus subtilis was evaluated by agar well diffusion method.Results: Antibacterial activity of 22’CD was analyzed with ciprofloxacin and miconazole standard and tested against E. coli, Pseudomonas aeruginosa, Salmonella paratyphi, Klebsiella pneumonia’s, Staphylococcus aureus, Streptococcus progenies, and B. subtilis.Conclusion: The 22’CD was found to be effective against E. coli and B. subtitles.

A new organically templated magnesium sulfate: structure, spectroscopic analysis, and thermal behaviour

2014 ◽  
Vol 68 (2) ◽  
Author(s):  
Dhouha Hassan ◽  
Walid Rekik ◽  
Houcine Naïli ◽  
Tahar Mhiri
Keyword(s):  
Thermal Decomposition ◽  
Hydrogen Bonds ◽  
Magnesium Sulfate ◽  
Spectroscopic Analysis ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Slow Evaporation ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
X Ray

AbstractA new magnesium sulfate templated by 2-methylpiperazine, (C5H14N2)[Mg(H2O)6](SO4)2, was prepared by the slow evaporation method. The obtained crystals were investigated by the Raman and FTIR spectroscopy and crystallographically characterised by single-crystal X-ray diffraction. The compound crystallises in the monoclinic system, space group P21/n. Supramolecular network of this hybrid material consists of Mg2+ cations octahedrally coordinated by six water molecules, sulfate tetrahedra and protonated and disordered diamine linked together by two types of hydrogen bonds: OW—H…O and N—H…O. Dehydration of the title compound takes place in three steps. Thermal decomposition of the anhydrous phase consists in the loss of the organic moiety and one sulfate group leading to the formation of magnesium sulfate.

The X-ray structure of a sodium peroxide hydrate, Na2O2•8H2O, and its reactions with carbon dioxide: relevance to the brightening of mechanical pulps

1997 ◽  
Vol 75 (1) ◽  
pp. 46-51 ◽  
Author(s):  
Geoffrey S. Hill ◽  
David G. Holah ◽  
Stephen D. Kinrade ◽  
Todd A. Sloan ◽  
Vincent R. Magnuson ◽  
...  
Keyword(s):  
Water Molecules ◽  
Monoclinic Space Group ◽  
Sodium Peroxide ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mechanical Pulps ◽  
Main Component ◽  
Key Words Sodium ◽  
Centrosymmetric Structure ◽  
Oxygen Atoms

The main component of the solid originally believed to be a peroxosilicate with pulp-brightening properties has been shown to be Na2O2•8H2O. The solid crystallizes in the monoclinic space group C2/c, with an empirical formula H8O5Na, and with a = 14.335(3), b = 6.461(1), c = 11.432(2) Å, β = 118.28(3)°, and Z = 8. The centrosymmetric structure consists of a peroxide anion with an O—O distance of 1.499(2) Å. Each of these oxygen atoms is at the apex of an approximate square-based pyramid, the base of which consists of four oxygen atoms of water molecules. The bases of the two pyramids are staggered when viewed down the peroxide bond. Each sodium is at the centre of an approximate octahedron of water molecules, four of which bridge other sodium atoms and two bridge to the peroxide anions. One hydrogen atom of each of these two water molecules is terminal and the other two are hydrogen bonded to peroxide oxygen atoms. The compound reacts very rapidly with CO2 in moist air to form Na2CO3, but in drier conditions, formation of the carbonate can take many days and proceeds via a percarbonate, believed to be Na2CO4. This has been identified by infrared spectroscopy and X-ray powder diffraction and can persist for long periods in dry air. Key words: sodium peroxide hydrate, sodium percarbonate, pulp brightening, X-ray diffraction, infrared.

scholarly journals On the Structure in Aqueous Superconcentrated Calcium Nitrate

1981 ◽  
Vol 36 (8) ◽  
pp. 831-835 ◽  
Author(s):  
R. Caminiti ◽  
A. Musinu ◽  
G. Paschina ◽  
G. Piccaluga ◽  
G. Pinna
Keyword(s):  
Experimental Data ◽  
Calcium Ions ◽  
Calcium Nitrate ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
Crystalline Hydrates ◽  
Oxygen Atoms

Abstract Liquid hydrous calcium nitrate of composition Ca(NO3)2 · 3.5 H2O was investigated by X-ray diffraction. Experimental data were interpreted in terms of geometrical models suggested by the structure of the crystalline hydrates Ca (NO3)2 · 3H2O and Ca(NO3)2 · 4H2O, in which calcium ions are coordinated to nine oxygen atoms, partly coming from water molecules, partly from NO3-ions.

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