scholarly journals Synthesis, Crystal Structure, Catalytic Properties, and Luminescent of a Novel Eu(III) Complex Material with 4-Imidazolecarboxaldehyde-pyridine-2-carbohydrazone

2017 ◽  
Vol 12 (2) ◽  
pp. 185 ◽  
Author(s):  
Li-Hua Wang ◽  
Lei Liang ◽  
Peng-Fei Li
Keyword(s):  
Crystal Structure ◽  
Catalytic Properties ◽  
Coupling Reaction ◽  
Reaction Engineering ◽  
Orthorhombic Space Group ◽  
Single Crystal Diffraction ◽  
Complex Material ◽  
X Ray ◽  
A3 Coupling ◽  
Luminescent Spectrum

A novel Eu(III) complex, [Eu(L)2(H2O)4]·(NO3)·(H2O)4 (1) (H2L = 4-imidazolecarboxaldehyde-pyridine-2-carbohydrazide), was synthesized. Its structure has been characterized by elemental analysis, IR, and X-ray single crystal diffraction analysis. Complex 1 is of orthorhombic, space group Fdd2 with a = 29.471(6) A˚, b = 10.287(2) A˚, c = 24.340(5) A˚, V = 7379(3) A˚3, Z = 8, Mr = 902.58, Dc = 1.625 µg·m-3, µ = 1.789 mm-1, F(000) = 3656, GOOF = 1.099, the final R= 0.0517, ωR= 0.1292 for 3043 observed reflections with I > 2σ(I).  The A3 coupling reaction has been investigated using the complex 1 as catalyst. The luminescent spectrum of the complex 1 gives two weak peaks (448 nm and 491 nm) and two strong peaks (596 nm and 620 nm) from excitation at 279 nm. Copyright © 2017 BCREC Group. All rights reserved.Received: 11st November 2016; Revised: 10th February 2017; Accepted: 23rd February 2017How to Cite: Wang, L.H., Liang, L., Li, P.F. (2017). Synthesis, Crystal Structure, Catalytic Properties, and Luminescent of a Novel Eu(III) Complex Material with 4-Imidazolecarboxaldehyde-pyridine-2-carbohydrazone. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (2): 185-190 (doi:10.9767/bcrec.12.2.764.185-190)Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.2.764.185-190

scholarly journals Synthesis, Crystal Structure of Mg(II) Complex Material and its Application as Catalysts for A3 Coupling Reaction

2015 ◽  
Vol 9 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Xi-Shi Tai ◽  
Li-Li Liu
Keyword(s):  
Crystal Structure ◽  
Coupling Reaction ◽  
Ethanol Solution ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Complex Molecules ◽  
X Ray ◽  
3D Network ◽  
A3 Coupling ◽  
Efficient Heterogeneous Catalyst

The ligand of 1, 2-phenylenedioxydiacetic acid (HL) has been employed to react with MgCl2·6H2O in water/ethanol solution (v:v = 1:1), to yield a novel Mg(II) complex [MgL(H2O]3·3.5H2O. The complex was characterized by infrared spectroscopy and single crystal X-ray diffraction structural analysis. The results show that the Mg(II) complex belongs to monoclinic, space group C2/c with a = 2.9160(6) nm, b = 0.67617(14) nm, c = 1.7319(4) nm, β = 109.06(3)°, V= 3.2275(11) nm, Z = 8, Dc= 1.562 µg·m-3, µ = 0.184 mm, F (000) = 1560, and final R1 = 0.0703, ωR2= 0.2256. The complex molecules form a 3D network structure through hydrogen bonds and π-π stack. The A3 coupling reaction of phenylacetylene, aldehyde and amine (piperidine) in the presence of Au@Mg(II) complex as an efficient heterogeneous catalyst has been studied.

Crystal structure of the anticancer drug carmustine determined by X-ray powder diffraction

2021 ◽  
pp. 1-3
Author(s):  
Carina Schlesinger ◽  
Edith Alig ◽  
Martin U. Schmidt
Keyword(s):  
Crystal Structure ◽  
Anticancer Drug ◽  
Powder Diffraction ◽  
Room Temperature ◽  
Powder Diffraction Data ◽  
Orthorhombic Space Group ◽  
Commercial Sample ◽  
One Dimensional ◽  
X Ray ◽  
Hydrogen Bond Pattern

The structure of the anticancer drug carmustine (1,3-bis(2-chloroethyl)-1-nitrosourea, C5H9Cl2N3O2) was successfully determined from laboratory X-ray powder diffraction data recorded at 278 K and at 153 K. Carmustine crystallizes in the orthorhombic space group P212121 with Z = 4. The lattice parameters are a = 19.6935(2) Å, b = 9.8338(14) Å, c = 4.63542(6) Å, V = 897.71(2) ų at 153 K, and a = 19.8522(2) Å, b = 9.8843(15) Å, c = 4.69793(6) Å, V = 921.85(2) ų at 278 K. The Rietveld fits are very good, with low R-values and smooth difference curves of calculated and experimental powder data. The molecules form a one-dimensional hydrogen bond pattern. At room temperature, the investigated commercial sample of carmustine was amorphous.

scholarly journals β-Y(BO2)3 – a new member of the β-Ln(BO2)3 (Ln=Nd, Sm, Gd–Lu) structure family

2017 ◽  
Vol 72 (12) ◽  
pp. 983-988 ◽  
Author(s):  
Martin K. Schmitt ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Lattice Parameters ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
X Ray

Abstractβ-Y(BO2)3 was synthesized in a Walker-type multianvil module at 5.9 GPa/1000°C. The crystal structure has been elucidated through single-crystal X-ray diffraction. β-Y(BO2)3 crystallizes in the orthorhombic space group Pnma (no. 62) with the lattice parameters a=15.886(2), b=7.3860(6), and c=12.2119(9) Å. Its crystal structure will be discussed in the context of the isotypic lanthanide borates β-Ln(BO2)3 (Ln=Nd, Sm, Gd–Lu).

Crystal Structure, Spectroscopic and Redox Properties of Copper(II) Bis{2-[(2,6-dimethylphenyl)iminomethyl-3-methoxyphenolate]}

2007 ◽  
Vol 62 (9) ◽  
pp. 1133-1138 ◽  
Author(s):  
Veli T. Kasumov ◽  
Ibrahim Uçar ◽  
Ahmet Bulut ◽  
Fevzi Kösal
Keyword(s):  
Crystal Structure ◽  
Title Complex ◽  
Redox Properties ◽  
Orthorhombic Space Group ◽  
Long Distance ◽  
X Ray ◽  
X Ray Crystallography ◽  
Square Planar ◽  
Planar Molecules ◽  
Exchange Interaction Parameter

The coordination chemistry of N-(2,6-di-methylphenyl)-2-hydroxy-3-methoxybenzaldimine (1) with Cu(II) has been investigated by X-ray crystallography, electronic and EPR spectroscopies, as well as by electro- and magnetochemistry. The title complex 2 crystallizes in the orthorhombic space group P212121 (a = 8.1538, b = 17.7466, c =19.8507 Å). The mononuclear square-planar molecules 2 featuring trans-N2O2 coordination are connected via weak intermolecular C-H· · ·π interactions into infinite chains parallel to the a axis. Although the intermolecular Cu· · ·Cu separations within individual chains and between chains are very long (8.154 and 9.726 Å ), the exchange interaction parameter G = 2.03 < 4, estimated from solid state EPR spectra, suggests the existence of long-distance superexchange pathways between adjacent Cu(II) centers. The electronic and electrochemical features of the compound are also discussed.

The molecular and crystal structure of [Pt(diethylenetriamine)(guanosine)](ClO4)2

1979 ◽  
Vol 57 (1) ◽  
pp. 57-61 ◽  
Author(s):  
R. Melanson ◽  
F. D. Rochon
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Least Squares ◽  
Platinum Atom ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
R Factor ◽  
Square Planar ◽  
Coordination Plane

The crystal structure of [Pt(diethylenetriamine)(guanosine)](ClO4)2 has been determined by X-ray diffraction. The crystals are orthorhombic, space group P212121, with a = 12.486(6), b = 13.444(7), c = 14.678(11) Å, and Z = 4. The structure was refined by block-diagonal least-squares analysis to a conventional R factor of 0.050 and a weighted Rw = 0.045.The coordination around the platinum atom is square planar. Guanosine is bonded to platinum through N(7). The purine planar ring makes an angle of 62.7° with the platinum coordination plane. The structure is stabilized by hydrogen bonding.

The preparation and catalytic properties of copper(II) complexes derived from a pyrazole containing ligand. X-ray crystal structure of [Cu(pzmhp)(BF4)](BF4)

1997 ◽  
Vol 257 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Mitchell R. Malachowski ◽  
Josephine Carden ◽  
Marilyn G. Davidson ◽  
Willem L. Driessen ◽  
Jan Reedijk
Keyword(s):  
Crystal Structure ◽  
Catalytic Properties ◽  
X Ray

scholarly journals Synthesis, Characterization, and Crystal Structure of [Co4(CH3CO2)2L4]2[BPh4]4·0.5H2O, Where HL = 4-(Salicylaldiminato)antipyrine

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Ramadan M. El-mehdawi ◽  
Abdussalam N. EL-dewik ◽  
Mufida M. Ben-Younes ◽  
Fathia A. Treish ◽  
Ramadan G. Abuhmaiera ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Schiff Base Ligand ◽  
Title Complex ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
Tridentate Schiff Base

The title complex was isolated as a red solid from the reaction of 4-(salicylaldiminato)antipyrine, HL, and cobalt (II) acetate in ethanol. The complex has been characterized by elemental analysis, FTIR, UV-Vis, and X-ray single crystal diffraction. Two crystallographically different cationic units, A and B, of the title complex are found. Both units are essentially isostructural; nevertheless, small differences exist between them. Both units contain four cobalt atoms arranged at the corners of distorted cubane-like core alternatively with phenoxy oxygen of the Schiff base. In both cases, one cobalt binds to three coordinated sites from the corresponding tridentate Schiff base ligand, and the fourth one was bonded by the acetate oxygen, and the fifth and the sixth donor sites come from the phenolate oxygen of another Schiff base ligand.

Determination of the Crystal Structure and Redefinition of Tsugaruite, Pb28As15S50Cl, the First Lead-Arsenic Chloro-Sulfosalt

2020 ◽  
Author(s):  
Cristian Biagioni ◽  
Luca Bindi ◽  
Koichi Momma ◽  
Ritsuro Miyawaki ◽  
Yoshitaka Matsushita ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Atomic Ratio ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Specific Position ◽  
Actual Classification ◽  
Aomori Prefecture

Abstract Tsugaruite was originally defined as a lead-arsenic sulfosalt from the Yunosawa mine, Aomori Prefecture, Japan. Until recently its crystal structure remained unsolved and its actual classification in the sulfosalt realm was unknown. Here the refinement of the crystal structure of tsugaruite using single-crystal X-ray diffraction data is reported. The mineral is orthorhombic, space group P2nn, with unit-cell parameters a = 8.0774(10), b = 15.1772(16), c = 38.129(4) Å, V = 4674.3(9) Å3, in agreement with previous studies. The solution of the crystal structure of this mineral revealed Cl occupying a specific position. Chlorine was thus sought and found using the electron microprobe; the average of six spot analyses gave (in wt.%): Pb 68.04, As 12.83, S 18.29, Cl 0.63, total 99.80. The empirical formula, calculated on the basis of Pb + As = 43 atoms per formula unit, is Pb28.26As14.74S49.08Cl1.52. Tsugaruite is an N = 4 plesiotypic derivative of the homologous series of Pb-Sb chloro-sulfosalts having the general formula Pb(2+2N)(Sb,Pb)(2+2N)S(2+2N)(S,Cl)(4+2N)ClN. It has a Cl/(Cl + S) atomic ratio close to that of other known Pb-Sb chloro-sulfosalts (pillaite, pellouxite) and slightly higher than that of dadsonite.

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