scholarly journals Coordination polymers of benzenediseleninate, the seleno analog of terephthalate

2014 ◽  
Vol 70 (a1) ◽  
pp. C1235-C1235
Author(s):  
Robert Burrow ◽  
Giancarlo Belmonte
Keyword(s):  
Coordination Polymers ◽  
Water Molecules ◽  
Gravimetric Analysis ◽  
The Novel ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Subsequent Formation ◽  
Metal Centers ◽  
Infrared Spectral

The proligand para-benzenediseleninic acid, (HO2SeC6H4SeO2H) (Figure), is the seleno analog to the commonly used MOF spacer proligand, terephthalic acid. Novel coordination polymers based on this proligand, and Mn(II), Fe(II), Co(II), Ni(II), Cu(II) or Zn(II) metal centers containing auxiliary water molecules, [M(O2SeC6H4SeO2)2(H2O)n], were synthesized. Depending on the reaction conditions, different pure or mixed phases can be produced. Crystal to crystal transformations of the novel coordination polymers were studied with powder X ray diffraction, infrared spectral analysis and thermal gravimetric analysis. These coordination polymers can be dehydrated with subsequent formation of new anhydrous coordination polymer phases. Some of these phases can be rehydrated to lead back to the crystalline starting materials or to new crystalline hydrated phases. We are working on the complete structural characterization of the phases.

Synthesis and Characterization of Superparamagnetic Fe3O4 Nanoparticles

2013 ◽  
Vol 750-752 ◽  
pp. 340-343 ◽  
Author(s):  
De Hui Sun ◽  
Jiao Wu ◽  
Ji Lin Zhang
Keyword(s):  
Room Temperature ◽  
Thermal Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Xrd Pattern ◽  
X Ray ◽  
Magnetic Investigation ◽  
Average Size

We synthesized Fe3O4 nanoparticles using a solvent thermal method and characterized the morphologies, structures, surface properties, thermal stability and magnetism of the products by Field emission scanning electron microscopy (FE-SEM), Powder X-ray diffraction (XRD), Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA) and vibrating sample magnetometer (VSM). The experimental results showed that the Fe3O4 nanoparticles have a tunable average size range from 55 nm to 85 nm. Their diameters decreased with increase of precursor FeCl24H2O concentration or increase of the reaction time under other reaction conditions held constant. The XRD pattern confirmed that the Fe3O4 nanoparticles belong to cubic structure. Magnetic investigation reveals that the Fe3O4 nanoparticles have higher saturation magnetization and negligible coercivity at room temperature.

Single Source Precursors for the Growth of Metal-Chalcogenide Thin Films

1992 ◽  
Vol 282 ◽  
Author(s):  
Allen L. Seligson ◽  
Philip J. Bonasia ◽  
John Arnold ◽  
Kin-Man Yu ◽  
Jim M. Walker ◽  
...  
Keyword(s):  
Thin Films ◽  
The Novel ◽  
Single Source ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Rutherford Back Scattering ◽  
Single Source Precursors ◽  
Back Scattering ◽  
Related Compounds

ABSTRACTWe have recently reported the growth of ZnTe and CdTe thin films from the novel volatile single-source precursors Zn(sitel)2 and Cd(sitel)2 [sitel = TeSi(TeSi(siMe3)3]. In an effort to understand the role played by the bulky substituents, we have prepared a number of related compounds and have investigated their potential for the growth of II-VI materials. We now describe the synthesis and characterization of M[EX(SiMe3)3]2 (M = Zn, Cd, Hg for E = Te, X = C; M = Zn for E = Se, X = C, Si) and their use as precursors molecules for the growth of ZnSe, ZnTe, CdTe and HgTe. The thin films were characterized by Rutherford Back scattering spectrometry (RBS) and X-ray diffraction. Pyrolysis reaction conditions for the alkyl and silyl chalcogenolates are also compared.

scholarly journals Rapid four-component synthesis of dihydropyrano[2,3-c]pyrazoles using nano-eggshell/Ti(IV) as a highly compatible natural based catalyst

BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Arefeh Dehghani Tafti ◽  
Bi Bi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri ◽  
Naeimeh Salehi
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Reaction Times ◽  
Diffraction Field ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Work Up

AbstractNano-eggshell/Ti(IV) as a novel naturally based catalyst was prepared, characterized and applied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. The characterization of nano-eggshell/Ti(IV) was performed using Fourier Transform Infrared spectroscopy, X-ray Diffraction, Field Emission Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and Thermo Gravimetric Analysis. Dihydropyrano[2,3-c]pyrazoles were synthesized in the presence of nano-eggshell/Ti(IV) via a four component reaction of aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate at room temperature under solvent free conditions. The principal affairs of this procedure are mild condition, short reaction times, easy work-up, high yields, reusability of the catalyst and the absence of toxic organic solvents.

scholarly journals Synthesis and Structural Characterization of (E)-4-[(2-Hydroxy-3-methoxybenzylidene)amino]butanoic Acid and Its Novel Cu(II) Complex

Molbank ◽  
10.3390/m1179 ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. M1179
Author(s):  
Eleftherios Halevas ◽  
Antonios Hatzidimitriou ◽  
Barbara Mavroidi ◽  
Marina Sagnou ◽  
Maria Pelecanou ◽  
...  
Keyword(s):  
Schiff Base ◽  
Gamma Aminobutyric Acid ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Polymeric Compound ◽  
Bridging Ligands ◽  
1H And 13C Nmr ◽  
One Dimensional ◽  
Ft Ir

A novel Cu(II) complex based on the Schiff base obtained by the condensation of ortho-vanillin with gamma-aminobutyric acid was synthesized. The compounds are physico-chemically characterized by elemental analysis, HR-ESI-MS, FT-IR, and UV-Vis. The complex and the Schiff base ligand are further structurally identified by single crystal X-ray diffraction and 1H and 13C-NMR, respectively. The results suggest that the Schiff base are synthesized in excellent yield under mild reaction conditions in the presence of glacial acetic acid and the crystal structure of its Cu(II) complex reflects an one-dimensional polymeric compound. The molecular structure of the complex consists of a Cu(II) ion bound to two singly deprotonated Schiff base bridging ligands that form a CuN2O4 chelation environment, and a coordination sphere with a disordered octahedral geometry.

Synthesis, crystal structure and properties of a 2-D Cd(II) coordination polymer based on ferrocenecarboxylate and 4,4′-bipyridine ligands

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Kai-Long Zhong ◽  
Jing Quan ◽  
Xian-Xiao Pan ◽  
Wei Song ◽  
Bing-Feng Li
Keyword(s):  
Coordination Polymer ◽  
Gravimetric Analysis ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Carboxylate Oxygen ◽  
Oxygen Chain ◽  
Crystal Structural

Abstract A new cadmium(II)-based coordination polymer [Cd3(FcCOO)6(4,4′-bipy)(H2O)2] n (FcCOO = ferrocenecarboxylato and 4,4′-bipy = 4,4′-bipyridine) has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The results of a crystal structural analysis has revealed that the title compound consists of two crystallographically unique CdII centers, one in a general position with a five-coordinated and one on an inversion center with a six-coordinated environment. The CdII centers are connected by FcCOO− units to form a metal carboxylate oxygen chain extending parallel to the [100] direction while the 4,4′-bipy ligands further act as bridging linkers of the CdII centers resulting in a layered polymer. In addition, an X-ray powder diffraction and thermal gravimetric analysis and a cyclo-voltammetric characterization of the complex have also been carried out.

Synthesis and Characterization of Y2O3 Nanoflowers

2012 ◽  
Vol 465 ◽  
pp. 76-79 ◽  
Author(s):  
Shuang Zhan ◽  
Xia Li
Keyword(s):  
Fourier Transform ◽  
Phase Composition ◽  
Electron Microscope ◽  
Synthesis And Characterization ◽  
The Novel ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Scanning Electron

The novel Y2O3 nanoflowers were synthesized through a facile hydrothermal method without using any catalyst or template. The phase composition and the microstructure of as-prepared products were characterized by field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD) as well as Fourier transform infrared spectrum. The formation mechanism for the Y2O3 flowers has been proposed.

Preparation and Characterization of Natural Hydroxyapatite from Animal Hard Tissues

2007 ◽  
Vol 342-343 ◽  
pp. 213-216 ◽  
Author(s):  
Xiao Ying Lü ◽  
Yong Bin Fan ◽  
Dachun Gu ◽  
Wei Cui
Keyword(s):  
Inductively Coupled Plasma ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Human Teeth ◽  
Inductively Coupled ◽  
Biological Source ◽  
Prepared Material ◽  
Different Temperatures ◽  
Natural Hydroxyapatite

The purpose of this study is to find out an effective method to prepare natural hydroxyapatite (HA) from biological source, i.e., pig bones, pig teeth, and extracted human teeth. For the preparation of natural HA a calcining method with different temperatures was used, in combination with the thermal gravimetric analysis (TGA). Three analysis methods, i.e., Fourier transform infrared spectroscope (FTIR), X-ray diffraction (XRD), and inductively coupled plasma (ICP) have been used to investigate the characteristics of the prepared materials. The spectrum of the prepared material, obtained by means of FTIR and XRD, are consistent with the standard FTIR spectrum and JCPDS index of XRD of hydroxyapitite. It confirms that the material prepared is hydroxyapitite indeed. The natural HA obtained by calcining at 850°C shows a desired quality.

Synthesis and crystallographic studies of two new 1,3,5-triazines

2020 ◽  
Vol 76 (4) ◽  
pp. 322-327
Author(s):  
Emmanuel Blas Patricio-Rangel ◽  
Margarita Tlahuextl ◽  
Hugo Tlahuext ◽  
Antonio Rafael Tapia-Benavides
Keyword(s):  
Noncovalent Interactions ◽  
Synthesis And Characterization ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
Positional Disorder ◽  
Hydrated Salt ◽  
Symmetry Space ◽  
Symmetry Space Group

The synthesis and characterization of two new 1,3,5-triazines containing 2-(aminomethyl)-1H-benzimidazole hydrochloride as a substituent are reported, namely, 2-{[(4,6-dichloro-1,3,5-triazin-2-yl)amino]methyl}-1H-benzimidazol-3-ium chloride, C11H9Cl2N6 +·Cl− (1), and bis(2,2′-{[(6-chloro-1,3,5-triazine-2,4-diyl)bis(azanediyl)]bis(methylene)}bis(1H-benzimidazol-3-ium)) tetrachloride heptahydrate, 2C19H18ClN9 2+·4Cl−·7H2O (2). Both salts were characterized using single-crystal X-ray diffraction analysis and IR spectroscopy. Moreover, the NMR (1H and 13C) spectra of 1 were obtained. Salts 1 and 2 have triclinic symmetry (space group P-1) and their supramolecular structures are stabilized by hydrogen bonding and offset π–π interactions. In hydrated salt 2, the noncovalent interactions yield pseudo-nanotubes filled with chloride anions and water molecules, which were modelled in the refinement with substitutional and positional disorder.

Syntheses, Structures, Thermal and Photoluminescence Properties of Two Zn(II) and Cd(II) Coordination Polymers Constructed from Taurine-derived Schiff Base and 4,4’-Bipyridine Ligands

2012 ◽  
Vol 67 (8) ◽  
pp. 774-782 ◽  
Author(s):  
Wei-Ting Guo ◽  
Zhi-Min Miao ◽  
Yun-Long Wang
Keyword(s):  
Schiff Base ◽  
Coordination Polymers ◽  
Tridentate Ligand ◽  
Supramolecular Architecture ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Monodentate Ligand ◽  
Metal Centers ◽  
X Ray ◽  
Ethanesulfonic Acid

Two chain-like coordination polymers, namely, {[Zn(saes)(4,4'-bipy)(H2O)]·H2O}n (1) and {[Cd (Hsaes)2(4,4'-bipy)(H2O)2]·2H2O}n (2), where H2saes=2-(2-hydroxybenzylideneamino)ethanesulfonic acid and 4,4'-bipy=4,4'-bipyridine, have been synthesized and characterized by singlecrystal X-ray diffraction, IR spectroscopy, elemental, thermogravimetric and photoluminescence analysis. X-Ray diffraction analyses indicate that 1and 2display octahedral metal centers with N3O3 and N2O4 donor sets, respectively. The Schiff base serves as a common N,O'-tridentate ligand in 1, and as a unique O-monodentate ligand in 2. In the crystal, both 1and 2form a 3D supramolecular architecture by O-H···O, C-H···O interactions or π···π stacking. The thermal and solid-state photoluminescence properties of both complexes have been investigated

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