Synthesis, Crystal Structure, Spectroscopic and Thermal Properties of a Novel Mixed Ligand Copper(II) Complex with 5,5-Dimethylhydantoin and Benzylamine

2006 ◽  
Vol 61 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Murat Taş ◽  
Serkan Soylu ◽  
Hümeyra Batı
Keyword(s):  
Crystal Structure ◽  
Thermal Analyses ◽  
Crystal Data ◽  
Monoclinic System ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Ft Ir ◽  
Complex Features ◽  
Water Ligands

AbstractThe crystal structure of the newly synthesized complex, trans-aqua-bis(benzylamino)-bis(5,5-dimethylhydantoinato) copper(II) was determined by X-Ray single crystal data. The thermal analyses, FT-IR and magnetic susceptibility data are also presented. The complex crystallizes in the monoclinic system, space group C2. The complex features a distorted square pyramidal [CuN4O] coordination with 5,5-dimethylhydantoinato, benzylamine and water ligands. The 5,5-dimethylhydantoinato anion is bonded to the copper(II) ion via its deprotonated N atom in the 3-position.

scholarly journals Synthesis, Crystal Structure and Interaction with Bovine Serum Albumin (BSA) of Two α-Aminophosphonic Acids Derivatives

2019 ◽  
pp. 1-7
Author(s):  
Wei Huang ◽  
Wen-Ling Wang
Keyword(s):  
Crystal Structure ◽  
Mass Spectrometry ◽  
Binding Constants ◽  
Ionization Mass ◽  
Monoclinic System ◽  
X Ray ◽  
X Ray Crystallography ◽  
Aminophosphonic Acids ◽  
Amino Phosphonate ◽  
Ft Ir

Two α-amino-phosphonate derivatives (1 & 2) were synthesized and their compositions and structures were characterized by Elemental Analysis (EA), FT-IR Spectrascopy (FT-IR), Electrospray Ionization Mass Spectrometry (ESI-MS), Nuclear Magnetic Resonance (NMR, 1H, 13C and 31P) and X-ray crystallography. Compound 1 & 2 were crystallized in monoclinic system with the space group P2(1)/n and P2(1)/c, respectively. The interaction effects of two α-aminophosphonate derivatives (1 & 2) with BSA were investigated and the binding constants were 1.07 × 104 M-1, 1.68 × 104 M-1, respectively. Besides, the values of n were indicated that 1:1 complex was formed between BSA and 1&2.

Coordination chemistry of thioether–pyridazine macrocycles II. Synthesis, structural and spectroscopic studies of dinuclear copper(II) and polynuclear copper(I) and silver(I) complexes of a tetrathiapyridazinophane macrocyclic ligand

1992 ◽  
Vol 70 (11) ◽  
pp. 2709-2716 ◽  
Author(s):  
Liqin Chen ◽  
Laurence K. Thompson ◽  
John N. Bridson
Keyword(s):  
Macrocyclic Ligand ◽  
Silver Ions ◽  
Spectroscopic Studies ◽  
Binuclear Complexes ◽  
Monoclinic System ◽  
Magnetic Susceptibility Data ◽  
Space Group ◽  
X Ray ◽  
X Ray Crystallography ◽  
Susceptibility Data

The preparation and properties of the thioether–pyridazine macrocycle (L3; C11H16N2S4) containing one pyridazine subunit, and its copper(II), copper(I), and silver(I) complexes are described. Magnetic susceptibility data (5–300 K) for the binuclear complexes [CuL3Cl2]2 (I) and [CuL3Br2]2 (II) have been fitted to the Friedberg magnetization expression with a molecular field correction. Intradimer antiferromagnetic exchange is weak (−2J < 18 cm−1), with even weaker interdimer exchange (−zJ′ < 0.3 cm−1). The complexes [CuL3Cl]x (III) and [AgL3ClO4]x (V) have been characterized by X-ray crystallography. III crystallizes in the triclinic system, space group [Formula: see text], with a = 9.410(2) Å, b = 10.291(2) Å, c = 9.208(2) Å, α = 108.56(1)°, β = 91.82(2)°, γ = 68.04(1)°, V = 780.1(2) Å3, and Z = 2(R = 0.035, Rw = 0.031 for 1856 reflections). The ligand acts as a bidentate, S2, bridge between dinuclear Cu2Cl2 units in a double stranded polymer. III crystallized in the monoclinic system, space group P21/n, with a = 9.382(4) Å, b = 19.274(4) Å, c = 10.190(3) Å, β = 106.35(3)°, V = 1768(1) Å3, and Z = 4 (R = 0.036, Rw = 0.029 for 1776 reflections). The structure consists of a polymeric, two dimensional sheet structure, involving pseudo-tetrahedral silver ions linked by exo-bidentate, S2, ligands and bidentate perchlorates.

The equiatomic intermetallics REPtCd (RE= La, Ce, Pr, Nd, Eu) and magnetic properties of CeAuCd

2015 ◽  
Vol 70 (3) ◽  
pp. 197-202 ◽  
Author(s):  
Michael Johnscher ◽  
Frank Tappe ◽  
Oliver Niehaus ◽  
Rainer Pöttgen
Keyword(s):  
Phase Transition ◽  
Three Dimensional ◽  
Induction Melting ◽  
Antiferromagnetic Phase ◽  
Crystal Data ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data

AbstractThe cadmium intermetallics REPtCd (RE = La, Ce, Pr, Nd, Eu) and CeAuCd were synthesized by induction-melting of the elements in sealed niobium ampoules followed by annealing in muffle furnaces. The samples were characterized by powder X-ray diffraction. The structures of CePtCd (ZrNiAl type, $P\bar 62m,$a = 763.8(6), c = 409.1(4) pm, wR2 = 0.0195, 298 F2 values, 14 variables) and EuPtCd (TiNiSi type, Pnma, a = 741.3(2), b = 436.4(1), c = 858.0(4) pm, wR2 = 0.0385, 440 F2 values, 20 variables) were refined from single-crystal data. The REPtCd structures exhibit three-dimensional networks of corner- and edge-sharing Cd@Pt2/6Pt2/3 and Cd@Pt4/4 tetrahedra, which leave cages for the rare earth atoms. Temperature-dependent magnetic susceptibility data of CeAuCd reveal a paramagnetic to antiferromagnetic phase transition at TN = 3.7(5) K.

scholarly journals Synthesis, High-resolution Crystal Structure Refinement and Magnetic Properties of the Manganese-rich Cementite-type Mn1.8Fe1.2C

2010 ◽  
Vol 65 (10) ◽  
pp. 1235-1239 ◽  
Author(s):  
Ludwig Stork ◽  
Paul Müller ◽  
Manfred Speldrich ◽  
Paul Kögerler ◽  
Jörg von Appen ◽  
...  
Keyword(s):  
Crystal Structure ◽  
High Resolution ◽  
Density Functional ◽  
Structure Refinement ◽  
Crystal Structure Refinement ◽  
Functional Theory ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Long Range Ordering

The manganese-rich ternary cementite phase Mn1.8Fe1.2C has been synthesized by a ceramic route in an almost quantitative yield, and the crystal structure refinement on the basis of high-resolution X-ray powder diffraction data using MoKα1 radiation has been performed. The carbon atom is found in a slightly distorted trigonal prism composed of Mn and Fe atoms, with a rather narrow bond length range from 1.95 to 2.09 Å . The magnetic susceptibility data clearly indicate long-range ordering phenomena, in particular dominant antiferromagnetic interactions, as predicted by density-functional theory.

Synthesis, crystal structure, and magnetic properties of the complex [(CH3)3NH]2 [Co(NCS)4]

2018 ◽  
Vol 73 (8) ◽  
pp. 571-575
Author(s):  
Yang Jie ◽  
Huang Yuan ◽  
Zhong YouQuan ◽  
Fang Ting ◽  
Hao Fan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Infrared Spectroscopy ◽  
Magnetic Measurements ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Ferromagnetic Interactions

AbstractA new complex [(CH3)3NH]2[Co(NCS)4], in which zero-dimensional [Co(NCS)4]n2− anions are balanced by 2n [(CH3)3NH]+ cations, was synthesized. The complex has been characterized by single X-ray diffraction, infrared spectroscopy, elemental analysis, and magnetic measurements. Magnetic susceptibility data indicate ferromagnetic interactions among the CoII ions.

Synthesis and Crystal Structure of 1-(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-iodopyrimidine-2,4(1H,3H)-dione

2014 ◽  
Vol 997 ◽  
pp. 196-199
Author(s):  
Wei Li ◽  
Qiang Xiao ◽  
Ru Chun Yang
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Title Compound ◽  
Nmr Spectra ◽  
Crystal Data ◽  
Single Crystal Diffraction ◽  
Monoclinic System ◽  
Synthesis And Crystal Structure ◽  
Space Group ◽  
X Ray

The title compound, 1-(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl) tetrahydrofuran-2-yl)-5-iodopyrimidine-2,4(1H,3H)-dione , C9H10FIN2O5, as potential drugs for anti-tumor, anti-viral have been synthesized and characterized by NMR spectra. Meanwhile, the crystal of 2b was obtained and determined by X-ray single-crystal diffraction. Crystal data: monoclinic system, space group P2(1),a= 9.0832(11) Ǻ,b= 5.4332(7) Ǻ,c= 12.2464(15) Ǻ,β= 107.809(4)°,V= 575.41(12) Ǻ3,Z= 2,F(000) = 360,Dx= 2.148 Mg m-3,μ= 2.813 mm-1,R= 0.014 andwR= 0.056 for 1988 independent reflections (Rint= 0.0209) and 1932 observed ones (I > 2σ (I)).

scholarly journals Synthesis, Characterization and Crystal Structure of 2-Pyridinecarboxamide

2019 ◽  
Vol 32 (1) ◽  
pp. 195-198
Author(s):  
Kai-Jin Sun ◽  
Zhao-Sheng Cai
Keyword(s):  
Crystal Structure ◽  
Stainless Steel ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Basic Solution ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
X Ray ◽  
Ft Ir ◽  
Uv Visible

2-Pyridinecarboxamide was synthesized from 2-picoline through two-steps reaction. Initially, 2-picoline was converted into 2-cyanopyridine by ammoxidation in a stainless-steel fixed-bed reactor at 370 ºC with V2O5 loaded on TiO2 as catalyst. The 2-cyanopyridine was transformed into 2-pyridinecarboxamide through oxidation hydrolysis in basic solution using MnO2 as oxidant at 70 ºC. The final product was characterized by FT-IR, NMR and UV-visible analysis, and 2-pyridinecarboxamide in the final product was determined using HPLC. The crystal structure of 2-pyridinecarboxamide was investigated using X-ray diffraction and SHELX 2018/3 (sh) software and the result indicated that 2-pyridinecarboxamide crystallized in the monoclinic system, space group P21/n with a = 5.207(2), b = 7.097(3), c = 16.243(6) Å, V = 595.7 (4) Å3; Z = 4.

Reactions of Bis(hexamethyldisilazanyl)manganese(II) with Nitrogen Containing Ligands: Syntheses and X-Ray Structures of [Mn( 1,10-phen){N(SiMe3)2}2] and [Mn(4,4' -bipy){N(SiMe3)2}2] ·THF

1994 ◽  
Vol 49 (1) ◽  
pp. 31-35 ◽  
Author(s):  
Marius Andruh ◽  
Herbert W. Roesky ◽  
Mathias Noltemeyer ◽  
Hans-Georg Schmidt
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Lattice Parameters ◽  
Crystal Data ◽  
Monoclinic System ◽  
Space Group ◽  
X Ray

Abstract The reaction of [Mn{N(SiMe3)2}2 (THF)] 1 with 2,2'-bipyridine (2,2'-bipy), 1,10-phenan-throline (1,10-phen) and 4,4'-bipyridine (4,4'-bipy) yields three new complexes: [Mn(2,2'-bipy){N(SiMe3)2}2] 2, [Mn(1,10-phen){N(SiMe3)2}2] 3, and [Mn(4,4'-bipy){N(SiMe3)2}2] · THF 4. The crystal structure of 3 reveals mononuclear species with pseudo-tetrahedral coordinated manganese(II) ions. Crystal data for 3: orthorhombic, a = 1741.0(2), b = 1879.3(3), c = 1967.0(3) pm, V = 6.436(2) nm3, Z = 8, space group Pbca. Compound 4 crystallizes in the monoclinic system, space group P 21/c; the lattice parameters are: a = 2139.5(3), b = 925.30(10), c = 1786.4(2) pm, β = 101.34(1)°, V= 3.4675(7) nm3, Z = 4. The molecular structure of 4 consists of zig-zag infinite chains, with bridging 4,4'-bipyridine groups.

Synthesis, crystal structure and magnetic properties of the complex [C(NH2)3]2[Mn(N3)4] with a polynuclear azido-bridged chain anion

2017 ◽  
Vol 72 (3) ◽  
pp. 171-174
Author(s):  
Kun Qian ◽  
Yan-hong Yu ◽  
Yao-Hui Ye ◽  
Hao Fan
Keyword(s):  
Crystal Structure ◽  
Magnetic Measurements ◽  
Antiferromagnetic Interaction ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Elemental Analyses ◽  
Chain Anion ◽  
Guanidinium Cation

Abstract A new complex [C(NH2)3]2[Mn(N3)4], in which MnII cations are alternatively bridged by double EE azide-bridges and the [Mn(N3)4]n2− chains are separated by guanidinium cation bilayers, has been synthesized and characterized by single crystal X-ray diffraction, infrared (IR) spectroscopy, elemental analyses, and magnetic measurements. Magnetic susceptibility data indicate antiferromagnetic interaction among the MnII ions.

scholarly journals Molekül- und Kristallstruktur von 1.1-Dimethylsilylentitanocendichlorid, (CH3)2Si(C5H4)2TiCl2 / Molecular and Crystal Structure of l,r-Dimethylsilylene Titanocene Dichloride, (CH3)2Si(C5H4)2TiCl2

1981 ◽  
Vol 36 (10) ◽  
pp. 1208-1210 ◽  
Author(s):  
Hartmut Köpf ◽  
Joachim Pickardt
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Structure Determination ◽  
Titanocene Dichloride ◽  
Molecular And Crystal Structure ◽  
Monoclinic Space Group ◽  
Crystal Data ◽  
Space Group ◽  
X Ray ◽  
Structural Dimensions

Abstract The molecular structure of the bridged [1]-titanocenophane 1,1'-dimethylsilylene titanocene dichloride, (CH3)2Si(C5H4)2TiCl2, has been investigated by an X-ray structure determination. Crystal data: monoclinic, space group C2/c, Z = 4, a = 1332.9(3), 6 = 988.7(3), c = 1068.9(3) pm, β = 113.43(2)°. The results are compared with the structural dimensions of similar compounds: 1,1'-methylene titanocene dichloride, CH2(C5H4)TiCl2, with the unbridged titanocene dichloride, (C5H5)2TiCl2 and the ethylene-bridged compound (CH2)2(C5H4)2TiCl2

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