Search results for "Susceptibility"
showing 10 items of 912 documents
Field-induced slow magnetic relaxation in mixed valence di- and tri-nuclear CoII–CoIII complexes
2020
Two novel mixed valence CoII–CoIII complexes, namely [CoIICoIII(L1)(ab)(mb)2(H2O)]·dmf (1) and [CoIII2CoII(L2)4(H2O)4]·2H2O (2) [H2L1 = (E)-2-((1-hydroxybutan-2-ylimino)methyl)-6-methoxyphenol, ab = 2-amino-butan-1-ol anion, mb = p-methyl benzoate, H2L2 = 3-((2-hydroxy-3-methoxy-benzylidene)-amino)-propionic acid, and dmf = N,N-dimethyl-formamide], were synthesized and characterized by single crystal X-ray diffraction and magnetic studies at low temperature. The structure determination reveals that both complexes belong to the monoclinic system with P21/c (1) and I2/a (2) space groups. Complex 1 is a dinuclear CoIIICoII compound with distorted octahedral cobalt centers showing different coo…
Towards Molecular Conductors with a Spin‐Crossover Phenomenon:Crystal Structures, Magnetic Properties and Mössbauer Spectra of[Fe(salten)Mepepy][M(dm…
2005
Three new iron(III) compounds of formula [Fe(salten)Mepepy][M(dmit)2]·CH3CN (M = Ni, Pd, Pt; H2salten = 4-azaheptamethylene-1,7-bis(salicylideneiminate); Mepepy = 1-(pyridin-4-yl)-2-(N-methylpyrrol-2-yl) ethane; dmit2– = 1,3-dithiole-2-thione-4,5-dithiolato) have been synthesised and the crystal structure of each compound has been solved at different temperatures. The structures consist of alternating layers of [M(dmit)2]– units and [Fe(salten)Mepepy] cations. In the Ni compound photo-isomerisation of the Mepepy ligand can be observed in dichloromethane solution. The temperature dependence of the magnetic susceptibility of the compounds reveals a gradual S = 5/2 blabla S = 1/2 spin crossove…
Thermal and Light-Induced Spin Transition in the High- and Low-Temperature Structure of [Fe0.35Ni0.65(mtz)6](ClO4)2
1996
The thermal and light induced spin transition in [Fe(0.35)Ni(0.65)(mtz)(6)](ClO(4))(2) (mtz = 1-methyl-1H-tetrazole) was studied by (57)Fe Mössbauer spectroscopy and magnetic susceptibility measurements. In addition to the spin transition of the iron(II) complexes the compound undergoes a structural phase transition. The high-temperature structure could be determined by X-ray crystallography of the isomorphous [Fe(0.25)Ni(0.75)(mtz)(6)](ClO(4))(2) complex at room temperature. The X-ray structural analysis shows this complex to be rhombohedric, space group Rthremacr;, with a = 10.865(2) Å and c = 23.65(1) Å with three molecules in the unit cell. The transition to the low-temperature structur…
Synthesis, crystal structure, magnetic properties and 57Fe Mossbauer spectroscopy of the new trinuclear [Fe3(4-(2'-hydroxyethyl)-1,2,4- triazole)6(H2…
2000
Hyetrz = 4-(2prime-hydroxyethyl)-1,2,4-triazole represents the first structurally characterized iron(II) spin crossover compound for which the structure has been solved above and below room temperature in both spin states. The compound crystallizes in the trigonal system, space group R3, a = 12.763(1) b= 67.144(1), V = 1684.3(1) 3, Z = 6 at 120K. At 330K the space group is retained and a = 13.0183(3) b=67.376(3), V = 1805.8(1) 3. The molecular structure consists of trinuclear FeII entities linked together by an unprecedented three-dimensional network of hydrogen bonds. This compound shows a gradual spin crossover behavior centered around room temperature, which has been followed by temperat…
Iron(II) Spin Transition Complexes with Dendritic Ligands, Part I
2008
The ligands G1- and G2-oligo (benzyl ether) (PBE) dendrons and their iron(II) complexes [Fe(Gn-PBE)3]A2·xH2O (with n = 1, 2 and A = triflate, tosylate) were prepared. The magnetic properties of the complexes were investigated by a SQUID magnetometer. All complexes exhibit gradual spin transition below room temperature. At very low temperatures the magnetic behaviour reflects zero-field splitting (ZFS) effects. 57Fe-Mossbauer spectroscopy was performed to distinguish between ZFS of high spin species and spin state conversion into the low spin state. Further characterisation was carried out by thermogravimetric analysis (TGA) and FT-IR spectroscopy. Structural features have been determined by…
A heptanuclear Fe(II)–Fe(III)6 system with twelve unpaired electrons
2000
Abstract The pentadentate ligand 5 LH2 = saldptn = N,N′-bis(1-hydroxy-2-benzyliden)-1,7-diamino-4-azaheptane has been prepared by a Schiff base condensation between 1,7-diamino-4-azaheptane and the corresponding salicyaldehyde. Its complexation with Fe(III) gave the high-spin (S=5/2) complex of [Fe III ( 5 L)Cl]. This precursor was combined with [Fe(CN)6]4− and a blue heptanuclear complex [FeII{(CN)Fe III ( 5 L)}6]Cl2 resulted. This system belongs to the class of high-spin molecules possessing twelve unpaired electrons (S=6) as proven by the magnetic susceptibility measurements and Mossbauer spectra.
( n -Bu 4 N) 2 [Fe(dcbdt) 2 ] 2 . Synthesis, crystal structure and magnetic characterisation
2003
Abstract The ( n -Bu 4 N) 2 [Fe(dcbdt) 2 ] 2 complex, where 4,5-dicyanobenzene-1,2-dithiolate (dcbdt), was prepared and characterised by X-ray diffraction, Mossbauer spectroscopy and magnetisation measurements. The crystal structure as determined by single crystal X-ray diffraction is triclinic, space group P 1 with cell parameters a =9.5660(1) A, b =13.0200(2) A, c =16.0850(2) A, α =67.554°(1), β =86.797°(1), γ =70.523°(1), V =1738.77(4) A 3 and it consists in strongly dimerised [Fe(dcbdt) 2 ] − units, which are stacked side by side as chains along a . The magnetic susceptibility shows that the [Fe(dcbdt) 2 ] − units have a low spin S =1/2 configuration and, besides a strong intradimer ant…
X-Ray structure of [ReCl4(μ-ox)Cu(pyim)2]: a new heterobimetallic ReIVCuIIferrimagnetic chain
2008
A new heterobimetallic Re(IV)Cu(II) compound has been prepared and its crystal structure determined by single-crystal X-ray diffraction; magnetic susceptibility measurements show that this compound behaves as a ferrimagnetic chain with significant antiferromagnetic interactions between Re(IV) and Cu(II) metal ions.
Synthesis, Structure, and Properties of BaVO2(AsO4): a New Vanadium Arsenate Containing the V2O42+ Core
1997
The new vanadium arsenate BaAsVO6 has been synthesized hydrothermally and structurally characterized by single-crystal X-ray diffraction, IR spectroscopy, and magnetic susceptibility measurements. It crystallizes in the monoclinic system, space group P21/c with unit cell parameters a = 5.645(1) A, b = 10.243(1) A, c = 8.945(1) A, β = 90.60(1)°, and Z = 2. The layered structure is built up from V2O42+ units and AsO43- anions, the AsO43- ligands being coordinated to two (V2O4)2+ units in both, terminal and bridging μ2-AsO43- fashion. The [VO2(AsO4)]2- layers are separated by Ba2+ cations. The V2O42+ unit has no precedence in oxo-vanadium chemistry.
Crystal structure, magnetic properties and esr studies of (4-apyH)4[CuIIBr4] [CuIBr2]2: a novel Cu(II)⧹Cu(I) system containing bromocuprate(I) chains…
1998
Abstract The synthesis, crystal structure, ESR spectra and magnetic properties are reported for the Cu(II)⧹Cu(I) compound (4-apyH)4[Cu3Br8] (4-apyH = C5H7N2 = 4-aminopyridinium). Single-crystals of the compound were grown by slow diffusion of n-hexane on an ethanolic solution of (4-apyH)2[CuBr4] · H2O. The crystal structure is made up of organic cations, isolated [CuIIBr4]2− anions and infinite [CuIBr2]nn− chains composed of edge-sharing CuIBr4 tetrahedra. N–H · · · Br hydrogen bond interactions between organic counter cations and inorganic anionic units are present and contribute to the cohesiveness of the crystal packing. Magnetic susceptibility measurements showed a good isolation of Cu(…