An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
A series of manganese(II) chelates of stoicheiometry [MnL] have been synthesized, where LH2 is a dibasic tridenate Schiff base formed between a 5-substituted salicylaldehyde and either a 5-substituted β- hydroxyaniline or anthranilic acid. The complexes are extremely susceptible to oxidation in solution but stable when dry. Some of the complexes were isolated as hemihydrates and others as mixed hydrate- ethanolates. Magnetic susceptibility measurements over the temperature range 80-300�K have been made for a number of the complexes. In some cases the magnetic moments at room temperature are reduced slightly from the spin-only S = 5/2 value and show θ values of c. 15-50�K. The results can be interpreted in terms of binuclear or polynuclear structures with very small values of the exchange integral J. Comparisons between observed and calculated data are not as good as those shown in related VO2+, NiII, CuII, and FeIII systems for which X-ray crystal structures are known.
The title compound (diphy) has been prepared from 2,2'-pyridil and 2-pyridylhydrazine and behaves as a quadridentate chelating agent with nicke1(11), copper(11), zinc(11) and cadmium(11) salts. The mono-(2-pyridylhydrazone) of 2,2'-pyridil (pmpy) is also described, together with its nickel(11) complex perchlorate.
The magnetic susceptibilities of iron(111) N-substituted salicylaldimine complexes of types Fe(sal-XR)3, Fe(sal-NR)2X, [Fe(salH-KR)2X]X, (X = Cl, Br), and [Fe(sal-NR)2]2O have been measured over the temperature range 90-300�K.? The mononuclear complexes exhibit normal high-spin (S = 5/2), Curie-Weiss behaviour. The binuclear oxygen-bridged complexes show antiferromagnetic behaviour and the results have been analysed using the spin-spin coupling mechanism. The exchange interaction is found to be independent of the nature of the N-substituent on the Schiff base. It appears that bulk susceptibility measurements alone cannot unambiguously specify the formal spin state of the ferric ion in these binuclear complexes.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
A number of solid complexes, most of which are extremely unstable in air, have been isolated from reactions between aqueous iron(II) and the sulphur-containing ligands thioglycollic acid, L-cysteine, L-cysteine methyl ester and DL-methionine. The 1 : 1 and 1 : 2 iron-ligand stoichiometries were obtained. Spectroscopic and magnetic measurements have been used to deduce possible structures and in most cases polymeric structures are indicated.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
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