Mossbauer studies in transition metal chemistry. III. Compounds of iron with some sulphur-containing Schiff base ligands

1974 ◽  
Vol 27 (11) ◽  
pp. 2307 ◽  
Author(s):  
M Bond ◽  
RL Martin ◽  
IAG Roos

M�ssbauer spectra are reported for a series of iron complexes with sulphur-containing Schiff base ligands. These tridentate ligands are based on the Schiff base formed by the condensation of dithiocarbazic acid and pyridine-2-carbaldehyde and form complexes with a metal-to-ligand ratio of 1 : 1 and 1 : 2. The M�ssbauer study confirms that most of these complexes contain iron(11) with examples of both high-and low-spin and one example of a spin crossover. Several iron(111) complexes were also studied. The quadrupole splittings show the anisotropy in bonding expected for metal atoms coordinated to different types of atoms within the same chelate ring. However, for some complexes the splittings are small, showing that low local symmetries need not produce large electric field gradients. In cases where it is applicable, the temperature dependence of the quadrupole splitting has been used to derive a splitting of the t2 and e orbitals produced by the non-cubic symmetry. For compounds of the form Fe(L)X2, where X is a halide and L the tridentate ligand, the Mossbauer results are best interpreted in terms of a five-coordinate structure rather than a six-coordinate bridged dimer.

2019 ◽  
Vol 4 (1) ◽  
pp. 30-36 ◽  
Author(s):  
Janusz Szklarzewicz ◽  
Anna Jurowska ◽  
Maciej Hodorowicz ◽  
Ryszard Gryboś

The synthesis and physicochemical properties of three new complexes of vanadium at +5, +4 and +3 oxidation state are described and discussed. The octahedral surrounding of vanadium for V(III) complexes of [V(L1)(HL1)] general formula is filled with two ONO tridentate ligand L, for V(IV) one ONO ligand L, oxido ligand and 1,10-phenanthroline (phen) as a co-ligand are presented in complexes of [VO(L2)(phen)]. For V(V) the complexes of [VO2(L1)(solv)] type were formed. As ligands, the H2L Schiff bases were formed in reaction between 5-hydroxysalcylaldehyde and phenylacetic hydrazide (H2L1) and 3,5-dichlorosalicyaldehyde and 4-hydroxybenzhydrazide (L2). The magnetic moment measurements, in 8 year period, show, that V(III) complexes slowly oxidise to V(IV) with preservation of the nonoxido character of the complexes, while V(IV) complexes were found to be stable. The TG and SDTA measurements indicate, that thermal stability depends mainly on the oxidation state of vanadium. The less thermally stable are the V(V) complexes, while V(IV) and V(III) are stable up to ca. 200oC. In solution, at pH 2 (similar to that in human digestion system), again the V(IV) are the most stable, only at pH 7.0 V(III) complexes had higher stability. The most stable, thus best for pharmaceutical use, are V(IV) complexes.


RSC Advances ◽  
2015 ◽  
Vol 5 (20) ◽  
pp. 15084-15095 ◽  
Author(s):  
Rupa Sarkar ◽  
Amar Hens ◽  
Kajal Krishna Rajak

Two mononuclear Re(v) complexes were synthesized using two different O, N, N coordinating Schiff base ligands. The X-ray structure and catalytic properties of the complexes are investigated and the electronic structure and absorption spectra were also calculated.


2019 ◽  
Vol 48 (40) ◽  
pp. 15012-15028 ◽  
Author(s):  
Emma V. Puttock ◽  
Jack D. Fradgley ◽  
Dmitry S. Yufit ◽  
J. A. Gareth Williams

Tridentate ligands, easily synthesised by condensation reactions of simple starting materials, can be used to prepare Pt(ii) complexes that are luminescent in solution, emitting in the red or deep-red spectral region, according to the substituents.


Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7301
Author(s):  
Karla-Alejandra López-Gastélum ◽  
Enrique F. Velázquez-Contreras ◽  
Juventino J. García ◽  
Marcos Flores-Alamo ◽  
Gerardo Aguirre ◽  
...  

Two new glycine-Schiff base copper(II) complexes were synthesized. Single crystal X-ray diffraction (SCXRD) allowed us to establish the structure of both complexes in the solid state. The glycine-Schiff base copper(II) complex derived from 2′-hydroxy-5′-nitroacetophenone showed a mononuclear hydrated structure, in which the Schiff base acted as a tridentate ligand, and the glycine-Schiff base copper(II) complex derived from 2′-hydroxy-5′-methylacetophenone showed a less common tetranuclear anhydrous metallocyclic structure, in which the Schiff base acted as a tetradentate ligand. In both compounds, copper(II) had a tetracoordinated square planar geometry. The results of vibrational, electronic, and paramagnetic spectroscopies, as well as thermal analysis, were consistent with the crystal structures. Both complexes were evaluated as catalysts in the olefin cyclopropanation by carbene transference, and both led to very high diastereoselectivity (greater than 98%).


2013 ◽  
Vol 1041 ◽  
pp. 44-49 ◽  
Author(s):  
Manas Sutradhar ◽  
Tannistha Roy Barman ◽  
Michael G.B. Drew ◽  
Eva Rentschler

1978 ◽  
Vol 31 (1) ◽  
pp. 35 ◽  
Author(s):  
RC Elder

A series of ligands has been formed by the 1 : 1 molar condensation of salicylaldehyde (sl) with the diamines, propane-1,3-diamine (p), butane-1,4-diamine (b) and 2,5-dimethylhexane-2,5-diamine (d). The potentially tridentate ligands are o-[N-(3- aminopropyl)formimidoyl]phenol (Hslp), o-[N-(4- aminobutyl)formimidoyl]phenol (Hslb) and o-[N-(4-amino-1,1,4- trimethylpentyl)formimidoyl]-phenol (Hsld), respectively. These form the bis-nickel(II) complexes Ni(slp)2, Ni(slb)2 and Ni(sld)2. All appear to have octahedral structures in the solid. Ni(slb)2 occurs in yellow and green forms in the solid. In solution Ni(sld)2 occurs in equilibrium between tetrahedral (amines uncoordinated) and an octahedral centrosymmetric form with facially bound sld ligands. Ni(slp)2 reacts with bis(5-chloro-salicylaldehyde)nickel(II) to give the unsymmetrical four-coordinate nickel complex formed from the 1 : 1 : 1 molar condensation of salicylaldehyde, propane-1,3-diamine and 5- chlorosalicylaldehyde. A dimeric, amido bridged complex has been produced by the vacuum thermolysis of Ni(slp)2. Mass spectroscopic evidence is cited for the formation of the analogous dimeric complexes from Ni(slb)2 and Ni(sld)2.


Author(s):  
Olga Yu. Vassilyeva ◽  
Vladimir N. Kokozay ◽  
Brian W. Skelton

The structure of the title compound, [Ni2(C9H10NO2)4], is built up by discrete centrosymmetric dimers. Two nitrogen and three oxygen atoms of two Schiff base ligands singly deprotonated at the phenolate site form a square-pyramidal environment for each metal atom. The ligands are bonded differently to the metal centre: one of the phenolic O atoms is bound to one nickel atom, whereas another bridges the two metal atoms to form the dimer. The Ni—N/O distances fall in the range 1.8965 (13)–1.9926 (15) Å, with the Ni—N bonds being slightly longer; the fifth contact of the metal to the bridging phenolate oxygen atom is substantially elongated [2.533 (1) Å]. A similar coordination geometry was observed in the isomorphous Cu analogue previously reported by us [Sydoruk et al. (2013). Acta Cryst. E69, m551–m552]. In the crystal, the [Ni2 L 4] molecules form sheets parallel to the ab plane with the polar methoxy groups protruding into the intersheet space and keeping the sheets apart. Within a sheet, the molecules are stacked relative to each other in such a way that the Ni2O2 planes of neighbouring molecules are orthogonal.


2015 ◽  
Vol 12 (2) ◽  
pp. 13
Author(s):  
Muhamad Faridz Osman ◽  
Karimah Kassim

The coordination complexes of Co(II) and Zn(II) with Schiff bases derived from o-phenylenediamine and substituted 2-hydroxybenzaldehyde were prepared All compounds were characterized by Fourier transform infrared (FTIR) spectroscopy and Nuclear magnetic resonance (NMR) spectroscopy elemental analyzers. They were analyzed using impedance spectroscopy in the frequency range of 100Hz-1 MHz. LI and L2 showed higher conductivity compared to their metal complexes, which had values of 1.3 7 x 10-7 and 6.13 x 10-8 S/cm respectively. 


2019 ◽  
Author(s):  
Swaraj Sengupta ◽  
Sahanwaj Khan ◽  
Shyamal K. Chattopadhyay ◽  
Indrani Banerjee ◽  
Tarun K. Panda ◽  
...  

Synthesis and characterisation of one trinuclear copper complex, ([Cu<sub>3</sub>L<sub>3</sub>O]ClO<sub>4</sub>) (<b>1</b>) and one nickel complex ([Ni(L'H)<sub>2</sub>(dmso)<sub>2</sub>](ClO<sub>4</sub>)<sub>2</sub>) (<b>2</b>) with Schiff base ligands: (3Z)-3-((Z)-(1-(thiophen-2-yl)ethylidene)hydrazono)butan-2-one oxime (LH) and 1-(pyridin-2-yl)ethylidene)hydrazono)butan-2-one oxime (L<sup>'</sup>H). <b>1</b> shows high catecholase activity and has also been tested as a catalyst for the synthesis of benzylimine. <b>2 </b> shows phenoxazinone synthase activity.


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