Search results for "SSB"

A Discrete μ 4 ‐Oxido Tetranuclear Iron(III) Cluster

2012

Reaction of a Schiff base ligand derived from salicyloyl hydrazide and diacetyl monooxime (H2L) with a triangular μ3-oxido-centered [Fe3(μ3-O)]7+ core yields a new tetranuclear iron(III) complex. FeIII4(μ4-O) crystallizes in the triclinic space group P. Structural studies reveal that this tetranuclear iron(III) complex is a new structure type of an uncharged (alkoxido)(oxido)iron(III) cluster in which the four iron(III) ions are located at the corners of a distorted tetrahedron. A study of the magnetic properties supports the presence of antiferromagnetic interactions through the central μ4-oxido ion as well as the μ2-methoxy groups present, giving an an S = 0 ground state. Mossbauer spectr…

Complexes of organometallic compounds. XLIX. A Mössbauer-zeeman spectroscopic study of glycylglycinato-O,N,N(2−) diphenyltin(IV), and the point-charg…

1978

Organometallic complexes with biological molecules: XII. Solid-state and solution studies on dialkyltin(IV)- and trialkyltin(IV)-thiaminepyrophosphat…

1999

Dialkyltin(IV) and trialkyltin(IV) derivatives of the coenzyme thiaminepyrophosphate (H2TPP) have been synthesized with general formula R2Sn(HTPP)2·nH2O (Alk = Me, n = 2; Alk = Bu, n = 4) and R3SnHTPP·nH2O (R=Me, n = 2; R = Bu, n = 1), respectively. The solid-state structure of the complexes has been investigated through infrared and Mossbauer spectroscopy. The infrared data suggest the involvement of only phosphate oxygen atoms in the coordination of both dialkyl- and trialkyl-tin(IV) moieties, with phosphate anions behaving as monoanionic bidentate bridging or chelating groups, with the tin(IV) involved in six- and five-fold coordination geometries, respectively, in R2Sn(HTPP)2·nH2O (R = …

( 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…

Complexes of organometallic compounds. LI. The correlation between 119Sn Mössbauer isomer shifts and partial atomic charges on tin in R3SnL compounds

1985

Abstract The 119Sn Mossbauer isomer shift parameters, δ, of compounds R3SnL (R = AlK, Ph; L = F, Cl, OH, OR′, CN, NCS, NCO, N3) have been correlated to partial atomic charges on tin QSn, calculated according to a valence state electronegativity equalization procedure carried out by the CHELEQ program. A unique δ/QSn correlation has been obtained for all the five-coordinated R3SnL species by using average δ parameters for the AlK3IV derivatives.

Mössbauer spectroscopy of mono-organotin(IV) derivatives

1974

Abstract The Mossbauer parameters isomer shift, δ, and quadrupole splitting, ΔE, of mono-organotin compounds insofar investigated have been collected and tabulated. It is demonstrated that isomer shifts consistently depend on ligand electronegativities and coordination numbers, from which it is deduced that RSn IV behave much more as Sn IV rather than R 2 Sn IV and R 3 Sn IV derivatives. The changes of δ for RSn IV are then interpreted by hypotheses analogous to those advanced for Sn IV and its adducts and complexes. It is also inferred that in RSn IV compounds there is a consistent s-character in all tin-ligand atom bonds.

Synthesis and spectroscopic characterization of dicyclohexyltin derivatives of dipeptides, andin vitro effects against MDA-MB 231 breast cancer cells…

1992

Dicyclohexyltin derivatives Cy2SnL (Cy = cyclohexyl) of the dipeptides H2L, glycylglycine, glycylalanine, alanylglycine, glycylvaline, glycylmethionine, glycylphenylalanine and glycyltyrosine, have been obtained by neutralization of Cy2SnO and H2L. The crystal structures of Cy2SnL (L = glycylglycinate, glycylalaninate) have been determined by single X-ray diffraction. Tin in each case has a distorted trigonal bipyramidal environment with the dipeptide acting as a tridentate NNO-ligand. From IR-data, and in some cases from 119Sn Mossbauer and 119Sn NMR data, analogous molecular structures are inferred for the other compounds Cy2SnL. Spectroscopic data indicate that the solid-state structures…

The hydrolysis of Me2SnIV and Me3SnIV moieties monitored through 119Sn Mössbauer spectroscopy

1991

Abstract The 119 Sn Mossbauer parameters δ, isomer shift, and Δ E , nuclear quadrupole splitting, have been determined in frozen aqueous solutions of Me 2 Sn IV and Me 3 Sn IV moieties at varying pH. The resulting functions n versus pH (where n is the average number of protons released per mole of the organotin aquocation) agree satisfactorily with functions from potentiometry. The structures of the aquocations, as well as of the hydroxides, and of the mono-hydroxo complex [Me 2 Sn(OH)(OH 2 ) n ] + , are correlated to the Δ E exp data by point-charge model calculations.

Infrared, Mössbauer and lattice dynamics studies of (3-mercaptopropionato)bis(trimethyltin(IV))

1981

Electronic Relaxation Phenomena Following 57Co(EC)57Fe Nuclear Decay in [MnII(terpy)2](ClO4)2·1/2H2O and in the Spin Crossover Complexes [CoII(terpy)…

2001

The valence states of the nucleogenic 57Fe arising from the nuclear disintegration of radioactive 57Co by electron capture decay, 57Co(EC)57Fe, have been studied by Mossbauer emission spectroscopy (MES) in the 57Co-labeled systems:  [57Co/Co(terpy)2]Cl2·5H2O (1), [57Co/Co(terpy)2](ClO4)2·1/2H2O (2), and [57Co/Mn(terpy)2](ClO4)2· 1/2H2O (3) (terpy = 2,2‘:6‘,2‘ ‘-terpyridine). The compounds 1, 2, and 3 were labeled with ca. 1 mCi of 57Co and were used as the Mossbauer sources at variable temperatures between 300 K and ca. 4 K. [Fe(terpy)2]X2 is a diamagnetic low-spin (LS) complex, independent of the nature of the anion X, while [Co(terpy)2]X2 complexes show gradual spin transition as the temp…