The title compound, [Fe(C(8)H(5))(C(22)H(16)P)(C(3)H(9)P)(3)], was synthesized by the addition of phenyl-ethine to a solution of the parent methyl iron complex Fe(CH(3)){P(C(6)H(5))(2)(C(10)H(6))}(PMe(3))(3) at 213 K, accompanied by evolution of methane. The coordination around the iron center can be described as slightly distorted octa-hedral [Fe-P 2.2485 (12)-2.2902 (12) Å; Fe-C 1.918 (5), 2....

[1] Iron solubility measurements in the Mauritanian upwelling and the adjacent Open Ocean of the Tropical Atlantic show for all stations lower values in the surface mixed layer than at depth below the pycnocline. We attribute this distribution to a combination of loss terms, chiefly photo-oxidation of organic ligands in the surface, and supply terms, predominantly from the release of ligands fr...

The maturation of cytosolic iron-sulfur (Fe/S) proteins in mammalian cells requires components of the mitochondrial iron-sulfur cluster assembly and export machineries. Little is known about the cytosolic components that may facilitate the assembly process. Here, we identified the cytosolic soluble P-loop NTPase termed huNbp35 (also known as Nubp1) as an Fe/S protein, and we defined its role in...

The atomic structure of a series sodium iron phosphate glasses is studied using different experimental techniques: X-ray and neutron diffraction (ND), infrared spectroscopy, extended absorption fine (EXAFS), near-edge (XANES). Detailed information about the pair correlations obtained. high resolution ND in real space resolves two P–O distances at 1.48 ? 1.59 as expected. All are found to consis...

We quantified the relationships among the specific growth rate, intracellular iron content, and steady state iron uptake rate for cultures of the marine diazotrophic cyanobacterium Trichodesmium (IMS 101) grown under differing conditions of Fe and N availability. The Fe quotas necessary to support a moderately Fe-limited growth rate (70% mmax) of 0.1 d21 under diazotrophy and ammonium were 38 a...

Mammalian ferritins are iron-storage proteins made of 24 subunits of two types: the H- and L-chains. L-chains, in contrast with H-chains, lack detectable ferroxidase activity. When ferritins were subjected to iron loading in vitro with increments near the saturation limit of 4000 Fe atoms per molecule, the homopolymers of human H-chains formed insoluble aggregates, caused by non-specific iron h...

Nitrogenase, the enzyme system responsible for biological nitrogen fixation, is believed to utilize two unique metalloclusters in catalysis. There is considerable interest in understanding how these metalloclusters are assembled in vivo. It has been presumed that immature iron-molybdenum cofactor-deficient nitrogenase MoFe proteins contain the P-cluster, although no biosynthetic pathway for the...

The catalysis of n-butane isomerization over iron-promoted tungstated zirconia (F1.2WZ) and platinum–iron-promoted tungstated zirconia (P/F1.2WZ) catalysts was studied and correlated to the catalyst characterization results. In the singly promoted F1.2WZ catalyst, we suggest that the iron species promotes the n-butane isomerization reaction through a redox effect. The formation of W–O–Fe linkag...

In dietary iron overload, excess hepatic iron promotes liver damage. The aim was to attenuate free radical-induced liver damage using vitamins. Four groups of 60 Wistar rats were studied: group 1 (control) was fed normal diet, group 2 (Fe) 2.5% pentacarbonyl iron (CI) followed by 0.5% Ferrocene, group 3 (Fe + V gp) CI, Ferrocene, plus vitamins A and E (42x and 10x RDA, respectively), group 4 (F...

X-ray absorption near edge structure (XANES) measurements at the C, N, and Fe K absorption edges were performed for iron(III)-tetraphenylporphyrin (FeTPP), iron(III)-tetrakis(p-carboxyphenyl)porphyrin (FeTCPP), and iron(III)-tetrakis(p-sulfonatophenyl)porphyrin (FeTSPP). The spectral shapes differ in the Fe K XANES, but not in C and N K XANES among FeTPP, FeTCPP, and FeTSPP. Crosschecks of XANE...