13C- and 57Fe-NMR spectra of several carbon monoxide hemoprotein models with varying polar and steric effects of the distal organic superstructure, constraints of the proximal side, and solvent polarity are reported. The 13C shieldings of heme models cover a 4.0 ppm range that is extended to 7.0 ppm
Chemical effects in x-ray fluorescence by study of Fe, Pt and U compounds
β Scribed by K. J. S. Sawhney; G. S. Lodha; S. K. Kataria; S. K. Kulshreshtha
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 95 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0049-8246
No coin nor oath required. For personal study only.
β¦ Synopsis
A systematic study of the relative x-ray intensity ratios of the K-and L-series lines was made on compounds of Fe, Pt and U to examine the influence of chemical state on energy-dispersive x-ray fluorescence analysis. The measurements were done using an energy-dispersive Si(Li) detector with photon excitation by radioisotopes. It was shown that reliable x-ray intensity ratios can be derived by employing well-defined experimental conditions. For Fe a significant dependence of the Ka and Kb x-ray yields per incident photon on the oxidation state of Fe was observed but no discernible effect on the Fe Kb/Ka intensity ratio was observed. Likewise, no significant effect of chemical state on the various L-series intensity ratios of Pt and U was observed. For the L-series the seldom quoted intensity ratios Lb 2 /La, Lb 1 /La, Lh/La and Lb 6 /La were also measured and reported. The measured intensity ratios agree fairly well with the theoretical values of Scofield.
π SIMILAR VOLUMES
The syntheses and X-ray structure determinations of single crystals and powders are reported for the compounds (Et 4 N) 3 M 2 F 9 (M = V 3+ , Cr 3+ , Fe 3+ ). The compounds are isostructural and represent a new structure type for A 3 M 2 X 9 compounds. They crystallize in the hexagonal space group P
A series of 3-substituted(X)bicyclo [ 1.1.1 ] pent-1-yltrimethylstannanes (3) were synthesized and their 119Sn and 13C NMR spectra were recorded. The 119Sn substituent chemical shifts (SCS) and the one-bond carbon-tin coupling constants [ 1J(13C,119Sn) ] were analyzed in terms of possible substituen