X-ray fluorescence in some rare earth and high Z elements excited by 661.6 keV γ-rays

The K-shell X-ray fluorescence cross sections are determined experimentally for 10 elements such as Pb, Hg, Ir, W, Lu, Tm, Dy, Tb, Gd and Nd at excitation energy of 661.6 keV associated with γ-rays of ¹³⁷Cs radioisotope. The technique employed involves the measurement of total intensity of fluorescent K X-rays that follow the photoeffect absorption of a known flux of γ-rays using a well type Nal(Tl) detector. The obtained results are compared with the available theoretical values and other measured values.     

Highly Efficient and Practical Syntheses of Lavendamycin Methyl Ester and Related Novel Quinolindiones

The novel 7-(N-formyl-, 7-(N-acetyl-, and 7-(N-isobutyrylamino)-2-methylquinoline-5,8-diones were synthesized in excellent overall yields in three steps via the nitration of the commercially available 8-hydroxy-2-methylquinoline followed by a reduction-acylation step and then oxidation. Acid hydrolysis of 7-(N-acetylamino)-2-methylquinoline-5,8-dione (14a) afforded the novel 7-aminoquinoline-5,8-dione 7 in excellent yields. Due to our efficient preparation of dione 14a, we now report a short and practical method for the total synthesis of the potent antitumor agent lavendamycin methyl ester (1b) with an excellent overall yield.     

Resonant neutron capture in 40Ca

The neutron capture cross section of ⁴⁰Ca has been measured with ≈ 0.2 % energy resolution below E_n = 300 keV. Resonance parameters have been extracted for many new p- and d-wave resonances. Gamma-ray spectra were also measured following capture in one doublet and two resolved resonances below 50 keV. Strong feeding of low-lying p-wave levels was observed in all cases. Calculations showed that valence transitions were inadequate to account for the observed dominance of these transitions and a further mechanism is required. The average resonance parameters obtained from the data are as follows: 〈D〉 = 37 + 4keV, 10⁴S₁ = 0.16 ± 0.05, 10⁴S₂ = 2.0 ± 0.7. The average radiative widths and standard deviations of their distributions were found to be strongly l-dependent as follows: 〈Γ_γ〉_s = 1.5 ± 0.9 eV, 〈Γ_γ〉_p = 0.36 ± 0.09 eV and 〈Γ_γ〉_d = 0.7 ± 0.4 eV.     

Mercury β-Diketonato complexes : II. The crystal and molecular structure of 3,3-bis(chloromercury)-2,4-pentanedione

The structure of 3,3-bis(chloromercury)-2,4-pentanedione is reported. The space group indicated is C2/c with unit cell dimensions: a = 15.048(2), b = 10.921(6), c = 16.080(4) Å, and β = 134.74(1)°. Three-dimensional absorption-corrected diffractometer data were used in the refinement of the structure to a conventional R(F) value of 0.079. Anisotropic temperature factors were used for Hg and Cl atoms while C and O atoms were refined isotropically. Both Hg atoms are bound to the γ-carbon of acetylacetone. Solid state Raman and infrared spectra are reported. Lowering of the C=O stretching frequency is discussed in terms of the crystal structure.     

The crystal and magnetic structures of Sr2YRuO6

Time-of-flight powder neutron diffraction data have been used to refine the crystal structure of the ordered, distorted perovskite Sr₂YRuO₆. Yttrium and ruthenium are octahedrally coordinated in this material with average MO bond lengths of 2.202 and 1.955 Å, respectively. Constant wavelength neutron diffraction data show that Sr₂YRuO₆ is a Type I antiferromagnet at 4.2 K with an ordered magnetic moment of 1.85 μ_B per Ru⁵⁺ ion. The Néel temperature of Sr₂YRuO₆ was determined to be 26 K. The data suggest that the 4d³ electrons in this material are localized rather than itinerant.