Mössbauer Spectroscopic Study on Vertical Distribution of Iron Species in Sediments from Qinghai Lake,China

In this study, ⁵⁷Fe Mössbauer spectroscopy has been applied to sediments collected from Qinghai Lake in Qinghai Province, China, to investigate the vertical distribution of iron species. Their Mössbauer spectra consisted of four doublets ascribable to one paramagnetic high-spin Fe³⁺, two paramagnetic high-spin Fe²⁺ with different quadrupole splittings, and one diamagnetic low-spin Fe²⁺ that corresponds to pyrite (FeS₂). The distribution of pyrite suggested climatic changes during the past nine thousand years. It was demonstrated that the iron speciation in the salt lake sediments by Mössbauer spectroscopy can be used to reconstruct the past environment.

     

Influence of reclamation on the concentrations and chemical states of elements in tideland sediment

In order to investigate the transition of tidelands, we collected sediments in Yatsu tideland and Nekozane river mouth in Tokyo Bay. The vertical distributions of elements were determined by instrumental neutron activation analysis and prompt gamma-ray analysis. In Yatsu tideland the vertical distribution changed in a great extent, which was considered as an influence of the neighboring reclamation. They were categorized into four groups, and two parameters were created by applying principal component analysis. Chemical states of iron and sulfur were also investigated by Mössbauer spectroscopy and X-ray absorption fine structure. These results show that Yatsu tideland became an anaerobic environment.     

Synthesis and Mesomorphic Properties of 2,6-Disubstituted Tetralins

Synthesis and mesomorphic behavior of nine members of each of the two classes of 6-phenyl- and 2-phenyltetralins and five members of the 2-trans-cyclohexyltetralins are reported. The synthesis of one member of each class is described in detail. Besides the target compounds, more than twenty intermediates showed liquid crystalline properties; their transition temperatures are recorded (see Tables 1-6).     

NMR studies on polarized12B implanted in highly oriented pyrolytic graphite

NMR measurements on¹²B nuclei implanted in a thin sheet of highly oriented pyrolytic graphite (Grafoil) have been made to study the magnitude of the polarization of¹²B and its electric quadrupole coupling. The magnitude of the residual polarization of¹²B held in carbon material is of crucial importance to the experiment measuring the average polarization of¹²B produced in the muon capture by¹²C. It was found that the polarization of¹²B can be maintained at 101.0±2.2% in Grafoil under a magnetic field of 3 kG. The electric quadrupole coupling was determined to bee ² qQ/h=+1207.3±8.2 kHz. From the magnitude and the sign of the electric field gradienteq, the location of¹²B was found to be a substitutional site in the carbon lattice. The anomalous B-C bond involving thesp ₂ hybrid orbitals with partially filledp _z electrons is also discussed.     

255. Additional bufadienolides from Ch'an Su. Toad venoms. 39

From the toad venom Ch'an Su the bufadienolides 1, 4, 9, 10, 12, 15, 17, 20, 22, 25 and 18 , the latter as diacetate 19 were isolated and their structure elucidated.     

μ- spin rotation studies on graphite and its second-stage rubidium intercalation compound. Evidence for a paramagnetic chemical shift

The precession frequencies of negative-muon spin rotation in highly oriented pyrolytic graphite and its second stage Rb compound were measured at room temperature. The results showed that a μ^- C-C bond is formed from sp² hybrid orbitals involving the partially filled p_z orbital and that intercalation influences the σ as well as the π bonds.     

Inversion of Optical Activity in the Synthesis of Mercury Sulfide Nanoparticles: Role of Ligand Coordination

Optical activity in inorganic colloidal materials was controlled through interactions of chiral molecules with the nanoparticle (NP) surface. An inversion of optical activity in the synthesis of mercury sulfide (HgS) NPs was demonstrated with an intrinsically chiral crystalline system in the presence of an identical chiral capping ligand. A continuous decrease in the positive first Cotton effect and an eventual reversal of CD profile were observed upon heating the aqueous solution of HgS NPs capped with N‐acetyl‐l ‐cysteine (Ac‐l ‐Cys) at 80 °C. Ac‐l ‐Cys afforded two bidentate coordination configurations with an almost mirror image of each other using the thiolate and either of carboxylate or acetyl–carbonyl groups on the HgS core. Experiment and calculation suggest that a shift in the distribution of the NP formation with energy in response to the combinations of ligand coordination structure and chiral crystalline surface is responsible for the inversion of optical activity.