On the origin of additional peaks in the photoelectron spectra of yttrium

Ultraviolet Photoemission analysis of yttrium metal reveals well defined features far below the conduction band. In order to elucidate their origin, we have used X-ray/Ultra violet photoelectron spectroscopy together with inverse photoemission. The comparison of the spectra of clean yttrium and of H exposed yttrium suggests that these structures are most probably due to hydrogen bands, hydrogen being either in a stable surface hydride form or as subsurface H.     

Slowly relaxing tunneling states in neutron-irradiated quartz: A study of the internal friction at audio-frequencies

The internal friction of two neutron-irradiated quartz samples was measured at audio-frequency as a function of temperature. This is an extension of acoustic measurements to much lower frequencies and thus to much longer time scales. A temperature independent behaviour has been observed and is discussed in the framework of the tunnelling model. One of the major assumptions of this model regarding the tunnelling states with long relaxation time could be verified for neutron-irradiated quartz.     

Characterization of reaction products formed during thin-layer chromatographic detection of thiocarbamate herbicides

The reaction between thiocarbamate herbicides and 2,6-dichlorobenzoquinone-N-chloroimine or 2,6-dibromobenzoquinone-N-chloroimine is suitable for the detection of these herbicides on thin-layer plates with high sensitivity. The reactions were followed by infrared, nuclear magnetic resonance and mass spectrometry. We have established the formation of 2,6-dichlorobenzoquinone-S-alkyl sulphenylimines. In the case of the bromo-derivative, halogen exchange and substitution on the quinone ring took place simultaneously leading to the formation of mixed halogenated 2,6-dihalo- and, in addition, 2,3,6-trihalobenzoquinone-S-alkyl sulphenylimines. The final product of the detection reaction, i.e. 2,6-dichlorobenzoquinone-S-alkyl sulphenylimine was reacted with 2,6-dibromobenzoquinone-N-chloroimine where 2,6-dichloro-3-bromobenzoquinone-S-alkyl sulphenylimine formed as a consequence of the looser bromine-carbon linkage on the 2 and 6 positions of the quinone ring.     

Humulenoids from plants of the family Apiaceae spatial structure of α-apienes

A conformational analysis has been made by the method of molecular mechanics of the -apienes — natural sesquiterpenes isolated from plants of the Apiaceae family. The results of the mathematical method with the inclusion of those x-ray structural studies have shown that in the molecules under consideration it is possible to expect the predominant realization of four conformations of the 11-membered ring:₁₄A ₈ ⁷ ,¹⁴A ₇ ⁸ ,₁₄A ₇ ⁸ , and¹⁴A ₈ ⁷ . These four conformations of unsubstituted -apiene and its natural derivatives have been characterized energetically, and the barriers to their interconversions have been evaluated.Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 197–202, March–April, 1992.     

Phytoecdysteroids of Rhaponticum carthamoides III. Rhapisterone C

A new ecdysteroid, rhapisterone C, has been isolated from seeds of the plantRhaponticum carthamoides (Willd) Iljin (family Compositae). It has been shown that rhapisterone C is 23-ethylecdysterone.Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 231–233, March–April, 1992.     

Base-atom recognition in protein adsorption to alkyl agaroses.

The three proteins phosphorylase b, calmodulin and fibrinogen are adsorbed onto thioalkyl derivatives of Sepharose much more strongly than onto gels carrying the same alkyl residue coupled via a carbamate linkage. This enhancement of binding onto alkyl-S-Sepharoses compared with alkyl-N-agaroses is not primarily due to an increase in the extent of conformational changes of the proteins occurring on the gel surface. This can be shown in experiments with the tripeptide Trp-Trp-Trp. The Trp tripeptide is also adsorbed with a much higher affinity to butyl-S-Sepharose than to butyl-N-Sepharose, showing that the primary interaction between the immobilized alkyl residue and the amino acids of the protein is decisive for adsorption. A model stressing the strong influence of an atom or a group of atoms at the base of an immobilized alkyl residue is described as "base-atom recognition".     

Variation of U-microdistribution in fossil Hipparion teeth as a complicating factor in dating studies

Five Upper Miocene fossil Hipparion molars were studied for U-distribution by Fission Track. U uptake has reached the whole mass of the teeth and no saturation fronts seem to occur in the interior layers. Mean U-concentration in dentine, cement and enamel was 157, 139 and 78 ppm, respectively. U_enamel/U_dentine 0.5 is considerably higher than 0.1 reported in the past for Upper-Quaternary mammoth teeth. These features are disadvantageous for ESR-dating in Hipparion enamel, although a long-lived signal (g=2.0018) is apparent. Leaching phenomena occur in the outer regions of these teeth. Inner enamel folding seems to have hindered a more uniform U-distribution in the teeth.     

A simple technique for surface labeling of solids with222Rn and its short-lived decay products

A simple radioactive labeling technique is described which is based on a recoil injection of atoms of²²²Rn and its decay products from a²²⁶Ra source into thin surface layers of solids.     

Calculation of exclusive processes with baryons

Using the nucleon andΔ ₃₃-resonance wave functions found out in previous papers [14, 15] we calculate the electromagnetic and weak nucleon formfactors, the transition formfactorγ \(\bar N\) Δ and the decay widths of charmonium levels³ S ₁,³ P ₂ and³ P ₁ into \(\bar N\) N and \(\bar \Delta \) Δ.     

C-odd exchange in high energypp andp \bar p elastic diffraction

Following the arguments of QCD, a proposed model takes into account the significant difference ofpp andp \(\bar p\) elasticd σ/dt discovered at the ISR. An expression forC-odd exchange is discussed and comparison with data is made. Starting from the ISR energies, the model is shown to describe well the data in a wide range of transverse momenta 0≦?t≦10 (GeV/c)² (including the Coulomb-nuclear interference region). Several peculiar predictions of the model will be testable in the TeV energy range and beyond.