Effect of extractant on arsenic(V) recovery from sulfuric acid solutions

Extraction of arsenic(V) from sulfuric acid solutions with various extractants in multistage counter-current extraction-stripping systems was compared. The extraction ability of the extractants studied showed the following order: ENIM 100>TBP=CYANEX 923>2-methylhexanol. The extraction depends significantly on the number of extraction stages and the phase ratios in extraction. The effects of the number of stripping stages and the phase ratio in stripping are less important.     

The mannan formed by the yeastBullera tsugae

The structure of an extracellular mannan formed by the yeastBullera tsugae has been studied. It has been shown that the repeating unit of this polysaccharide contains -(13)- and -(14)-bound D-mannopyranose residues in equimolar ratio. A comparison has been made of the polymer under investigation with the extracellular mannan from a yeast of the genusRhodotorula. Leningrad Institute of Pharmaceutical Chemistry. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 746–750, November–December, 1985.     

N,N-bis[2-oxo-3-oxazolidinyl]phosphorodiamidic chloride: a novel coupling reagent in the synthesis of oligodeoxyribonucleotides

Use of a novel coupling reagent, N,N-bis[2-oxo-3-oxazolidinyl]phosphorodiamidic chloride (BOPDC) in the synthesis of oligodeoxyribonucleotides is described. This reagent allows the synthesis of phosphotriesters in high yields (70–80%) without detectable side reactions. Synthesis of a hexanucleotide, d(A-A-C-C-C-G) is presented as an example.     

Polymerization of mono- and α,ω-dicarbanionic polystyryl-barium—II. Effect of added lithium salt in THF

The propagation rate of polystyryl-barium was studied in THF at 20°, in the presence of small amounts of lithium chloride. These kinetic results furnish a new method for the determination of triple ion formation in both mono- and α,ω-dicarbanionic polystyryl-barium. The constant of triple ion association of monocarbanionic (PS^?)₂Ba, K_T, was found to be 3.7 × 10⁵ l M^?1, close to the value calculated from published data.

The triple ion association constant of α,ω-dicarbanionic PS^2?Ba²⁺, K_DT, is about 1.2 × 10⁶ l M^?1.

Taking into account the cyclic structure of α,ω-dicarbanionic PS^2?Ba²⁺ and a statistical factor 3 between K_T and K_DT, it is concluded that mono- and dicarbanionic polystyryl-barium have similar abilities for triple ion formation. Nevertheless, stronger associations are observed for dicarbanionic oligomers with a degree of polymerization lower than 5–7.     

Alkaloids of Aconitum kirinense. Structure of akirine

The known alkaloid lepenine and the new diterpene alkaloid akirine have been isolated from the epigeal part ofAconitum kirinense Nakai. To establish the structure of akirine, its spectral characteristics have been studied and an x-ray structural analysis has been made. It is 1α,8β-dihydroxy-16β-methoxy-9β,14β-methylenedioxy-3β,4β-epoxy-N-ethylaconitane — the first diterpene alkaloid with a lycoctonine skeleton containing a 9,14-methylenedioxy group and a β-oriented substituent at C14.     

Crystal and molecular structure of the sesquiterpene humulane alcohol juniferol

The spatial structure of the sesquiterpene humulane alcohol juniferol, which is represented in the crystal by two conformers, IA and IB, differing by the conformation of the C2...C9 section, has been established by the x-ray structural method. The strain energies of the conformers have been calculated by the method of molecular mechanics. The barrier to the interconversion of the conformers by rotation of the C2...C9 section has been calculated; it amounts to 7–8 kcal/mole. This value of the transformation barrier permits the assumption that the two conformers also exist in solution, their interconversion being hindered.Institute of Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Institute of Crystallography, Academy of Sciences of the USSR, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 757–762, November–December, 1990.     

Isolation and identification of the sex pheromone of females of Heliothis maritima (Lepidoptera,Noctuidae)

Four components have been isolated from an extract of the sex pheromone of the mothHeliothis maritima and have been identified: hexadecanal, hexadec-cis-11-enal, hexadec-cis-9-enal, and hexadec-cis-11-en-1-ol. All-Union Scientific-Research Institute for Biological Methods of Plant Protection, Kishinev. Don Zonal Scientific-Research Institute of Agriculture. Don Scientific-Production Combine. Ecology Division of Lund University, Lund, Sweden. Translated from Khimiya Priorodnykh Soedinenii, No. 4, pp. 574–577, July–August, 1991.     

Encapsulation of pesticides in a starch-calcium adduct

A simple method of encapsulating water-insoluble pesticides in a starch matrix is described. The method consists of mixing the pesticide with alkali starch followed by precipitation with a calcium chloride solution. A starch–calcium adduct that entraps the pesticide in small cells within granular particles is formed. Liquid and solid pesticides were successfully encapsulated by the new method. By use of the herbicide trifluralin [2,6-dinitro-N,N-dipropyl-4-(trifluoromethyl) benzenamine] as core material more than 90% recovery and encapsulation was achieved. Use of acid-modified starches and flours resulted in a lower percentage of encapsulation. Effective encapsulation was also achieved by replacing calcium chloride with strontium chloride or barium chloride.     

Pimaricin—VIII : Structural and configurational studies by electron impact and field desorption mass spectrometry, 13C (25.2MHz) and 1H (270 MHz)-NMR spectroscopy

Attempts to obtain a molecular ion from the polyene macrolide antibiotic pimaricin by EI and FD mass spectrometry were unsuccessful The loss of carbon dioxide and a varying number of water molecules from the molecular ion made a molecular-weight determination impossible ¹³C NMR spectroscopy of N-acetylpimaricin, its dodecahydroderivative, and of HH-2, a hydrogenation-hydrogenolysis product of N-acetylpimaricin, confirmed that the antibiotic has structure 3 containing a hemi-ketalic ring and lacking an OH group at C-8. The value of the anomeric coupling constant, J_c-1-h-1, indicates that the mycosamine moiety is β-glycosidically bound to the aglycone.The structure and configuration of the antibiotic have been studied by analysis of the 270 MHz ¹H-NMR spectra of N acetylpimaricin and HH-2. By comparison of the two spectra and by extensive decoupling experiments, all signals in the spectrum of N-acetylpimaricin have been assigned to the protons in structure 3. From chemical-shift, coupling constant, and integral values, it was deduced that the mycosamine ring is pyranoid with a chair conformation, the hemi-ketal is 6 membered and occupies a chair conformation with the substituents in equatorial positions, the epoxy protons as well as the olefinic protons are trans to each other, and the antibiotic is diastereomerically pure.     

Structure of the alkaloid kalidine

The spatial structure of the alkaloid kalidine obtained from the epigeal part ofKalidium gracile Fenzl. has been determined by IR and NMR spectroscopy and x-ray structural analysis. It has been established that it is the chloride of the trimethyl derivative of glycinamide.Institute of the Chemistry of Plant Substances of the Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 558–561, July–August, 1987.