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.     

Synthesis of 24-epiteasterone

Starting from ergosterol, the synthesis of the brassinosteroid 24-epiteasterone has been achieved by the use of a new scheme for introducing a 3-hydroxy-6-keto group as the result of the Birch reduction of the corresponding 5-hydroxy-⁷-3,6-dione.Institute of Bioorganic Chemistry, Belorussian Academy of Sciences, Minsk. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 224–227, March–April, 1992.     

Determination of gallium by anodic stripping square-wave voltammetry Detection of a GaZn intermetallic compound and its destruction by Sb in an NaSCNNaClO(4) supporting electrolyte

Reproducibility for successive determinations with a hanging mercury drop electrode is assessed in relation to solution stirring, drop size and back-diffusion to the mercury thread. The effect of experimental parameters such as drop size, deposition time and gallium concentration on the observed stripping current is investigated. The interference of zinc present in a 0.5M NaSCN + 4.2M NaClO(4) supporting electrolyte on the gallium detection limit and calibration plots is described. Formation of an intermetallic compound with a Zn:Ga ratio of 2:3 and its destruction by co-deposition of zinc with Sb are reported. A detection limit of 10(-8)M gallium was obtained in the presence of 10(-5)M Sb(III).     

Lepton phenomenology and neutrinoless double β-decay in superstring inspired theories

The properties of neutrinos,s-leptons,s-quarks as well as the coloured isosinglet \(\tilde D\) and \(\tilde D^c \) are studied in superstring inspired models. Furthermore the neutrinoless double β-decay process is investigated, including light and heavy majorana neutrinos, as well as the contribution of the exotic Higgs scalars of the theory. From the current experimental limits onov-ββ-decay, useful constraints are imposed on the masses and Yukawa couplings of the theory.     

Speeding-up and scaling of domain-wall relaxation nearT c of a uniaxial ferromagnet

The dynamic susceptibility () measured between 10 Hz and 10 MHz on different GdCl₃-ellipsoids (T _c=2.21 K) reveals a completely reversible motion of the domain walls. Taking into account the contribution of the fast adiabatic intradomain magnetization to the nearly Debye-shaped (), we determine for the first time the kinetic Onsager coefficientL _d of the domain wall relaxation of a ferromagnet. Approaching the CurietemperatureL _d speeds up critically, which by a novel simple relaxational model can be related to the increasing width (=correlation length) of linear Bulaevskii-Ginzburg domain-walls and to the shrinking domain period. The reduction ofL _d by an external field can be represented by a universal scaling function, and within the same dynamical model, this effect is ascribed to the increase of the domain period, predicted for a bubble phase. However, the effect of sample size onL _d is much smaller than expected.     

Light-induced starch degradation in non-dormant turions of Spirodela polyrhiza

Continuous red light controls starch degradation in turions of Spirodela polyrhiza[Dölger, K., U. K. Tirlapur and K.‐J. Appenroth [1997]Photochem. Photobiol. 66, 126–127 (1997)]. This light could be replaced by repeated red light pulses with the reciprocity law fulfilled over a large range of fluence rates. The effect of red light pulses repeated every 24 or 12 h for 6 days was reversible by subsequent far‐red light pulses. In contrast, hourly applied red pulses were irreversible by far‐red light. This discrepancy was explained by showing the starch degradation activity of far‐red pulses themselves. The investigated process was categorized as a phytochrome low fluence response with an unusual property: requirement of light treatment for several days. A partial fulfillment of this requirement was obtained with a red pulse followed by a dark period and a 24 h continuous irradiation. These results suggest the existence of two separate steps in the process of starch degradation in turions: formation of a sprout (=sink) during the pulse‐induced germination, and starch degradation in the storage tissue (=source) induced by the second light treatment.     

Structure of the products of the cyclization in acetic anhydride of β-(2-carboxy-5-chlorophenylamino) propionic acid and its nitrile

-(2-Carboxy-5-chlorophenylamino)propionic acid cyclizes in acetic anhydride to form 4-chloro-2-(2,4-dioxopiperidino)benzoic acid, which subsequently undergoes conversion into its lactone. Under the same conditions, -[acetyl(2-carboxy-5-chlorophenyl)amino]-propionitrile forms 7-chloro-1--cyanoethyl-1,2,3,4-tetrahydroquinoline-2,4-dione. The structures of the compounds obtained were confirmed by their IR, UV, and PMR spectra. An evaluation of the stability of the ketonic and enolic forms of the compounds obtained on the basis of calculations by Hückel's method has been made.Translated from Khimiya Geterotsiklicheskikh Soedinenii, Vol. 6, No. 7, pp. 879–884, July, 1970.