Structure–activity studies on the fungitoxicity of some triorganotin(IV) compounds

Seventeen triorganotin(IV) compounds, with the general formula R₃SnX, containing symmetrical and unsymmetrical combinations of alkyl and aryl groups on tin and with a wide variation in the non-carbon-bonded anionic (X) residues, were examined along with three formally pentacoordinated adducts of triaryltin chlorides with triphenylphosphine oxide for their antifungal activity against nine plant pathogenic and saprophytic fungi. The in vitro tests included inhibitory studies on radial growth, mycelial growth, spore germination, and germ tube elongation. A significant finding was the dependence of fungitoxicity on the nature of the X group in both the tributyltin and triaryltin series, in contrast to earlier published reports on the negligible influence of the X groups on overall toxicity relative to the R group. This suggests that the X group is significantly involved in transporting the biocide to the reactive sites, and that the X group which tends to confer increased solubility to the triorganotin compound gives rise to increased activity. In studies of R group variations, tri-iso-butyltin bromide was found to be much less fungitoxic than tri-n-butyltin compounds, a result which is reconcilable in terms of increased steric encumbrance at the tin site in the former case. The steric factor is also implicated in the reduced activities observed for tris(p-tolyl)tin and tris(p-chlorophenyl)tin compounds relative to (Ph₃SnX) towards most of the fungi screened in this study. In general, it was also noted that the triaryltins were more selective in their antifungal action than the trialkyltins, which exhibited broad spectral activity when applied at the concentration level of 10 μg cm^?3.     

Fluctuations of the energy absorption of electron-photon radiation in a model with collision-grouping elements

In the present work, the general method proposed earlier for calculating the distribution density and moments of the absorbed energy in isolated sensitive regions of absorbers irradiated by ionizing particles is developed and made specific for the electron-photon problem. Electron transfer is considered within the framework of a model using grouping of excitations and slipping ionization; the presence of electron equilibrium in the vicinity of sensitive regions is assumed. Two similar methods of calculating these characteristics are developed. Both reduce the initial problem to two independent problems: determining the electron spectrum in the sensitive region (in one of the methods, the spectrum of electron sources is also needed) and calculating the coefficients characterizing electron transfer in the sensitive region and its immediate vicinity.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 9, pp. 89–94, September.     

Narrow linewidth 2 μm optical parametric oscillation in periodically poled LiNbO<Subscript>3</Subscript> with volume Bragg grating outcoupler

An optical parametric oscillator using a periodically poled LiNbO₃ crystal and a volume Bragg grating output coupler is presented. Signal and idler wavelengths of 2008 and 2264 nm were generated from the 1064 nm Nd:YVO₄ pump laser. The Bragg grating was reflecting in a narrow band around 2008 nm, creating a purely singly resonant cavity. Signal and idler linewidths of approximately 0.44 and 0.72 nm, respectively, were measured. This is a reduction of 80 and 60 times compared to when using a mirror as output coupler. A total output energy of 156 μJ was measured with 47% slope efficiency. PACS 42.65.Yj; 42.72.Ai; 42.40.Eq     

Envelopes of holomorphy of Jordan curves in ℂn

A comprehensive answer is given to two related questions: (i) Can continuous functions be approximated by holomorphic ones on Jordan curves in ?ⁿ (A.G. Vitushkin, 1964)? (ii) Is any Jordan curve in ?ⁿ holomorphically convex (E.L. Stout, 1970)?     

Catalytic supports on the base of activated anthracites and synthetic carbons

Selective adsorption of platinum group metals (PMG) on activated carbons from a multi-component model and technological solutions was proposed for the preparation of heterogeneous-supported catalysts. Activated natural anthracites and a nitrogen-containing synthetic carbon are considered as carriers for Pd-supported catalysts. Their catalytic activity was studied in the Pd-catalyzed reactions of hydrogen peroxide decomposition and chloride ions oxidation by manganese(III). On the base of the obtained results, novel high sensitive analytical methods both for direct determination of supported-metal quantity and palladium oxidation states on the surface of spent adsorbents are suggested.