Synthesis of 4- and 6-methyl derivatives of 5,7-dioxo(4h,6h)-1,3-dithiolo[4,5-d]pyrimidine based on methylbarbituric acids,spectroscopic characteristics and acidity constants

We have obtained previously unknown 1-methyl- and 1,3-dimethyl-5-diethylaminothiocarbonylthiobarbituric acids by reaction of sodium diethyldithiocarbamate with 5-phenyliodonium betaines of 1-methyl- and 1,3-dimethylbarbituric acids. Cyclization of these compounds upon heating in conc. H₂SO₄ gives methyl-substituted 5,7-dioxo(4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2-diethylimmonium hydrosulfates; the derivative of 1-methylbarbituric acid forms a mixture of 4-methyl- and 6-methyl-substituted compounds (21). We isolated perchlorates of 4-methyl- and 4,6-dimethyl-substituted derivatives in pure form. By treatment of the immonium salt with sodium sulfide or selenide, we obtained 4-methyl- and 4,6-dimethyl-5,7-dioxo(4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2-thiones and 4-methyl-, 6-methyl-, and 4,6-dimethyl-2-selenones. We characterized the isomeric 4- and 6-methyl-substituted selenones by electronic absorption spectra and ionization constants (7.65 and 4.0). The differences in the pK values and in the electronic absorption spectra makes it possible to distinguish the substitution site in N-mono-substituted derivatives of 5,7-dioxo(4H,6H)-1,3-dithiolo[4,5-d]pyrimidine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1526–1533, November, 1993.     

Dynamic light scattering,a probe of brownian particle dynamics

The principles and techniques of dynamic light scattering (DLS) are outlined and its application to the study of suspensions of interacting colloidal particles is discussed. We show how, under appropriate conditions, DLS can measure long-time collective and self-diffusion coefficients as well as study short-time motions (characterized by the cumulants). These theoretical considerations are illustrated by experimental data. Finally, we discuss the relevance of certain characteristic timescales to theories of the diffusion of interacting particles.     

Extractive spectrophotometric determination of uranium with Malachite Green

A sensitive spectrophotometric method based on the extraction of a uranium-benzoate-Malachite Green complex by chlorobenzene is described. The absorption maximum is at 635 nm and the molar absorptivity is 8.3 x 10(4) 1 mole(-1), cm(-1). A preliminary separation of uranium by extraction with methyl isobutyl ketone from acid-deficient aluminium nitrate solution is used to avoid interferences. An aliquot of the extract is then diluted with chlorobenzene and shaken with benzoate buffer containing Malachite Green (MG). The method has been applied for the determination of uranium in a synthetic leach solution. The complex extracted is probably [MG(2)(C(6)H(5)COO)(3)][MG(+)].     

Construction and analytical applications of an extractive electrode sensitive to mercury(I)

The construction and characteristics of a new type of extractive electrode sensitive to Hg(2+)(2) are described. The performance of the electrode is compared with that of an ion-selective electrode with mercurous dithizonate as the active substance. The Hg(2+)(2) -extractive electrode contains Pd(HDz)(2) in its membrane. Its stability and sensitivity are remarkable. It has been used as indicator electrode for the titration of halides alone and in mixtures, and for determination of mercury(I), mercury(II), silver, and of substances containing or reacting with mercury. The basis of the electrode response is discussed.     

Dispersion interaction between helium atoms

Accurate values for the coefficients of the R^?6, R^?8 and R^?10 in the series representation of the dispersion interaction between two helium atoms at distance R are obtained by a simple variation method.     

Offene und cyclische Methylstibonigsäureester. II

Esters of Methylstibonous Acid. II. The reaction of methyldibromstibine with sodium alcoholates and phenolates yield methyldialkoxi and methyldiphenoxistibines. Interchange reactions of the methyldiethoxistibine with thiols, 1,2-diols, 1,2-dithiols, and 2-mercapto-1-oles form dithioesters and cyclic esters of the methylstibonous acid in nearly quantitativ amount and high purity.     

Extractive substances ofLarix dahurica

Summary The quantitative determination of quercetin and dihydroquercetin in the total flavonoids ofLatrix dahurica has been effected by the use of thin-layer chromatography on Kapron for separating the mixture with subsequent elution of the spots and colorimetry of the eluates obtained. The methanol-dimethylformamide (1:1) system was used as the eluate. It has been found that the flavonoids of the heartwood ofLatrix dahurica contain a predominating amount, 69% of dihydroquercetin, the amount of quercetin being 11%.Khimiya Prirodnykh Soedinenii, Vol. 3, No. 5, pp. 298–301, 1967     

Intramolecular hydrogen bond in substituted 3-hydroxypyridines

To explain the character of the intramolecular hydrogen bond in substituted 3-hydroxypyridines, the chemical shifts in the NMR spectra of the hydroxyl group and the IR spectra were studied. It was established that the stability of the intramolecular hydrogen bond of the O-HNR₂ type in substituted 3-hydroxypyridines increases when compared with the corresponding phenols, while an opposite pattern is observed for bonds of the O-H0₂ N type. An approximate evaluation of the energy of the intramolecular hydrogen bond in substituted 3-hydroxypyridines was achieved. When reacting with bases of the same strength, 3-hydroxypyridine forms more stable complexes than phenol.     

Arylhydroxyacetic acids and amino acids derived from ethinylphenols

Conclusions A method of synthesis of arylhydroxyacetic acids and ammo acids derived from ethinylphenols has been developed in view of possible physiological activity of these compounds.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1170–1172, May, 1970.