Conversions of 2-thioxo-1,3-dithiol-4,5-dicarboxylic acid dimethyl ester — The path to a new heterocyclic system, (4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2,5,7-trione and 5,6-dimercaptouracil derivatives

The conversions of 2-thioxo-1,3-dithiol-4,5-dicarboxylic acid methyl ester into anhydride, mono- and diamide, and monoamide methyl ester were demonstrated. The new heterocyclic system, (4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2,5,7-trione, was obtained by oxidative rearrangement-cyclization of 2-oxo-1,3-dithiol-4,5-dicarboxylic acid diamide with phenyliodosyl(hydroxy)tosylate and used to synthesize previously unknown 5,6-dimercaptouracil derivatives, including nickel dithiolene complex.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1270–1275, September, 1992.     

Belousov-Zhabotinskii oscillatory chemical reactions involving complexes of transition metals with 1,10-phenanthroline and 2,2′-bipyridyl

An analysis is given of features of the catalytic effect of complexes of manganese, iron and ruthenium with 1,10-phenanthroline and with 2,2-bipyridyl on the oscillatory Belousov-Zhabotinskii chemical reaction. On the basis of the experimental results, the redox properties of the various complexes and the composition of their coordination spheres consideration is given to the possibility (not previously taken into account) of the conversion of the catalyst during the formation and consumption of key substances [bromide ion, bromous acid HBrO₂, the bromyl and malonyl radicalsBrO₂ andCO(COOH)₂], the concentrations of which govern the oscillatory regime of the reaction. A scheme is proposed for the action of the complexes of transition metals with 1,10-phenanthroline and 2,2-bipyridyl which removes the discrepancies between the usually accepted mechanism for the Belousov-Zhabotinskii reaction and the experimental results.Sonar Scientific Research Center for the Automation of Biotechnical Systems, Cybernetics Institute of the Ukrainian SSR, Kiev. Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 27, No. 3, pp. 346–353, June, 1991. Original article submitted March 14, 1991.     

Equilibria in complexes of N-heterocyclic molecules,part XII. The reaction of hydroxide and alkoxide Ions with platinum(II) complexes of 5-nitro-1,10-phenanthroline and 2,2′-bipyridyl

Summary Bis-(5-nitro-1,10-phenanthroline)platinum(II) dichloride and diperchlorate have been prepared. The reaction between the parent cation and hydroxide ion has been studied using 1 FI n.m.r. spectroscopy and found to involve attack at the ligand. The bis-(2,2-bipyridyl)platinum(II) ion has been shown to be highly reactive towards methoxide ion. The dissociation of a 2,2-bipyridyl ligand is preceded by attack at the ligand.Part XI: R. D. Gillard, t.. A. P. Kane-Maguire and P. A. Williams,Transition Met. Chem., 2, 47 (1977).On leave from the University of Baghdad, Iraq.     

Microbiological transformations of 19-oxygenated ent-kauranes

The microbiological transformations of three 19-oxygenated ent-kauranes with Rhizopus nigricans, Aspergillus ochraceous and Calonectria decora have been investigated. The most common transformation observed is hydroxylation at the C-1 and C-7 positions. For ent-kaur-16-en-19-oic acid allylic hydroxylation and hydration of the double bond also occur.     

Glass transition in the lower homologues of polyethyleneoxide

Experimental measurements of T_g for two series of lower homologues of polyethyleneoxide. differing in their end-groups, are discussed in terms of existing theories. Simple free-volume considerations predicting linear dependence of T_g on (molecular weight)^?1 are inadequate in systems with end-groups capable of specific interactions (hydrogen bonding). Thermodynamic arguments show that the true T_g of infinitely long PEO chain is 220 ± 5°K. Suitable modification of parameters of the Gibbs-DiMarzio equations to account for the dependence of the free volume fraction on the concentration of end-groups results in good fit of the experimental data for hydroxyl-terminated samples and correctly predicts T_g(∞). Analysis of the data for chlorine-substituted oligomers suggests the existence of specific intermolecular interactions in the latter, involving chlorine atoms.     

Special features in the chemical structure of phosphorus isocyanates

The UV and IR absorption spectra and the NMR and NQR spectra of certain isocyanates of three- and four-coordinated phosphorus have been investigated. The reciprocal effect of the phosphorus atom and the NCO group is discussed on the basis of spectral analysis, quantum chemical calculations of the electron systems, and calculations of the normal vibrational forms. Comparison of the (PO) frequencies in the IR spectra of the phosphorus isocyanates with the Taft gives a linear relationship which testifies to the predominant inductive effect of the NCO group on the P(O)R₁R₂ grouping. A similar relationship is observed between the resonance frequency _res in the NMR spectra and for C1P(O)R₁R₂ compounds. The effect of the phosphorus atom on the electronic system in the NCO group is shown by the hypsochromic shift of the absorption band in the210-m region and an appreciable increase in its intensity, compared with alkyl isocyanates. This fact, which agrees with the NMR spectral data and the quantum chemical calculations, indicates the presence of conjugation in the P-N bond. We found the order of the P-N bond to be approximately 1.2. This partial double-bond nature of the P-N bond results from the interaction of the p electrons of nitrogen in the NCO group with the d orbitals of the phosphorus atom.We are grateful to our colleagues at the Kazan Physicotechnical Institute AS USSR A. I. Rivkind, S. G. Salikhov, and I. A. Safin for recording the spectra.     

Thiazolocyanines

A method was developed for the preparation of 2-methyl-N-(2-thiazolyl)-, 2-methyl-N-(2-pyridyl)-, and 2-methyl-N-(2-benzothiazolyl)thiazolium salts. Cyanine dyes were synthesized from these salts. A comparison of the absorption spectra of dyes with various substituents (ethyl, phenyl, and 2-hetaryl) attached to the nitrogen atoms of the thiazole rings of the dyes demonstrated that the color deepens as the electronegativity of these substituents increases.See [1] for communication XIV.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 933–936, July, 1972.     

Some developments in the chemical direct oxygen determination

This paper discusses modifications of the direct determination of oxygen in organic compounds by reduction with carbon. Two versions are considered, (a) a microscale method for compounds containing metals, phosphorus or boron, and including automatic non-aqueous carbon dioxide titration, and (b) a manometric method capable of analysing samples containing traces of oxygen down to 5ppm.     

Hydrolyse und Alkoholyse von Reaktivfarbstoffen: III. Sorbitolyse von Monochlortriazin-Farbstoffen. 3. Mitteilung über reaktionsmechanistische Untersuchungen an Reaktivfarbstoffen

• 1 The kinetics of the competitive reactions of three monochlorotriazine reactive dyes with water and with sorbitol have been investigated.
• 2 The reactions of the monochlorotriazine dyes with sorbitol anions and hydroxyl ions can be divided as follows: (a) With dyes without a NH-group between the triazine nucleus and the other part of the molecule, the reaction follows the simple addition-elimination mechanism (A_N2E), in which the addition of the nucleophile is ratelimiting. (b) The reactions of dyes containing a NH-group can be explained by assuming that more than one of the tautomeric isomers are reactive. With one isomer the addition of the nucleophile is the slowest step; with another the base-catalysed decomposition of the addition complex is rate-limiting.
• 3 The first acid dissociation constant of sorbitol is evaluated (pK_a = 13.14;60°).