A novel heterocyclic system — dihydro-2H-1,5,2,4-dioxadiazine. 2,4-Dimethyldihydro-2H-1,5,2,4-dioxadiazine hydrochloride: synthesis and NMR study

The first representative of a novel heterocyclic system, namely, 2,4-dimethyldihydro-2H-1,5,2,4-dioxadiazine hydrochloride, was synthesized.     

Investigation of the chemical heterogeneity of polyphenylenes using the condensation of methyl aryl ketones as a model reaction

The chemical heterogeneity of polyphenylenes obtained by trimerization poiycycio-condensation of acetylaromatic compounds has been investigated by GLC-MS analysis of the products of trimerization cyclocondensation of acetophenone. The mechanism for the formation of side products of the reaction is discussed. The presence of dypnone fragments in the polyphenylene structure results in a decrease in the thermal stability of these polymers.Deceased March, 1993.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1595–1601, September, 1993.     

Synthesis and structure of 5,5-dialkyl-3-arylamino-2-thiohydantoins

The reaction of arylhydrazides of -alkyl--chlorocarboxylic acids with thiocyanate ions gave intermediate thiocyanates which rearranged to isothiocyanates on heating and the latter cyclized to 5,5-dialkyl-3-arylamino-2-thiohydantoins.Institute of Technical Chemistry, Urals Branch, Russian Academy of Sciences, Perm' 614000. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 898–903, July, 1997.     

The effect of polyamine homologation on the transport and cytotoxicity properties of polyamine-(DNA-intercalator) conjugates

An efficient five-step synthetic method was developed to access a homologous series of spermidine-acridine and spermidine-anthracene conjugates. The derivatives were comprised of a spermidine fragment covalently tethered at its N4 position to either an acridine or anthracene nucleus via an aliphatic chain (e.g., spermidine-[aliphatic tether]-acridine). The distance separating the spermidine and aromatic nucleus was altered by using different tethers comprised of four or five methylene units, respectively. These ligands (2-5) were shown to inhibit human DNA topoisomerase-II (TOPO-II) activity at 10 microM. Enzymatic activity was assessed as the ability to unknot (decatenate) and cleave kinetoplast DNA (kDNA). Polyamine conjugation did not disrupt the ability of the acridine-spermidine conjugates 2 and 3 to inhibit TOPO-II activity as compared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at 10 microM). In general, the acridine derivatives (2 and 3) showed higher TOPO-II inhibitory activity than their anthracene counterparts (4 and 5). However, this trend was reversed in a whole cell assay with L1210 (murine leukemia) cells, wherein the anthracene analogues were more potent than their acridine counterparts. In this regard the qualitative enzyme-based assay did not predict the trends in the corresponding IC(50) values. Within either series insertion of an additional methylene unit did not significantly alter activity. While the appended spermidine unit did not disrupt TOPO II inhibition by the tethered DNA intercalator, it did provide an alternative mode of entry into the cell as demonstrated by spermidine protection assays. These results were compared with a spermine-intercalator analogue. Of all the conjugates tested the N(4)-(4-(9-aminoacridinyl)butyl)spermine hexahydrochloride (conjugate 16)resulted in the highest degree of L1210 cell rescue upon cotreatment of the cells with exogenous spermidine. It was concluded that the monoalkylated spermine motif present in 16 holds promise as a better vector than its N4 monoalkylated spermidine counterpart.     

Simulating Unstable States during the Coumarin Adsorption on a Mercury Electrode

Dependences of differential capacitance C on potential E of a stationary electrode (hanging mercury drop) in aqueous 0.1 M NaF solutions containing 4.6 × 10^–4 to 3 × 10^–3 M C₉H₆O₂ are obtained using an automatic impedancemeter. At coumarin concentrations below 0.001 M and potential slowly scanned near –1.1 V (SCE) the capacitance is unstable, which results in differently-shaped C vs. E curves in this potential range. The obtained results are attributed to nonequilibrium phase transitions in the adsorption layer, during which the orientation of coumarin molecules at the electrode surface alters. These phenomena are explained semiquantitatively on the basis of a developed theory.     

Problems of Quantitative Spectroscopic Measurements in Heterogeneous Catalysis: Molar Absorption Coefficients of Vibrations in Adsorbed Substances

Published data on the molar absorption coefficients and integral intensities A ₀ of vibrations in physically and chemically adsorbed molecules are reviewed. Analysis of published data shows that bonds characterized by high values of the dipole momentum derivative with respect to the normal coordinate change during adsorption toward decreasing this derivative, whereas bonds characterized by a low value of the derivative change toward increasing the derivative. Thus, adsorption results in a decrease in the difference in values of the dipole momentum derivative with respect to the normal coordinate of different bonds compared with the same bonds in the individual molecules. In addition, the interval of changing the molar absorption coefficients for the surface complexes are at least two orders of magnitude lower than that for the same bonds in the molecules in the gas phase. A series for the degree of easiness in detecting complexes on the catalyst surface (the series of decreasing the molar absorption coefficient) is proposed.     

Synthesis and transformations of metallacycles. 23. Cp2TiCl2-Catalyzed cyclometallation of fullerene C60 with EtAlCl2

1-Ethyl-2,3-fullerenoaluminacyclopropanes (EtAl)_n(²-C₆₀) were synthesized by the reaction of fullerene C₆₀ with an excess of EtAlCl₂ in the presence of Mg and using Cp₂TiCl₂ as the catalyst in a THF--toluene solution at 20 °C. Deuterolysis of fullerenoaluminacyclopropanes afforded a mixture of deuteriofullerenes C₆₀D_m, where m = 6--12.     

Coulometric determination of NAD+ and NADH in normal and cancer cells using LDH, RVC and a polymer mediator

An electrochemical method for the measurement of NAD(+) and NADH in normal and cancer tissues using flow injection analysis (FIA) is reported. Reticulated vitreous carbon (RVC) electrodes with entrapped l-lactate dehydrogenase (LDH) and a new redox polymer containing covalently bound toluidine blue O (TBO) were employed for this purpose. Both NAD(+) and NADH were estimated coulometrically based on their reaction with LDH. The latter was immobilized on controlled pore glass (CPG) by cross-linking with glutaraldehyde and packed within the RVC. The concentrations of NAD(+) and NADH in the tissues, estimated using different electron mediators such as ferricyanide (FCN), meldola blue (MB) and TBO have also been compared. The effects of flow rate, pH, applied potential (versus Ag/AgCl reference) and adsorption of the mediators have also been investigated. Based on the measurements of NAD(+) and NADH in normal and cancer tissues it has been concluded that the NADH concentration is lower, while the NAD(+) concentration is higher in cancer tissues. Amongst the electron mediators TBO was found to be a more stable mediator for such measurements.     

Synthesen in der Naphthalinreihe: Methoxylierte Tetralone und Naphthole

Ohne ZusammenfassungHerrn Prof. Dr.A. Franke in aufrichtiger Verehrung zum 80. Geburtstag gewidmet.