Experience with using aclarubicin in the treatment of acute leukemia and blast crisis of chronic myeloid leukemia]

The clinical efficacy of aclarubicin, an anthracycline antibiotic, was studied in 48 patients with leukemia. The antibiotic was used in the following combinations with cytarabine: "7 + 7", "5 + 5" and "7 & 3". A complete remission was stated in 14 (42.4 per cent) out of 33 patients with acute nonlymphoid leukemia, 6 (43 per cent) out of the 14 patients having relapses. The combined therapy was effective in 4 out of 5 pre-resistant patients. The "7 + 3" scheme was the most beneficial. The most common adverse reactions were nausea and vomiting.     

Use of carminomycin on adult patients with acute leukemias]

The data on the clinical trials of karminomycin, a new antitumor antibiotic are presented. The drug was used in the treatment of 46 adult patients with leukemia. Karminomycin was used in primary inducing therapy and treatment of relapses. The results of the trials showed that karminomycin had a definite therapeutic activity in treatment of acute myeloblast leukemia at various stages of the process. A rapid effect of the antibiotic provided its use in emergency cases with rapidly progressing variants of the disease.     

Synthesis and structures of bimetallic silicon-containing imido alkylidene complexes of molybdenum Me2Si[CHMo(NAr)(ORF3)2]2 and PhVinSi[CHMo(NAr)(ORF3)2]2

Bimetallic alkylidene complexes of molybdenum (R_F3O)₂(ArN)MoCH-SiMe₂-CHMo(NAr)(OR_F3)₂ (1) and (R_F3O)₂(ArN)MoCH-SiPhVin-CHMo(NAr)(OR_F3)₂ (2) (Ar = 2,6-C₆H₃; R_F3 = CMe₂CF₃) have been prepared by the reactions of vinyl silicon reagents Me₂Si(CHCH₂)₂ and PhSi(CHCH₂)₃ with known alkylidene compound PhMe₂C-CHMo(NAr)(OR_F3)₂. Complexes 1 and 2 were structurally characterized. Ring opening metathesis polymerization (ROMP) of cyclooctene using compounds 1 and 2 as initiators led to the formation of high molecular weight polyoctenamers with predominant trans-units content in the case of 1 and predominant cis-units content in the case of 2.     

Use of water-soluble 2-nitro-4-sulfophenyl ester of adipic acid for preparation of peptide protein conjugates]

Two synthetic peptides were conjugated with bovine serum albumin by means of 2-nitro-4-sulfophenyl ester of adipic acid. The amino acid analysis of the conjugates has shown that 14-15 molecules of the peptide are coupled per 1 molecule of the albumin during 10 min. The number of coupled molecules is the same when the reaction time increases to 24 hours. So, 2-nitro-4-sulfophenyl ester of adipic acid may be used parallel with the known bifunctional reagents to obtain peptide-protein conjugates.     

Technical Aspects of Using Rank Distributions of Phytoplankton Abundance for the Analysis of Mass Data of Freshwater Ecological Monitoring. Approximate Calculations

Rank distribution parameters for the abundance of phytoplankton species was calculated based on long-term hydrobiological monitoring (1978–1997) of water bodies in the Azov, Caspian, and Kara hydrographic regions. Two model relationships between species abundance and the rank were used in data analysis: exponential and hyperbolic. Parameter variability related to changes in environmental quality in time and space was analyzed. The dependencies of parameters on the region, time, and season of sampling were determined. Possible factors underlying the parameter dependence on phytoplankton sample processing in the system of biological monitoring were analyzed.     

Manganese(III) and rhenium(II) complexes with bulky 4,6-di-tert-butyl-N-(2,6-di-iso-propylphenyl)-o-iminobenzoquinonato ligands via carbonyls of corresponding metals

Four-coordinate complex Mn^III(ISQ-Prⁱ)(AP-Prⁱ) (1), where ISQ-Prⁱ = 4,6-di-tert-butyl-N-(2,6-di-iso-propylphenyl)-o-iminobenzosemiquinonate anion-radical, AP-Prⁱ = 4,6-di-tert-butyl-N-(2,6-di-iso-propylphenyl)-o-amidophenolate dianion, has been prepared by the reaction of Mn₂(CO)₁₀ with free 4,6-di-tert-butyl-N-(2,6-di-iso-propylphenyl)-o-iminobenzoquinone (IBQ-Prⁱ) in the molar ratio 1:4 in toluene. In contrast to manganese, rhenium carbonyl reacts with o-iminobenzoquinone to form complex Re^II(ISQ-Prⁱ)₂(CO)₂ (2) with the retention of two carbonyls in coordination sphere of rhenium. The complexes have been characterized by IR, UV-Vis, and EPR spectroscopies. Molecular structures of compounds 1 and 2 have been determined by single-crystal X-ray crystallography. Compound 1 is centro-symmetric square-planar molecule with delocalized mixed valent state of AP-Prⁱ and ISQ-Prⁱ ligands. EPR spectrum of 1 in solid at 300-77 K is typical for manganese complexes with S = 3/2 state. The effective magnetic moment of 1 is 1.96 μ_B at temperature 5 K as it was established by variable-temperature magnetic susceptibility measurements. Six-coordinate octahedral complex 2 possesses an S = 1/2 ground state, which is attained via strong intramolecular antiferromagnetic interaction between t_2g orbital unpaired electron of the low spin Re^II ion and the unpaired electron on π-orbital of the radical ligand.     

The Role of the Electrode Surface in Na–Air Batteries: Insights in Electrochemical Product Formation and Chemical Growth of NaO2

The Na–air battery, because of its high energy density and low charging overpotential, is a promising candidate for low‐cost energy storage, hence leading to intensive research. However, to achieve such a battery, the role of the positive electrode material in the discharge process must be understood. This issue is herein addressed by exploring the electrochemical reduction of oxygen, as well as the chemical formation and precipitation of NaO₂ using different electrodes. Whereas a minor influence of the electrode surface is demonstrated on the electrochemical formation of NaO₂, a strong dependence of the subsequent chemical precipitation of NaO₂ is identified. In the origin, this effect stems from the surface energy and O₂/O₂^? affinity of the electrode. The strong interaction of Au with O₂/O₂^? increases the nucleation rate and leads to an altered growth process when compared to C surfaces. Consequently, thin (3 µm) flakes of NaO₂ are found on Au, whereas on C large cubes (10 µm) of NaO₂ are formed. This has significant impact on the cell performance and leads to four times higher capacity when C electrodes with low surface energy and O₂/O₂^? affinity are used. It is hoped that these findings will enable the design of new positive electrode materials with optimized surfaces.     

Proton Ion Exchange Reaction in Li3IrO4: A Way to New H3+xIrO4 Phases Electrochemically Active in Both Aqueous and Nonaqueous Electrolytes

Progress over the past decade in Li‐insertion compounds has led to a new class of Li‐rich layered oxide electrodes cumulating both cationic and anionic redox processes. Pertaining to this new class of materials are the Li/Na iridate phases, which present a rich crystal chemistry. This work reports on a new protonic iridate phase H_3+xIrO₄ having a layered structure obtained by room temperature acid‐leaching of Li₃IrO₄. This new phase shows reversible charge storage properties of 1.5 e^? per Ir atom with high rate capabilities in both nonaqueous (vs Li⁺/Li) and aqueous (vs capacitive carbon) media. It is demonstrated that Li‐insertion in carbonate LiPF₆‐based electrolyte occurs through a classical reduction process (Ir⁵⁺ ? Ir³⁺), which is accompanied by a well‐defined structural transition. In concentrated H₂SO₄ electrolyte, this work provides evidence that the overall capacity of 1.7 H⁺ per Ir results from two additive redox processes with the low potential one showing ohmic limitations. Altogether, the room temperature protonation approach, which can be generalized to various Li‐rich phases containing either 3d, 4d or 5d metals, offers great opportunities for the judicious design of attractive electrode materials.     

The Principle of Competitive Exception in a Two-Species Community with One Metabolic Regulation Factor

The validity of the competitive exclusion principle (the Gause’s principle) at one metabolic regulation factor is demonstrated for a general model of two-species community. The competitive exclusion principle postulates that a long-term coexistence of species is impossible if their number exceeds the number of density-dependent growth-regulating factors. Previously, this principle was proved for the stationary states in a general model of a community with any number of factors. In the dynamic modes, the number of species in a community may exceed the number of regulating factors. However, under the influence of one factor, only one species survives.