47 research outputs found

    Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid

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    The electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid (3,4-dichloro-5-hydroxyfuran-2(5H)-one) in MeCN-Bu 4NBF4 (0.1 mol L-1) was investigated. It was shown that all sulfides are electrochemically active, from one to five oxidation steps of sulfur-containing groups were observed for them. The ease and direction of oxidation of the thio group depend on its nature and position in the furanone ring. 3-Substituted 2(5H)-furanones possess the lowest oxidation potential. 4-Substituted 2(5H)-furanones are predominantly oxidized to sulfoxides, 5-aryl- and -alkylthio derivatives undergo fragmentation to give mucochloric acid, and 3-arylthio derivative gives complex unidentified mixture of products. In the case of 3,4-bis(4-methylphenylthio) derivative, the oxidation product of the arylthio group at the 3 position to the corresponding sulfoxide was isolated. Based on the data from cyclic voltammetry with different concentrations of a substrate and water added, the results of preparative electrolysis and quantum chemical calculations, possible mechanisms of electrochemical oxidation of mucochloric acid-derived sulfides are discussed. The initial common step is a reversible single-electron transfer from the substrate molecule to form highly reactive radical cation. Β© 2009 Springer Science+Business Media, Inc

    Strategic Planning of Regional Forest Development Based on the Principles of Green Economy.

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    Π’ послСдниС дСсятилСтия ΠΎΠ±ΠΎΡΡ‚Ρ€ΠΈΠ»ΠΈΡΡŒ ΠΏΡ€ΠΎΠ±Π»Π΅ΠΌΡ‹ поиска Π½Π°ΠΏΡ€Π°Π²Π»Π΅Π½ΠΈΠΉ Ρ€Π°Ρ†ΠΈΠΎΠ½Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ использования ΠΏΡ€ΠΈΡ€ΠΎΠ΄Π½Ρ‹Ρ… рСсурсов, устойчивого развития экосистСм, ΠΎΠ΄Π½ΠΈΠΌ ΠΈΠ· Π±Π°Π·ΠΎΠ²Ρ‹Ρ… элСмСнтов ΠΊΠΎΡ‚ΠΎΡ€Ρ‹Ρ… ΠΎΡΡ‚Π°ΡŽΡ‚ΡΡ лСса. ΠŸΡ€ΠΎΠ±Π»Π΅ΠΌΡ‹ развития лСсного хозяйства Π΄ΠΈΠΊΡ‚ΡƒΡŽΡ‚ Π½Π΅ΠΎΠ±Ρ…ΠΎΠ΄ΠΈΠΌΠΎΡΡ‚ΡŒ Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ Π½ΠΎΠ²Ρ‹Ρ… ΠΏΠΎΠ΄Ρ…ΠΎΠ΄ΠΎΠ² ΠΊ Ρ„ΠΎΡ€ΠΌΠΈΡ€ΠΎΠ²Π°Π½ΠΈΡŽ стратСгии развития лСсного хозяйства Π² соотвСтствии с ΠΏΡ€ΠΈΠ½Ρ†ΠΈΠΏΠ°ΠΌΠΈ Π·Π΅Π»Π΅Π½ΠΎΠΉ экономики, Π² Ρ‚ΠΎΠΌ числС Π½Π° ΡƒΡ€ΠΎΠ²Π½Π΅ ΠΎΡ‚Π΄Π΅Π»ΡŒΠ½Ρ‹Ρ… Ρ€Π΅Π³ΠΈΠΎΠ½ΠΎΠ². Π’ настоящСй ΡΡ‚Π°Ρ‚ΡŒΠ΅ прСдставлСны Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚Π°Π½Π½Ρ‹Π΅ Π°Π²Ρ‚ΠΎΡ€Π°ΠΌΠΈ основныС полоТСния ΠΊΠΎΠ½Ρ†Π΅ΠΏΡ†ΠΈΠΈ стратСгичСского управлСния лСсным хозяйством Ρ€Π΅Π³ΠΈΠΎΠ½Π° с ΠΏΠΎΠ·ΠΈΡ†ΠΈΠΈ устойчивого развития, ΠΊΠ»ΡŽΡ‡Π΅Π²Ρ‹ΠΌΠΈ ΠΈΠ· ΠΊΠΎΡ‚ΠΎΡ€Ρ‹Ρ… ΡΠ²Π»ΡΡŽΡ‚ΡΡ ΡƒΡ‡Π΅Ρ‚ Π΄ΠΎΡ…ΠΎΠ΄Π½ΠΎ-рСсурсного ΠΏΠΎΡ‚Π΅Π½Ρ†ΠΈΠ°Π»Π° систСмы лСсопользования Ρ€Π΅Π³ΠΈΠΎΠ½Π° ΠΏΡ€ΠΈ ΠΏΠ»Π°Π½ΠΈΡ€ΠΎΠ²Π°Π½ΠΈΠΈ Π΅Π³ΠΎ ΡΠΎΡ†ΠΈΠ°Π»ΡŒΠ½ΠΎ-экономичСского развития ΠΈ достиТСниС баланса ΠΌΠ΅ΠΆΠ΄Ρƒ лСсоосвоСниСм ΠΈ лСсовосстановлСниСм. Π’ связи с Ρ‡Π΅ΠΌ сформулированы ΠΊΠ»ΡŽΡ‡Π΅Π²Ρ‹Π΅ ΠΏΠ°Ρ€Π°ΠΌΠ΅Ρ‚Ρ€Ρ‹ Π²Ρ‹Π±ΠΎΡ€Π° стратСгичСских Π°Π»ΡŒΡ‚Π΅Ρ€Π½Π°Ρ‚ΠΈΠ² развития: ΡƒΡ€ΠΎΠ²Π΅Π½ΡŒ интСнсивности лСсопользования (лСсоосвоСния) ΠΈ ΡƒΡ€ΠΎΠ²Π΅Π½ΡŒ лСсовосстановлСния. Ѐиксация Π·Π½Π°Ρ‡Π΅Π½ΠΈΠΉ ΠΏΠΎΠΊΠ°Π·Π°Ρ‚Π΅Π»Π΅ΠΉ ΠΏΠΎ ΠΊΠΎΠ½ΠΊΡ€Π΅Ρ‚Π½Ρ‹ΠΌ Ρ‚Π΅Ρ€Ρ€ΠΈΡ‚ΠΎΡ€ΠΈΠ°Π»ΡŒΠ½Ρ‹ΠΌ Π΅Π΄ΠΈΠ½ΠΈΡ†Π°ΠΌ лСсохозяйствования позволяСт ΠΏΠΎΡΡ‚Ρ€ΠΎΠΈΡ‚ΡŒ ΠΊΠ°Ρ€Ρ‚Ρƒ позиционирования ΠΊΠ°ΠΊ основу для Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ Π΄ΠΎΡ€ΠΎΠΆΠ½Ρ‹Ρ… ΠΊΠ°Ρ€Ρ‚ ΠΈΡ… стратСгичСского развития. ΠŸΡ€Π΅Π΄Π»ΠΎΠΆΠ΅Π½Π½Ρ‹ΠΉ ΠΏΠΎΠ΄Ρ…ΠΎΠ΄ Π°ΠΏΡ€ΠΎΠ±ΠΈΡ€ΠΎΠ²Π°Π½ Π½Π° основС Π΄Π°Π½Π½Ρ‹Ρ… ΠΎ лСсничСствах Π˜Ρ€ΠΊΡƒΡ‚ΡΠΊΠΎΠΉ области министСрства лСсного хозяйства Π˜Ρ€ΠΊΡƒΡ‚ΡΠΊΠΎΠΉ области ΠΈ министСрства ΠΏΡ€ΠΈΡ€ΠΎΠ΄Π½Ρ‹Ρ… рСсурсов ΠΈ экологии Π˜Ρ€ΠΊΡƒΡ‚ΡΠΊΠΎΠΉ области. ΠžΡ‚ΠΌΠ΅Ρ‡Π°Π΅Ρ‚ΡΡ, Ρ‡Ρ‚ΠΎ Π² послСдниС дСсятилСтия лСсноС хозяйство Π˜Ρ€ΠΊΡƒΡ‚ΡΠΊΠΎΠΉ области Π½Π°ΠΏΡ€Π°Π²Π»Π΅Π½ΠΎ Π½Π° ΡƒΠ²Π΅Π»ΠΈΡ‡Π΅Π½ΠΈΠ΅ Ρ‚Π΅ΠΌΠΏΠΎΠ² роста лСсодобычи. ΠŸΡ€ΠΈ этом Π½Π°Π±Π»ΡŽΠ΄Π°ΡŽΡ‚ΡΡ чрСзмСрная ΠΈΠ½Ρ‚Π΅Π½ΡΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΈ Π±Π΅ΡΡΠΈΡΡ‚Π΅ΠΌΠ½ΠΎΡΡ‚ΡŒ Π·Π°Π³ΠΎΡ‚ΠΎΠ²ΠΊΠΈ дрСвСсины ΠΏΡ€ΠΈ нСэффСктивном воспроизводствС ΠΈ Π½ΠΈΠ·ΠΊΠΎΠΉ продуктивности лСсов, усугубляСмыС ΠΌΠ°ΡΡˆΡ‚Π°Π±Π½Ρ‹ΠΌΠΈ ΠΏΠΎΠΆΠ°Ρ€Π°ΠΌΠΈ. ΠšΠ°Ρ€Ρ‚Π° позиционирования Ρ€Π΅Π³ΠΈΠΎΠ½Π°Π»ΡŒΠ½Ρ‹Ρ… лСсничСств наглядно продСмонстрировала, Ρ‡Ρ‚ΠΎ стратСгичСскиС ΠΏΠΎΠ·ΠΈΡ†ΠΈΠΈ Π±ΠΎΠ»Π΅Π΅ ΠΏΠΎΠ»ΠΎΠ²ΠΈΠ½Ρ‹ Ρ‚Π΅Ρ€Ρ€ΠΈΡ‚ΠΎΡ€ΠΈΠ°Π»ΡŒΠ½Ρ‹Ρ… Π΅Π΄ΠΈΠ½ΠΈΡ† лСсопользования Π˜Ρ€ΠΊΡƒΡ‚ΡΠΊΠΎΠΉ области ΡΠ²Π»ΡΡŽΡ‚ΡΡ Π½Π΅ΠΎΠΏΡ‚ΠΈΠΌΠ°Π»ΡŒΠ½Ρ‹ΠΌΠΈ для Ρ€Π΅Π°Π»ΠΈΠ·Π°Ρ†ΠΈΠΈ стратСгии устойчивого развития лСсного хозяйства Ρ€Π΅Π³ΠΈΠΎΠ½Π° Π² Ρ€Π°ΠΌΠΊΠ°Ρ… Π·Π΅Π»Π΅Π½ΠΎΠΉ экономики.In recent decades, the issues of rational use of natural resources and sustainable development of ecosystems (where forests are an important element) became acute. Forest management requires new approaches in order to create a forestry development strategy in accordance with the principles of green economy, including at the regional level. The article presents conceptual provisions of strategic forest management of regions from the perspective of sustainable development. When planning the socio-economic development of a region, it is necessary to consider the revenue and resource potential of its forest management system and strive to achieve a balance between forest exploitation and reforestation. In this connection, the key parameters for choosing strategic alternatives are the intensity of forest use (forest exploitation) and reforestation. After recording the values of indicators for specific forest territorial units, we constructed a positioning map as the basis for strategic development maps. The proposed approach was tested using data on regional forestry retrieved from the Ministry of Forestry of the Irkutsk Region and Ministry of Natural Resources and Environment of the Irkutsk region. Over the past decades, an increase in forest resource extraction in the Irkutsk region was noted. Regional forest development is characterised by excessive intensity and irregularity of timber harvest, as well as by ineffective reproduction and low productivity of forests, aggravated by large-scale fires. The positioning map of regional forestry in the Irkutsk region clearly demonstrates that the forestry development strategy based on the principles of green economy cannot be implemented in more than half of forest territorial units due to their strategic positioning

    Structural diversity of interaction products of mucochloric acid and its derivatives with 1,2-ethanedithiol

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    The synthesis and characterization of previously unknown sulfur-containing products from the reaction of mucochloric acid (3,4-dichloro-5-hydroxy-2(5H)- furanone) and its 5-alkoxy derivatives with 1,2-ethanedithiol is reported. Under basic and acidic conditions both SH-groups of the reagent show nucleophilic activity, leading to the formation of substitution products of different structural types. Novel fused (7-hydroxy-2,3-dihydro[1,4]dithiino[2,3-c]furan- 5(7H)-one) and spiro (9-chloro-6-methoxy-7-oxa-1,4-dithiaspiro[4.4]nonan-8-one) bicyclic compounds, as well as various bis-thioethers have been obtained and characterized by NMR spectroscopy and single crystal X-ray diffraction. Β© 2010 Elsevier Ltd. All rights reserved

    Synthesis of novel arylthio derivatives of mucochloric acid

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    Stable reaction products of mucochloric acid with aromatic and heterocyclic thiols were synthesized and characterized. Under basic conditions the reactions proceeded with the substitution of the chlorine atom(s) by arylthiogroup(s), while in an acidic medium the hydroxy group at C5 was substituted. Different types of new sulfur-containing products of di- and trisubstitution on the basis of mucochloric acid were obtained. In one case a new acyclic product - di-p-tolyl-2,3-bis-(p-tolylthio)butanedithioate - was isolated. The structure of all synthesized compounds was confirmed by IR, 1H, and 13C NMR spectroscopy; three compounds were characterized by single crystal X-ray diffraction. Copyright Β© Taylor & Francis Group, LLC

    ELECTROCATALYTIC PROPERTIES OF PALLADIUM (II) ORGANIC COMPLEXES IN THE NESPHERE ELECTROCHEMICAL OXIDATION OF GLUCOSE

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    The aim of this work was to study the electrocatalytic properties of palladium (II) com-plexes immobilized on the surface of a working electrode in a neutral medium in relation to the electrochemical oxidation of glucose.Π Π°Π±ΠΎΡ‚Π° Π²Ρ‹ΠΏΠΎΠ»Π½Π΅Π½Π° ΠΏΡ€ΠΈ финансовой ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΠ΅ Российского Научного Π€ΠΎΠ½Π΄Π° (ΠΏΡ€ΠΎΠ΅ΠΊΡ‚ β„– 20-13-00142)

    Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid

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    The electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid (3,4-dichloro-5-hydroxyfuran-2(5H)-one) in MeCN-Bu 4NBF4 (0.1 mol L-1) was investigated. It was shown that all sulfides are electrochemically active, from one to five oxidation steps of sulfur-containing groups were observed for them. The ease and direction of oxidation of the thio group depend on its nature and position in the furanone ring. 3-Substituted 2(5H)-furanones possess the lowest oxidation potential. 4-Substituted 2(5H)-furanones are predominantly oxidized to sulfoxides, 5-aryl- and -alkylthio derivatives undergo fragmentation to give mucochloric acid, and 3-arylthio derivative gives complex unidentified mixture of products. In the case of 3,4-bis(4-methylphenylthio) derivative, the oxidation product of the arylthio group at the 3 position to the corresponding sulfoxide was isolated. Based on the data from cyclic voltammetry with different concentrations of a substrate and water added, the results of preparative electrolysis and quantum chemical calculations, possible mechanisms of electrochemical oxidation of mucochloric acid-derived sulfides are discussed. The initial common step is a reversible single-electron transfer from the substrate molecule to form highly reactive radical cation. Β© 2009 Springer Science+Business Media, Inc

    Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid

    No full text
    The electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid (3,4-dichloro-5-hydroxyfuran-2(5H)-one) in MeCN-Bu 4NBF4 (0.1 mol L-1) was investigated. It was shown that all sulfides are electrochemically active, from one to five oxidation steps of sulfur-containing groups were observed for them. The ease and direction of oxidation of the thio group depend on its nature and position in the furanone ring. 3-Substituted 2(5H)-furanones possess the lowest oxidation potential. 4-Substituted 2(5H)-furanones are predominantly oxidized to sulfoxides, 5-aryl- and -alkylthio derivatives undergo fragmentation to give mucochloric acid, and 3-arylthio derivative gives complex unidentified mixture of products. In the case of 3,4-bis(4-methylphenylthio) derivative, the oxidation product of the arylthio group at the 3 position to the corresponding sulfoxide was isolated. Based on the data from cyclic voltammetry with different concentrations of a substrate and water added, the results of preparative electrolysis and quantum chemical calculations, possible mechanisms of electrochemical oxidation of mucochloric acid-derived sulfides are discussed. The initial common step is a reversible single-electron transfer from the substrate molecule to form highly reactive radical cation. Β© 2009 Springer Science+Business Media, Inc

    Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid

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    The electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid (3,4-dichloro-5-hydroxyfuran-2(5H)-one) in MeCN-Bu 4NBF4 (0.1 mol L-1) was investigated. It was shown that all sulfides are electrochemically active, from one to five oxidation steps of sulfur-containing groups were observed for them. The ease and direction of oxidation of the thio group depend on its nature and position in the furanone ring. 3-Substituted 2(5H)-furanones possess the lowest oxidation potential. 4-Substituted 2(5H)-furanones are predominantly oxidized to sulfoxides, 5-aryl- and -alkylthio derivatives undergo fragmentation to give mucochloric acid, and 3-arylthio derivative gives complex unidentified mixture of products. In the case of 3,4-bis(4-methylphenylthio) derivative, the oxidation product of the arylthio group at the 3 position to the corresponding sulfoxide was isolated. Based on the data from cyclic voltammetry with different concentrations of a substrate and water added, the results of preparative electrolysis and quantum chemical calculations, possible mechanisms of electrochemical oxidation of mucochloric acid-derived sulfides are discussed. The initial common step is a reversible single-electron transfer from the substrate molecule to form highly reactive radical cation. Β© 2009 Springer Science+Business Media, Inc

    Endometriosis management prior to IVF

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    Endometriosis affects up to 10% of reproductive-aged women; with higher prevalence among patients suffering from dysmenorrhea, infertility and chronic pelvic pain (CPP). Early detection is the basis of targeting at time therapy. Administration of GnRH-agonists (GnRHa) is limited with its safety and portability. Dienogest administration as the stage of preparation to in vitro fertilization (IVF) may provide the preparative pre-gravid reserve. Fifty-six infertile patients with adenomyosis and previous IVF failures were recruited for prospective cohort study. The treatment followed the unique algorithm created using clinical experience. Post-transfer support was also considered. The aims included evaluation of dienogest effectiveness for different stages of adenomyosis; working out the schemes of dienogest therapy prior to IVF; evaluation of IVF effectiveness after dienogest administration. Patients with adenomyosis grade I-II demonstrated encouraging results: normalisation of menstrual function in 68.6% cases; decreasing of CPP in 74.3% of patients; better uterine vascularisation in 48.6% cases; IVF effectiveness increased up to 48.6%. Thus, in cases of adenomyosis and previous IVF failures dienogest should be administrated prior to IVF, which results in higher IVF effectiveness. Β© 2015 Β© 2015 Taylor & Francis

    2004–2016 Wintertime Atmospheric Blocking Events over Western Siberia and Their Effect on Surface Temperature Anomalies

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    Western Siberia is a large area in Northern Eurasia, which lies between the Urals and the Yenisei River. The atmospheric blocking events are not a frequent phenomenon in this region. Nevertheless, they noticeably affect the weather and living conditions of people there. We have investigated 14 winter blocking events, identified over Western Siberia, over 2004–2016, and have studied their effect on the surface temperature in this region. We have compared each of the 14 blocking events to the corresponding surface temperature anomalies in the north and in the south of Western Siberia. As a result, the temperature anomalies were separated into two groups: (1) dipole, with a positive surface temperature anomaly (or close to the norm) in the north, and with a negative anomaly (or close to the norm) in the south, and (2) non-dipole. Ten events were attributed to Group 1, four events were referred to Group 2. Analyzing the potential temperature on the dynamic tropopause (advection characteristic) showed that the Group 1 events feature strong advection over the investigated territory. In the non-dipole situations from Group 2 Western Siberia are away from strong blocking events
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