47 research outputs found
Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid
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.
Π ΠΏΠΎΡΠ»Π΅Π΄Π½ΠΈΠ΅ Π΄Π΅ΡΡΡΠΈΠ»Π΅ΡΠΈΡ ΠΎΠ±ΠΎΡΡΡΠΈΠ»ΠΈΡΡ ΠΏΡΠΎΠ±Π»Π΅ΠΌΡ ΠΏΠΎΠΈΡΠΊΠ° Π½Π°ΠΏΡΠ°Π²Π»Π΅Π½ΠΈΠΉ ΡΠ°ΡΠΈΠΎΠ½Π°Π»ΡΠ½ΠΎΠ³ΠΎ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ ΠΏΡΠΈΡΠΎΠ΄Π½ΡΡ
ΡΠ΅ΡΡΡΡΠΎΠ², ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΠ³ΠΎ ΡΠ°Π·Π²ΠΈΡΠΈΡ ΡΠΊΠΎΡΠΈΡΡΠ΅ΠΌ, ΠΎΠ΄Π½ΠΈΠΌ ΠΈΠ· Π±Π°Π·ΠΎΠ²ΡΡ
ΡΠ»Π΅ΠΌΠ΅Π½ΡΠΎΠ² ΠΊΠΎΡΠΎΡΡΡ
ΠΎΡΡΠ°ΡΡΡΡ Π»Π΅ΡΠ°. ΠΡΠΎΠ±Π»Π΅ΠΌΡ ΡΠ°Π·Π²ΠΈΡΠΈΡ Π»Π΅ΡΠ½ΠΎΠ³ΠΎ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²Π° Π΄ΠΈΠΊΡΡΡΡ Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎΡΡΡ ΡΠ°Π·ΡΠ°Π±ΠΎΡΠΊΠΈ Π½ΠΎΠ²ΡΡ
ΠΏΠΎΠ΄Ρ
ΠΎΠ΄ΠΎΠ² ΠΊ ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΡΡΡΠ°ΡΠ΅Π³ΠΈΠΈ ΡΠ°Π·Π²ΠΈΡΠΈΡ Π»Π΅ΡΠ½ΠΎΠ³ΠΎ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²Π° Π² ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΠΈΠΈ Ρ ΠΏΡΠΈΠ½ΡΠΈΠΏΠ°ΠΌΠΈ Π·Π΅Π»Π΅Π½ΠΎΠΉ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠΈ, Π² ΡΠΎΠΌ ΡΠΈΡΠ»Π΅ Π½Π° ΡΡΠΎΠ²Π½Π΅ ΠΎΡΠ΄Π΅Π»ΡΠ½ΡΡ
ΡΠ΅Π³ΠΈΠΎΠ½ΠΎΠ². Π Π½Π°ΡΡΠΎΡΡΠ΅ΠΉ ΡΡΠ°ΡΡΠ΅ ΠΏΡΠ΅Π΄ΡΡΠ°Π²Π»Π΅Π½Ρ ΡΠ°Π·ΡΠ°Π±ΠΎΡΠ°Π½Π½ΡΠ΅ Π°Π²ΡΠΎΡΠ°ΠΌΠΈ ΠΎΡΠ½ΠΎΠ²Π½ΡΠ΅ ΠΏΠΎΠ»ΠΎΠΆΠ΅Π½ΠΈΡ ΠΊΠΎΠ½ΡΠ΅ΠΏΡΠΈΠΈ ΡΡΡΠ°ΡΠ΅Π³ΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ Π»Π΅ΡΠ½ΡΠΌ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²ΠΎΠΌ ΡΠ΅Π³ΠΈΠΎΠ½Π° Ρ ΠΏΠΎΠ·ΠΈΡΠΈΠΈ ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΠ³ΠΎ ΡΠ°Π·Π²ΠΈΡΠΈΡ, ΠΊΠ»ΡΡΠ΅Π²ΡΠΌΠΈ ΠΈΠ· ΠΊΠΎΡΠΎΡΡΡ
ΡΠ²Π»ΡΡΡΡΡ ΡΡΠ΅Ρ Π΄ΠΎΡ
ΠΎΠ΄Π½ΠΎ-ΡΠ΅ΡΡΡΡΠ½ΠΎΠ³ΠΎ ΠΏΠΎΡΠ΅Π½ΡΠΈΠ°Π»Π° ΡΠΈΡΡΠ΅ΠΌΡ Π»Π΅ΡΠΎΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ ΡΠ΅Π³ΠΈΠΎΠ½Π° ΠΏΡΠΈ ΠΏΠ»Π°Π½ΠΈΡΠΎΠ²Π°Π½ΠΈΠΈ Π΅Π³ΠΎ ΡΠΎΡΠΈΠ°Π»ΡΠ½ΠΎ-ΡΠΊΠΎΠ½ΠΎΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΡΠ°Π·Π²ΠΈΡΠΈΡ ΠΈ Π΄ΠΎΡΡΠΈΠΆΠ΅Π½ΠΈΠ΅ Π±Π°Π»Π°Π½ΡΠ° ΠΌΠ΅ΠΆΠ΄Ρ Π»Π΅ΡΠΎΠΎΡΠ²ΠΎΠ΅Π½ΠΈΠ΅ΠΌ ΠΈ Π»Π΅ΡΠΎΠ²ΠΎΡΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½ΠΈΠ΅ΠΌ. Π ΡΠ²ΡΠ·ΠΈ Ρ ΡΠ΅ΠΌ ΡΡΠΎΡΠΌΡΠ»ΠΈΡΠΎΠ²Π°Π½Ρ ΠΊΠ»ΡΡΠ΅Π²ΡΠ΅ ΠΏΠ°ΡΠ°ΠΌΠ΅ΡΡΡ Π²ΡΠ±ΠΎΡΠ° ΡΡΡΠ°ΡΠ΅Π³ΠΈΡΠ΅ΡΠΊΠΈΡ
Π°Π»ΡΡΠ΅ΡΠ½Π°ΡΠΈΠ² ΡΠ°Π·Π²ΠΈΡΠΈΡ: ΡΡΠΎΠ²Π΅Π½Ρ ΠΈΠ½ΡΠ΅Π½ΡΠΈΠ²Π½ΠΎΡΡΠΈ Π»Π΅ΡΠΎΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ (Π»Π΅ΡΠΎΠΎΡΠ²ΠΎΠ΅Π½ΠΈΡ) ΠΈ ΡΡΠΎΠ²Π΅Π½Ρ Π»Π΅ΡΠΎΠ²ΠΎΡΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½ΠΈΡ. Π€ΠΈΠΊΡΠ°ΡΠΈΡ Π·Π½Π°ΡΠ΅Π½ΠΈΠΉ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»Π΅ΠΉ ΠΏΠΎ ΠΊΠΎΠ½ΠΊΡΠ΅ΡΠ½ΡΠΌ ΡΠ΅ΡΡΠΈΡΠΎΡΠΈΠ°Π»ΡΠ½ΡΠΌ Π΅Π΄ΠΈΠ½ΠΈΡΠ°ΠΌ Π»Π΅ΡΠΎΡ
ΠΎΠ·ΡΠΉΡΡΠ²ΠΎΠ²Π°Π½ΠΈΡ ΠΏΠΎΠ·Π²ΠΎΠ»ΡΠ΅Ρ ΠΏΠΎΡΡΡΠΎΠΈΡΡ ΠΊΠ°ΡΡΡ ΠΏΠΎΠ·ΠΈΡΠΈΠΎΠ½ΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΠΊΠ°ΠΊ ΠΎΡΠ½ΠΎΠ²Ρ Π΄Π»Ρ ΡΠ°Π·ΡΠ°Π±ΠΎΡΠΊΠΈ Π΄ΠΎΡΠΎΠΆΠ½ΡΡ
ΠΊΠ°ΡΡ ΠΈΡ
ΡΡΡΠ°ΡΠ΅Π³ΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΡΠ°Π·Π²ΠΈΡΠΈΡ. ΠΡΠ΅Π΄Π»ΠΎΠΆΠ΅Π½Π½ΡΠΉ ΠΏΠΎΠ΄Ρ
ΠΎΠ΄ Π°ΠΏΡΠΎΠ±ΠΈΡΠΎΠ²Π°Π½ Π½Π° ΠΎΡΠ½ΠΎΠ²Π΅ Π΄Π°Π½Π½ΡΡ
ΠΎ Π»Π΅ΡΠ½ΠΈΡΠ΅ΡΡΠ²Π°Ρ
ΠΡΠΊΡΡΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ ΠΌΠΈΠ½ΠΈΡΡΠ΅ΡΡΡΠ²Π° Π»Π΅ΡΠ½ΠΎΠ³ΠΎ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²Π° ΠΡΠΊΡΡΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ ΠΈ ΠΌΠΈΠ½ΠΈΡΡΠ΅ΡΡΡΠ²Π° ΠΏΡΠΈΡΠΎΠ΄Π½ΡΡ
ΡΠ΅ΡΡΡΡΠΎΠ² ΠΈ ΡΠΊΠΎΠ»ΠΎΠ³ΠΈΠΈ ΠΡΠΊΡΡΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ. ΠΡΠΌΠ΅ΡΠ°Π΅ΡΡΡ, ΡΡΠΎ Π² ΠΏΠΎΡΠ»Π΅Π΄Π½ΠΈΠ΅ Π΄Π΅ΡΡΡΠΈΠ»Π΅ΡΠΈΡ Π»Π΅ΡΠ½ΠΎΠ΅ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²ΠΎ ΠΡΠΊΡΡΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ Π½Π°ΠΏΡΠ°Π²Π»Π΅Π½ΠΎ Π½Π° ΡΠ²Π΅Π»ΠΈΡΠ΅Π½ΠΈΠ΅ ΡΠ΅ΠΌΠΏΠΎΠ² ΡΠΎΡΡΠ° Π»Π΅ΡΠΎΠ΄ΠΎΠ±ΡΡΠΈ. ΠΡΠΈ ΡΡΠΎΠΌ Π½Π°Π±Π»ΡΠ΄Π°ΡΡΡΡ ΡΡΠ΅Π·ΠΌΠ΅ΡΠ½Π°Ρ ΠΈΠ½ΡΠ΅Π½ΡΠΈΠ²Π½ΠΎΡΡΡ ΠΈ Π±Π΅ΡΡΠΈΡΡΠ΅ΠΌΠ½ΠΎΡΡΡ Π·Π°Π³ΠΎΡΠΎΠ²ΠΊΠΈ Π΄ΡΠ΅Π²Π΅ΡΠΈΠ½Ρ ΠΏΡΠΈ Π½Π΅ΡΡΡΠ΅ΠΊΡΠΈΠ²Π½ΠΎΠΌ Π²ΠΎΡΠΏΡΠΎΠΈΠ·Π²ΠΎΠ΄ΡΡΠ²Π΅ ΠΈ Π½ΠΈΠ·ΠΊΠΎΠΉ ΠΏΡΠΎΠ΄ΡΠΊΡΠΈΠ²Π½ΠΎΡΡΠΈ Π»Π΅ΡΠΎΠ², ΡΡΡΠ³ΡΠ±Π»ΡΠ΅ΠΌΡΠ΅ ΠΌΠ°ΡΡΡΠ°Π±Π½ΡΠΌΠΈ ΠΏΠΎΠΆΠ°ΡΠ°ΠΌΠΈ. ΠΠ°ΡΡΠ° ΠΏΠΎΠ·ΠΈΡΠΈΠΎΠ½ΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΡΠ΅Π³ΠΈΠΎΠ½Π°Π»ΡΠ½ΡΡ
Π»Π΅ΡΠ½ΠΈΡΠ΅ΡΡΠ² Π½Π°Π³Π»ΡΠ΄Π½ΠΎ ΠΏΡΠΎΠ΄Π΅ΠΌΠΎΠ½ΡΡΡΠΈΡΠΎΠ²Π°Π»Π°, ΡΡΠΎ ΡΡΡΠ°ΡΠ΅Π³ΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΏΠΎΠ·ΠΈΡΠΈΠΈ Π±ΠΎΠ»Π΅Π΅ ΠΏΠΎΠ»ΠΎΠ²ΠΈΠ½Ρ ΡΠ΅ΡΡΠΈΡΠΎΡΠΈΠ°Π»ΡΠ½ΡΡ
Π΅Π΄ΠΈΠ½ΠΈΡ Π»Π΅ΡΠΎΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ ΠΡΠΊΡΡΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ ΡΠ²Π»ΡΡΡΡΡ Π½Π΅ΠΎΠΏΡΠΈΠΌΠ°Π»ΡΠ½ΡΠΌΠΈ Π΄Π»Ρ ΡΠ΅Π°Π»ΠΈΠ·Π°ΡΠΈΠΈ ΡΡΡΠ°ΡΠ΅Π³ΠΈΠΈ ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΠ³ΠΎ ΡΠ°Π·Π²ΠΈΡΠΈΡ Π»Π΅ΡΠ½ΠΎΠ³ΠΎ Ρ
ΠΎΠ·ΡΠΉΡΡΠ²Π° ΡΠ΅Π³ΠΈΠΎΠ½Π° Π² ΡΠ°ΠΌΠΊΠ°Ρ
Π·Π΅Π»Π΅Π½ΠΎΠΉ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠΈ.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
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
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
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±ΠΎΡΠ° Π²ΡΠΏΠΎΠ»Π½Π΅Π½Π° ΠΏΡΠΈ ΡΠΈΠ½Π°Π½ΡΠΎΠ²ΠΎΠΉ ΠΏΠΎΠ΄Π΄Π΅ΡΠΆΠΊΠ΅ Π ΠΎΡΡΠΈΠΉΡΠΊΠΎΠ³ΠΎ ΠΠ°ΡΡΠ½ΠΎΠ³ΠΎ Π€ΠΎΠ½Π΄Π° (ΠΏΡΠΎΠ΅ΠΊΡ β 20-13-00142)
Electron transfer and subsequent reactions during electrochemical oxidation of aryl- and alkylthio derivatives of mucochloric acid
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
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
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
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
2004β2016 Wintertime Atmospheric Blocking Events over Western Siberia and Their Effect on Surface Temperature Anomalies
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 2004β2016, 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