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Decavanadate
Sodium decavanadate describes any member of the family of inorganic compounds with the formula Na6 10O28H2O)n. These are sodium salts of the orange-colored decavanadate anion 10O28sup>6−. Numerous other decavanadate salts have been isolated and studied since 1956 when it was first characterized. Preparation The preparation of decavanadate is achieved by acidifying an aqueous solution of ortho-vanadate: :10 Na3 O4 + 24 HOAc → Na6 10O28 + 12 H2O + 24 NaOAc The formation of decavanadate is optimized by maintaining a pH range of 4–7. Typical side products include metavanadate, O3sup>−, and hexavanadate, 6O16sup>2−, ions. Structure The decavanadate ion consists of 10 fused VO6 octahedra and has D2h symmetry. The structure of Na6 10O28·18H2O has been confirmed with X-ray crystallography. The decavanadate anions contains three sets of equivalent V atoms (see fig. 1). These include two central VO6 octahedra (Vc) and four each peripheral tetragonal-pyramidal VO5 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Decavanadate Structure
Sodium decavanadate describes any member of the family of inorganic compounds with the formula Na6[V10O28](H2O)n. These are sodium salts of the orange-colored decavanadate anion [V10O28]6−. Numerous other decavanadate salts have been isolated and studied since 1956 when it was first characterized. Preparation The preparation of decavanadate is achieved by acidifying an aqueous solution of ortho-vanadate: :10 Na3[VO4] + 24 HOAc → Na6[V10O28] + 12 H2O + 24 NaOAc The formation of decavanadate is optimized by maintaining a pH range of 4–7. Typical side products include metavanadate, [VO3]−, and hexavanadate, [V6O16]2−, ions. Structure The decavanadate ion consists of 10 fused VO6 octahedra and has D2h symmetry. The structure of Na6[V10O28]·18H2O has been confirmed with X-ray crystallography. The decavanadate anions contains three sets of equivalent V atoms (see fig. 1). These include two central VO6 octahedra (Vc) and four each peripheral tetragonal-pyramidal ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Vanadate
In chemistry, a vanadate is an anionic coordination complex of vanadium. Often vanadate refers to oxoanions of vanadium, most of which exist in its highest oxidation state of +5. The complexes and are referred to as hexacyanovanadate(III) and nonachlorodivanadate(III), respectively. A simple vanadate ion is the tetrahedral orthovanadate anion, (which is also called vanadate(V)), which is present in e.g. sodium orthovanadate and in solutions of in strong base ( pH > 13). Conventionally this ion is represented with a single double bond, however this is a resonance form as the ion is a regular tetrahedron with four equivalent oxygen atoms. Additionally a range of polyoxovanadate ions exist which include discrete ions and "infinite" polymeric ions. There are also vanadates, such as rhodium vanadate, , which has a statistical rutile structure where the and ions randomly occupy the positions in the rutile lattice, that do not contain a lattice of cations and balancing ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Vanadium
Vanadium is a chemical element with the symbol V and atomic number 23. It is a hard, silvery-grey, malleable transition metal. The elemental metal is rarely found in nature, but once isolated artificially, the formation of an oxide layer ( passivation) somewhat stabilizes the free metal against further oxidation. Spanish scientist Andrés Manuel del RÃo discovered compounds of vanadium in 1801 in Mexico by analyzing a new lead-bearing mineral he called "brown lead". Though he initially presumed its qualities were due to the presence of a new element, he was later erroneously convinced by French chemist Hippolyte Victor Collet-Descotils that the element was just chromium. Then in 1830, Nils Gabriel Sefström generated chlorides of vanadium, thus proving there was a new element, and named it "vanadium" after the Scandinavian goddess of beauty and fertility, VanadÃs (Freyja). The name was based on the wide range of colors found in vanadium compounds. Del Rio's lead mineral was ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Huemulite
Huemulite is a mineral with formula Na4Mg(V10O28)·24H2O that is yellow to orange in color. It was first discovered in Argentina in 1959 and described in 1966. The mineral is named for the Huemul mine in which it was discovered. Occurrence and properties Huemulite is yellowish orange to orange and bright in color. The mineral occurs as thin films, aggregates of fine fibers, botryoidal masses, and interstitial filling in host sandstone. Huemulite has been found in Argentina, the Czech Republic, the United Kingdom, and the United States. It occurs in association with epsomite, gypsum, hummerite, rossite, and thenardite. Huemulite is a member of the pascoite group. It melts at to become a red liquid. Huemulite dissolves readily in cold water to produce an orange-yellow solution with a pH of 5.5 to 6.5.Gordillo, p. 12. Formation and synthesis In Argentina, the mineral formed after mine tunnels were cut through Cu- U deposits in sandstone and conglomerate.Gordillo, p. 3. The va ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Magnesiopascoite
Magnesiopascoite is a bright orange mineral with formula Ca2Mg(V10O28)·16H2O. It was discovered in the U.S. state of Utah and formally described in 2008. The mineral's name derives from its status as the magnesium analogue of pascoite. Description Magnesiopascoite is a member of the pascoite group and is the magnesium analogue of pascoite. It is transparent and bright orange in color, occurring as intergrown, parallel stackings of crystals up to several millimeters in the largest dimension. The crystals vary from tabular to equant to prismatic. The mineral dissolves slowly in water and quickly in cold, dilute hydrochloric acid. It decomposes rapidly when mildly heated, likely as a result of dehydration. Structure and composition The crystal structure of magnesiopascoite consists of the decavanadate anion (V10O28)6− and interstitial 6+ consisting of Mg(H2O)6 octahedra and seven-fold coordinated CaO2(H2O)5. The structure differs from that of pascoite primarily in cation coordina ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pascoite
Pascoite is a mineral with formula Ca3V10O28·17H2O that is red-orange to yellow in color. It was discovered in the Pasco Province of Peru, for which it is named, and described in 1914. Description Crystals of pascoite, which occur in granular crusts, are minute and lath-like with oblique terminations. The mineral is dark red-orange to yellow-orange in color and dirty yellow when partially dehydrated. It occurs as efflorescences in mine tunnels or as a product leached out of surficial vanadium oxides by ground water. Pascoite has been found in association with carnotite. Pascoite melts readily to form a deep red liquid. Pascoite is a member of the eponymous pascoite group. The magnesium analogue of pascoite is magnesiopascoite. Structure A 2005 study determined that pascoite has a C 2/m disordered crystal structure. It consists of decavanadate anions (V10O28)6− linked together by the interstitial complex 6+. Synthesis Pascoite can be easily synthesized by leaching oxides of ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Vanadium-51 Nuclear Magnetic Resonance
Vanadium-51 nuclear magnetic resonance (51V NMR spectroscopy) is a method for the characterization of vanadium-containing compounds and materials. 51V comprises 99.75% of naturally occurring element. The nucleus is quadrupolar with I = 7/2, which is not favorable for NMR spectroscopy. The quadrupole moment is small, thus the linewidths are small. The magnetogyric ratio is relatively high (+7.0492 rad T−1s−1), such that 51V has 38% receptivity vs 1H. Its resonance frequency is close to that of 13C (gyromagnetic ratio = 6.728284 rad T−1s−1). The chemical shift dispersion is great as illustrated by this series: 0 for VOCl3 (chemical shift standard), −309 for VOCl2(O-i-Pr), −506 VOCl(O-i-Pr)2, and −629 VO(O-i-Pr)3. For vanadates, the parent orthovanadate and its conjugate acid absorb at −541 ( O4sup>3-) and 534 ( VO4sup>2-). For decavanadate Sodium decavanadate describes any member of the family of inorganic compounds with the formula Na6 10O28H2O)n. These are ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Inorganic Compound
In chemistry, an inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds, that is, a compound that is not an organic compound. The study of inorganic compounds is a subfield of chemistry known as '' inorganic chemistry''. Inorganic compounds comprise most of the Earth's crust, although the compositions of the deep mantle remain active areas of investigation. Some simple carbon compounds are often considered inorganic. Examples include the allotropes of carbon (graphite, diamond, buckminsterfullerene, etc.), carbon monoxide, carbon dioxide, carbides, and the following salts of inorganic anions: carbonates, cyanides, cyanates, and thiocyanates. Many of these are normal parts of mostly organic systems, including organisms; describing a chemical as inorganic does not necessarily mean that it does not occur within living things. History Friedrich Wöhler's conversion of ammonium cyanate into urea in 1828 is often cited as the starting point of modern ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Glycolysis
Glycolysis is the metabolic pathway that converts glucose () into pyruvate (). The free energy released in this process is used to form the high-energy molecules adenosine triphosphate (ATP) and reduced nicotinamide adenine dinucleotide (NADH). Glycolysis is a sequence of ten reactions catalyzed by enzymes. Glycolysis is a metabolic pathway that does not require oxygen (In anaerobic conditions pyruvate is converted to lactic acid). The wide occurrence of glycolysis in other species indicates that it is an ancient metabolic pathway. Indeed, the reactions that make up glycolysis and its parallel pathway, the pentose phosphate pathway, occur in the oxygen-free conditions of the Archean oceans, also in the absence of enzymes, catalyzed by metal. In most organisms, glycolysis occurs in the liquid part of cells, the cytosol. The most common type of glycolysis is the ''Embden–Meyerhof–Parnas (EMP) pathway'', which was discovered by Gustav Embden, Otto Meyerhof, and Jakub Karol ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Journal Of Inorganic Biochemistry
The ''Journal of Inorganic Biochemistry'' is a monthly peer-reviewed scientific journal covering research on the inorganic aspects of biochemistry, such as metalloenzymes and metallobiomolecules. The journal was established in 1971 as ''Bioinorganic Chemistry'', obtaining its current name in 1979. Since 1996, the editor-in-chief has been John H. Dawson ( University of South Carolina). According to the ''Journal Citation Reports'', the journal has a 2020 impact factor The impact factor (IF) or journal impact factor (JIF) of an academic journal is a scientometric index calculated by Clarivate that reflects the yearly mean number of citations of articles published in the last two years in a given journal, as i ... of 4.155, ranking it 7th out of 44 journals in the category "Chemistry, Inorganic and Nuclear". References External links * Biochemistry journals Elsevier academic journals Monthly journals Publications established in 1971 Inorganic chemistry journals Eng ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Enzyme Inhibitor
An enzyme inhibitor is a molecule that binds to an enzyme and blocks its activity. Enzymes are proteins that speed up chemical reactions necessary for life, in which substrate molecules are converted into products. An enzyme facilitates a specific chemical reaction by binding the substrate to its active site, a specialized area on the enzyme that accelerates the most difficult step of the reaction. An enzyme inhibitor stops ("inhibits") this process, either by binding to the enzyme's active site (thus preventing the substrate itself from binding) or by binding to another site on the enzyme such that the enzyme's catalysis of the reaction is blocked. Enzyme inhibitors may bind reversibly or irreversibly. Irreversible inhibitors form a chemical bond with the enzyme such that the enzyme is inhibited until the chemical bond is broken. By contrast, reversible inhibitors bind non-covalently and may spontaneously leave the enzyme, allowing the enzyme to resume its function. Reve ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Leishmania
''Leishmania'' is a parasitic protozoan, a single-celled organism of the genus '' Leishmania'' that are responsible for the disease leishmaniasis. They are spread by sandflies of the genus ''Phlebotomus'' in the Old World, and of the genus ''Lutzomyia'' in the New World. At least 93 sandfly species are proven or probable vectors worldwide.WHO (2010) Annual report. Geneva Their primary hosts are vertebrates; ''Leishmania'' commonly infects hyraxes, canids, rodents, and humans. History Members of an ancient genus of the ''Leishmania'' parasite, ''Paleoleishmania'', have been detected in fossilized sand flies dating back to the early Cretaceous period. The first written reference to the conspicuous symptoms of cutaneous leishmaniasis surfaced in the Paleotropics within oriental texts dating back to the 7th century BC (allegedly transcribed from sources several hundred years older, between 1500 and 2000 BC). Due to its broad and persistent prevalence throughout antiquity as a mys ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
