Names | |
---|---|
IUPAC name Sodium technetate(V) | |
Other names Sodium metatechnetate | |
Identifiers | |
3D model (JSmol) | |
| |
Properties | |
NaTcO3 | |
Molar mass | 168.8942 g/mol |
Appearance | black solid [1] |
Melting point | 800 °C (1,470 °F; 1,070 K) (decomposes) [1] |
insoluble | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | toxic, radioactive |
Related compounds | |
Other anions | Sodium pertechnetate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Sodium technetate(V) is an inorganic compound with the chemical formula NaTcO3. It is a perovskite material and a rare example of an insoluble sodium salt. [2]
Sodium technetate(V) can be prepared by co-heating technetium, sodium pertechnetate and sodium oxide, and decomposition occurs at high temperature. [3] In addition, Na99
2MoO4 decomposed in a NaOH solution will also produce NaTcO3. [4] The NaTcO3 puckering effect resembles NaMoO3 and the band between the eπ
g and a1g state disappears. [5]
NaTcO3 is a black solid that is a member of the Na2O–Tc2O5 system. It is stable to 800 °C (1,470 °F; 1,070 K). [1]
In chemistry, azide is a linear, polyatomic anion with the formula N−3 and structure −N=N+=N−. It is the conjugate base of hydrazoic acid HN3. Organic azides are organic compounds with the formula RN3, containing the azide functional group. The dominant application of azides is as a propellant in air bags.
Group 7, numbered by IUPAC nomenclature, is a group of elements in the periodic table. It contains manganese (Mn), technetium (Tc), rhenium (Re) and bohrium (Bh). This group lies in the d-block of the periodic table, and are hence transition metals. This group is sometimes called the manganese group or manganese family after its lightest member; however, the group itself has not acquired a trivial name because it belongs to the broader grouping of the transition metals.
Praseodymium(III) chloride is the inorganic compound with the formula PrCl3. Like other lanthanide trichlorides, it exists both in the anhydrous and hydrated forms. It is a blue-green solid that rapidly absorbs water on exposure to moist air to form a light green heptahydrate.
In inorganic nomenclature, a manganate is any negatively charged molecular entity with manganese as the central atom. However, the name is usually used to refer to the tetraoxidomanganate(2−) anion, MnO2−
4, also known as manganate(VI) because it contains manganese in the +6 oxidation state. Manganates are the only known manganese(VI) compounds.
In chemistry, an aluminate is a compound containing an oxyanion of aluminium, such as sodium aluminate. In the naming of inorganic compounds, it is a suffix that indicates a polyatomic anion with a central aluminium atom.
A uranate is a ternary oxide involving the element uranium in one of the oxidation states 4, 5 or 6. A typical chemical formula is MxUyOz, where M represents a cation. The uranium atom in uranates(VI) has two short collinear U–O bonds and either four or six more next nearest oxygen atoms. The structures are infinite lattice structures with the uranium atoms linked by bridging oxygen atoms.
Technetium hexafluoride or technetium(VI) fluoride (TcF6) is a yellow inorganic compound with a low melting point. It was first identified in 1961. In this compound, technetium has an oxidation state of +6, the highest oxidation state found in the technetium halides. In this respect, technetium differs from rhenium, which forms a heptafluoride, ReF7. Technetium hexafluoride occurs as an impurity in uranium hexafluoride, as technetium is a fission product of uranium (spontaneous fission in natural uranium, possible contamination from induced fission inside the reactor in reprocessed uranium). The fact that the boiling point of the hexafluorides of uranium and technetium are very close to each other presents a problem in using fluoride volatility in nuclear reprocessing.
Technetium compounds are chemical compounds containing the chemical element technetium. Technetium can form multiple oxidation states, but often forms in the +4 and +7 oxidation states. Because technetium is radioactive, technetium compounds are extremely rare on Earth.
Pertechnetic acid (HTcO4) is a compound of technetium that is produced by reacting technetium(VII) oxide (Tc2O7) with water or reacting Tc metal or TcO2 with strong oxidizing acids, such as nitric acid, mixture of concentrated sulfuric acid with hydrogen peroxide or aqua regia. The dark red hygroscopic substance is a strong acid, with a pKa of 0.32, as such it exists almost entirely as the pertechnetate ion in aqueous solution. The red color in solution is thought to be due to the formation of the polyoxometallate Tc20O4−68, while fresh HTcO4 is white.
The perrhenate ion is the anion with the formula ReO−
4, or a compound containing this ion. The perrhenate anion is tetrahedral, being similar in size and shape to perchlorate and the valence isoelectronic permanganate. The perrhenate anion is stable over a broad pH range and can be precipitated from solutions with the use of organic cations. At normal pH, perrhenate exists as metaperrhenate, but at high pH mesoperrhenate forms. Perrhenate, like its conjugate acid perrhenic acid, features rhenium in the oxidation state of +7 with a d0 configuration. Solid perrhenate salts takes on the color of the cation.
Technetium(IV) chloride is the inorganic compound with the formula TcCl4. It was discovered in 1957 as the first binary halide of technetium. It is the highest oxidation binary chloride of technetium that has been isolated as a solid. It is volatile at elevated temperatures and its volatility has been used for separating technetium from other metal chlorides. Colloidal solutions of technetium(IV) chloride are oxidized to form Tc(VII) ions when exposed to gamma rays.
In chemistry, germanate is a compound containing an oxyanion of germanium. In the naming of inorganic compounds it is a suffix that indicates a polyatomic anion with a central germanium atom, for example potassium hexafluorogermanate, K2GeF6.
Sodium bismuthate is an inorganic compound, and a strong oxidiser with chemical formula NaBiO3. It is somewhat hygroscopic, but not soluble in cold water, which can be convenient since the reagent can be easily removed after the reaction. It is one of the few water insoluble sodium salts. Commercial samples may be a mixture of bismuth(V) oxide, sodium carbonate and sodium peroxide.
In chemistry, molybdenum bronze is a generic name for certain mixed oxides of molybdenum with the generic formula A
xMo
yO
z where A may be hydrogen, an alkali metal cation (such as Li+, Na+, K+), and Tl+. These compounds form deeply coloured plate-like crystals with a metallic sheen, hence their name. These bronzes derive their metallic character from partially occupied 4d bands. The oxidation states in K0.28MoO3 are K+1, O2−, and Mo+5.72. MoO3 is an insulator, with an unfilled 4d band.
Sodium hyponitrite is a solid ionic compound with formula Na
2N
2O
2 or (Na+
)2[ON=NO]2−.
Silver hyponitrite is an ionic compound with formula Ag2N2O2 or (Ag+
)2[ON=NO]2−, containing monovalent silver cations and hyponitrite anions. It is a bright yellow solid practically insoluble in water and most organic solvents, including DMF and DMSO.
Nitride fluorides containing nitride and fluoride ions with the formula NF4-. They can be electronically equivalent to a pair of oxide ions O24-. Nitride fluorides were discovered in 1996 by Lavalle et al. They heated diammonium technetium hexafluoride to 300 °C to yield TcNF. Another preparation is to heat a fluoride compound with a nitride compound in a solid state reaction. The fluorimido ion is F-N2- and is found in a rhenium compound.
Rhenium compounds are compounds formed by the transition metal rhenium (Re). Rhenium can form in many oxidation states, and compounds are known for every oxidation state from -3 to +7 except -2, although the oxidation states +7, +4, and +3 are the most common. Rhenium is most available commercially as salts of perrhenate, including sodium and ammonium perrhenates. These are white, water-soluble compounds. The tetrathioperrhenate anion [ReS4]− is possible.
Protactinium compounds are compounds containing the element protactinium. These compounds usually have protactinium in the +5 oxidation state, although these compounds can also exist in the +2, +3 and +4 oxidation states.
{{cite journal}}
: CS1 maint: multiple names: authors list (link){{cite journal}}
: CS1 maint: multiple names: authors list (link){{cite journal}}
: CS1 maint: multiple names: authors list (link)