Sodium technetate(V)

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Sodium technetate(V)
Sodium technetate(V).png
Names
IUPAC name
Sodium technetate(V)
Other names
Sodium metatechnetate
Identifiers
3D model (JSmol)
  • [Na+].[O-][Tc](=O)=O
Properties
NaTcO3
Molar mass 168.8942 g/mol
Appearanceblack 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. [2]

Contents

Preparation

Sodium technetate(V) can be prepared by co-heating technetium, sodium pertechnetate and sodium oxide, and decomposition occurs at high temperature. [3] In addition, Na299MoO4 decomposed in a NaOH solution will also produce NaTcO3. [4] The NaTcO3 puckering effect resembles NaMoO3 and the band between the egπ and a1g state disappears. [5]

Properties

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]

Related Research Articles

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.

Molybdenum trioxide describes a family of inorganic compounds with the formula MoO3(H2O)n where n = 0, 1, 2. The anhydrous compound is produced on the largest scale of any molybdenum compound since it is the main intermediate produced when molybdenum ores are purified. The anhydrous oxide is a precursor to molybdenum metal, an important alloying agent. It is also an important industrial catalyst. It is a yellow solid, although impure samples can appear blue or green.

<span class="mw-page-title-main">Manganate</span> Chemical compound

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.

<span class="mw-page-title-main">Ozonide</span> Polyatomic ion (O3, charge –1), or cyclic compounds made from ozone and alkenes

Ozonide is the polyatomic anion O−3. Cyclic organic compounds formed by the addition of ozone to an alkene are also called ozonides.

<span class="mw-page-title-main">Uranate</span>

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.

<span class="mw-page-title-main">Technetium hexafluoride</span> Chemical compound

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.

<span class="mw-page-title-main">Potassium nonahydridorhenate</span> Chemical compound

Potassium nonahydridorhenate(VII) is an inorganic compound having the formula K2[ReH9]. This colourless salt is soluble in water but only poorly soluble in most alcohols. This salt contains the nonahydridorhenate(VII) anion, [ReH9]2−, which is a rare example of a coordination complex bearing only hydride ligands.

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.

<span class="mw-page-title-main">Technetium(IV) chloride</span> Chemical compound

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.

<span class="mw-page-title-main">Germanate</span> Chemical compound

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.

In chemistry, molybdenum bronze is a generic name for certain mixed oxides of molybdenum with the generic formula A
x
Mo
y
O
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.

<span class="mw-page-title-main">Sodium hyponitrite</span> Chemical compound

Sodium hyponitrite is a solid ionic compound with formula Na
2
N
2
O
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 canary yellow solid practically insoluble in water and most organic solvents, including DMF and DMSO.

<span class="mw-page-title-main">Yttrium(III) nitrate</span> Chemical compound

Yttrium(III) nitrate is an inorganic compound, a salt with the formula Y(NO3)3. The hexahydrate is the most common form commercially available.

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.

<span class="mw-page-title-main">Terbium compounds</span> Chemical compounds with at least one terbium atom

Terbium compounds are compounds formed by the lanthanide metal terbium (Tb). Terbium generally exhibits the +3 oxidation state in these compounds, such as in TbCl3, Tb(NO3)3 and Tb(CH3COO)3. Compounds with terbium in the +4 oxidation state are also known, such as TbO2 and BaTbF6. Terbium can also form compounds in the 0, +1 and +2 oxidation states.

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.

References

  1. 1 2 3 Keller, C.; Kanellakopulos, B. (1965-04-01). "Ternäre oxide des drei-bis siebenwertigen technetiums mit alkalien". Journal of Inorganic and Nuclear Chemistry (in German). 27 (4): 787–795. doi:10.1016/0022-1902(65)80438-9. ISSN   0022-1902.
  2. Sabine Körbel, Miguel A. L. Marques, Silvana Botti (25 February 2016). "Stability and electronic properties of new inorganic perovskites from high-throughput ab initio calculations". Journal of Materials Chemistry C. 4 (15): 3157–3167. doi:10.1039/C5TC04172D. ISSN   2050-7526 . Retrieved 3 May 2023.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. 无机化学丛书. 第九卷 锰分族 铁系 铂系, pg. 122. 3.11 氧化数为V的锝和铼化合物.
  4. M. Fis̆er, V. Brabec, O. Dragoun, A. Kovalík, J. Frána, M. Rys̆avý (1985). "Determination of 99mTc valent form in solids by measurement of internal conversion electrons". The International Journal of Applied Radiation and Isotopes. 36 (3): 219–222. doi:10.1016/0020-708X(85)90071-7. Archived from the original on 2018-07-02. Retrieved 3 May 2023.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. M. H. N. Assadi, Masashi Okubo, Atsuo Yamada, Yoshitaka Tateyama (8 February 2018). "Oxygen redox in hexagonal layered NaxTMO3 (TM = 4d elements) for high capacity Na ion batteries". Journal of Materials Chemistry A. 6 (8): 3747–3753. doi:10.1039/C7TA10826E. ISSN   2050-7488 . Retrieved 3 May 2023.{{cite journal}}: CS1 maint: multiple names: authors list (link)

External reading