Protactinium(IV) chloride

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Protactinium(IV) chloride
Kristallstruktur Uran(IV)-chlorid.png
Names
IUPAC name
Protactinium(IV) chloride
Identifiers
3D model (JSmol)
  • InChI=1S/4ClH.Pa/h4*1H;/q;;;;+4/p-4
    Key: YVRMMEYNJWFJEX-UHFFFAOYSA-J
  • [Pa](Cl)(Cl)(Cl)Cl
Properties
PaCl4
Molar mass 372.848 g mol−1
Appearance chartreuse
Density 4.72 g/cm3
Structure
tetragonal [1] ,tI20
I41/amd , No. 141
Related compounds
Other anions
Protactinium(IV) fluoride
Protactinium(IV) bromide
Protactinium(IV) iodide
Other cations
Uranium(IV) chloride
Thorium(IV) chloride
Praseodymium(III) chloride
Related compounds
Protactinium(V) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Protactinium(IV) chloride is an inorganic compound. It is an actinide halide, a salt composed of protactinium and chlorine. It is radioactive, and has the chemical formula of PaCl4. It is a chartreuse-coloured (yellowish-green) crystal [1] of the tetragonal crystal system.

Contents

Preparation

Protactinium(IV) chloride can be prepared by the reduction of protactinium(V) chloride: [2]

It can also be obtained by the chlorination of protactinium(IV) oxide: [2]

It can also be formed during the thermal decomposition of protactinium oxychloride at 500 °C in a vacuum: [3]

Properties

Protactinium(IV) chloride is a chartreuse, hygroscopic, crystalline solid that can be sublimed at 400 °C in a vacuum. It is soluble in strong mineral acids, forming green solutions. The complex PaCl4·4CH3CN is formed with acetonitrile. It has a tetragonal crystal structure with the space group I41/amd (space group no. 141) and the lattice parameters a = 837.7 pm, c = 747.9 pm [2] of the uranium(IV) chloride type. [4]

Related Research Articles

<span class="mw-page-title-main">Protactinium</span> Chemical element, symbol Pa and atomic number 91

Protactinium is a chemical element; it has symbol Pa and atomic number 91. It is a dense, radioactive, silvery-gray actinide metal which readily reacts with oxygen, water vapor, and inorganic acids. It forms various chemical compounds, in which protactinium is usually present in the oxidation state +5, but it can also assume +4 and even +3 or +2 states. Concentrations of protactinium in the Earth's crust are typically a few parts per trillion, but may reach up to a few parts per million in some uraninite ore deposits. Because of its scarcity, high radioactivity, and high toxicity, there are currently no uses for protactinium outside scientific research, and for this purpose, protactinium is mostly extracted from spent nuclear fuel.

<span class="mw-page-title-main">Silane</span> Chemical compound (SiH4)

Silane (Silicane) is an inorganic compound with chemical formula SiH4. It is a colourless, pyrophoric, toxic gas with a sharp, repulsive, pungent smell, somewhat similar to that of acetic acid. Silane is of practical interest as a precursor to elemental silicon. Silane with alkyl groups are effective water repellents for mineral surfaces such as concrete and masonry. Silanes with both organic and inorganic attachments are used as coupling agents. They are commonly used to apply coatings to surfaces or as an adhesion promoter.

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).

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

Thorium(IV) chloride describes a family of inorganic compounds with the formula ThCl4(H2O)n. Both the anhydrous and tetrahydrate (n = 4) forms are known. They are hygroscopic, water-soluble white salts.

<span class="mw-page-title-main">Organoactinide chemistry</span> Study of chemical compounds containing actinide-carbon bonds

Organoactinide chemistry is the science exploring the properties, structure, and reactivity of organoactinide compounds, which are organometallic compounds containing a carbon to actinide chemical bond.

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

Niobium(IV) chloride, also known as niobium tetrachloride, is the chemical compound of formula NbCl4. This compound exists as dark violet crystals, is highly sensitive to air and moisture, and disproportiates into niobium(III) chloride and niobium(V) chloride when heated.

<span class="mw-page-title-main">Berkelium compounds</span> Chemical compounds

Berkelium forms a number of chemical compounds, where it normally exists in an oxidation state of +3 or +4, and behaves similarly to its lanthanide analogue, terbium. Like all actinides, berkelium easily dissolves in various aqueous inorganic acids, liberating gaseous hydrogen and converting into the trivalent oxidation state. This trivalent state is the most stable, especially in aqueous solutions, but tetravalent berkelium compounds are also known. The existence of divalent berkelium salts is uncertain and has only been reported in mixed lanthanum chloride-strontium chloride melts. Aqueous solutions of Bk3+ ions are green in most acids. The color of the Bk4+ ions is yellow in hydrochloric acid and orange-yellow in sulfuric acid. Berkelium does not react rapidly with oxygen at room temperature, possibly due to the formation of a protective oxide surface layer; however, it reacts with molten metals, hydrogen, halogens, chalcogens and pnictogens to form various binary compounds. Berkelium can also form several organometallic compounds.

<span class="mw-page-title-main">Thorium compounds</span> Chemical compounds

Many compounds of thorium are known: this is because thorium and uranium are the most stable and accessible actinides and are the only actinides that can be studied safely and legally in bulk in a normal laboratory. As such, they have the best-known chemistry of the actinides, along with that of plutonium, as the self-heating and radiation from them is not enough to cause radiolysis of chemical bonds as it is for the other actinides. While the later actinides from americium onwards are predominantly trivalent and behave more similarly to the corresponding lanthanides, as one would expect from periodic trends, the early actinides up to plutonium have relativistically destabilised and hence delocalised 5f and 6d electrons that participate in chemistry in a similar way to the early transition metals of group 3 through 8: thus, all their valence electrons can participate in chemical reactions, although this is not common for neptunium and plutonium.

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

Rhenium(IV) chloride is the inorganic compound with the formula ReCl4. This black solid is of interest as a binary phase but otherwise is of little practical value. A second polymorph of ReCl4 is also known.

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

Neptunium(III) chloride or neptunium trichloride is an inorganic compound with a chemical formula NpCl3. This salt is strongly radioactive.

Curium compounds are compounds containing the element curium (Cm). Curium usually forms compounds in the +3 oxidation state, although compounds with curium in the +4, +5 and +6 oxidation states are also known.

Protactinium(V) bromide is an inorganic compound. It is a halide of protactinium, consisting of protactinium and bromine. It is radioactive and has a chemical formula of PaBr5, which is a red crystal of the monoclinic crystal system.

<span class="mw-page-title-main">Protactinium(V) fluoride</span> Chemical compound

Protactinium(V) fluoride is a fluoride of protactinium with the chemical formula PaF5.

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

Protactinium(IV) bromide is an inorganic compound. It is an actinide halide, composed of protactinium and bromine. It is radioactive, and has the chemical formula of PaBr4. It may be due to the brown color of bromine that causes the appearance of protactinium(IV) bromide to be brown crystals. Its crystal structure is tetragonal. Protactinium(IV) bromide is sublimed in a vacuum at 400 °C. The protactinium(IV) halide closest in structure to protactinium(IV) bromide is protactinium(IV) chloride.

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.

Americium compounds are compounds containing the element americium (Am). These compounds can form in the +2, +3, and +4, although the +3 oxidation state is the most common. The +5, +6 and +7 oxidation states have also been reported.

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

Neptunium tetrachloride is a binary inorganic compound of neptunium metal and chlorine with the chemical formula NpCl4.

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

Protactinium tetrafluoride is a binary inorganic compound of protactinium metal and fluorine with the chemical formula PaF4.

Protactinium tetraiodide is a binary inorganic compound of protactinium metal and iodine with the chemical formula PaI4.

References

  1. 1 2 Brown D., Hall T.L., Moseley P.T (1973). "Structural parameters and unit cell dimensions for the tetragonal actinide tetrachlorides(Th, Pa, U, and Np) and tetrabromides (Th and Pa)". J. Chem. Soc., Dalton Trans. (6): 686–691. doi:10.1039/DT9730000686.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. 1 2 3 Georg Brauer (Hrsg.), unter Mitarbeit von Marianne Baudler u. a.: Handbuch der Präparativen Anorganischen Chemie. 3., umgearbeitete Auflage. Band I, Ferdinand Enke, Stuttgart 1975, ISBN   3-432-02328-6, pp. 1176.
  3. Harry Julius Emeleus, A. G. Sharpe (1970), ADVANCES IN INORGANIC CHEMISTRY AND RADIOCHEMISTRY (in German), Academic Press, p. 15, ISBN   978-0-08057861-3
  4. Lester R. Morss, Norman M. Edelstein, J. Fuger (Hrsg.): . Bände 1-6. Springer, Dordrecht 2010, ISBN   978-94-007-0211-0, S. 201 (English, in Google Books).