Rubidium chloride

Last updated
Rubidium chloride
Rubidium-chloride-3D-ionic.png
Rubidium-chloride-CsCl-structure-3D-ionic.png
Names
Other names
rubidium(I) chloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.029.310 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
RTECS number
  • VL8575000
UNII
  • InChI=1S/ClH.Rb/h1H;/q;+1/p-1 Yes check.svgY
    Key: FGDZQCVHDSGLHJ-UHFFFAOYSA-M Yes check.svgY
  • InChI=1/ClH.Rb/h1H;/q;+1/p-1
  • [Rb+].[Cl-]
Properties
RbCl
Molar mass 120.921 g/mol
Appearancewhite crystals
hygroscopic
Density 2.80 g/cm3 (25 °C)
2.088 g/mL (750 °C)
Melting point 718 °C (1,324 °F; 991 K)
Boiling point 1,390 °C (2,530 °F; 1,660 K)
77 g/100mL (0 °C)
91 g/100 mL (20 °C)
130 g/100 mL (100 °C)
Solubility in methanol 1.41 g/100 mL
46.0·10−6 cm3/mol
1.5322
Thermochemistry
52.4 JK1mol1
Std molar
entropy
(S298)
95.9 JK1mol1
435.14 kJ/mol
Hazards
NFPA 704 (fire diamond)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
4440 mg/kg (rat)
Safety data sheet (SDS) Fisher Scientific
Related compounds
Other anions
Rubidium fluoride
Rubidium bromide
Rubidium iodide
Rubidium astatide
Other cations
Lithium chloride
Sodium chloride
Potassium chloride
Caesium chloride
Francium chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Rubidium chloride is the chemical compound with the formula RbCl. This alkali metal halide salt is composed of rubidium and chlorine, and finds diverse uses ranging from electrochemistry to molecular biology.

Contents

Structure

In its gas phase, RbCl is diatomic with a bond length estimated at 2.7868 Å. [1] This distance increases to 3.285 Å for cubic RbCl, reflecting the higher coordination number of the ions in the solid phase. [2]

Depending on conditions, solid RbCl exists in one of three arrangements or polymorphs as determined with holographic imaging: [3]

Sodium chloride (octahedral 6:6)

The sodium chloride (NaCl) polymorph is most common. A cubic close-packed arrangement of chloride anions with rubidium cations filling the octahedral holes describes this polymorph. [4] Both ions are six-coordinate in this arrangement. The lattice energy of this polymorph is only 3.2 kJ/mol less than the following structure's. [5]

Caesium chloride (cubic 8:8)

At high temperature and pressure, RbCl adopts the caesium chloride (CsCl) structure (NaCl and KCl undergo the same structural change at high pressures). Here, the chloride ions form a simple cubic arrangement with chloride anions occupying the vertices of a cube surrounding a central Rb+. This is RbCl's densest packing motif. [2] Because a cube has eight vertices, both ions' coordination numbers equal eight. This is RbCl's highest possible coordination number. Therefore, according to the radius ratio rule, cations in this polymorph will reach their largest apparent radius because the anion-cation distances are greatest. [4]

Sphalerite (tetrahedral 4:4)

The sphalerite polymorph of rubidium chloride has not been observed experimentally. This is consistent with the theory; the lattice energy is predicted to be nearly 40.0 kJ/mol smaller in magnitude than those of the preceding structures. [5]

Synthesis and reaction

The most common preparation of pure rubidium chloride involves the reaction of its hydroxide with hydrochloric acid, followed by recrystallization: [6]

RbOH + HCl → RbCl + H2O

Because RbCl is hygroscopic, it must be protected from atmospheric moisture, e.g. using a desiccator. RbCl is primarily used in laboratories. Therefore, numerous suppliers (see below) produce it in smaller quantities as needed. It is offered in a variety of forms for chemical and biomedical research.

Rubidium chloride reacts with sulfuric acid to give rubidium hydrogen sulfate.

Radioactivity

Every 18 mg of rubidium chloride is equivalent to approximately one banana equivalent dose due to the large fraction (27.8%) of naturally-occurring radioactive isotope rubidium-87.

Uses

Related Research Articles

<span class="mw-page-title-main">Alkali metal</span> Group of highly reactive chemical elements

The alkali metals consist of the chemical elements lithium (Li), sodium (Na), potassium (K), rubidium (Rb), caesium (Cs), and francium (Fr). Together with hydrogen they constitute group 1, which lies in the s-block of the periodic table. All alkali metals have their outermost electron in an s-orbital: this shared electron configuration results in their having very similar characteristic properties. Indeed, the alkali metals provide the best example of group trends in properties in the periodic table, with elements exhibiting well-characterised homologous behaviour. This family of elements is also known as the lithium family after its leading element.

<span class="mw-page-title-main">Caesium</span> Chemical element, symbol Cs and atomic number 55

Caesium is a chemical element; it has symbol Cs and atomic number 55. It is a soft, silvery-golden alkali metal with a melting point of 28.5 °C, which makes it one of only five elemental metals that are liquid at or near room temperature. Caesium has physical and chemical properties similar to those of rubidium and potassium. It is pyrophoric and reacts with water even at −116 °C (−177 °F). It is the least electronegative element, with a value of 0.79 on the Pauling scale. It has only one stable isotope, caesium-133. Caesium is mined mostly from pollucite. Caesium-137, a fission product, is extracted from waste produced by nuclear reactors. It has the largest atomic radius of all elements whose radii have been measured or calculated, at about 260 picometers.

<span class="mw-page-title-main">Ionic bonding</span> Chemical bonding involving attraction between ions

Ionic bonding is a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions, or between two atoms with sharply different electronegativities, and is the primary interaction occurring in ionic compounds. It is one of the main types of bonding, along with covalent bonding and metallic bonding. Ions are atoms with an electrostatic charge. Atoms that gain electrons make negatively charged ions. Atoms that lose electrons make positively charged ions. This transfer of electrons is known as electrovalence in contrast to covalence. In the simplest case, the cation is a metal atom and the anion is a nonmetal atom, but these ions can be more complex, e.g. molecular ions like NH+
4
or SO2−
4
. In simpler words, an ionic bond results from the transfer of electrons from a metal to a non-metal to obtain a full valence shell for both atoms.

<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">Rubidium</span> Chemical element, symbol Rb and atomic number 37

Rubidium is a chemical element; it has symbol Rb and atomic number 37. It is a very soft, whitish-grey solid in the alkali metal group, similar to potassium and caesium. Rubidium is the first alkali metal in the group to have a density higher than water. On Earth, natural rubidium comprises two isotopes: 72% is a stable isotope 85Rb, and 28% is slightly radioactive 87Rb, with a half-life of 48.8 billion years—more than three times as long as the estimated age of the universe.

<span class="mw-page-title-main">Salt (chemistry)</span> Chemical compound involving ionic bonding

In chemistry, a salt or ionic compound is a chemical compound consisting of an ionic assembly of positively charged cations and negatively charged anions, which results in a neutral compound with no net electric charge. The constituent ions are held together by electrostatic forces termed ionic bonds.

<span class="mw-page-title-main">Cubic crystal system</span> Crystallographic system where the unit cell is in the shape of a cube

In crystallography, the cubiccrystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.

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

Zinc chloride is the name of inorganic chemical compounds with the formula ZnCl2·nH2O, with x ranging from 0 to 4.5, forming hydrates. Zinc chloride, anhydrous and its hydrates are colorless or white crystalline solids, and are highly soluble in water. Five hydrates of zinc chloride are known, as well as four forms of anhydrous zinc chloride. This salt is hygroscopic and even deliquescent. Zinc chloride finds wide application in textile processing, metallurgical fluxes, and chemical synthesis. No mineral with this chemical composition is known aside from the very rare mineral simonkolleite, Zn5(OH)8Cl2·H2O.

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

Barium chloride is an inorganic compound with the formula BaCl2. It is one of the most common water-soluble salts of barium. Like most other water-soluble barium salts, it is a white powder, highly toxic, and imparts a yellow-green coloration to a flame. It is also hygroscopic, converting to the dihydrate BaCl2·2H2O, which are colourless crystals with a bitter salty taste. It has limited use in the laboratory and industry.

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

Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.

<span class="mw-page-title-main">Madelung constant</span> Constant in crystallography

The Madelung constant is used in determining the electrostatic potential of a single ion in a crystal by approximating the ions by point charges. It is named after Erwin Madelung, a German physicist.

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

Caesium chloride or cesium chloride is the inorganic compound with the formula CsCl. This colorless salt is an important source of caesium ions in a variety of niche applications. Its crystal structure forms a major structural type where each caesium ion is coordinated by 8 chloride ions. Caesium chloride dissolves in water. CsCl changes to NaCl structure on heating. Caesium chloride occurs naturally as impurities in carnallite, sylvite and kainite. Less than 20 tonnes of CsCl is produced annually worldwide, mostly from a caesium-bearing mineral pollucite.

Ionic radius, rion, is the radius of a monatomic ion in an ionic crystal structure. Although neither atoms nor ions have sharp boundaries, they are treated as if they were hard spheres with radii such that the sum of ionic radii of the cation and anion gives the distance between the ions in a crystal lattice. Ionic radii are typically given in units of either picometers (pm) or angstroms (Å), with 1 Å = 100 pm. Typical values range from 31 pm (0.3 Å) to over 200 pm (2 Å).

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

Rubidium perchlorate, RbClO4, is the perchlorate of rubidium. It is an oxidizing agent, as are all perchlorates.

In chemistry, the lattice energy is the energy change upon formation of one mole of a crystalline ionic compound from its constituent ions, which are assumed to initially be in the gaseous state. It is a measure of the cohesive forces that bind ionic solids. The size of the lattice energy is connected to many other physical properties including solubility, hardness, and volatility. Since it generally cannot be measured directly, the lattice energy is usually deduced from experimental data via the Born–Haber cycle.

A Schottky defect is an excitation of the site occupations in a crystal lattice leading to point defects named after Walter H. Schottky. In ionic crystals, this defect forms when oppositely charged ions leave their lattice sites and become incorporated for instance at the surface, creating oppositely charged vacancies. These vacancies are formed in stoichiometric units, to maintain an overall neutral charge in the ionic solid.

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

Gold compounds are compounds by the element gold (Au). Although gold is the most noble of the noble metals, it still forms many diverse compounds. The oxidation state of gold in its compounds ranges from −1 to +5, but Au(I) and Au(III) dominate its chemistry. Au(I), referred to as the aurous ion, is the most common oxidation state with soft ligands such as thioethers, thiolates, and organophosphines. Au(I) compounds are typically linear. A good example is Au(CN)−2, which is the soluble form of gold encountered in mining. The binary gold halides, such as AuCl, form zigzag polymeric chains, again featuring linear coordination at Au. Most drugs based on gold are Au(I) derivatives.

In chemistry, crystallography, and materials science, the coordination number, also called ligancy, of a central atom in a molecule or crystal is the number of atoms, molecules or ions bonded to it. The ion/molecule/atom surrounding the central ion/molecule/atom is called a ligand. This number is determined somewhat differently for molecules than for crystals.

Cobalt compounds are chemical compounds formed by cobalt with other elements.

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.

References

  1. Lide, D. R.; Cahill, P.; Gold, L. P. (1963). "Microwave Spectrum of Lithium Chloride". Journal of Chemical Physics. 40 (1): 156–159. doi:10.1063/1.1724853.
  2. 1 2 Wells, A. F. (1984). Structural Inorganic Chemistry. Oxford University Press. pp. 410, 444.
  3. Kopecky, M.; Fábry, J.; Kub, J.; Busetto, E.; Lausi, A. (2005). "X-ray diffuse scattering holography of a centrosymmetric sample". Applied Physics Letters. 87 (23): 231914. Bibcode:2005ApPhL..87w1914K. doi:10.1063/1.2140084.
  4. 1 2 Shriver, D. F.; Atkins, P. W.; Cooper, H. L. (1990). "Chapter 2". Inorganic Chemistry. Freeman.
  5. 1 2 Pyper, N. C.; Kirkland, A. I.; Harding, J. H. (2006). "Cohesion and polymorphism in solid rubidium chloride". Journal of Physics: Condensed Matter. 18 (2): 683–702. Bibcode:2006JPCM...18..683P. doi:10.1088/0953-8984/18/2/023. S2CID   93595759.
  6. Winter, M. (2006). "Compounds of Rubidium". WebElements.
  7. Budavari, S. (1996). The Merck index: an encyclopedia of chemicals, drugs, and biologicals. Rahway, NJ, U.S.A.: Merck. ISBN   0-911910-12-3.
  8. Hallonquist, J.; Lindegger, M.; Mrosovsky, N. (1994). "Rubidium chloride fuses split circadian activity rhythms in hamsters housed in bright constant light". Chronobiology International. 11 (2): 65–71. doi:10.3109/07420529409055892. PMID   8033243.
  9. Hougardy, E.; Pernet, P.; Warnau, M.; Delisle, J.; Grégoire, J.-C. (2003). "Marking bark beetle parasitoids within the host plant with rubidium for dispersal studies". Entomologia Experimentalis et Applicata. 108 (2): 107. Bibcode:2003EEApp.108..107H. doi:10.1046/j.1570-7458.2003.00073.x. S2CID   85691705.
  10. "RbCl Transformation Protocol". New England Biolabs. 2006. Archived from the original on 2006-03-19.
  11. Gian F. Placidi; Liliana Dell'Osso; Giuseppe Nistico; Hagop S. Akiskal (6 December 2012). Recurrent Mood Disorders: New Perspectives in Therapy. Springer Science & Business Media. pp. 293–. ISBN   978-3-642-76646-6.