Francium

    group 1 · period 7 · s-block · alkali metal

    Identity

    Name and symbol
    Francium, Fr
    Atomic number
    87 protons
    Position
    group 1 · period 7 · s-block · alkali metal
    CAS number
    7440-73-5

    Atomic structure

    Atomic mass
    223 u
    Electron configuration
    1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s² 4d¹⁰ 5p⁶ 6s² 4f¹⁴ 5d¹⁰ 6p⁶ 7s¹
    [Rn] 7s¹
    Electrons per shell
    2, 8, 18, 32, 18, 8, 1
    Valence electrons
    1 outer shell
    nuclidehalf-lifedecay
    223Fr22.00 mβ-≈100%; α=0.006%
    212Fr20.0 mβ+=57±0.2%; α=43±0.2%
    222Fr14.2 mβ-=100%
    221Fr4.801 mα≈100%; β-=0.0048±1.5%; 14C=8.8e-11±1.1%
    no stable isotope; the longest-lived nuclides

    Physical properties

    State at room temperature
    Solid
    Melting point
    300 K (26.85 °C)
    Boiling point
    680 K (406.85 °C)
    Density
    not in sources
    Appearance
    not in sources
    Thermal conductivity
    15 W/(m·K)
    Electrical resistivity
    3 µΩ·m
    Electrical conductivity
    333,333.333 S/m
    Crystal structure
    body-centered cubic
    Molar heat capacity
    not in sources

    Chemical properties

    Oxidation states
    +1
    Electronegativity
    0.67 (Allen Scale)
    Ionisation energy
    3.9 eV
    1st 380 kJ/mol
    Electron affinity
    0.47 eV
    Atomic radius
    empirical 260, covalent 260, van der Waals 348 pm
    Ionic radius
    Fr⁺ 180 pm
    Reactivity
    The heaviest alkali metal (7s1) and the second most electropositive element after caesium, but its longest-lived isotope lasts 22 minutes and no more than about 30 g exist in the crust at once, so bulk francium has never been seen; every fact about its chemistry comes from tracer solutions of the Fr+ ion coprecipitated with caesium salts.
    with water
    Not known: no bulk sample has ever existed to test, though by analogy with caesium the reaction would be explosive; in water francium is simply the soluble Fr+ ion.
    with oxygen, air
    Not known: no oxidation of the metal has been observed; the oxide is predicted to disproportionate to the peroxide and the metal, and the superoxide FrO2 to be more covalent than its lighter congeners.
    with acids
    Not known for the metal; francium salts are handled only in solution, where the perchlorate, iodate, picrate, tartrate, chloroplatinate and silicotungstate coprecipitate with the caesium salts and the rest stay dissolved.
    with halogens
    Not known: the halides are expected to be white, water-soluble solids formed from the elements, but none has been made by direct reaction.
    Typical compounds
    • FrClO₄ francium perchlorate tiny amounts coprecipitated with caesium perchlorate

    Occurrence, production and use

    Crustal abundance
    Not Applicable
    Oceanic abundance
    Not Applicable
    Occurrence and sources
    • transient decay product in actinium and uranium ore detected in purified actinium; made artificially from radium or thorium
    Extraction, production
    Neutron bombardment of radium in a reactor, or proton bombardment of thorium

    no equation printed

    Uses

    Due to the small amounts produced and its short half-life, there are currently no uses for francium outside of basic scientific research.

    Safety, toxicity
    not in sources

    Discovery and name

    Discovered by
    Marguerite Perey
    Discovered
    1939
    First isolated
    not in sources
    Named by
    not in sources
    Origin of the name
    after France, homeland of the discoverer

    Francium was discovered in 1939 by Marguerite Perey, a physicist at the Curie Institute in Paris, France (Fig. IUPAC.87.1). 223Fr (with a half-life of 22 min) occurs naturally in uranium minerals as a result of actinium decay. However, it is estimated that no more than approximately 30 g of francium is present in the Earth’s crust at any time. Francium can be produced artificially for research by bombarding thorium with protons. Francium was named in honor of Perey’s home country, France [575], [576], [577]. Francium has no known isotopic applications outside of scientific research.

    Conventions

    Valence electrons are counted by the usual convention: the outer shell for s- and p-block elements, ns and (n-1)d for the d-block, ns, (n-1)d and (n-2)f for the f-block. Lanthanides and actinides are placed in the f-block with no group number. Electrical conductivity is the reciprocal of the printed resistivity. Ionic radii are Shannon effective radii, six-coordinate unless noted. Where a field reads “not in sources” the value was not found; it is a gap, not a zero. Regulatory limits are the published values and change often, so check the standard in force at your site and the numbers written into your own permit before you design to them.

    Data

    Element records, isotopes, radii and the descriptive text come from PubChem (NCBI), the Los Alamos National Laboratory periodic table, IUPAC CIAAW and the IAEA Atomic Mass Data Center. Appearance, thermal conductivity, electrical resistivity, crystal structure, discovery and the origin of each name come from Wikipedia and Periodic-Table-JSON, used under CC BY-SA 4.0. Hazard classifications come from the ECHA C&L inventory via PubChem. Ionic radii follow R. D. Shannon (1976). The water chapters cite their own sources at the foot of each entry, and are written to the level of Snoeyink and Jenkins, Stumm and Morgan, MWH's Water Treatment and Metcalf and Eddy.