Seaborgium

    group 6 · period 7 · d-block · transition metal

    Identity

    Name and symbol
    Seaborgium, Sg
    Atomic number
    106 protons
    Position
    group 6 · period 7 · d-block · transition metal
    CAS number
    54038-81-2

    Atomic structure

    Atomic mass
    271 u
    Electron configuration
    1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s² 4d¹⁰ 5p⁶ 6s² 4f¹⁴ 5d¹⁰ 6p⁶ 7s² 5f¹⁴ 6d⁴
    [Rn] 7s²⁵f¹⁴⁶d⁴
    Electrons per shell
    2, 8, 18, 32, 32, 12, 2
    Valence electrons
    6 ns and (n-1)d
    nuclidehalf-lifedecay
    269Sg5 mα≈100%; SF ?
    273Sg5 m [Estimated]SF ?
    272Sg4 m [Estimated]α ?; SF ?
    270Sg3 m [Estimated]α ?; SF ?
    no stable isotope; the longest-lived nuclides

    Physical properties

    State at room temperature
    Solid
    Melting point
    not in sources
    Boiling point
    not in sources
    Density
    not in sources
    Appearance
    not in sources
    Thermal conductivity
    not in sources
    Electrical resistivity
    not in sources
    Electrical conductivity
    not in sources
    Crystal structure
    body-centered cubic
    Molar heat capacity
    not in sources

    Chemical properties

    Oxidation states
    6, (5), (4), (3), 0 ​(parenthesized oxidation states are predictions)
    Electronegativity
    not in sources
    Ionisation energy
    7.8 eV
    Electron affinity
    not in sources
    Atomic radius
    not in sources
    Ionic radius
    not in sources
    Reactivity
    A group 6 transactinide studied a few atoms at a time; gas-phase and ion-exchange experiments confirm a stable +6 state and molybdenum- and tungsten-like chemistry, plus a zero-valent hexacarbonyl Sg(CO)6 made in 2014.
    with water
    Not known for the element; single atoms oxidized in moist oxygen gave the oxide hydroxide: SgOX3+HX2OSgOX2(OH)X2\ce{SgO3 + H2O -> SgO2(OH)2}.
    with oxygen, air
    Single atoms react with oxygen, the inferred first step of the 2001 gas-phase experiment being the trioxide: 2Sg+3OX22SgOX3\ce{2 Sg + 3 O2 -> 2 SgO3}, the species actually detected being its hydrate SgO2(OH)2.
    with acids
    In nitric and hydrofluoric acid seaborgium elutes from cation-exchange resin most likely as neutral SgO2F2 or the anion SgO2F3^-, while in 0.1 M nitric acid it stays cationic, hydrolyzing less than molybdenum and tungsten.
    with halogens
    With oxygen and hydrogen chloride single atoms form the volatile oxychloride: Sg+OX2+2HClSgOX2ClX2+HX2\ce{Sg + O2 + 2 HCl -> SgO2Cl2 + H2}, the least volatile of the group 6 oxychlorides.
    Typical compounds
    • SgO₂Cl₂ seaborgium dioxide dichloride volatile oxychloride, first seaborgium compound (1995)
    • SgO₂(OH)₂ seaborgium oxide hydroxide formed from the trioxide with water vapor
    • Sg(CO)₆ seaborgium hexacarbonyl volatile zero-valent carbonyl, made in 2014

    Occurrence, production and use

    Crustal abundance
    Not Applicable
    Oceanic abundance
    Not Applicable
    Occurrence and sources
    • synthetic only californium-249 bombarded with oxygen-18 nuclei
    Extraction, production
    not in sources
    Uses

    Since only a few atoms of seaborgium have ever been made, there are currently no uses for seaborgium outside of basic scientific research.

    Safety, toxicity
    not in sources

    Discovery and name

    Discovered by
    Lawrence Berkeley National Laboratory
    Discovered
    1974
    First isolated
    not in sources
    Named by
    not in sources
    Origin of the name
    after Glenn T. Seaborg

    Seaborgium does not occur naturally in the Earth’s crust. In 1974, seaborgium was first synthesized by Albert Ghiorso and his team at the University of California in Berkeley using the nuclear reaction 249Cf (18O, 4n) 263Sg. The element is named for Glenn T. Seaborg (Fig. IUPAC.106.1), who synthesized a number of trans-uranium elements [634], [648].

    Seaborgium has no commercial applications. However, 265Sg was one of the decay products used to confirm the synthesis of copernicium in a particle accelerator experiment.

    Seaborgium is named after Glenn Seaborg.

    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.