Dubnium

    group 5 · period 7 · d-block · transition metal

    Identity

    Name and symbol
    Dubnium, Db
    Atomic number
    105 protons
    Position
    group 5 · period 7 · d-block · transition metal
    CAS number
    53850-35-4

    Atomic structure

    Atomic mass
    268 u
    Electron configuration
    1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s² 4d¹⁰ 5p⁶ 6s² 4f¹⁴ 5d¹⁰ 6p⁶ 7s² 5f¹⁴ 6d³
    [Rn] 7s²⁵f¹⁴⁶d³
    Electrons per shell
    2, 8, 18, 32, 32, 11, 2
    Valence electrons
    5 ns and (n-1)d
    nuclidehalf-lifedecay
    268Db29 hSF≈100%; β+ ?; α ?
    269Db3 h [Estimated]α ?; SF ?
    267Db2.0 hSF=100%
    270Db1.7 hSF≈87%; α≈13%
    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
    5, (4), (3) ​(parenthesized oxidation states are predictions)
    Electronegativity
    not in sources
    Ionisation energy
    6.8 eV
    Electron affinity
    not in sources
    Atomic radius
    not in sources
    Ionic radius
    not in sources
    Reactivity
    A group 5 transactinide known only from tracer experiments on single atoms; aqueous studies confirm a dominant +5 state like niobium and tantalum, with complexing behavior closer to niobium and protactinium than to tantalum.
    with water
    Not known; no experiment with water alone is reported.
    with oxygen, air
    Not known; gas-phase runs with traces of oxygen gave a less volatile species assigned to the oxybromide DbOBr3, and oxychlorides less volatile than the chlorides.
    with acids
    Single atoms in concentrated hydrochloric or hydrofluoric acid form anionic Db(V) halide complexes, probably DbOX4^- or Db(OH)2X4^-, which sorb on glass like the group 5 elements and extract like niobium rather than tantalum.
    with halogens
    Gas-phase experiments with bromine and chlorine gave volatile dubnium bromide and chloride, the bromide less volatile than niobium bromide and about as volatile as hafnium bromide.
    Typical compounds
    not in sources

    Occurrence, production and use

    Crustal abundance
    Not Applicable
    Oceanic abundance
    Not Applicable
    Occurrence and sources
    • synthetic only californium-249 bombarded with nitrogen-15 nuclei
    Extraction, production
    not in sources
    Uses

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

    Safety, toxicity
    not in sources

    Discovery and name

    Discovered by
    independently by the Lawrence Berkeley Laboratory and the Joint Institute for Nuclear Research
    Discovered
    1970
    First isolated
    not in sources
    Named by
    not in sources
    Origin of the name
    after Dubna, Moscow Oblast, Russia, site of Joint Institute for Nuclear Research

    Dubnium does not occur naturally in the Earth’s crust. Credit for the first synthesis of this element is given jointly to Albert Ghiorso and his team at the University of California in Berkeley and Georgi Flerov and his team at the Joint Institute for Nuclear Research (JINR) in Dubna, Russia (Fig. IUPAC.105.1). The element is named for the location of the Joint Institute for Nuclear Research (JINR) laboratory in Dubna, Russia [646], [647]. Dubnium has no isotopic applications outside of scientific research.

    Dubnium is named after the site of the Joint Institute for Nuclear Research in Dubna, Russia.

    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.