Einsteinium

    no group (f-block) · period 7 · f-block · actinide

    Identity

    Name and symbol
    Einsteinium, Es
    Atomic number
    99 protons
    Position
    no group (f-block) · period 7 · f-block · actinide
    CAS number
    7429-92-7

    Atomic structure

    Atomic mass
    252 u
    Electron configuration
    1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s² 4d¹⁰ 5p⁶ 6s² 4f¹⁴ 5d¹⁰ 6p⁶ 7s² 5f¹¹
    [Rn] 7s²⁵f¹¹
    Electrons per shell
    2, 8, 18, 32, 29, 8, 2
    Valence electrons
    13 ns, (n-1)d and (n-2)f
    nuclidehalf-lifedecay
    252Es471.7 dα=78±0.2%; ε=22±0.2%
    254Es275.7 dα≈100%; ε ?; β-=1.74e-4±0.8%; SF<3e-6%
    255Es39.8 dβ-=92.0±0.4%; α=8.0±0.4%; SF=0.0041±0.2%
    253Es20.47 dα=100%; SF=8.7e-6±0.3%
    no stable isotope; the longest-lived nuclides

    Physical properties

    State at room temperature
    Solid
    Melting point
    1,133 K (859.85 °C)
    Boiling point
    996 K (722.85 °C)
    Density
    not in sources
    Appearance
    silvery; glows blue in the dark
    Thermal conductivity
    not in sources
    Electrical resistivity
    not in sources
    Electrical conductivity
    not in sources
    Crystal structure
    face-centered cubic
    Molar heat capacity
    not in sources

    Chemical properties

    Oxidation states
    +3
    Electronegativity
    1.3 (Pauling Scale)
    Ionisation energy
    6.42 eV
    1st 619 kJ/mol
    Electron affinity
    not in sources
    Atomic radius
    van der Waals 245 pm
    Ionic radius
    Es³⁺ 84 pm
    Reactivity
    A soft, silvery, rather reactive late actinide and the heaviest element studied in bulk: +3 dominates in solids and in solution (pale pink), and it is the first actinide in which a +2 state is firmly established, made by reducing Es(III) with samarium(II) chloride.
    with water
    The sources do not describe the metal with water; Es3+ is the stable aqueous ion and the trihalides react with water vapor to oxyhalides such as EsOCl.
    with oxygen, air
    The sources do not describe the metal with oxygen; the oxide Es2O3 was obtained by burning the nitrate and exists in cubic, monoclinic and hexagonal forms that interconvert under self-irradiation.
    with acids
    Tracer studies show trivalent actinide behavior in acid solution, giving the pale pink Es3+ ion whose luminescence has been observed in hydrochloric acid.
    with halogens
    No reaction of the metal with the halogens is reported; the trihalides EsF3, EsCl3, EsBr3 and EsI3 are made from the oxide or from solution, and hydrogen reduces them to the dihalides: 2EsClX3+HX22EsClX2+2HCl\ce{2 EsCl3 + H2 -> 2 EsCl2 + 2 HCl}.
    Typical compounds
    • Es₂O₃ einsteinium(III) oxide colorless cubic crystals, from burning the nitrate
    • EsF₃ einsteinium(III) fluoride precipitated from Es(III) chloride solution with fluoride
    • EsCl₃ einsteinium(III) chloride orange, from the oxide in dry hydrogen chloride
    • EsCl₂ einsteinium(II) chloride divalent, from hydrogen reduction of the trichloride

    Occurrence, production and use

    Crustal abundance
    Not Applicable
    Oceanic abundance
    Not Applicable
    Occurrence and sources
    • synthetic only milligram quantities from neutron bombardment of plutonium in a reactor
    Extraction, production
    not in sources
    Uses

    Since only small amounts of einsteinium have ever been produced, it currently has no uses outside of basic scientific research.

    Safety, toxicity
    not in sources

    Discovery and name

    Discovered by
    Lawrence Berkeley National Laboratory
    Discovered
    1952
    First isolated
    not in sources
    Named by
    not in sources
    Origin of the name
    after Albert Einstein

    Einsteinium does not occur naturally in the Earth’s crust. It was first identified in December 1952 by American scientists from the Argonne National Laboratory near Chicago, Illinois, the Los Alamos National Laboratory in Los Alamos, New Mexico, and The University of California Laboratory in Berkeley, California in the debris of thermonuclear weapons. The element was named for Albert Einstein (Fig. IUPAC.99.1). 253Es was the first isotope identified; it has a half-life of 20.47 days. The isotope with the longest half-life is 252Es, with a half-life of 472 days [630], [631].

    There are no uses for isotopes of einsteinium outside of basic scientific research for the production of higher transuranic elements and studies of actinide science. Due to the radiation and heat given off by einsteinium isotopes, it is difficult to use them in experiments and studies [631].

    Tracer studies using 253Es show that einsteinium has chemical properties typical of a heavy trivalent, actinide element. Oxidation states of II and III for einsteinium have been reported and oxidation state IV has been postulated from vapor transport studies but not established unequivocally. Einsteinium is the first divalent metal in the actinide series (two bonding electrons rather than three). The self-irradiation properties of einsteinium make it extremely difficult, for example, to obtain x-ray crystallographic data. The intense gamma and x-rays from einsteinium decay to daughter products over-exposes the x-ray film/detector. This intense self-irradiation can be exploited however to study accelerated aging and radiation damage studies, and for targeted radiation medical treatments. An example of einsteinium chemical studies is the chemical consequences of radioactive decay. With the relatively short half-life of Es-253 (20.47 days) one can study the in-growth of daughter Bk-249 (half-life 330 days) and grand-daughter Cf-249 (half-life 351 years). Evidence suggests that divalent Es might decay into a divalent Bk daughter and subsequently into as of yet unknown divalent Cf. There are no commercial uses for einsteinium however it is the heaviest element for which bulk studies can be performed that allows for fundamental studies of the role of 5-f electrons in actinide systematics.

    Further reading:

    Richard G. Haire (2006) Chapter 12, The Chemistry of the Actinide and Transactinide Elements, Third Edition, L. R. Morss, J. Fuger, and N. M. Edelstein, Eds, Springer Publishers.

    This element reviewed and Updated by Dr. David Hobart, 2011

    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.