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Californium(III) polyborate

From Wikipedia, the free encyclopedia
Californium(III) polyborate
Names
Other names
Californium borate
Identifiers
3D model (JSmol)
  • InChI=1S/B6H5O13.Cf/c7-1-13-2(8)16-6(12)18-4(10)14-3(9)17-5(11,15-1)19-6;/h7-9,11-12H;/q-3;+3
    Key: DIULMIKRPOXUQF-UHFFFAOYSA-N
  • [Cf+3].O1B(O)OB(O)O[B-]2(O)O[B-]1(O)OB(O)OB([O-])O2
Properties
Cf[B6O8(OH)5]
Molar mass526.90 g/mol[1]
Appearancepale green plates
Density3.842 g/cm3, solid
Structure
monoclinic[1]
C2/c
a = 6.849 Å,b = 18.809 Å,c = 101.36 Å
α = 90°, β = 124.72°, γ = 90°
910.9
4
8 coordinatesquare antiprism
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Californium polyborate is a covalent compound with formula Cf[B6O8(OH)5]. In this compound thecalifornium is in a +3 oxidation state. This compound is the highest atomic number borate with a visible solid phase. Heavier elements than californium decay too fast to make macroscopic amounts of solid crystals.[1]

Californium polyborate is unusual in that californium is covalently bound to the borate. Californium was expected to resemblelanthanide elements in being highly ionic. Thepolyborate anion is polarisable and flexible.[2] The 5f, 6d, 7s, and 7p orbitals of californium are all involved on the bonding.[2] Most valence electrons are in the 5f orbital, and a significant fraction (23) in the 6d orbital, and smaller fractions of one electron are in the 7s and 7p orbitals.[1]

Formation

[edit]

Californium(III) polyborate can be made by autoclaving acalifornium(III) chloride solution in water with excess boric acid for a week at 240°C. This is then cooled slowly to room temperature for another three days. Water dissolves excess boric acid to leave insoluble crystals of the borate.[1]

Properties

[edit]

The californium(III) polyborate solid undergoes a green fluorescence of 525 nm with ultraviolet light of wavelengths 365 or 420 nm.[1] There is also an invisible near infrared fluorescence at 1020 nm induced by green light at 546 nm.[1]

Safety

[edit]

Californium polyborate is dangerous because of the radioactivity of californium and its decay daughtercurium. Between them these elements emitα particles,gamma rays andneutrons.[1]

References

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  1. ^abcdefghPolinski, Matthew J.; Garner, Edward B.; Maurice, Rémi; Planas, Nora; Stritzinger, Jared T.; Parker, T. Gannon; Cross, Justin N.; Green, Thomas D.; Alekseev, Evgeny V.; Van Cleve, Shelley M.; Depmeier, Wulf; Gagliardi, Laura; Shatruk, Michael; Knappenberger, Kenneth L.; Liu, Guokui; Skanthakumar, S.; Soderholm, Lynda; Dixon, David A.;Albrecht-Schmitt, Thomas E. (23 March 2014)."Unusual structure, bonding and properties in a californium borate".Nature Chemistry.6 (5):387–392.Bibcode:2014NatCh...6..387P.CiteSeerX 10.1.1.711.6947.doi:10.1038/nchem.1896.PMID 24755589.S2CID 104331283.
  2. ^ab"Unusual structure, bonding, and properties may provide a new possibility for a californium borate". 1 June 2015. Retrieved29 July 2015.
Cf(II)
Cf(III)
Organocalifornium(III) compounds
Cf(IV)
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