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Californium compounds
 

Few compounds of californium have been made and studied.[1] The only californium ion that is stable in aqueous solutions is the californium(III) cation.[2] The other two oxidation states are IV (strong oxidizing agents) and II (strong reducing agents).[3] The element forms a water-soluble chloride, nitrate, perchlorate, and sulfate and is precipitated as a fluoride, oxalate or hydroxide.[4] If problems of availability of the element could be overcome, then CfBr2 and CfI2 would likely be stable.[5]

Californium(III) nitrate

The +3 oxidation state is represented by californium(III) oxide (yellow-green, Cf2O3), californium(III) fluoride (bright green, CfF3) and californium(III) iodide (lemon yellow, CfI3).[3] Other +3 oxidation states include the sulfide and metallocene.[6] Californium(IV) oxide (black brown, CfO2), californium(IV) fluoride (green, CfF4) represent the IV oxidation state. The II state is represented by californium(II) bromide (yellow, CfBr2) and californium(II) iodide (dark violet, CfI2).[3]

Compounds

Californium(IV) oxide (CfO2) is a black-brown solid that has a cubic crystal structure with a lattice parameter, the distance between unit cells in the crystal, of 531.0 ± 0.2 pm.[7] Crystals of californium(III) oxide normally have a body-centered cubic symmetry. They convert to a monoclinic form upon heating to about 1400 °C and melt at 1750 °C.[7]

Californium(III) chloride (CfCl3) is an emerald green compound with a hexagonal structure that can be prepared by reacting Cf2O3 with hydrochloric acid at 500 °C.[8] CfCl3 is then used as a feeder stock to form the yellow-orange triiodide CfI3, which in turn can be reduced to the lavender-violet diiodide CfI2.[9]

Californium(III) fluoride (CfF3) is a yellow-green solid with a crystal symmetry that gradually changes from orthorhombic to trigonal when heated above room temperature.[10] Californium(IV) fluoride (CfF4) is a bright green solid with a monoclinic crystal structure.[11]

Californium(II) iodide (CfI2) is a deep purple solid with a stable rhombohedral structure at room temperature and an unstable hexagonal structure. Californium(III) iodide (CfI3) is a lemon-yellow solid that has a rhombohedral structure and sublimes at ~800 °C.[12]

Californium(III) oxyfluoride (CfOF) is prepared by hydrolysis of californium(III) fluoride (CfF3) at high temperature.[13] Californium(III) oxychloride (CfOCl) is prepared by hydrolysis of the hydrate of californium(III) chloride at 280–320 °C.[14]

Heating the sulfate in air at about 1200 °C and then reducing with hydrogen at 500 °C produces the sesquioxide (Cf2O3).[8] The hydroxide Cf(OH)3 and the trifluoride CfF3 are slightly soluble.[8]

Californium(III) oxychloride (CfOCl) was the first californium compound to be discovered.[15]

Californium(III) polyborate is unusual in that californium is covalently bound to the borate.[16]

Tris(cyclopentadienyl)californium(III) (Cp3Cf) presents itself as ruby red crystals. This cyclopentadienyl complex has been prepared by the reaction between Cp2Be and CfCl3 on a microgram scale and characterized by X-ray crystallography.[17] Californium is the second-heaviest element for which an organometallic compound is known. A bent californium metallocene has also been isolated and characterized.[18]

See also

References

  1. ^ Krebs, Robert (2006). The History and Use of our Earth's Chemical Elements: A Reference Guide. Westport, Connecticut: Greenwood Publishing Group. pp. 327–328. ISBN 978-0-313-33438-2.
  2. ^ CRC 2006, p. 4-8.
  3. ^ a b c Jakubke 1994, p. 166.
  4. ^ Seaborg 2004.
  5. ^ Greenwood 1997, p. 1272.
  6. ^ Cotton 1999, p. 1163.
  7. ^ a b Baybarz, R. D.; Haire, R. G.; Fahey, J. A (1972). "On the Californium Oxide System". Inorganic and Nuclear Chemistry. 34 (2): 557–565. doi:10.1016/0022-1902(72)80435-4.
  8. ^ a b c Cunningham 1968, p. 105.
  9. ^ Cotton, Simon (2006). Lanthanide and Actinide Chemistry. West Sussex, England: John Wiley & Sons. p. 168. ISBN 978-0-470-01006-8.
  10. ^ Stevenson, J. N.; Peterson, J. R. (1973). "The Trigonal and Orthorhombic Crystal Structures of CfF3 and their Temperature Relationship". Inorganic and Nuclear Chemistry. 35 (10): 3481–3486. doi:10.1016/0022-1902(73)80356-2.
  11. ^ Chang, C-T. P.; Haire, R. G.; Nave, S. E. (1990). "Magnetic Susceptibility of Californium Fluorides". Physical Review B. 41 (13): 9045–9048. Bibcode:1990PhRvB..41.9045C. doi:10.1103/PhysRevB.41.9045. PMID 9993248.
  12. ^ Macintyre, J. E.; Daniel, F. M.; Stirling, V. M. (1992). Dictionary of inorganic compounds. London: Chapman and Hall, CRC Press. p. 2826. ISBN 978-0-412-30120-9.
  13. ^ Peterson, J. R.; Burns, John H. (1968). "Preparation and Crystal Structure of Californium Oxyfluoride, CfOF". Inorganic and Nuclear Chemistry. 30 (11): 2955–2958. doi:10.1016/0022-1902(68)80155-1.
  14. ^ Copeland, J. C.; Cunningham, B. B. (1969). "Crystallography of the Compounds of Californium. II. Crystal Structure and Lattice Parameters of Californium Oxychloride and Californium Sesquioxide" (PDF). Inorganic and Nuclear Chemistry. 31 (3): 733–740. doi:10.1016/0022-1902(69)80020-5.
  15. ^ Seaborg, Glenn T. (1963). Man-Made Transuranium Elements. Prentice-Hall.
  16. ^ "Unusual structure, bonding, and properties may provide a new possibility for a californium borate". 1 June 2015. Retrieved 29 July 2015.
  17. ^ Laubereau, Peter G.; Burns, John H. (1970). "Microchemical preparation of tricyclopentadienyl compounds of berkelium, californium, and some lanthanide elements". Inorganic Chemistry. 9 (5): 1091–1095. doi:10.1021/ic50087a018.
  18. ^ Goodwin, Conrad A. P.; Su, Jing; Stevens, Lauren M.; White, Frankie D.; Anderson, Nickolas H.; Auxier, John D.; Albrecht-Schönzart, Thomas E.; Batista, Enrique R.; Briscoe, Sasha F.; Cross, Justin N.; Evans, William J.; Gaiser, Alyssa N.; Gaunt, Andrew J.; James, Michael R.; Janicke, Michael T.; Jenkins, Tener F.; Jones, Zachary R.; Kozimor, Stosh A.; Scott, Brian L.; Sperling, Joseph. M.; Wedal, Justin C.; Windorff, Cory J.; Yang, Ping; Ziller, Joseph W. (18 November 2021). "Isolation and characterization of a californium metallocene" (PDF). Nature. 599 (7885): 421–424. Bibcode:2021Natur.599..421G. doi:10.1038/s41586-021-04027-8. PMID 34789902. S2CID 244347582.

Bibliography

Zdroj:https://en.wikipedia.org?pojem=Californium_compounds
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Chemical compound
Californium
Ion
Aqueous solution
Cation
Oxidation state
Oxidizing agent
Reducing agent
Chloride
Nitrate
Perchlorate
Sulfate
Fluoride
Oxalate
Hydroxide
File:Cf-251.png
Metallocene
Californium(IV) oxide
Lattice constant
Unit cell
Picometre
Monoclinic crystal system
Californium(III) chloride
Hydrochloric acid
Californium(III) fluoride
Orthorhombic crystal system
Trigonal crystal system
Californium(IV) fluoride
Monoclinic crystal system
Californium(II) iodide
Californium(III) iodide
Sublimation (phase transition)
Californium(III) oxyfluoride
Hydrolysis
Californium(III) fluoride
Californium(III) oxychloride
Hydrate
Californium(III) chloride
Redox
Hydroxide
Solubility
Californium oxychloride
Californium(III) polyborate
Cyclopentadienyl complex
Bent metallocene
Californium
Compounds of berkelium
Einsteinium compounds
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Californium dichloride
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Californium(III) nitrate
Californium(III) oxybromide
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