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Organopolonium chemistry

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Study of the carbon-polonium bond

Organopolonium chemistry describes the synthesis and properties of chemical compounds containing a carbon to polonium chemical bond.

As polonium is a highly radioactive element (its most commonly used isotope, Po, has a half-life of about 138 days), organopolonium chemistry is mostly unexplored, and what is known is mostly confined to tracer-level studies due to self-destruction and charring of the compounds by the energetic alpha decay of polonium. Moreover, the C–Po bond is even weaker than the C–Te and C–Se bonds; compounds with those bonds tend to decompose over time to form elemental tellurium and selenium respectively.

Identification of such compounds has mostly been accomplished using chromatography, with analogous tellurium compounds as references, as classical chemical methods cannot be applied. Their production is often accomplished by the beta decay of Bi-containing organobismuth compounds. Some compounds have been claimed but not securely identified.

Relatively well-characterised derivatives are mostly restricted to dialkyl and diaryl polonides (R2Po), triarylpolonium halides (Ar3PoX), and diarylpolonium dihalides (Ar2PoX2). Polonium also forms soluble compounds with some ligands, such as 2,3-butanediol and thiourea.

References

  1. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 786. ISBN 978-0-08-037941-8.
  2. ^ Zingaro, Ralph A. (2011). "Polonium: Organometallic Chemistry". Encyclopedia of Inorganic and Bioinorganic Chemistry. John Wiley & Sons. p. 1–3. doi:10.1002/9781119951438.eibc0182. ISBN 9781119951438.
  3. ^ Murin, A. N.; Nefedov, V. D.; Zaitsev, V. M.; Grachev, S. A. (1960). "Production of organopolonium compounds by using chemical alterations taking place during the β-decay of RaE" (PDF). Dokl. Akad. Nauk SSSR (in Russian). 133 (1): 123–125. Retrieved 12 April 2020.
Compounds of carbon with other elements in the periodic table
CH He
CLi CBe CB CC CN CO CF Ne
CNa CMg CAl CSi CP CS CCl CAr
CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr
CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe
CCs CBa 1 asterisk CLu CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn
Fr CRa 2 asterisks Lr Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
1 asterisk CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb
2 asterisks Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No
Legend
  • Chemical bonds to carbon
  • Core organic chemistry
  • Many uses in chemistry
  • Academic research, no widespread use
  • Bond unknown


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