Cyclopentadienylthallium

Cyclopentadienylthallium
Names
IUPAC name
Thallium(I) cyclopentadienide
Other names
Thallium cyclopentadienide
5-Cyclopentadienyl)thallium
Identifiers
34822-90-7
ChemSpider 24721800 Yes
Jmol-3D images Image
Properties
Molecular formula
C5H5Tl
Molar mass 269.48 g·mol−1
Appearance Light yellow solid
Melting point 300 °C (572 °F; 573 K)
Insoluble
Hazards
EU classification T+
R-phrases R26/28, R33, R36/37/38
S-phrases S13, S28, S45
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
0
3
0
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Cyclopentadienylthallium, also known as thallium cyclopentadienide, is an organothallium compound with formula C5H5Tl. This light yellow solid is insoluble in most organic solvents, but sublimes readily, and is useful as a precursor to transition metal and main group cyclopentadienyl complexes, as well as organic cyclopentadiene derivatives.[1]

Preparation

Cyclopentadienylthallium is prepared by the reaction of thallium(I) sulfate, sodium hydroxide, and cyclopentadiene:[2]

Tl2SO4 + 2 NaOH → 2 TlOH + Na2SO4
TlOH + C5H6 → TlC5H5 + H2O

Applications

Compared to most of other cyclopentadienyl (Cp) transfer reagent such as cyclopentadienyl sodium, CpMgBr and Cp2Mg, cyclopentadienylthallium is less air sensitive. It is also much less of a reducing agent.

References

  1. C. Elschenbroich, (2006). Organometallics. Wiley-VCH, Weinheim. p. 130. ISBN 3-527-29390-6.
  2. A.J. Nielson, C.E.F. Rickard, J.M. Smith (1986). "Cyclopentadienylthallium (Thallium Cyclopentadienide)". Inorg. Synth. 24: 97–99. doi:10.1002/9780470132555.ch31.