Cyclopentadienylthallium
Names | |
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IUPAC name
Thallium(I) cyclopentadienide | |
Other names
Thallium cyclopentadienide (η5-Cyclopentadienyl)thallium | |
Identifiers | |
34822-90-7 | |
ChemSpider | 24721800 |
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Jmol-3D images | Image |
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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 | |
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
- ↑ C. Elschenbroich, (2006). Organometallics. Wiley-VCH, Weinheim. p. 130. ISBN 3-527-29390-6.
- ↑ A.J. Nielson, C.E.F. Rickard, J.M. Smith (1986). "Cyclopentadienylthallium (Thallium Cyclopentadienide)". Inorg. Synth. 24: 97–99. doi:10.1002/9780470132555.ch31.