Trioctylphosphine oxide
Structural formula of trioctylphosphine oxide
Names
Preferred IUPAC name
Trioctyl-λ5-phosphanone
Other names
Tri-n-octylphosphine oxide
Identifiers
3D model (JSmol)
Abbreviations TOPO
1796648
ChemSpider
ECHA InfoCard 100.001.020
EC Number
  • 201-121-3
MeSH Trioctyl+phosphine+oxide
RTECS number
  • SZ1662500
UNII
UN number 3077
  • InChI=1S/C24H51OP/c1-4-7-10-13-16-19-22-26(25,23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3 checkY
    Key: ZMBHCYHQLYEYDV-UHFFFAOYSA-N checkY
  • InChI=1/C24H51OP/c1-4-7-10-13-16-19-22-26(25,23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3
    Key: ZMBHCYHQLYEYDV-UHFFFAOYAY
  • CCCCCCCCP(=O)(CCCCCCCC)CCCCCCCC
Properties
C24H51OP
Molar mass 386.645 g·mol−1
Appearance White, opaque crystals
Melting point 50 to 54 °C (122 to 129 °F; 323 to 327 K)
Boiling point 411.2 °C (772.2 °F; 684.3 K) at 760 mmHg[1]
Hazards[2]
GHS labelling:
GHS05: Corrosive
Danger
H315, H318
P264, P280, P302+P352, P305+P351+P338, P310, P332+P313, P362
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond
3
1
0
Flash point 110 °C (230 °F; 383 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Trioctylphosphine oxide (TOPO) is an organophosphorus compound with the formula OP(C8H17)3. Frequently referred to as TOPO, this compound is used as an extraction or stabilizing agent. It is an air-stable white solid at room temperature.

Preparation and use

TOPO is usually prepared by oxidation of trioctylphosphine, which in turn is produced by alkylation of phosphorus trichloride.

The main use of TOPO is in solvent extraction of metals, especially uranium.[3] The high lipophilicity and high polarity are properties key to this application. Its high polarity, which results from the dipolar phosphorus-oxygen bond, allows this compound to bind to metal ions. The octyl groups confer solubility in low polarity solvents such as kerosene.[4]

In the research laboratory, both trioctylphosphine and TOPO are frequently useful as a capping ligand for the production of quantum dots such as those consisting of CdSe. In these cases, TOPO serves as solvent for the synthesis and solubilizes the growing nanoparticles. TOPO-coated quantum dots are typically soluble in chloroform, toluene, and (to a lesser extent) hexane.[5]

References

  1. ↑ Nakhutin, I. E. (1971). Zhurnal Obshchei Khimii. 41 (5): 940–943. {{cite journal}}: Missing or empty |title= (help)
  2. ↑ "C&L Inventory". echa.europa.eu.
  3. ↑ Kumar, Jyothi Rajesh; Kim, Joon-Soo; Lee, Jin-Young; Yoon, Ho-Sung (18 February 2011). "A Brief Review on Solvent Extraction of Uranium from Acidic Solutions". Separation & Purification Reviews. 40 (2): 77–125. doi:10.1080/15422119.2010.549760. S2CID 95358600.
  4. ↑ Watson, E. K.; Rickelton, W. A. "A review of the industrial and recent potential applications of trioctylphosphine oxide" Solvent Extraction and Ion Exchange 1992, volume 10, pp. 879-89. doi:10.1080/07366299208918141
  5. ↑ García-Rodríguez, Raúl; Hendricks, Mark P.; Cossairt, Brandi M.; Liu, Haitao; Owen, Jonathan S. (2013). "Conversion Reactions of Cadmium Chalcogenide Nanocrystal Precursors". Chemistry of Materials. 25 (8): 1233–1249. doi:10.1021/cm3035642.
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