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Phosphinate Chemistry in the 21st Century: A Viable Alternative to the Use of Phosphorus Trichloride in Organophosphorus Synthesis.
Abstract
Organophosphorus compounds are important in everyday applications ranging from agriculture to medicine and are used in flame retardants and other materials. Although organophosphorus chemistry is known as a mature and specialized area, researchers would like to develop new methods for synthesizing organophosphorus compounds to improve the safety and sustainability of these chemical processes. The vast majority of compounds that contain a phosphorus-carbon bond are manufactured using phosphorus trichloride (PCl3) as an intermediate. However, these reactions require chlorine, and researchers would like to avoid the use of PCl3 and develop safer chemistry that also decreases energy consumption and minimizes waste. Researchers have already proposed and discussed two primary strategies based on elemental phosphorus (P4 or Pred) or on phosphine (PH3) as alternatives to PCl3. However, phosphinates, an important class of phosphorus compounds defined as any compound with a phosphorus atom attached to two oxygens, R(1)R(2)P(O)(OR) (R(1)/R(2) = hydrogen/carbon), offer another option. This Account discusses the previously neglected potential of these phosphinates as replacements of PCl3 for the preparation of organophosphorus compounds. Because of their strong reductive properties, industry currently uses the simplest members of this class of compounds, hypophosphites, for one major application: electroless plating. In comparison with other proposed PCl3 surrogates, hypophosphorous derivatives can offer improved stability, lower toxicity, higher solubility, and increased atom economy. When their reducing power is harnessed to form phosphorus-carbon or phosphorus-oxygen bonds, these compounds are also rich and versatile precursors to organophosphorus compounds. This Account examines the use of transition metal-catalyzed reactions such as cross-coupling and hydrophosphinylation for phosphorus-carbon bond formation. Because the most important industrial organophosphorus compounds include compounds triply or quadruply bound to oxygen, I also discuss controlled transfer hydrogenation for phosphorus-oxygen bond formation. I hope that this Account will further promote research in this novel and exciting yet much underdeveloped area of phosphinate activation.
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Cites
Westheimer, F. H. (1987) · Science · doi:10.1126/science.2434996 · Cited by 1,711
Elser, J., & Bennett, E. (2011) · Nature · doi:10.1038/478029a · Cited by 931
Towards global phosphorus security: A systems framework for phosphorus recovery and reuse options
Cordell, D., Rosemarin, A., Schröder, J. J., & Smit, A. L. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.02.032 · Cited by 915
Environment: The disappearing nutrient
Gilbert, N. (2009) · Nature · doi:10.1038/461716a · Cited by 817
Stable singlet carbenes as mimics for transition metal centers
Martin, D., Soleilhavoup, M., & Bertrand, G. (2011) · Chem. Sci. · doi:10.1039/c0sc00388c · Cited by 666
The Global Phosphorus Cycle: Past, Present, and Future
Filippelli, G. M. (2008) · Elements · doi:10.2113/gselements.4.2.89 · Cited by 591
P4Activation by Main Group Elements and Compounds
Scheer, M., Balázs, G., & Seitz, A. (2010) · Chemical Reviews · doi:10.1021/cr100010e · Cited by 489
Early-Transition-Metal-Mediated Activation and Transformation of White Phosphorus
Cossairt, B. M., Piro, N. A., & Cummins, C. C. (2010) · Chemical Reviews · doi:10.1021/cr9003709 · Cited by 463
P4 Activation by Late-Transition Metal Complexes
Caporali, M., Gonsalvi, L., Rossin, A., & Peruzzini, M. (2010) · Chemical Reviews · doi:10.1021/cr900349u · Cited by 448
A brief history of phosphorus: From the philosopher’s stone to nutrient recovery and reuse
Ashley, K., Cordell, D., & Mavinic, D. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.03.001 · Cited by 384
Global potential of phosphorus recovery from human urine and feces
Mihelcic, J. R., Fry, L. M., & Shaw, R. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.02.046 · Cited by 378
Improved phosphorus use efficiency in agriculture: A key requirement for its sustainable use
Schröder, J. J., Smit, A. L., Cordell, D., & Rosemarin, A. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.01.065 · Cited by 371
Industrial Inorganic Chemistry
Büchel, K. H., Moretto, H., & Woditsch, P. (2000) · Wiley eBooks · doi:10.1002/9783527613328 · Cited by 303
Solvent extraction in hydrometallurgy: the role of organophosphorus extractants
Flett, D. S. (2005) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2004.11.037 · Cited by 294
Vaccari, D. A. (2009) · Scientific American · doi:10.1038/scientificamerican0609-54 · Cited by 289
Karl, D. M. (2000) · Nature · doi:10.1038/35017683 · Cited by 258
Antonini, S., Arias, M. A., Eichert, T., & Clemens, J. (2012) · Chemosphere · doi:10.1016/j.chemosphere.2012.07.026 · Cited by 137
Phosphorus Recovery from Wastewater—Expert Survey on Present Use and Future Potential
Sartorius, C., von Horn, J., & Tettenborn, F. (2012) · Water Environment Research · doi:10.2175/106143012x13347678384440 · Cited by 95
Extrapolating phosphorus production to estimate resource reserves
Vaccari, D. A., & Strigul, N. S. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.01.052 · Cited by 95
A novel approach to phosphonic acids from hypophosphorous acid
Bravo‐Altamirano, K., & Montchamp, J. (2007) · Tetrahedron Letters · doi:10.1016/j.tetlet.2007.06.090 · Cited by 61
Self-citationRadical-mediated reduction of the dithiocarbamate group under tin-free conditions
McMaster, C., Bream, R. N., & Grainger, R. S. (2012) · Organic & Biomolecular Chemistry · doi:10.1039/c2ob25434d · Cited by 51
Cited by
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Metadata
- Authors
- Montchamp, J.-L.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-08-02
- Volume
- 47
- Issue
- 1
- Pages
- 77-87
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W2333758883
- Cited by
- 435
- References
- 21
- FWCI
- 9.19
- Type
- journal article
- Language
- en
- Open access
- closed
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