Phosphine oxides (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Phosphine oxides" in English language version.

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10doi.org

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4harvard.edu

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4nih.gov

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3semanticscholar.org

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2handle.net

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2worldcat.org

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1rsc.org

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1orgsyn.org

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1radtech.org

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doi.org

D. B. Chesnut (1999). "The Electron Localization Function (ELF) Description of the PO Bond in Phosphine Oxide". Journal of the American Chemical Society. 121 (10): 2335–2336. Bibcode:1999JAChS.121.2335C. doi:10.1021/ja984314m.
Gilheany, Declan G. (1994). "No d Orbitals but Walsh Diagrams and Maybe Banana Bonds: Chemical Bonding in Phosphines, Phosphine Oxides, and Phosphonium Ylides". Chemical Reviews. 94 (5): 1339–1374. doi:10.1021/cr00029a008. PMID 27704785.
Gallen, Albert; Riera, Antoni; Verdaguer, Xavier; Grabulosa, Arnald (2019). "Coordination Chemistry and Catalysis with Secondary Phosphine oxides". Catalysis Science & Technology. 9 (20): 5504–5561. doi:10.1039/C9CY01501A. hdl:2445/164459. S2CID 202885438.
Ackermann, Lutz (2007). "Catalytic Arylations with Challenging Substrates: From Air-Stable HASPO Preligands to Indole Syntheses and C-H-Bond Functionalizations". Synlett. 2007 (4): 0507–0526. doi:10.1055/s-2007-970744.
Horký, Filip; Císařová, Ivana; Štěpnička, Petr (2021). "A Stable Primary Phosphane Oxide and Its Heavier Congeners". Chemistry – A European Journal. 27 (4): 1282–1285. doi:10.1002/chem.202003702. PMID 32846012. S2CID 221346479.
Denniston, Michael L.; Martin, Donald R. (1977). "Methyldiphenylphosphine Oxide and Dimethylphenylphosphine Oxide". Inorganic Syntheses. Vol. 17. pp. 183–185. doi:10.1002/9780470132487.ch50. ISBN 9780470132487.
Podyacheva, Evgeniya; Kuchuk, Ekaterina; Chusov, Denis (2019). "Reduction of phosphine oxides to phosphines". Tetrahedron Letters. 60 (8): 575–582. doi:10.1016/j.tetlet.2018.12.070. S2CID 104364715.
van Kalkeren, Henri A.; van Delft, Floris L.; Rutjes, Floris P. J. T. (2013). "Organophosphorus Catalysis to Bypass Phosphine Oxide Waste". ChemSusChem. 6 (9): 1615–1624. Bibcode:2013ChSCh...6.1615V. doi:10.1002/cssc.201300368. hdl:2066/117145. ISSN 1864-5631. PMID 24039197.
Klaus Naumann; Gerald Zon; Kurt Mislow (1969). "Use of hexachlorodisilane as a reducing agent. Stereospecific deoxygenation of acyclic phosphine oxides". Journal of the American Chemical Society. 91 (25): 7012–7023. Bibcode:1969JAChS..91.7012N. doi:10.1021/ja01053a021.
Li, Yuehui; Lu, Liang-Qiu; Das, Shoubhik; Pisiewicz, Sabine; Junge, Kathrin; Beller, Matthias (2012). "Highly Chemoselective Metal-Free Reduction of Phosphine Oxides to Phosphines". Journal of the American Chemical Society. 134 (44): 18325–18329. Bibcode:2012JAChS.13418325L. doi:10.1021/ja3069165. ISSN 0002-7863. PMID 23062083.

handle.net

hdl.handle.net

Gallen, Albert; Riera, Antoni; Verdaguer, Xavier; Grabulosa, Arnald (2019). "Coordination Chemistry and Catalysis with Secondary Phosphine oxides". Catalysis Science & Technology. 9 (20): 5504–5561. doi:10.1039/C9CY01501A. hdl:2445/164459. S2CID 202885438.
van Kalkeren, Henri A.; van Delft, Floris L.; Rutjes, Floris P. J. T. (2013). "Organophosphorus Catalysis to Bypass Phosphine Oxide Waste". ChemSusChem. 6 (9): 1615–1624. Bibcode:2013ChSCh...6.1615V. doi:10.1002/cssc.201300368. hdl:2066/117145. ISSN 1864-5631. PMID 24039197.

harvard.edu

ui.adsabs.harvard.edu

D. B. Chesnut (1999). "The Electron Localization Function (ELF) Description of the PO Bond in Phosphine Oxide". Journal of the American Chemical Society. 121 (10): 2335–2336. Bibcode:1999JAChS.121.2335C. doi:10.1021/ja984314m.
van Kalkeren, Henri A.; van Delft, Floris L.; Rutjes, Floris P. J. T. (2013). "Organophosphorus Catalysis to Bypass Phosphine Oxide Waste". ChemSusChem. 6 (9): 1615–1624. Bibcode:2013ChSCh...6.1615V. doi:10.1002/cssc.201300368. hdl:2066/117145. ISSN 1864-5631. PMID 24039197.
Klaus Naumann; Gerald Zon; Kurt Mislow (1969). "Use of hexachlorodisilane as a reducing agent. Stereospecific deoxygenation of acyclic phosphine oxides". Journal of the American Chemical Society. 91 (25): 7012–7023. Bibcode:1969JAChS..91.7012N. doi:10.1021/ja01053a021.
Li, Yuehui; Lu, Liang-Qiu; Das, Shoubhik; Pisiewicz, Sabine; Junge, Kathrin; Beller, Matthias (2012). "Highly Chemoselective Metal-Free Reduction of Phosphine Oxides to Phosphines". Journal of the American Chemical Society. 134 (44): 18325–18329. Bibcode:2012JAChS.13418325L. doi:10.1021/ja3069165. ISSN 0002-7863. PMID 23062083.

nih.gov

pubmed.ncbi.nlm.nih.gov

Gilheany, Declan G. (1994). "No d Orbitals but Walsh Diagrams and Maybe Banana Bonds: Chemical Bonding in Phosphines, Phosphine Oxides, and Phosphonium Ylides". Chemical Reviews. 94 (5): 1339–1374. doi:10.1021/cr00029a008. PMID 27704785.
Horký, Filip; Císařová, Ivana; Štěpnička, Petr (2021). "A Stable Primary Phosphane Oxide and Its Heavier Congeners". Chemistry – A European Journal. 27 (4): 1282–1285. doi:10.1002/chem.202003702. PMID 32846012. S2CID 221346479.
van Kalkeren, Henri A.; van Delft, Floris L.; Rutjes, Floris P. J. T. (2013). "Organophosphorus Catalysis to Bypass Phosphine Oxide Waste". ChemSusChem. 6 (9): 1615–1624. Bibcode:2013ChSCh...6.1615V. doi:10.1002/cssc.201300368. hdl:2066/117145. ISSN 1864-5631. PMID 24039197.
Li, Yuehui; Lu, Liang-Qiu; Das, Shoubhik; Pisiewicz, Sabine; Junge, Kathrin; Beller, Matthias (2012). "Highly Chemoselective Metal-Free Reduction of Phosphine Oxides to Phosphines". Journal of the American Chemical Society. 134 (44): 18325–18329. Bibcode:2012JAChS.13418325L. doi:10.1021/ja3069165. ISSN 0002-7863. PMID 23062083.

orgsyn.org

W. B. McCormack (1973). "3-Methyl-1-Phenylphospholene oxide". Organic Syntheses; Collected Volumes, vol. 5, p. 787.

radtech.org

"Boosting the cure of phosphine oxide photoinitiators.Sensitisation or Synergy?" (PDF). Retrieved 2025-03-27.

rsc.org

pubs.rsc.org

In fact, the N-O bonds in amine oxides are more likely to be closer to double bonds than are those of the P-O bonds in phosphine oxides; see e.g. https://pubs.rsc.org/en/content/articlelanding/2015/sc/c5sc02076j#:~:text=Quantitative%20analysis%20of%20known%20species%20of%20general%20formulae,high%20degree%20of%20covalent%20rather%20than%20ionic%20bonding.

semanticscholar.org

api.semanticscholar.org

Gallen, Albert; Riera, Antoni; Verdaguer, Xavier; Grabulosa, Arnald (2019). "Coordination Chemistry and Catalysis with Secondary Phosphine oxides". Catalysis Science & Technology. 9 (20): 5504–5561. doi:10.1039/C9CY01501A. hdl:2445/164459. S2CID 202885438.
Horký, Filip; Císařová, Ivana; Štěpnička, Petr (2021). "A Stable Primary Phosphane Oxide and Its Heavier Congeners". Chemistry – A European Journal. 27 (4): 1282–1285. doi:10.1002/chem.202003702. PMID 32846012. S2CID 221346479.
Podyacheva, Evgeniya; Kuchuk, Ekaterina; Chusov, Denis (2019). "Reduction of phosphine oxides to phosphines". Tetrahedron Letters. 60 (8): 575–582. doi:10.1016/j.tetlet.2018.12.070. S2CID 104364715.

worldcat.org

search.worldcat.org

van Kalkeren, Henri A.; van Delft, Floris L.; Rutjes, Floris P. J. T. (2013). "Organophosphorus Catalysis to Bypass Phosphine Oxide Waste". ChemSusChem. 6 (9): 1615–1624. Bibcode:2013ChSCh...6.1615V. doi:10.1002/cssc.201300368. hdl:2066/117145. ISSN 1864-5631. PMID 24039197.
Li, Yuehui; Lu, Liang-Qiu; Das, Shoubhik; Pisiewicz, Sabine; Junge, Kathrin; Beller, Matthias (2012). "Highly Chemoselective Metal-Free Reduction of Phosphine Oxides to Phosphines". Journal of the American Chemical Society. 134 (44): 18325–18329. Bibcode:2012JAChS.13418325L. doi:10.1021/ja3069165. ISSN 0002-7863. PMID 23062083.