Metal-phosphine complex (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Metal-phosphine complex" in English language version.

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archive.org

doi.org

  • Iaroshenko, Viktor (4 January 2019). "Phosphines and Related Tervalent Phosphorus Systems". In Van Leeuwen, Piet W. N. M. (ed.). Organophosphorus Chemistry: From Molecules to Applications. pp. 1–58. doi:10.1002/9783527672240.ch1. ISBN 9783527672240.
  • Miyaura, Norio; Suzuki, Akira (1993). "Palladium-Catalyzed Reaction of 1-Alkenylboronates with Vinylic Halides: (1Z,3E)-1-Phenyl-1,3-octadiene". Org. Synth. 68: 130. doi:10.15227/orgsyn.068.0130.
  • Osborn, J. A.; Wilkinson, G. (1967). "Tris(triphenylphosphine)halorhodium(I)". Inorganic Syntheses. Vol. 10. p. 67. doi:10.1002/9780470132418.ch12. ISBN 9780470131695.
  • Tolman, C. A. (1977). "Steric effects of Phosphorus Ligands in Organometallic Chemistry and Homogeneous Catalysis". Chemical Reviews. 77 (3): 313–348. doi:10.1021/cr60307a002.
  • Orpen, A. G.; Connelly, N. G. (1990). "Structural Systematics: the Role of P-A σ* Orbitals in Metal-Phosphorus π-Bonding in Redox-Related Pairs of M-PA3 Complexes (A = R, Ar, OR; R = alkyl)". Organometallics. 9 (4): 1206–1210. doi:10.1021/om00118a048.
  • Gilheany, D. G. (1994). "No d Orbitals but Walsh Diagrams and Maybe Banana Bonds: Chemical Bonding in Phosphines, Phosphine Oxides, and Phosphonium Ylides". Chem. Rev. 94 (5): 1339–1374. doi:10.1021/cr00029a008. PMID 27704785.
  • Newman-Stonebraker, Samuel H.; Smith, Sleight R.; Borowski, Julia E.; Peters, Ellyn; Gensch, Tobias; Johnson, Heather C.; Sigman, Matthew S.; Doyle, Abigail G. (2021). "Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis". Science. 374 (6565): 301–308. Bibcode:2021Sci...374..301N. doi:10.1126/science.abj4213. PMID 34648340. S2CID 238991361.
  • Garrou, Philip E. (1985). "Transition-Metal-Mediated Phosphorus-Carbon Bond Cleavage and Its Relevance to Homogeneous Catalyst Deactivation". Chem. Rev. 85 (3): 171–185. doi:10.1021/cr00067a001.
  • Reppe, W.; Schweckendiek, W. J. (31 July 1948). "Cyclisierende Polymerisation von Acetylen. III Benzol, Benzolderivate und hydroaromatische Verbindungen". Justus Liebigs Annalen der Chemie. 560 (1): 104–116. doi:10.1002/jlac.19485600104.
  • Slaugh, L; Mullineaux, R. (1968). "Novel Hydroformylation catalysts". J. Organomet. Chem. 13 (2): 469. doi:10.1016/S0022-328X(00)82775-8.
  • Herrmann, W. A.; Kohlpaintner, C. W. (1998). "Syntheses of Water-Soluble Phosphines and their Transition Metal Complexes". Inorganic Syntheses. Vol. 32. pp. 8–25. doi:10.1002/9780470132630.ch2. ISBN 9780471249214. {{cite book}}: |journal= ignored (help)

harvard.edu

ui.adsabs.harvard.edu

  • Newman-Stonebraker, Samuel H.; Smith, Sleight R.; Borowski, Julia E.; Peters, Ellyn; Gensch, Tobias; Johnson, Heather C.; Sigman, Matthew S.; Doyle, Abigail G. (2021). "Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis". Science. 374 (6565): 301–308. Bibcode:2021Sci...374..301N. doi:10.1126/science.abj4213. PMID 34648340. S2CID 238991361.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Gilheany, D. G. (1994). "No d Orbitals but Walsh Diagrams and Maybe Banana Bonds: Chemical Bonding in Phosphines, Phosphine Oxides, and Phosphonium Ylides". Chem. Rev. 94 (5): 1339–1374. doi:10.1021/cr00029a008. PMID 27704785.
  • Newman-Stonebraker, Samuel H.; Smith, Sleight R.; Borowski, Julia E.; Peters, Ellyn; Gensch, Tobias; Johnson, Heather C.; Sigman, Matthew S.; Doyle, Abigail G. (2021). "Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis". Science. 374 (6565): 301–308. Bibcode:2021Sci...374..301N. doi:10.1126/science.abj4213. PMID 34648340. S2CID 238991361.

semanticscholar.org

api.semanticscholar.org

  • Newman-Stonebraker, Samuel H.; Smith, Sleight R.; Borowski, Julia E.; Peters, Ellyn; Gensch, Tobias; Johnson, Heather C.; Sigman, Matthew S.; Doyle, Abigail G. (2021). "Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis". Science. 374 (6565): 301–308. Bibcode:2021Sci...374..301N. doi:10.1126/science.abj4213. PMID 34648340. S2CID 238991361.