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Volumn 53, Issue 1, 2014, Pages 568-577

1′-(diphenylphosphino)-1-cyanoferrocene: A simple ligand with complicated coordination behavior toward copper(I)

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EID: 84891765912     PISSN: 00201669     EISSN: 1520510X     Source Type: Journal    
DOI: 10.1021/ic4026848     Document Type: Article
Times cited : (35)

References (121)
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    • 2CN easily undergoes deprotonation at the methylene group. The resulting C anion can be used as a ligand in transition-metal complexes
    • 2CN easily undergoes deprotonation at the methylene group. The resulting C anion can be used as a ligand in transition-metal complexes. For a review, see: Braunstein, P. Chem. Rev. 2006, 106, 134-159
    • (2006) Chem. Rev. , vol.106 , pp. 134-159
    • Braunstein, P.1
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    • 2OH·HCl/KI/ZnO in hot acetonitrile, which was shown to work well with (unsubstituted) ferrocenecarboxaldehyde, gave disappointing results in the case of 1. Using this procedure, nitrile 3 was not only isolated in a low yield but was also contaminated with the difficult-to-separate starting aldehyde
    • 2OH·HCl/KI/ZnO in hot acetonitrile, which was shown to work well with (unsubstituted) ferrocenecarboxaldehyde, gave disappointing results in the case of 1. Using this procedure, nitrile 3 was not only isolated in a low yield but was also contaminated with the difficult-to-separate starting aldehyde. See: Kivrak, A.; Zora, M. J. Organomet. Chem. 2007, 692, 2346-2349
    • (2007) J. Organomet. Chem. , vol.692 , pp. 2346-2349
    • Kivrak, A.1    Zora, M.2
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    • 2 at 0.19 and 0.53, respectively
    • 2, at 0.19 and 0.53, respectively. Data from: Hansch, C.; Leo, A.; Taft, R. W. Chem. Rev. 1991, 91, 165-195
    • (1991) Chem. Rev. , vol.91 , pp. 165-195
    • Hansch, C.1    Leo, A.2    Taft, R.W.3
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    • Wilkinson, G. Gillard, R. D. McCleverty, J. A. Pergamon Press: New York, Vol. Chapter 53
    • Hathaway, B. J. In Comprehensive Coordination Chemistry; Wilkinson, G.; Gillard, R. D.; McCleverty, J. A., Eds.; Pergamon Press: New York, 1987; Vol. 5, Chapter 53, p 533-774.
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    • Hathaway, B.J.1
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    • 3: Lippard, S. J.; Ucko, D. A. Inorg. Chem. 1968, 7, 1051-1056 and references therein
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    • Lippard, S.J.1    Ucko, D.A.2
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    • version 5.33, in Nov 2011 with updates from Nov 2011 and from Feb, May, and Aug 2012.
    • According to a search in the Cambridge Structural Database, version 5.33, in Nov 2011 with updates from Nov 2011 and from Feb, May, and Aug 2012.
    • According to a Search in the Cambridge Structural Database
  • 120
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    • For an overview of the chemistry of ferrocene ligands, see: Wiley: Chichester, U.K.
    • For an overview of the chemistry of ferrocene ligands, see: Ferrocenes: Ligands, Materials and Biomolecules; Štěpnička, P., Ed.; Wiley: Chichester, U.K., 2008.
    • (2008) Ferrocenes: Ligands, Materials and Biomolecules
    • Štěpnička, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.