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Volumn 31, Issue 6, 2012, Pages 2219-2230

Synthesis, structure, spectroscopy, and reactivity of azapentadienyl- cobalt-phosphine complexes 1

Author keywords

[No Author keywords available]

Indexed keywords

BOND DISTANCE; DICATIONIC PRODUCTS; LIGAND EXCHANGES; LIGAND SUBSTITUTION REACTIONS; RESONANCE STRUCTURE; TRIFLIC ACIDS; TRIMETHYL PHOSPHITE; X RAY CRYSTAL STRUCTURES;

EID: 84859145861     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om2011326     Document Type: Article
Times cited : (7)

References (21)
  • 8
    • 0001129470 scopus 로고
    • For azapentadienyl-metal-phosphine complexes, see
    • For azapentadienyl-metal-phosphine complexes, see: Bleeke, J. R.; Luaders, S. T.; Robinson, K. D. Organometallics 1994, 13, 1592-1600
    • (1994) Organometallics , vol.13 , pp. 1592-1600
    • Bleeke, J.R.1    Luaders, S.T.2    Robinson, K.D.3
  • 9
    • 0002796181 scopus 로고
    • For phosphapentadienyl-metal-phosphine complexes, see
    • For phosphapentadienyl-metal-phosphine complexes, see: Bleeke, J. R.; Rohde, A. M.; Robinson, K. D. Organometallics 1995, 14, 1674-1680
    • (1995) Organometallics , vol.14 , pp. 1674-1680
    • Bleeke, J.R.1    Rohde, A.M.2    Robinson, K.D.3
  • 10
    • 45449103106 scopus 로고    scopus 로고
    • For silapentadienyl-metal-phosphine complexes, see
    • For silapentadienyl-metal-phosphine complexes, see: Bleeke, J. R.; Thananatthanachon, T.; Rath, N. P. Organometallics 2008, 27, 2436-2446
    • (2008) Organometallics , vol.27 , pp. 2436-2446
    • Bleeke, J.R.1    Thananatthanachon, T.2    Rath, N.P.3
  • 13
    • 0000531567 scopus 로고
    • For synthesis of the analogous Li salt, see
    • For synthesis of the analogous Li salt, see: Wolf, G.; Wurthwein, E.-U. Chem. Ber. 1991, 124, 889-896
    • (1991) Chem. Ber. , vol.124 , pp. 889-896
    • Wolf, G.1    Wurthwein, E.-U.2
  • 14
    • 33847089848 scopus 로고
    • Alternatively, a Berry pseudorotation may be responsible, but the small "bite angle" of the allyl moiety makes this pathway more strained and, in our view, less likely. See
    • Alternatively, a Berry pseudorotation may be responsible, but the small "bite angle" of the allyl moiety makes this pathway more strained and, in our view, less likely. See: Albright, T. A.; Hofmann, P.; Hoffmann, R. J. Am. Chem. Soc. 1977, 99, 7546-7557
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 7546-7557
    • Albright, T.A.1    Hofmann, P.2    Hoffmann, R.3
  • 19
    • 84859126850 scopus 로고    scopus 로고
    • MiTeGen, LLC, PO Box 3867, Ithaca, NY, 14852.
    • MiTeGen, LLC, PO Box 3867, Ithaca, NY, 14852.
  • 20
    • 67651050932 scopus 로고    scopus 로고
    • Bruker Analytical X-Ray, Madison, WI.
    • Apex II and SAINT; Bruker Analytical X-Ray, Madison, WI, 2008.
    • (2008) Apex II and SAINT


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.