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Volumn 15, Issue 13, 1996, Pages 2918-2922

Metal-promoted oxidative π-conjugation and coupling of substituted-fulvalene-type ligands: Synthesis and crystal structures of π-conjugated C24H12(SiMe3)2 and the dimer [C24H13(SiMe3)2]2

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Indexed keywords


EID: 0002954546     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om950954b     Document Type: Article
Times cited : (8)

References (39)
  • 1
    • 0040966194 scopus 로고
    • and references cited therein
    • Meyer, A. Y.; Yinnon, H. Tetrahedron 1972, 28, 3915-3928 and references cited therein.
    • (1972) Tetrahedron , vol.28 , pp. 3915-3928
    • Meyer, A.Y.1    Yinnon, H.2
  • 3
    • 0007063953 scopus 로고
    • Butterworths: London
    • Pentafulvalene was first reported by Doering and DeMore, see: (a) Doering, W. v. E. Theoretical Organic Chemistry (The Kekulé Symposium); Butterworths: London, 1959; pp 35-48. (b) DeMore, W. B.; Pritchard, H. O.; Davidson, M. J. Am. Chem. Soc. 1959, 81, 5874-5879.
    • (1959) Theoretical Organic Chemistry (The Kekulé Symposium) , pp. 35-48
    • Doering, W.V.E.1
  • 4
    • 1542543939 scopus 로고
    • Pentafulvalene was first reported by Doering and DeMore, see: (a) Doering, W. v. E. Theoretical Organic Chemistry (The Kekulé Symposium); Butterworths: London, 1959; pp 35-48. (b) DeMore, W. B.; Pritchard, H. O.; Davidson, M. J. Am. Chem. Soc. 1959, 81, 5874-5879.
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 5874-5879
    • DeMore, W.B.1    Pritchard, H.O.2    Davidson, M.3
  • 22
    • 0001136816 scopus 로고
    • Experimental Organometallic Chemistry: A Practicum in Synthesis and Characterization
    • American Chemical Society: Washington, DC
    • Wadya, A. L.; Daresbourg, N. Y. Experimental Organometallic Chemistry: A Practicum in Synthesis and Characterization; ACS Symposium Series 357; American Chemical Society: Washington, DC, 1987.
    • (1987) ACS Symposium Series 357
    • Wadya, A.L.1    Daresbourg, N.Y.2
  • 26
    • 5344232360 scopus 로고    scopus 로고
    • Siemens Analytical Instrument, Inc., Madison, WI, 1990
    • Siemens Analytical Instrument, Inc., Madison, WI, 1990.
  • 27
    • 5344252623 scopus 로고    scopus 로고
    • note
    • The cis assignment is made relative to the least-squares plane of the fused cyclic portion of the molecule.
  • 32
    • 5344270126 scopus 로고    scopus 로고
    • note
    • Bailey et al. reported a C=C twist with an average value of 40° and length of 1.39 Å for 1,1′-bis(isopropoxycarbonyl)-9,9′-bis-(fluorenylidene) and ascribed a diradical character to the bond (see ref 5d).
  • 38
    • 5344267713 scopus 로고    scopus 로고
    • note
    • The trimethylsilyl groups were not included in the determination of the best least-squares plane of each of the substituted-fulvalene fragments.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.