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Volumn 24, Issue 22, 2005, Pages 5407-5423

Cyclopentadienyl and olefin substituent effects on insertion and β-hydrogen elimination with group 4 metallocenes. kinetics, mechanism, and thermodynamics for zirconocene and hafnocene alkyl hydride derivatives

Author keywords

[No Author keywords available]

Indexed keywords

HYBRID COMPLEXES; HYDRIDE TRANSFER; METAL COMPLEXES; METALLOCENE;

EID: 27544433061     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om0580351     Document Type: Article
Times cited : (81)

References (67)
  • 33
    • 0000839180 scopus 로고
    • 3)(H). However, addition of excess ethylene results in reductive elimination of ethane and formation of the zirconocyclopentane. McAlister, D. R.; Erwin, D. R.; Bercaw, J. E. J. Am. Chem. Soc. 1978, 100, 5966.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 5966
    • McAlister, D.R.1    Erwin, D.R.2    Bercaw, J.E.3
  • 36
    • 0004105856 scopus 로고
    • John Wiley and Sons: New York
    • + were taken from: Isaacs, N. S. Physical Organic Chemistry; John Wiley and Sons: New York, 1986; p 131.
    • (1986) Physical Organic Chemistry , pp. 131
    • Isaacs, N.S.1
  • 39
    • 27544464072 scopus 로고    scopus 로고
    • Brandow, C. G.; Bercaw, J. E. Unpublished results
    • Brandow, C. G.; Bercaw, J. E. Unpublished results.
  • 44
    • 27544511644 scopus 로고
    • Advances in Chemistry Series 167; Chapter 10
    • (a) Bercaw, J. E. In Transition Metal Hydrides; Advances in Chemistry Series 167; 1978; Chapter 10, p 136.
    • (1978) Transition Metal Hydrides , pp. 136
    • Bercaw, J.E.1
  • 48
    • 27544506328 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford; Chapter 3.9
    • Labinger, J. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Chapter 3.9.
    • (1991) Comprehensive Organic Synthesis
    • Labinger, J.A.1
  • 61
    • 27544476720 scopus 로고    scopus 로고
    • note
    • Although a correlation exists between M-C and C-H bond strengths, it is not absolute, and as a result, differences in M-C bond dissociation energies often exceed the differences in the corresponding C-H bond strengths.
  • 64
    • 0002522541 scopus 로고
    • ACS Symposium Series No. 357; Wayda, A. L., Darensbourg, M. Y., Eds.; American Chemical Society: Washington, DC; Chapter 4
    • Burger, B. J.; Bercaw, J. E. In Experimental Organometallic Chemistry; ACS Symposium Series No. 357; Wayda, A. L., Darensbourg, M. Y., Eds.; American Chemical Society: Washington, DC, 1987; Chapter 4.
    • (1987) Experimental Organometallic Chemistry
    • Burger, B.J.1    Bercaw, J.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.