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Volumn 70, Issue 10, 2005, Pages 3806-3813

An evolved explanation for the molecular geometry and electronic structure of diphenyl-substituted cyclic trimethylenemethane in the ground state: A nearly planar conformation with a considerably localized electronic state

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION SPECTROSCOPY; CHEMICAL BONDS; CONFORMATIONS; ELECTRONIC STRUCTURE; EMISSION SPECTROSCOPY; MOLECULAR STRUCTURE; PROBABILITY DENSITY FUNCTION;

EID: 18744395229     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo047893o     Document Type: Article
Times cited : (21)

References (72)
  • 1
    • 0004536241 scopus 로고
    • Mayo, P. d., Ed.; Academic: New York
    • For books or recent experimental reviews for TMMs, see: (a) Berson, J. A. In Rearrangements in Ground and Excited States; Mayo, P. d., Ed.; Academic: New York, 1980; Vol. 1, pp 311-390.
    • (1980) Rearrangements in Ground and Excited States , vol.1 , pp. 311-390
    • Berson, J.A.1
  • 2
    • 0002366798 scopus 로고
    • Borden, W. T., Ed.; John Wiley & Sons: New York
    • (b) Borden, W. T. In Diradicals; Borden, W. T., Ed.; John Wiley & Sons: New York, 1982; pp 1-72.
    • (1982) Diradicals , pp. 1-72
    • Borden, W.T.1
  • 3
    • 0003621829 scopus 로고
    • Borden, W. T., Ed.; John Wiley & Sons: New York
    • (c) Berson, J. A. In Diradicals; Borden, W. T., Ed.; John Wiley & Sons: New York, 1982; pp 151-194.
    • (1982) Diradicals , pp. 151-194
    • Berson, J.A.1
  • 4
    • 4744348454 scopus 로고    scopus 로고
    • Moss, R. A., Platz, M. S., Jones, M., Eds.; John Wiley & Sons: Hoboken
    • (d) Berson, J. A. In Reactive Intermediate Chemistry; Moss, R. A., Platz, M. S., Jones, M., Eds.; John Wiley & Sons: Hoboken, 2004; pp 165-203.
    • (2004) Reactive Intermediate Chemistry , pp. 165-203
    • Berson, J.A.1
  • 14
    • 18744392090 scopus 로고    scopus 로고
    • note
    • Later studies of the Berson group demonstrated that the single molecular species postulate was actually correct. For the details, see the Conclusion.
  • 35
    • 18744377616 scopus 로고    scopus 로고
    • note
    • 14
  • 37
    • 18744403822 scopus 로고    scopus 로고
    • note
    • An apparent emission maximum was observed at 544 nm. See the Supporting Information.
  • 38
    • 18744389875 scopus 로고    scopus 로고
    • note
    • p with planar geometry (θ = 0°, Chart 2), indicating that substitution of two phenyl groups induces elongation of the C-2-C-3 bond, which is probably due to the essentially localized electronic state.
  • 40
    • 18744389601 scopus 로고    scopus 로고
    • note
    • 20 in cycloadditions of other TMMs.
  • 48
    • 18744397058 scopus 로고    scopus 로고
    • note
    • 9b
  • 49
    • 18744363180 scopus 로고    scopus 로고
    • note
    • .., and this was also one of the factors motivating our work.
  • 51
    • 18744387831 scopus 로고    scopus 로고
    • note
    • ..
  • 53
    • 18744376709 scopus 로고    scopus 로고
    • note
    • As one of the reviewers stressed, a spectroscopically undetectable amount of largely twisted TMMs could be a critical reactive species in trapping experiment in solution. We think that more work is needed to establish the reactivity of TMMs in solution.
  • 56
    • 18744375303 scopus 로고    scopus 로고
    • note
    • For further discussion, see refs 1c and 1d.
  • 57
    • 18744411958 scopus 로고    scopus 로고
    • note
    • For example, the results will provide meaningful information on the problem of the difficulty in simulating the |D/hc| value of various TMMs.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.