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Volumn 118, Issue 41, 1996, Pages 9988-9989

Decisive evidence for nonclassical bonding in five-vertex closo-boranes X2B3H3, X = N, CH, P, SiH, BH-

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOBORON DERIVATIVE;

EID: 0029966162     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja962036q     Document Type: Article
Times cited : (48)

References (35)
  • 7
    • 10344243783 scopus 로고    scopus 로고
    • 2- was deduced to be zero, using graph theoretical approaches in ref 4a
    • 2- was deduced to be zero, using graph theoretical approaches in ref 4a.
  • 9
    • 0003500644 scopus 로고
    • Liebman, J. F., Greenberg, A., Williams, R E.. Eds.; VCH Publishers: New York, and references cited therein
    • Beaudet, R. A. In Advances in Boron and the Boranes; Liebman, J. F., Greenberg, A., Williams, R E.. Eds.; VCH Publishers: New York, 1988 and references cited therein.
    • (1988) Advances in Boron and the Boranes
    • Beaudet, R.A.1
  • 18
    • 0011083499 scopus 로고
    • and references therein
    • (b) Reed, A. E.; Weinhold, F. Chem. Rev. 1988, 88, 899 and references therein,
    • (1988) Chem. Rev. , vol.88 , pp. 899
    • Reed, A.E.1    Weinhold, F.2
  • 23
    • 0000239121 scopus 로고
    • Diamagnetic Susceptibility Exaltation as Criterion of Aromaticity
    • Snyder, Ed.; Academic Press: New York
    • (b) Dauben, H. J., Jr.; Wilson, J. D.; Laity, J. L. Diamagnetic Susceptibility Exaltation as Criterion of Aromaticity In Non-Benzenoid Aromatks; Snyder, Ed.; Academic Press: New York, 1971; Vol. 2.
    • (1971) Non-Benzenoid Aromatks , vol.2
    • Dauben Jr., H.J.1    Wilson, J.D.2    Laity, J.L.3
  • 29
    • 0011190497 scopus 로고    scopus 로고
    • (a) The nucleus independent chemical shift (NICS) is defined as the negative of the absolute magnetié shielding computed, for example, at the geometrical center or other points of a ring (cage) molecule. Aromatic (diatropic) compounds have significant negative NICS, while antiaromatic molecules (paratropic) are characterized by positive NICS values. Schleyer, P. v. R.; Maerker, C.; Dransfeld, A.; Jiao, H.; Hommes, N. J. v. E. J. Am. Chem. Soc. 1996, 118, 6317.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 6317
    • Schleyer, P.V.R.1    Maerker, C.2    Dransfeld, A.3    Jiao, H.4    Hommes, N.J.V.E.5
  • 33
    • 10344227996 scopus 로고    scopus 로고
    • 2h) are 1.008 and 0.892, respectively
    • 2h) are 1.008 and 0.892, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.