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Volumn 18, Issue 16, 1997, Pages 2060-2074

Hydrogen bonding properties of oxygen and nitrogen acceptors in aromatic heterocycles

Author keywords

Cambridge Structural Database (CSD); Distributed multipole analysis (DMA); Heterocycle; Hydrogen bond; Intermolecular perturbation theory (IMPT)

Indexed keywords


EID: 0000826617     PISSN: 01928651     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-987X(199712)18:16<2060::AID-JCC10>3.0.CO;2-S     Document Type: Article
Times cited : (114)

References (37)
  • 14
    • 85033189869 scopus 로고    scopus 로고
    • personal communication
    • J. P. M. Lommerse, personal communication.
    • Lommerse, J.P.M.1
  • 20
    • 5244358598 scopus 로고
    • University of Cambridge, Cambridge, U.K., This is a suite of quantum chemistry programs developed by R. D. Amos with contributions from I. L. Alberts, J. S. Andrews, S. M. Colwell, N. C. Handy, D. Jayatilaka, P. J. Knowles, R. Kobayashi, N. Koga, K. E. Laidig, P. E. Maslen, C. W. Murray, J. E. Rice, J. Sanz, E. D. Simandiras, A. J. Stone, and M.-D. Su
    • CADPAC5, The Cambridge Analytic Derivatives Package, Issue 5, University of Cambridge, Cambridge, U.K., 1992. This is a suite of quantum chemistry programs developed by R. D. Amos with contributions from I. L. Alberts, J. S. Andrews, S. M. Colwell, N. C. Handy, D. Jayatilaka, P. J. Knowles, R. Kobayashi, N. Koga, K. E. Laidig, P. E. Maslen, C. W. Murray, J. E. Rice, J. Sanz, E. D. Simandiras, A. J. Stone, and M.-D. Su.
    • (1992) The Cambridge Analytic Derivatives Package , Issue.5
  • 28
    • 0004286868 scopus 로고    scopus 로고
    • contributions from A. Dullweber, M. P. Hodges, P. L. A. Popelier, and D. J. Wales, University of Cambridge
    • A. J. Stone, ORIENT Version 3.2, contributions from A. Dullweber, M. P. Hodges, P. L. A. Popelier, and D. J. Wales, University of Cambridge, 1996.
    • (1996) ORIENT Version 3.2
    • Stone, A.J.1
  • 29
    • 85033177047 scopus 로고    scopus 로고
    • note
    • When statistical correction is applied, the range of θ values will be greater than that of φ, and so in the θ-φ scattergram, θ will look more scattered than φ.
  • 33
    • 0004148869 scopus 로고
    • Cornell University Press, Ithaca, NY
    • L. Pauling, The Chemical Bond, Cornell University Press, Ithaca, NY, 1967, p. 223.
    • (1967) The Chemical Bond , pp. 223
    • Pauling, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.