메뉴 건너뛰기




Volumn 13, Issue 3, 2012, Pages 695-698

Do cation⋯π interactions always need to be 1:1?

Author keywords

cation pi interactions; charge transfer; density functional theory; intermolecular forces; supramolecular chemistry

Indexed keywords

CHARGE TRANSFER; CHEMICAL BONDS; CRYSTAL STRUCTURE; POSITIVE IONS; SUPRAMOLECULAR CHEMISTRY;

EID: 84857314406     PISSN: 14394235     EISSN: 14397641     Source Type: Journal    
DOI: 10.1002/cphc.201100996     Document Type: Article
Times cited : (41)

References (44)
  • 22
    • 33845301210 scopus 로고    scopus 로고
    • For a discussion on the limit to the puckering of benzene and yet sustaining aromaticity.
    • For a discussion on the limit to the puckering of benzene and yet sustaining aromaticity:, A. Datta, S. K. Pati, Chem. Phys. Lett. 2006, 433, 67.
    • (2006) Chem. Phys. Lett. , vol.433 , pp. 67
    • Datta, A.1    Pati, S.K.2
  • 42
    • 0011190497 scopus 로고    scopus 로고
    • GIAO NMR shielding at M06-2X/6-31+G(d,p) for NICS(0) and NICS(1) in HAB are -11.2 ppm and -37.8 ppm respectively suggesting its aromatic character. For discussion on the GIAO method
    • GIAO NMR shielding at M06-2X/6-31+G(d,p) for NICS(0) and NICS(1) in HAB are -11.2 ppm and -37.8 ppm respectively suggesting its aromatic character. For discussion on the GIAO method:, P. v. R. Schleyer, C. Maerker,;, A. Dransfeld, H. Jiao, N. J. R. v. Eikema-Hommas, J. Am. Chem. Soc. 1996, 118, 6317
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 6317
    • Schleyer V. P, R.1    Maerker, C.2    Dransfeld, A.3    Jiao, H.4    Eikema-Hommas, N.J.R.V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.