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Volumn 62, Issue 9, 2006, Pages 2036-2044

Supramolecular complexation studies of [60]fullerene with calix[4]naphthalenes - A reinvestigation

Author keywords

60 Fullerene; Association constants; Binding constants; Calixarenes; Calixnaphthalenes; Contact pair transitions; Supramolecular complexation

Indexed keywords

(60)FULLERENE; CALIX(4)NAPHTHALENE; CARBON DISULFIDE; FULLERENE DERIVATIVE; NAPHTHALENE DERIVATIVE; TOLUENE; UNCLASSIFIED DRUG;

EID: 31844449499     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.09.151     Document Type: Article
Times cited : (33)

References (43)
  • 2
    • 0003277099 scopus 로고    scopus 로고
    • Calixarenes Revisited
    • J.F. Stoddard Royal Society of Chemistry Cambridge
    • For recent monographs see: (a) C.D. Gutsche J.F. Stoddard Calixarenes Revisited Monographs in Supramolecular Chemistry 1998 Royal Society of Chemistry Cambridge
    • (1998) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 8
    • 0004287470 scopus 로고    scopus 로고
    • Z. Asfari V. Böhmer J. Harrowfield J. Vicens Kluwer Academic Dordrecht
    • Z.-L. Zhong, A. Ikeda, and S. Shinkai Z. Asfari V. Böhmer J. Harrowfield J. Vicens Calixarenes 2001 2001 Kluwer Academic Dordrecht 476 495 Chapter 26
    • (2001) Calixarenes 2001 , pp. 476-495
    • Zhong, Z.-L.1    Ikeda, A.2    Shinkai, S.3
  • 28
    • 31844452340 scopus 로고    scopus 로고
    • note
    • 1H NMR studies see Ref. 16.
  • 36
    • 31844452483 scopus 로고    scopus 로고
    • note
    • The numbering for the protons are based upon the naphthalene ring numbering system.
  • 37
    • 31844433035 scopus 로고    scopus 로고
    • note
    • Molecular modeling was conducted using Spartan'04 Windows version 1.0.3 Molecular Modeling Software from Wavefunction Inc., Irvine, CA, USA. Molecular mechanics (MMFF94) calculations were conducted on the optimized geometry of the host and/or complexes.
  • 40
    • 13844308335 scopus 로고    scopus 로고
    • 60 for a different naphthalene-ring based molecular receptor lacking tert-butyl substituents, which we have recently studied, see: A.H. Tran, D.O. Miller, and P.E. Georghiou J. Org. Chem. 70 2005 1115 1121
    • (2005) J. Org. Chem. , vol.70 , pp. 1115-1121
    • Tran, A.H.1    Miller, D.O.2    Georghiou, P.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.