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Volumn 47, Issue 39, 2008, Pages 7485-7488

Halide recognition by tetraoxacalix[2]arene[2]triazine receptors: Concurrent noncovalent halide-π and lone-pair-π interactions in host-halide-water ternary complexes

Author keywords

interactions; Anion recognition; Calixarenes; Host guest systems; Noncovalent interactions

Indexed keywords

CHLORINE COMPOUNDS;

EID: 54749125347     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801705     Document Type: Article
Times cited : (245)

References (40)
  • 1
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    • Supramolecular Chemistry of Anions (Eds: A. Bianchi, K, Bowman-James, E. Garcia-Espana), Wiley-VCH, New York, 1997.
    • Supramolecular Chemistry of Anions (Eds: A. Bianchi, K, Bowman-James, E. Garcia-Espana), Wiley-VCH, New York, 1997.
  • 2
    • 54749130823 scopus 로고    scopus 로고
    • Anion Sensing (Ed.: I. Stibor) in Top. Curr. Chem. 2005, 255, pp. 1-299.
    • Anion Sensing (Ed.: I. Stibor) in Top. Curr. Chem. 2005, 255, pp. 1-299.
  • 6
    • 54749102014 scopus 로고    scopus 로고
    • All review articles in a special issue devoted to anion complexation, Coord. Chem. Rev. 2006, 250(23-24), 2917-3244.
    • d) All review articles in a special issue devoted to anion complexation, Coord. Chem. Rev. 2006, 250(23-24), 2917-3244.
  • 17
    • 54749129558 scopus 로고    scopus 로고
    • D. W. Johnson, B. P. Hay, and co-workers reported that no examples of anion-π complexes for the arenes have been studied theoretically, and the majority of reported contacts between anions and arenes fail to exhibit the expected geometry for an anion-π complex. See refs. [6] and [10].
    • b) D. W. Johnson, B. P. Hay, and co-workers reported that no examples of anion-π complexes for the arenes have been studied theoretically, and the majority of reported contacts between anions and arenes fail to exhibit the expected geometry for an anion-π complex. See refs. [6] and [10].
  • 20
    • 54749096813 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 4182.
    • (2008) Angew. Chem , vol.120 , pp. 4182
  • 22
    • 0033766193 scopus 로고    scopus 로고
    • For a useful overview of heteroatom-bridged calixarenes,see
    • a) For a useful overview of heteroatom-bridged calixarenes,see : B. König, M. H. Fonseca, Eur. J. Inorg. Chem. 2000, 2303;
    • (2000) Eur. J. Inorg. Chem , pp. 2303
    • König, B.1    Fonseca, M.H.2
  • 24
    • 9644275229 scopus 로고    scopus 로고
    • For overviews on recent developments of heteroatom bridged calixaromatics, see: c
    • For overviews on recent developments of heteroatom bridged calixaromatics, see: c) M.-X. Wang, H.-B. Yang, J. Am. Chem. Soc. 2004, 126, 15412;
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 15412
    • Wang, M.-X.1    Yang, H.-B.2
  • 36
    • 34748909971 scopus 로고    scopus 로고
    • Hyperquad2003 software
    • b) Hyperquad2003 software, Protonic Software,http://www.hyperquad.co.uk.
    • Protonic Software
  • 37
    • 54749093665 scopus 로고    scopus 로고
    • Crystallographic data for 1·Cl-(CH 3CH2)4N+·(H 2O)1.5 (C26H31Cl3N 7O5.5, Mr, 635.93, orthorhombic, space group Pnma, a, 24.168(5, b, 16.852(3, c, 14.967(3) Å, α, 90.00, β, 90.00, γ, 90.00°, V, 6096(2) Å3, T, 173(2) K, full-matrix least-squares refinement on F2 converged to RF, 0.1050 [I > 2σ(I, 0.1688 (all data) and Rw(F2, 0.2292 [I > 2σ(I, 0. 2515 (all data),goodness of fit 1.232. Crystallographic data for 1·Br-(CH3CH2)4N +·H2O C26H28BrCl 2N7O5, Mr, 669.35
    • 2) = 0.2746 [I > 2s(I)], 0.2906 (all data),goodnes s of fit 1.644. CCDC 684393 and CCDC 684394 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.