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Volumn 7, Issue 6, 2007, Pages 1154-1162

Guest-dependent cavities in two-dimensional metal - Organic frameworks sustained by tetrafluoro-1,3-benzenedicarboxylate

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Indexed keywords


EID: 34347248450     PISSN: 15287483     EISSN: None     Source Type: Journal    
DOI: 10.1021/cg070055d     Document Type: Article
Times cited : (58)

References (82)
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    • See the following reviews and references therein: a
    • See the following reviews and references therein: (a) Kitagawa, S.; Kitaura, R.; Noro, S. Angew. Chem., Int. Ed. 2004, 43, 2334-2375.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 2334-2375
    • Kitagawa, S.1    Kitaura, R.2    Noro, S.3
  • 14
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    • (b) Corma, A. Chem. Rev. 1997, 97, 2373-2419.
    • (1997) Chem. Rev , vol.97 , pp. 2373-2419
    • Corma, A.1
  • 28
    • 33750145134 scopus 로고    scopus 로고
    • and references therein
    • (i) Halder, G. J.; Kepert, C. J. Aust. J. Chem. 2006, 59, 597-604 and references therein.
    • (2006) Aust. J. Chem , vol.59 , pp. 597-604
    • Halder, G.J.1    Kepert, C.J.2
  • 34
    • 33750174534 scopus 로고    scopus 로고
    • and references therein
    • (f) Suh, M. P.; Cheon, Y. E. Aust. J. Chem. 2006, 59, 605-612 and references therein.
    • (2006) Aust. J. Chem , vol.59 , pp. 605-612
    • Suh, M.P.1    Cheon, Y.E.2
  • 79
    • 34347262530 scopus 로고    scopus 로고
    • 2 (all data) = 0.107, GOF = 0.89. CCDC deposit number: xxxxxx.Single crystals of TFBDC were grown from a benzene/ethanol mixture.
    • 2 (all data) = 0.107, GOF = 0.89. CCDC deposit number: xxxxxx.Single crystals of TFBDC were grown from a benzene/ethanol mixture.
  • 80
    • 34347241199 scopus 로고    scopus 로고
    • Presumably, the strong electron-withdrawing effects of fluorine atoms interfere with the planar conjugation system of BDC and therefore allow for larger torsion angles and a wider distribution of torsion angles for carboxyl groups
    • Presumably, the strong electron-withdrawing effects of fluorine atoms interfere with the planar conjugation system of BDC and therefore allow for larger torsion angles and a wider distribution of torsion angles for carboxyl groups.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.