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Volumn 119, Issue 51, 1997, Pages 12503-12513

Controlling catenations, properties and relative ring-component movements in catenanes with aromatic fluorine substituents

Author keywords

[No Author keywords available]

Indexed keywords

FLUORINE DERIVATIVE;

EID: 0031585689     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja970640a     Document Type: Article
Times cited : (68)

References (55)
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    • note
    • 1H NMR dilution experiment.
  • 40
    • 2642600309 scopus 로고    scopus 로고
    • note
    • A macrocyclic polyether of similar size to bis-p-phenylene-34-crown-10 but with no aromatic units, i.e. 36-crown-12, is unable to template the formation of a [2]catenane with cyclobis(paraquat-p-phenylene), as the other ring component, either at ambient or ultrahigh pressure.
  • 42
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    • Directing of the C-F bond into the π face of the p-phenylene ring is not altogether surprising given the reluctance of organic fluorine, despite the high electronegativity of fluorine, to function as a hydrogen bond acceptor see: Dunitz, J. D.; Taylor, R. Chem. Eur. J. 1997, 3, 89-98.
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    • note
    • 3CN solution at 303 K: it revealed that irradiation of a low intensity signal at δ 6.18 for the "alongside" hydroquinone ring protons leads to an enhancement of a signal at δ 3.75, for the "inside" hydroquinone ring protons.
  • 48
    • 2642599273 scopus 로고    scopus 로고
    • note
    • 6 (25% at 12 kbar).
  • 54
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    • note
    • 4-). We feel that this nomenclature system facilitates the comparison of the UV-vis spectroscopic and electrochemical properties of the macrocyclic polyethers and catenanes with those of the reference compounds.
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    • Spartan V4.1, Wavefunction Inc., 18401 Von Karman Ave., 370 Irvine CA 92715.


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