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Volumn 76, Issue 2, 2011, Pages 492-499

Double-threaded dimer and supramolecular oligomer formed by stilbene modified cyclodextrin: Effect of acyl migration and photostimuli

Author keywords

[No Author keywords available]

Indexed keywords

ACYL MIGRATION; AQUEOUS SOLUTIONS; CDS; DIFFUSION COEFFICIENTS; EQUILIBRIUM STATE; HYDROXYL GROUPS; MIGRATION RATES; MODIFIED CYCLODEXTRINS; NEUTRAL CONDITIONS; PHOTO-IRRADIATION; PHOTOINDUCED ISOMERIZATION; PHOTOSTATIONARY STATE; SUPRAMOLECULAR STRUCTURE; THERMAL ISOMERIZATIONS;

EID: 78651469914     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101936t     Document Type: Article
Times cited : (21)

References (81)
  • 3
    • 33749554122 scopus 로고    scopus 로고
    • Pearson Education: Upper Saddle River, NJ
    • Liu, C. Foundations of MEMS; Pearson Education: Upper Saddle River, NJ, 2006.
    • (2006) Foundations of MEMS
    • Liu, C.1
  • 27
    • 0004240038 scopus 로고    scopus 로고
    • Ed.; Willey, VCH: Weinheim, Germany, Sec. 7, "Switchable Catenanes and Molecular Shuttles"
    • Raymo, F. M.; Stoddart, J. F. Molecular Switches; Feringa, B. L., Ed.; Willey, VCH: Weinheim, Germany, 2001, Sec. 7, "Switchable Catenanes and Molecular Shuttles".
    • (2001) Molecular Switches
    • Raymo, F.M.1    Stoddart, J.F.2    Feringa, B.L.3
  • 49
    • 0004240038 scopus 로고    scopus 로고
    • Ed.; Willey, VCH: Weinheim, Germany,; Sec. 2, "Photoswitchable Molecular Systems Based on Diarylethenes"
    • Irie, M. Molecular Switches; Feringa, B. L., Ed.; Willey, VCH: Weinheim, Germany, 2001; Sec. 2, "Photoswitchable Molecular Systems Based on Diarylethenes".
    • (2001) Molecular Switches
    • Irie, M.1    Feringa, B.L.2
  • 61
    • 84855619663 scopus 로고    scopus 로고
    • Although three kinds of StiO-α-CD (2-trans -StiO-α-CD, 3-trans -StiO-α-CD, and 6-trans -StiO-α-CD) are prepared by in the mixture of α-CD and Succinimidyl-N -(4-stilbene carboxylate), 6-trans -StiO-α-CD having the StiO group at the primary hydroxyl group forms little. Main product of the reaction gives 2-trans -StiO-α-CD and 3-trans -StiO-α-CD because the secondary hydroxyl group forms the hydrogen bond network to activate the nucleophilicity
    • Although three kinds of StiO-α-CD (2-trans -StiO-α-CD, 3-trans -StiO-α-CD, and 6-trans -StiO-α-CD) are prepared by in the mixture of α-CD and Succinimidyl-N -(4-stilbene carboxylate), 6-trans -StiO-α-CD having the StiO group at the primary hydroxyl group forms little. Main product of the reaction gives 2-trans -StiO-α-CD and 3-trans -StiO-α-CD because the secondary hydroxyl group forms the hydrogen bond network to activate the nucleophilicity.


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