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Volumn 5, Issue 5, 2001, Pages 465-473

Heteroassociation of meso-sulfonatophenylporphyrins with β- and γ-cyclodextrin

Author keywords

Cyclodextrin inclusion complexes; Nuclear Overhauser effect (NOE); Rotational nuclear Overhauser effect spectroscopy (ROESY); Water soluble porphyrins

Indexed keywords

BETA CYCLODEXTRIN; GAMMA CYCLODEXTRIN; PHENYL GROUP; PORPHYRIN DERIVATIVE; SULFONIC ACID DERIVATIVE;

EID: 0035007882     PISSN: 10884246     EISSN: None     Source Type: Journal    
DOI: 10.1002/jpp.346.abs     Document Type: Article
Times cited : (14)

References (43)
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    • Side-to-side aggregates, characterized by a well-defined bathochromic shifted absorption [6-10]
    • Side-to-side aggregates, characterized by a well-defined bathochromic shifted absorption [6-10].
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    • Jelley EE. 1937; 139: 631.
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    • White WI. In The Porphyrins, vol. 5. Dolphin D. (ed). Academic Press: New York, 1978; 303-339.
    • (1978) The Porphyrins , vol.5 , pp. 303-339
    • White, W.I.1
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    • note
    • 4 and β-CD both the 1:1 and 1:2 stoichiometry hypotheses give estimations of equilibrium constant values ranging about four orders of magnitude.
  • 27
    • 85037131744 scopus 로고    scopus 로고
    • note
    • The overlap in some of the NMR samples of some of the proton signals does not allow the straightforward assignment of all detected NOEs, but this does not affect the distinction between both types of structures.
  • 28
    • 0002468584 scopus 로고    scopus 로고
    • Atwood JL, Davis JED, MacNicol D, Vögtle F eds. Pergamon, Elsevier, Oxford
    • Szejtli J. In Comprehensive Supramolecular Chemistry (Atwood JL, Davis JED, MacNicol D, Vögtle F eds.) vol. 3, Pergamon, Elsevier, Oxford, 1996, p. 12.
    • (1996) Comprehensive Supramolecular Chemistry , vol.3 , pp. 12
    • Szejtli, J.1
  • 35
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    • Coordinate files TPHPOR10, TPPPFEC, SIKJOL, BAJJAX, BCDEXDO3 and CIWMIE10 from Cambridge Data Base: Allen FH, Kennard O, Taylor R. Acc. Chem. Res. 1983; 16: 146.
    • (1983) Acc. Chem. Res. , vol.16 , pp. 146
    • Allen, F.H.1    Kennard, O.2    Taylor, R.3
  • 38
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    • note
    • The correlation between H′-6 and H-2 is not clear because of the small differences in their chemical shifts. However, we assume that the detected NOE is with H′-6.
  • 41
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    • note
    • The CD spectra described in Ref. [25] could not be reproduced. We attribute the published signals to a too strongly absorbing solution.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.