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Volumn 37, Issue 24, 1999, Pages 3394-3397

Sapphyrin supramolecules through C-H · · · S and C-H · · · Se hydrogen bonds - First structural characterization of meso-arylsapphyrins bearing heteroatoms

Author keywords

Hydrogen bonds; Porphyrinoids; Supramolecular chemistry

Indexed keywords

PORPHYRIN DERIVATIVE;

EID: 0033521582     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19981231)37:24<3394::AID-ANIE3394>3.0.CO;2-4     Document Type: Article
Times cited : (83)

References (29)
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    • and references therein
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    • note
    • Such an intermediate (sapphyrinogen) has been proposed by Latos-Grazyński for the formation of sapphyrins; see reference [6]. Experiments are in progress to monitor the formation of rubyrinogen by UV absorption spectroscopy.
  • 21
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    • We would like to thank the referee who brought to our attention a recent paper by Latos-Grazyński and co-workers published after submission of this manuscript in which an asymmetric tautomer for 5,10,15,20-tetraphenyl-26,28-dithiasapphyrin was proposed. For details see: K. Rachlewicz, N. Sprutta, P. J. Chmielewski, L. Latos-Grazyński, J. Chem. Soc. Perkin Trans. 2 1998, 969-975.
    • (1998) J. Chem. Soc. Perkin Trans. 2 , pp. 969-975
    • Rachlewicz, K.1    Sprutta, N.2    Chmielewski, P.J.3    Latos-Grazyński, L.4
  • 22
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    • note
    • 2 using SHELXTL Version 5.03.5. Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-101 360. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: (+44)1223-336-033; e-mail: deposit@ccdc.cam. ac.uk) .
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    • [10b]
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    • note
    • 3 solution of 6 resulted in gradual broadening of the signals, suggesting the existence of aggregates due to intermolecular interactions in solution.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.