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Volumn 38, Issue 11, 1999, Pages 1658-1660

Self-assembly of quinodimethanes through covalent bonds: A novel principle for the synthesis of functional macrocycles

Author keywords

Dendrimers; Ferrocene; Macrocycles; Quinodimethane; Supramolecular chemistry

Indexed keywords

DENDRIMER; FERROCENE; MACROCYCLIC COMPOUND; QUINONE DERIVATIVE; TETRAMER;

EID: 0033152162     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990601)38:11<1658::AID-ANIE1658>3.0.CO;2-L     Document Type: Article
Times cited : (31)

References (30)
  • 1
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    • Eds.: J.-M. Lehn, J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle, Pergamon, Oxford
    • Self-assembly and supramolecular chemistry: a) Comprehensive Supramolecular Chemistry, Vol. 1-11 (Eds.: J.-M. Lehn, J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle), Pergamon, Oxford, 1996;
    • (1996) Comprehensive Supramolecular Chemistry , vol.1-11
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    • 0000633029 scopus 로고    scopus 로고
    • f) D. Philp, J. F. Stoddart, Angew. Chem. 1996, 108, 1242-1286; Angew. Chem. Int. Ed. Engl. 1996, 35, 1154-1196;
    • (1996) Angew. Chem. , vol.108 , pp. 1242-1286
    • Philp, D.1    Stoddart, J.F.2
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    • 0029811409 scopus 로고    scopus 로고
    • f) D. Philp, J. F. Stoddart, Angew. Chem. 1996, 108, 1242-1286; Angew. Chem. Int. Ed. Engl. 1996, 35, 1154-1196;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1154-1196
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    • 0000892335 scopus 로고
    • e) J. Issberner, R. Moors, F. Vögtle, Angew. Chem. 1994, 106, 2507-2514; Angew. Chem. Int. Ed. Engl. 1994, 33, 2413-2420;
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 2413-2420
  • 19
    • 0000134533 scopus 로고
    • Macrocycles of type 3 and 5 contain 9,9′-diphenyl-9,9′-bi[9H-fluorene] as a partial structure. For the conformational analysis of bifluorenyls, see also a) G. A. Olah, L. D. Field, M. I. Watkins, R. Malhotra, J. Org. Chem. 1981, 46, 1761;
    • (1981) J. Org. Chem. , vol.46 , pp. 1761
    • Olah, G.A.1    Field, L.D.2    Watkins, M.I.3    Malhotra, R.4
  • 23
    • 0345659396 scopus 로고    scopus 로고
    • unpublished results
    • P. Schlaf, unpublished results; R. Hosseinzadeh, unpublished results.
    • Schlaf, P.1
  • 24
    • 0344364733 scopus 로고    scopus 로고
    • unpublished results
    • P. Schlaf, unpublished results; R. Hosseinzadeh, unpublished results.
    • Hosseinzadeh, R.1
  • 25
    • 0345659395 scopus 로고    scopus 로고
    • note
    • 4 symmetrie is possible which leads to the observation of time-averaged NMR spectra. This information serves as the basis for assigning the structures of 3 and 5.
  • 26
    • 0344364735 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum. The individual assignments of all signals is difficult as they are partially hidden by substituent absorptions or overlap which each other. Therefore, the low-field and high-field signals were used for the structure elucidation.
  • 27
    • 0344364734 scopus 로고    scopus 로고
    • note
    • -1.
  • 28
    • 0344796548 scopus 로고    scopus 로고
    • note
    • Of the six chemically different protons on each fluorene ring, two can be observed separately shifted towards high field.
  • 30
    • 85021621670 scopus 로고
    • Dissociation energies of 9,9′-bifluorenyl derivatives: K. Rakus, S.-P. Verevkin, J. Schätzer, H.-D. Beckhaus, C. Rüchardt, Chem. Ber. 1994, 127, 1095-1103; E. M. Arnett, S. Venimadhavan, J. Am. Chem. Soc. 1991, 113, 6967-6975.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6967-6975
    • Arnett, E.M.1    Venimadhavan, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.