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Volumn 78, Issue 12, 2005, Pages 2214-2227

Chemistry of anthracene-acetylene oligomers. II. Synthesis, structure, and properties of 1,8-anthrylene-ethynylene cyclic tetramers and related acyclic oligomers

Author keywords

[No Author keywords available]

Indexed keywords

DIAMOND PRISM; HEPTAMER; ORANGE CRYSTALS; TETRAMERS;

EID: 33644916053     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.78.2214     Document Type: Article
Times cited : (48)

References (91)
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    • 0001854116 scopus 로고
    • ed by P. J. Stang and F. Diederich, VCH, Weinheim, Chap. 12
    • a) J. K. Young and J. S. Moore, "Modern Acetylene Chemistry," ed by P. J. Stang and F. Diederich, VCH, Weinheim (1995), Chap. 12.
    • (1995) Modern Acetylene Chemistry
    • Young, J.K.1    Moore, J.S.2
  • 6
    • 33750614974 scopus 로고    scopus 로고
    • ed by D. Astruc, VCH, Weinheim Chap. 7
    • c) U. H. F. Bunz, "Modern Arene Chemistry," ed by D. Astruc, VCH, Weinheim (2002), Chap. 7.
    • (2002) Modern Arene Chemistry
    • Bunz, U.H.F.1
  • 41
    • 0141570824 scopus 로고    scopus 로고
    • Our recent works on the rotational isomerism of diarylethynes. a) S. Toyota and T. Makino, Tetrahedron Lett., 44, 7775 (2003).
    • (2003) Tetrahedron Lett. , vol.44 , pp. 7775
    • Toyota, S.1    Makino, T.2
  • 60
    • 33750633368 scopus 로고    scopus 로고
    • note
    • Careful measurements revealed that this type of hypochromic effect was insignificant in the Bu-substituted tetramer 2b. We consider that the steric effect of the Bu groups is one of the reasons for the difference between 2a and 2b.
  • 61
    • 0003559584 scopus 로고
    • John Wiley & Sons, Ltd., Chichester
    • a) F. Vögtle, "Cyclophane Chemistry," John Wiley & Sons, Ltd., Chichester (1993), p. 77.
    • (1993) Cyclophane Chemistry , pp. 77
    • Vögtle, F.1
  • 70
    • 0003718955 scopus 로고    scopus 로고
    • The lifetime of the monomer emission of anthracene is ca. 5.2 ns in solution. B. Valeur, "Molecular Fluorescence," (2002), Ref. 26, p. 190.
    • (2002) Molecular Fluorescence , pp. 190
    • Valeur, B.1
  • 79
  • 82
    • 84943076505 scopus 로고
    • It was proposed that the limit of distance required for the photocyclization between two π-systems was ca. 4.2 Å under a topochemical environment. G. M. J. Schmidt, Pure Appl. Chem., 27, 647 (1971).
    • (1971) Pure Appl. Chem. , vol.27 , pp. 647
    • Schmidt, G.M.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.