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Volumn 49, Issue 11, 2010, Pages 1995-1999

Two-component gel formation by pseudoenantiomeric ethynylhelicene oligomers

Author keywords

Circular dichroism; Gels; Pseudoenantiomers; Sol gel processes

Indexed keywords

CHEMICAL EQUATIONS; CIRCULAR DICHROISM; GEL FORMATION; HELICENES; ORGANOGELS; THERMOREVERSIBILITY; TWO-COMPONENT;

EID: 77949353705     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.200906693     Document Type: Article
Times cited : (52)

References (25)
  • 2
    • 34247160897 scopus 로고    scopus 로고
    • Eds, R. G. Weiss, P. Terech, Springer, Dodrecht
    • b) Molecular Gels, (Eds.: R. G. Weiss, P. Terech), Springer, Dodrecht, 2006;
    • (2006) Molecular Gels
  • 7
    • 36348935693 scopus 로고    scopus 로고
    • For recent examples: a
    • For recent examples: a) D. Haldar, Tetrahedron 2008, 64, 186-190;
    • (2008) Tetrahedron , vol.64 , pp. 186-190
    • Haldar, D.1
  • 13
    • 0346076610 scopus 로고    scopus 로고
    • For examples of racemic mixtures forming better gels than enantiomers: a J. Makarević, M. Jokić, Z. Raza, Z. Š tefanić, B. Kojić-Prodić, M. Žinić, Chem. Eur. J. 2003, 9, 5567-5580;
    • For examples of racemic mixtures forming better gels than enantiomers: a) J. Makarević, M. Jokić, Z. Raza, Z. Š tefanić, B. Kojić-Prodić, M. Žinić, Chem. Eur. J. 2003, 9, 5567-5580;
  • 15
    • 18844402447 scopus 로고    scopus 로고
    • For examples of racemic mixtures forming gels but not enantiomers: c M. de Loos, A. Friggeri, J. van Esch, R. M. Kellogg, B. L. Feringa, Org. Biomol. Chem. 2005, 3, 1631-1639;
    • For examples of racemic mixtures forming gels but not enantiomers: c) M. de Loos, A. Friggeri, J. van Esch, R. M. Kellogg, B. L. Feringa, Org. Biomol. Chem. 2005, 3, 1631-1639;
  • 18
    • 23744457908 scopus 로고    scopus 로고
    • Effect of oligomer length on one-component gel: a S. Kawano, N. Fujita S. Shinkai, Chem. Eur. J. 2005, 11, 4735-4742;
    • Effect of oligomer length on one-component gel: a) S. Kawano, N. Fujita S. Shinkai, Chem. Eur. J. 2005, 11, 4735-4742;
  • 21
    • 26844495356 scopus 로고    scopus 로고
    • Use of hydrophobic interactions in a two-component gel: J.-H. Ryu, M. Lee, J. Am. Chem. Soc. 2005, 127, 14170-14171.
    • Use of hydrophobic interactions in a two-component gel: J.-H. Ryu, M. Lee, J. Am. Chem. Soc. 2005, 127, 14170-14171.
  • 24
    • 52449099845 scopus 로고    scopus 로고
    • We recently reported that a (P)-pentamer with a perfluorooctyl side chain interacted with an (M)-pentamer with decyloxycarbonyl side chain forming a hetero-double helix. Thus, a slight change in the side chain structure substantially affected the aggregate structure. R. Amemiya, N. Saito, M. Yamaguchi, J. Org. Chem. 2008, 73, 7137-7144
    • We recently reported that a (P)-pentamer with a perfluorooctyl side chain interacted with an (M)-pentamer with decyloxycarbonyl side chain forming a hetero-double helix. Thus, a slight change in the side chain structure substantially affected the aggregate structure. R. Amemiya, N. Saito, M. Yamaguchi, J. Org. Chem. 2008, 73, 7137-7144.
  • 25
    • 34248551763 scopus 로고    scopus 로고
    • Effect of the ee value on gel formation: A. R. Hirst, B. Huang, V. Castelletto, I. W Hamley, D. K. Smith, Chem. Eur. J. 2007, 13, 2180-2188.
    • Effect of the ee value on gel formation: A. R. Hirst, B. Huang, V. Castelletto, I. W Hamley, D. K. Smith, Chem. Eur. J. 2007, 13, 2180-2188.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.