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Volumn 46, Issue 43, 2010, Pages 8258-8260

Shape-persistent arylenevinylene macrocycles (AVMs) prepared via acyclic diene metathesis macrocyclization (ADMAC)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; AROMATIC COMPOUND; ARYLENEVINYLENE MACROCYCLE; MACROCYCLIC COMPOUND; MONOMER; NANOFIBRIL; NANOMATERIAL; UNCLASSIFIED DRUG;

EID: 77958507508     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc02941f     Document Type: Article
Times cited : (45)

References (34)
  • 23
    • 0043194171 scopus 로고    scopus 로고
    • Presumably the presence of cis double bonds results in high angle strain in the macrocycles, so the unfavored cyclic products were converted into the most stable cyclohexamer 1 under the reversible, thermodynamically-controlled condition
    • A. K. Chatterjee T.-L. Choi D. P. Sanders R. H. Grubbs J. Am. Chem. Soc. 2003 125 11360
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 11360
    • Chatterjee, A.K.1    Choi, T.-L.2    Sanders, D.P.3    Grubbs, R.H.4
  • 28
    • 0345603311 scopus 로고
    • Linear decyl group was installed to enhance the solubility of AVM 2 and oligomeric reaction intermediates. For the effect of side chain substituents on the self assembly process, see
    • J. Zhang J. S. Moore J. Am. Chem. Soc. 1992 114 9701
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9701
    • Zhang, J.1    Moore, J.S.2
  • 30
    • 40549145875 scopus 로고    scopus 로고
    • Previously the preparation of nanofibrils from carbazole-based AEMs has been reported, and the fibril formation is primarily due to the columnar stacking of the macrocycles, see
    • Y. Che X. Yang L. Zang Chem. Commun. 2008 1413
    • (2008) Chem. Commun. , pp. 1413
    • Che, Y.1    Yang, X.2    Zang, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.