메뉴 건너뛰기




Volumn 12, Issue 9, 2006, Pages 2482-2487

Chemistry of anthracene-acetylene oligomers: Synthesis and enantiomeric resolution of a chiral 1,8-anthrylene-ethynylene cyclic tetramer

Author keywords

Arylene ethynylenes; Chiral resolution; Cross coupling; Macrocycles; Nanostructures

Indexed keywords

CRYSTAL SYMMETRY; NANOSTRUCTURED MATERIALS; SYNTHESIS (CHEMICAL);

EID: 33644919106     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200501111     Document Type: Article
Times cited : (28)

References (26)
  • 1
    • 33644909009 scopus 로고    scopus 로고
    • Poly(arylene ethynylene)s (Ed.: C. Weder), Springer, Heidelberg
    • a) Advances in Polymer Science, Vol. 117: Poly(arylene ethynylene)s (Ed.: C. Weder), Springer, Heidelberg, 2005;
    • (2005) Advances in Polymer Science , vol.117
  • 2
    • 84891029339 scopus 로고    scopus 로고
    • Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski, Wiley-VCH, Weinheim
    • b) Acetylene Chemistry (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim, 2005;
    • (2005) Acetylene Chemistry
  • 3
    • 0042291889 scopus 로고    scopus 로고
    • Ed.: D. Astruc, Wiley-VCH, Weinheim
    • Modern Arene Chemistry (Ed.: D. Astruc), Wiley-VCH, Weinheim, 2002.
    • (2002) Modern Arene Chemistry
  • 7
    • 4544308030 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1722-1724;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1722-1724
  • 15
    • 4544339165 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 2248-2251;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2248-2251
  • 17
    • 0035938215 scopus 로고    scopus 로고
    • For selected examples of chiral π-conjugated hydrocarbons in enantiopure forms see: a) A. Rajca, H. Wang, P. Bolshov, S. Rajca, Tetrahedron 2001, 57, 3725-3735;
    • (2001) Tetrahedron , vol.57 , pp. 3725-3735
    • Rajca, A.1    Wang, H.2    Bolshov, P.3    Rajca, S.4
  • 23
    • 33644897534 scopus 로고    scopus 로고
    • note
    • The desilylation of the TMS group with KF proceeded very slowly for 10 as a result of steric hindrance and therefore, TBAF was used in this step. The desilylation of the triisopropylsilyl (TIPS) group was not observed when the reaction was carried out in chloroform. In contrast, the desilylation of the TMS and TIPS groups took place rapidly for 13 in THF.
  • 25
    • 33644896753 scopus 로고    scopus 로고
    • note
    • The bathochromic shift could be attributed to the through-space interactions between the chromophores. Further studies will reveal this point.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.