메뉴 건너뛰기




Volumn 68, Issue 25, 2003, Pages 9813-9815

Effect of Ring Fusion on the Electronic Absorption and Emission Properties of Oligothiophenes

Author keywords

[No Author keywords available]

Indexed keywords

PLANARIZATION;

EID: 0344666656     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035241e     Document Type: Article
Times cited : (112)

References (27)
  • 8
    • 0037419460 scopus 로고    scopus 로고
    • A related approach to a mixed thiophene-pyrrole fused-ring system, N-functionalized dithieno[3,2-b:2′,3′-d]pyrroles, has recently been demonstrated: Ogawa, K.; Rasmussen, S. C. J. Org. Chem. 2003, 68, 2921-2928.
    • (2003) J. Org. Chem. , vol.68 , pp. 2921-2928
    • Ogawa, K.1    Rasmussen, S.C.2
  • 22
    • 0344969722 scopus 로고    scopus 로고
    • note
    • 2, oligomer 7 is the most soluble, followed by 8, 6, 5 and finally the nonfused oligomer α-quaterthiophene (4) is the least soluble.
  • 27
    • 0038236400 scopus 로고    scopus 로고
    • The thieno[3,2-b]thiophene-based copolymer poly(9,9′ -dioctylfluorene-alt-thieno[3,2-b]thiophene) was recently reported to exhibit better electroluminescence performance than the corresponding bithiophene-based copolymers. Lim, E.; Jung, B.; Shim, H. Macromolecules 2003, 36, 4288-4293.
    • (2003) Macromolecules , vol.36 , pp. 4288-4293
    • Lim, E.1    Jung, B.2    Shim, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.