메뉴 건너뛰기




Volumn 11, Issue 21, 2009, Pages 4794-4797

Tuning the optical properties of aryl-substituted dispirofluorenelndenofluorene isomers through intramolecular excimer formation

Author keywords

[No Author keywords available]

Indexed keywords


EID: 70350627542     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901750x     Document Type: Article
Times cited : (50)

References (25)
  • 1
    • 70350650306 scopus 로고    scopus 로고
    • Thematic issue: Organic Electronics and Optoelectronics. Guest editors: Forrest, S. R., Thompson, M. E..
    • Chem. Reu. 2007, 107, 4 (Thematic issue: Organic Electronics and Optoelectronics. Guest editors: Forrest, S. R., Thompson, M. E.).
    • (2007) , vol.107 , pp. 4
    • Reu, C.1
  • 8
    • 70350676127 scopus 로고    scopus 로고
    • 2) = 0.2013, GOF = 1.082.
    • 2) = 0.2013, GOF = 1.082.
  • 13
    • 70350654193 scopus 로고    scopus 로고
    • note
    • Comparison of the cyclic voltammograms shows the different solubility of lb and 2b polycations. Indeed, an adsorption/desorption process is evident on the CV of lb, while the three redox waves of 2b are all diffusion controlled. This observation is consistent with the fact that DSFIFs 2 are always more soluble than their corresponding DSF-IF 1 congeners.
  • 21
    • 70350633260 scopus 로고    scopus 로고
    • abs (in nm).
    • abs (in nm).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.