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Volumn 42, Issue 23, 2004, Pages 5891-5899

Synthesis and properties of the [2.2]paracyclophane-containing conjugated polymer with benzothiadiazole as an electron acceptor

Author keywords

2.2 paracyclophane; Conjugated polymers; Fluorescence; Light emitting diodes (LED); Through space

Indexed keywords

ABSORPTION SPECTROSCOPY; AROMATIC COMPOUNDS; ELECTRON TRANSITIONS; LIGHT EMITTING DIODES; MATHEMATICAL MODELS; PHOTOLUMINESCENCE; SYNTHESIS (CHEMICAL); ULTRAVIOLET RADIATION;

EID: 10044260792     PISSN: 0887624X     EISSN: None     Source Type: Journal    
DOI: 10.1002/pola.20443     Document Type: Article
Times cited : (41)

References (49)
  • 10
    • 0002206460 scopus 로고
    • Optical nonlinearities in chemistry
    • Optical Nonlinearities in Chemistry, special issue of Chem Rev 1994, 94, 1-278.
    • (1994) Special Issue of Chem Rev , vol.94 , pp. 1-278
  • 22
    • 0035028906 scopus 로고    scopus 로고
    • See also refs. 23-25
    • Independently, synthesis of the π-conjugated polymers with thiophene and [2.2]paracyclophane as a repeating unit by electrochemical polymerization has been reported. Guyard, L.; Audebert, P. Elecrochem Commun 2001, 3, 164. See also refs. 23-25.
    • (2001) Elecrochem Commun , vol.3 , pp. 164
    • Guyard, L.1    Audebert, P.2
  • 38
    • 0035879209 scopus 로고    scopus 로고
    • See also refs. 39 and 40
    • Yamamoto and coworkers reported the CT-type conjugated polymers containing dialkoxybenzene as a donor and benzothiadiazole as an acceptor that formed a D-A π-stacked structure in the solid state: Yamamoto, T.; Kokubo, H.; Morikita, T. J Polym Sci Part B: Polym Phys 2001, 39, 1713. See also refs. 39 and 40.
    • (2001) J Polym Sci Part B: Polym Phys , vol.39 , pp. 1713
    • Yamamoto, T.1    Kokubo, H.2    Morikita, T.3
  • 47
    • 10044233315 scopus 로고    scopus 로고
    • note
    • D = 1.344) were used]. See refs. 48 and 49 for refractive indices.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.