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Volumn 44, Issue 7, 2011, Pages 2276-2281

Thermally polymerized rylene nanoparticles

Author keywords

[No Author keywords available]

Indexed keywords

A-THERMAL; DIIMIDE; DYNAMIC LIGHT SCATTERING MEASUREMENT; EMISSION COLOR; FLUORESCENCE QUANTUM YIELD; FUNCTIONALIZED; MONOMER CONCENTRATION; NANO-EMULSIONS; PERYLENES; PHOTOPHYSICAL PROPERTIES; TERRYLENE; WATER SUSPENSIONS;

EID: 79953878352     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma2000866     Document Type: Article
Times cited : (18)

References (49)
  • 43
    • 0037816260 scopus 로고    scopus 로고
    • As previously reported, these isomers were difficult to separate by conventional purification methods:;;;;; J. Org. Chem. 2004, 69, 7933 A mixture of 1,6-and 1,7-dibromo isomers was used to synthesize M3 (see note 17); however, compound 4 is shown as the 1,7-isomer in Scheme 1 for simplicity
    • Ahrens, M. J.; Fuller, M. J.; Wasielewski, M. R. Chem. Mater. 2003, 15, 2684 As previously reported, these isomers were difficult to separate by conventional purification methods: Würthner, F.; Stepanenko, V.; Chen, Z.; Saha-Möller, C. R.; Kocher, N.; Stalke, D. J. Org. Chem. 2004, 69, 7933 A mixture of 1,6-and 1,7-dibromo isomers was used to synthesize M3 (see note 17); however, compound 4 is shown as the 1,7-isomer in Scheme 1 for simplicity.
    • (2003) Chem. Mater. , vol.15 , pp. 2684
    • Ahrens, M.J.1    Fuller, M.J.2    Wasielewski, M.R.3    Würthner, F.4    Stepanenko, V.5    Chen, Z.6    Saha-Möller, C.R.7    Kocher, N.8    Stalke, D.9
  • 44
    • 79953859512 scopus 로고    scopus 로고
    • 1H NMR spectrum of the final mixture (see Supporting Information). The chemical shifts of the 1,6-and 1,7-isomers were assigned based on previous assignments made for similar PDIs (see note 16)
    • 1H NMR spectrum of the final mixture (see Supporting Information). The chemical shifts of the 1,6-and 1,7-isomers were assigned based on previous assignments made for similar PDIs (see note 16).
  • 49
    • 0008662621 scopus 로고
    • Fluorescence quantum yields for NP1-3 were measured against Rhodamine B in ethanol, which has a quantum yield of 0.71:;, Fluorescence quantum yields for NP4, 5 were measured against zinc phthalocyanine in 1% pyridine in toluene, which has a quantum yield of 0.30:;; J. Chem. Phys. 1971, 55, 4131-4140
    • Fluorescence quantum yields for NP1-3 were measured against Rhodamine B in ethanol, which has a quantum yield of 0.71: Demas, J. N.; Crosby, G. A. J. Phys. Chem. 1971, 75, 991-1024 Fluorescence quantum yields for NP4, 5 were measured against zinc phthalocyanine in 1% pyridine in toluene, which has a quantum yield of 0.30: Vincett, P. S.; Voigt, E. M.; Rieckhoff, K. E. J. Chem. Phys. 1971, 55, 4131-4140
    • (1971) J. Phys. Chem. , vol.75 , pp. 991-1024
    • Demas, J.N.1    Crosby, G.A.2    Vincett, P.S.3    Voigt, E.M.4    Rieckhoff, K.E.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.