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Volumn 112, Issue 13, 2008, Pages 3910-3917

Effect of dual fullerenes on lifetimes of charge-separated states of subphthalocyanine - triphenylamine - fullerene molecular systems

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBONS; NANOSTRUCTURES;

EID: 45849130221     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp7108658     Document Type: Article
Times cited : (53)

References (54)
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    • Leznoff, C. C, Lever, A. B. P, Eds, VCH: Weinheim, Germany
    • Phthalocyanines: Properties and Applications; Leznoff, C. C., Lever, A. B. P., Eds.; VCH: Weinheim, Germany, 1996; Vol. 4.
    • (1996) Phthalocyanines: Properties and Applications , vol.4
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    • Schauman, E, Ed, Georg Thieme Verlag: Stuttgart, Germany, 94, p
    • (a) Hanack, M.; Heckman, H.; Polley, R. In Methods in Organic Chemistry; Schauman, E., Ed.; Georg Thieme Verlag: Stuttgart, Germany, 1998; Vol. E 94, p 717.
    • (1998) Methods in Organic Chemistry , vol.E , pp. 717
    • Hanack, M.1    Heckman, H.2    Polley, R.3
  • 32
    • 84906379134 scopus 로고    scopus 로고
    • Electron Transfer in Functionalized Fullerenes. In Fullerenes: From Synthesis to Optoelectronic Properties; Guldi, D. M., Martin, N., Eds.; Kluwer Academic Publishers: Norwell, MA, 2002; pp 163-212.
    • (d) Electron Transfer in Functionalized Fullerenes. In Fullerenes: From Synthesis to Optoelectronic Properties; Guldi, D. M., Martin, N., Eds.; Kluwer Academic Publishers: Norwell, MA, 2002; pp 163-212.
  • 33
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    • Fujutsuka, M.; Ito, O. Photochemistry of Fullernes. In Handbook of Photochemistry and Photobiology; Nalwa, H. S., Ed.; American Scientific Publishers: Stevenson Ranch, CA, 2003; 2 Organic Photochemistry, pp 111-145.
    • (e) Fujutsuka, M.; Ito, O. Photochemistry of Fullernes. In Handbook of Photochemistry and Photobiology; Nalwa, H. S., Ed.; American Scientific Publishers: Stevenson Ranch, CA, 2003; Vol. 2 Organic Photochemistry, pp 111-145.
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    • (2003) Gaussian 03
  • 38
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    • SubPc, TPA dyad shows different absorption characters compared with the reported subphthalocyanine functionalized with TPA, which shows absorption maxima at 618 and 450 nm.12c This observation reflects the change of the linkage style between the SubPc and TPA, shifting the B-and Q-bands
    • 12c This observation reflects the change of the linkage style between the SubPc and TPA, shifting the B-and Q-bands.
  • 39
    • 84906379131 scopus 로고    scopus 로고
    • 60 moiety considerably changes the electronic character of SubPc - TPA unit in this non-polar solvent.
    • 60 moiety considerably changes the electronic character of SubPc - TPA unit in this non-polar solvent.
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    • 12b
    • 12b
  • 44
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    • Compared with the reported SubPc, ferrocene dyad with its extremely long-lived charge-separated state up to 231 μs,12b the charge-recombination of SubPc--TPA+ in our present study occurs rapidly <6 ns, further producing 3SubPc*. This difference may be attributed to the shorter distance between SubPc and TPA, in addition to the position of TPA right overhead of SubPc as shown in Figure 2, which are quite different from SubPc-ferrocene dyad with longer linkage and side position of the ferrocene donor
    • 3SubPc*. This difference may be attributed to the shorter distance between SubPc and TPA, in addition to the position of TPA right overhead of SubPc as shown in Figure 2, which are quite different from SubPc-ferrocene dyad with longer linkage and side position of the ferrocene donor.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.