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Volumn 119, Issue 39, 1997, Pages 9230-9236

Significant effect of salt bridges on electron transfer

Author keywords

[No Author keywords available]

Indexed keywords

CHARGE TRANSFER; ELECTRON ENERGY LEVELS; HYDROGEN BONDS; INTERFACES (MATERIALS); PHOTOCHEMICAL REACTIONS; REACTION KINETICS; RUTHENIUM COMPOUNDS; SALTS;

EID: 0031260356     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja970176+     Document Type: Article
Times cited : (195)

References (62)
  • 9
    • 0000777214 scopus 로고
    • Molybdenum Enzymes, Cofactors, and Model Systems; Stiefel, E. I., Coucouvanis, D., Newton, W. E., Eds.; American Chemical Society: Washington, DC
    • (b) Stiefel, E. I. In Molybdenum Enzymes, Cofactors, and Model Systems; ACS Symposium Series 535; Stiefel, E. I., Coucouvanis, D., Newton, W. E., Eds.; American Chemical Society: Washington, DC, 1993; p 1.
    • (1993) ACS Symposium Series 535 , pp. 1
    • Stiefel, E.I.1
  • 41
    • 1842300559 scopus 로고    scopus 로고
    • to be published
    • Saari, E. A., to be published.
    • Saari, E.A.1
  • 57
    • 1842324732 scopus 로고    scopus 로고
    • note
    • as of 2.5 (see ref 30). Hence, the observed intramolecular electron transfer decay rates well exceed equilibration rates, and intramolecular electron transfer occurs for a static complex. This is not the case for 3, however, where the off rates are expected to be commensurate with the electron transfer kinetics. For this system, the interpretation of the observed PCET rate constant reported in Table 1 is complicated by a dynamic equilibrium between acceptor and donor.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.