메뉴 건너뛰기




Volumn 75, Issue 17, 2010, Pages 5875-5881

Electron transfer properties of alkoxyl radicals. A time-resolved kinetic study of the reactions of the tert -butoxyl, cumyloxyl, and benzyloxyl radicals with alkyl ferrocenes

Author keywords

[No Author keywords available]

Indexed keywords

ALKOXYL RADICALS; AROMATIC RINGS; ELECTRON RELAY; ELECTRON TRANSFER; FERROCENES; IN-LINE; MARCUS EQUATION; ORDERS OF MAGNITUDE; OXYGEN RADICAL; PREREACTION COMPLEXES; REDUCTION POTENTIAL; TIME-RESOLVED KINETIC STUDY; UNPAIRED ELECTRONS;

EID: 77956147516     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100931a     Document Type: Article
Times cited : (19)

References (81)
  • 2
    • 0000647193 scopus 로고    scopus 로고
    • For a definition, see
    • For a definition, see: Mayer, J. M. Acc. Chem. Res. 1998, 31, 441-450
    • (1998) Acc. Chem. Res. , vol.31 , pp. 441-450
    • Mayer, J.M.1
  • 25
    • 0347938954 scopus 로고    scopus 로고
    • Rappoport Z., Ed.; John Wiley & Sons: New York,; Chapter 16
    • Steenken, S.; Neta, P. In The Chemistry of Phenols; Rappoport, Z., Ed.; John Wiley & Sons: New York, 2003; Chapter 16, pp 1107 - 1152.
    • (2003) The Chemistry of Phenols , pp. 1107-1152
    • Steenken, S.1    Neta, P.2
  • 53
    • 77956148460 scopus 로고    scopus 로고
    • · undergoes a rapid 1,2-H-atom shift reaction in water and alcohols (see ref 42). Accordingly, in MeCN the decay of this radical can be accelerated by the presence of small amounts of water
    • · undergoes a rapid 1,2-H-atom shift reaction in water and alcohols (see ref 42). Accordingly, in MeCN the decay of this radical can be accelerated by the presence of small amounts of water.
  • 61
    • 77956162398 scopus 로고    scopus 로고
    • · with both OMFc and DcMFc proceed, at least in part, by hydrogen atom abstraction from the ferrocene methyl groups.
    • · with both OMFc and DcMFc proceed, at least in part, by hydrogen atom abstraction from the ferrocene methyl groups.
  • 63
    • 77956158002 scopus 로고    scopus 로고
    • For a critical discussion on the factors controlling reactivity in hydrogen abstractions by radicals, see, for example, refs 6, 52, and 53
    • For a critical discussion on the factors controlling reactivity in hydrogen abstractions by radicals, see, for example, refs 6, 52, and 53.
  • 71
    • 77956144326 scopus 로고    scopus 로고
    • · due to the limited kinetic information obtained for their reactions with alkylferrocenes
    • · due to the limited kinetic information obtained for their reactions with alkylferrocenes.
  • 79
    • 77956133859 scopus 로고    scopus 로고
    • · with OMFc (see Table 1) appears also to be in contrast with an outer sphere ET mechanism. Further studies are underway in our laboratories to provide a better understanding of the role of solvent effects on these processes
    • · with OMFc (see Table 1) appears also to be in contrast with an outer sphere ET mechanism. Further studies are underway in our laboratories to provide a better understanding of the role of solvent effects on these processes.
  • 80
    • 77956141737 scopus 로고    scopus 로고
    • ·, where only electronic effects are expected to operate
    • ·, where only electronic effects are expected to operate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.