Journal article

Photoinduced energy and electron transfer between ketone triplets and organic dyes

Jockusch S, Timpe H, Schnabel W, Turro N ...see all

Journal of Physical Chemistry A, vol. 101, issue 4 (1997) pp. 440-445 Published by American Chemical Society

  • 12


    Mendeley users who have this article in their library.
  • 76


    Citations of this article.
Sign in to save reference


Cationic organic dyes (phenosafranine, safranine T (ST+), thiopyronine, and methylene blue) are efficient quenchers of the triplet states of aromatic ketones. The triplets of benzophenone (BP), xanthone, thioxanthone, benzil, and N-methylacridone are quenched by the dyes via energy transfer, generating triplet excited dyes (typically kq = 5.5 × 109 M-1 s-1 for 3BP* + ST+ in acetonitrile solution). Regarding Michler's ketone, p-(dimethylamino)benzophenone, and 3,6-bis(dimethylamino)thioxanthone, the mechanism of triplet quenching is solvent-dependent. Electron transfer occurs in polar solvents like acetonitrile, and energy transfer is the dominant reaction pathway in less polar solvents, such as dichloromethane. Delayed fluorescence of the dye caused by heterotriplet−triplet annihilation involving ketone and dye was detected upon studying the reaction of the dyes with triplet excited ketones (BP, xanthone, thioxanthone, and benzil). By applying two successive laser pulses (λex = 532 and 308 nm, respectivel...

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document

Get full text


  • S. Jockusch

  • H. J. Timpe

  • W. Schnabel

  • N. J. Turro

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free