Triplet‐Singlet Transitions in Organic Molecules. Lifetime Measurements of the Triplet State

1949 ◽  
Vol 17 (10) ◽  
pp. 905-913 ◽  
Author(s):  
Donald S. McClure
1968 ◽  
Vol 46 (6) ◽  
pp. 1031-1033 ◽  
Author(s):  
N. C. Lang ◽  
K. O. Kutschke

The ratio of the relative yield for fluorescence to that for phosphorescence of hexafluoroacetone excited at 3130 Å was measured; the ratio was a linear function of mercury concentration. This observation confirms that the deactivation of the triplet state proceeds by a reaction which is first order in [Hg]. A quenching constant was obtained which is in excellent agreement with that based on lifetime measurements under mercury-free and mercury-saturated conditions.


2000 ◽  
Vol 331 (5-6) ◽  
pp. 489-496 ◽  
Author(s):  
Tran-Chin Yang ◽  
David J. Sloop ◽  
S.I. Weissman ◽  
Tien-Sung Lin

2001 ◽  
Vol 73 (3) ◽  
pp. 431-434 ◽  
Author(s):  
M. F. García-Parajó ◽  
J.-A. Veerman ◽  
L. Kuipers ◽  
N. F. van Hulst

The photodynamics of individual molecules and fluorescent proteins has been investigated in real time. In the case of organic molecules, both the triplet state lifetime and intersystem crossing yield appear to vary in time and space. In the case of autofluorescent proteins, light-driven "on-off" fluorescence emission has been observed, with a behavior that is consistent with the existence of a long-lived dark state.


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