scholarly journals Heavy-atom effect on optically excited triplet state kinetics

PLoS ONE ◽  
2017 ◽  
Vol 12 (11) ◽  
pp. e0184239
Author(s):  
Christian Hintze ◽  
Tobias O. Morgen ◽  
Malte Drescher
2020 ◽  
Vol 56 (11) ◽  
pp. 1721-1724 ◽  
Author(s):  
Yuqi Hou ◽  
Qingyun Liu ◽  
Jianzhang Zhao

Heavy atom-free dyads showing a red light-absorbing and exceptionally long-lived triplet state based on a spin–orbital charge transfer intersystem crossing mechanism.


1987 ◽  
Vol 42 (9) ◽  
pp. 1041-1042 ◽  
Author(s):  
H. Hopf ◽  
E. Hermann

Phosphorescence and fluorescence spectra, quantum yields of phosphorescence and fluorescence as well as phosphorescence lifetimes have been measured of six methyl-, chloro- and bromo-derivatives of [2.2] paracyclophane in ethanol at 77 K. While the chloro-derivatives as well as dibromo-paracyclophane exhibit a normal internal heavy-atom effect behaviour the momobromo-compound shows anomalies. These possibly indicate that in the monobromo-compound an additional pathway of the radiationless deactivation of the lowest triplet state is effective which does not occur with the other compounds.


2020 ◽  
Author(s):  
Wenbin Hu ◽  
XIan-Fu Zhang ◽  
Mingyu Liu

The attachement of SR (R is alkyl or phenyl) makes BODIPY efficiently generate excited triplet state (T<sub>1</sub>) and singlet oxygen with quantum yield up to 0.82 (compared to 0.10 of parent BODIPY). This affords an efficient method to synthesize heavy atom free photosensitizers. This efficient T<sub>1</sub> formation is because SR presence leads to a new excited state S<sub>1</sub>(n,pi*) with an energy smaller but close to the usual S<sub>1</sub>(pi,pi*) state.


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