Interaction of excited dioxouranium(VI) ion with amino-acids: a laser flash photolysis, quantum yield and ESR investigation

1986 ◽  
Vol 114 (2) ◽  
pp. 215-220 ◽  
Author(s):  
Terence J. Kemp ◽  
Mark A. Shand
2004 ◽  
Vol 52 (21) ◽  
pp. 6602-6606 ◽  
Author(s):  
Daniel R. Cardoso ◽  
Douglas W. Franco ◽  
Karsten Olsen ◽  
Mogens L. Andersen ◽  
Leif H. Skibsted

1977 ◽  
Vol 24 (2) ◽  
pp. 211-217 ◽  
Author(s):  
I. Arnold ◽  
F.J. Comes ◽  
G.K. Moortgat

2009 ◽  
Vol 62 (5) ◽  
pp. 434 ◽  
Author(s):  
Xian-Fu Zhang ◽  
Yakuan Chang ◽  
Yanling Peng ◽  
Fushi Zhang

The photophysical properties of five novel phthalocyanine analogues, dihydroxy phosphorus(v) triazatetrabenzocorrole (PTBC) substituted with –NO2, –SO3H, OiPr, and –NH2, respectively, were studied by a combination of absorption, steady-state emission, time-resolved fluorescence, and laser flash photolysis. All substituents, even for the strong electron-donating –NH2, cause only a slight red shift of their absorption and emission maxima. These complexes are generally monomeric in organic solution, whereas the sulfonated derivative, PTBC(SO3H)4, slightly aggregates in aqueous buffer. Distinct from phthalocyanines, PTBCs substituted with –NO2 or –NH2 still show high photo activities. The electron-withdrawing –NO2 and –SO3H decrease the fluorescence quantum yield but increase the triplet formation yield to 0.76 and 0.82, respectively. All PTBCs have long triplet lifetimes and hence generate singlet oxygen efficiently with a quantum yield from 0.43 to 0.75. Together with the ground-state absorption properties, the results suggest that these PTBCs may be used as excellent photosensitizers for photodynamic therapy.


2000 ◽  
Vol 26 (7-8) ◽  
pp. 715-725 ◽  
Author(s):  
Zhenyu Sheng ◽  
Qinhua Song ◽  
Fan Gao ◽  
Xiaoguo Zhou ◽  
Jiang Li ◽  
...  

2017 ◽  
Vol 33 (5) ◽  
pp. 1051-1056
Author(s):  
Hai-Xia LI ◽  
◽  
Yan-Cheng LIU ◽  
Rui-Zhi TANG ◽  
Peng ZHANG ◽  
...  

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