Molecular and Crystal Structures of Uranyl Nitrate Complexes withN-Alkylated 2-Pyrrolidone Derivatives: Design and Optimization of Promising Precipitant for Uranyl Ion

2008 ◽  
Vol 8 (7) ◽  
pp. 2364-2376 ◽  
Author(s):  
Koichiro Takao ◽  
Kyoko Noda ◽  
Yasuji Morita ◽  
Kenji Nishimura ◽  
Yasuhisa Ikeda
2017 ◽  
Vol 56 (21) ◽  
pp. 13530-13534 ◽  
Author(s):  
Hiroyuki Kazama ◽  
Satoru Tsushima ◽  
Yasuhisa Ikeda ◽  
Koichiro Takao

2010 ◽  
Vol 10 (5) ◽  
pp. 2033-2036 ◽  
Author(s):  
Seong-Yun Kim ◽  
Koichiro Takao ◽  
Yoshinori Haga ◽  
Etsuji Yamamoto ◽  
Yoshihisa Kawata ◽  
...  

2007 ◽  
Vol 62 (2) ◽  
pp. 109-111 ◽  
Author(s):  
A. I. Sizov ◽  
T. M. Zvukova ◽  
Z. A. Starikova ◽  
B. M. Bulychev

2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Qingchun Zhang ◽  
Bo Jin ◽  
Rufang Peng ◽  
Xiaofang Wang ◽  
Zhaotao Shi ◽  
...  

A series of uranyl complexes have been synthesized by reacting hexadentate ligands CH2[COO (CH2)nCAM; n=2, 3, 4]2 [CAM = 2,3-Ph(OH)2CONH] containing the catecholamide (CAM) group and β-diketonates framework with uranyl nitrate. They were characterized by FTIR, UV-vis, 1H NMR, XPS, TGA, and elemental analysis. The analysis revealed that oxygen atom of β-diketonate did not bind to uranyl ion in complexes 1–3. The photocatalytic degradation properties of the target complexes for degradation of rhodamine B (RhB) were investigated. The result indicated that approximately 74%, 71%, and 67% RhB were degraded in the presence of complexes 1–3 after about 210 min, respectively. Consequently, complexes 1–3 have excellent photocatalytic degradation property.


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