Rational Design and Convenient Synthesis of a Novel Family of Ruthenium Complexes with O,N-Bidentate Ligands

ChemInform ◽  
2006 ◽  
Vol 37 (39) ◽  
Author(s):  
Renate Drozdzak ◽  
Nele Ledoux ◽  
Bart Allaert ◽  
Ileana Dragutan ◽  
Valerian Dragutan ◽  
...  
2005 ◽  
Vol 3 (3) ◽  
pp. 404-416 ◽  
Author(s):  
Renate Drozdzak ◽  
Nele Ledoux ◽  
Bart Allaert ◽  
Ileana Dragutan ◽  
Valerian Dragutan ◽  
...  

AbstractA two step procedure for the synthesis of a novel family of homogeneous and immobilized Ru-complexes containing Schiff bases as O,N-bidentate ligands is described. The new Ru-complexes have been structurally characterized by IR, Raman,1H-,13C-NMR spectroscopy. The Schiff bases were associated with a diversity of inorganic and organic ligands such as chloride, phosphane, arenes, various carbenes (alkylidene, vinylidene, indenylidene and allenylidene as well as N-heterocyclic carbenes) and cyclodienes. By choosing a selective range of substituents for the Schiff base, useful physical and chemical properties of the prepared Rucomplexes can be induced. This synthetic approach is promising in creating a valuable and diverse selection of Ru-complexes, valuable for future applications.


2015 ◽  
Vol 51 (13) ◽  
pp. 2637-2640 ◽  
Author(s):  
Zhiqin Deng ◽  
Lianling Yu ◽  
Wenqiang Cao ◽  
Wenjie Zheng ◽  
Tianfeng Chen

We have described the rational design of selenium-containing ruthenium complexes and their use as cancer radiosensitizers through regulating ROS-mediated pathways.


2010 ◽  
Vol 636 (7) ◽  
pp. 1380-1385 ◽  
Author(s):  
Roberto Menzel ◽  
Eric Täuscher ◽  
Dieter Weiß ◽  
Rainer Beckert ◽  
Helmar Görls

ChemMedChem ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. 991-998 ◽  
Author(s):  
Zhiqin Deng ◽  
Lianling Yu ◽  
Wenqiang Cao ◽  
Wenjie Zheng ◽  
Tianfeng Chen

1995 ◽  
Vol 24 (9) ◽  
pp. 833-834 ◽  
Author(s):  
Yasutaka Kataoka ◽  
Yoshinori Saito ◽  
Koji Nagata ◽  
Kenichi Kitamura ◽  
Atsushi Shibahara ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (19) ◽  
pp. 5806
Author(s):  
Liang Liu ◽  
Hui Chen ◽  
Zhenqiang Yang ◽  
Junnian Wei ◽  
Zhenfeng Xi

Copper-catalyzed and organocopper-involved reactions are of great significance in organic synthesis. To have a deep understanding of the reaction mechanisms, the structural characterizations of organocopper intermediates become indispensable. Meanwhile, the structure-function relationship of organocopper compounds could advance the rational design and development of new Cu-based reactions and organocopper reagents. Compared to the mono-carbonic ligand, the C,N- and C,C-bidentate ligands better stabilize unstable organocopper compounds. Bidentate ligands can chelate to the same copper atom via η2-mode, forming a mono-cupra-cyclic compounds with at least one acute C-Cu-C angle. When the bidentate ligands bind to two copper atoms via η1-mode at each coordinating site, the bimetallic macrocyclic compounds will form nearly linear C-Cu-C angles. The anionic coordinating sites of the bidentate ligand can also bridge two metals via μ2-mode, forming organocopper aggregates with Cu-Cu interactions and organocuprates with contact ion pair structures. The reaction chemistry of some selected organocopper compounds is highlighted, showing their unique structure–reactivity relationships.


2012 ◽  
Vol 41 (45) ◽  
pp. 13800 ◽  
Author(s):  
Stephanie J. Lucas ◽  
Rianne M. Lord ◽  
Rachel L. Wilson ◽  
Roger M. Phillips ◽  
Visuvanathar Sridharan ◽  
...  

Author(s):  
Noriko Dodo ◽  
Yuji Matsushima ◽  
Mitsunari Uno ◽  
Kiyotaka Onitsuka ◽  
Shigetoshi Takahashi

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