A Series of Copper Complexes of a Dinucleating Bis(tetradentate) Nitrogen Ligand: Synthesis, Structural, Spectroscopic, Electrochemical, and Magnetic Characterization

2017 ◽  
Vol 2017 (29) ◽  
pp. 3570-3579 ◽  
Author(s):  
Thomas Limpke ◽  
Christoph Butenuth ◽  
Anja Stammler ◽  
Hartmut Bögge ◽  
Thorsten Glaser
2020 ◽  
Vol 39 (4) ◽  
pp. 500-504 ◽  
Author(s):  
Seiji Akiyama ◽  
Satoru Ikemoto ◽  
Satoshi Muratsugu ◽  
Mizuki Tada ◽  
Makoto Yamashita

2007 ◽  
Vol 46 (10) ◽  
pp. 4298-4307 ◽  
Author(s):  
Angelina Prokofieva ◽  
Alexander I. Prikhod'ko ◽  
Eva Anna Enyedy ◽  
Etelka Farkas ◽  
Walter Maringgele ◽  
...  

1968 ◽  
Vol 46 (2) ◽  
pp. 139-148 ◽  
Author(s):  
Patrick T. T. Wong ◽  
D. G. Brewer

Infrared spectra, including the lower frequency region, of copper (II) complexes of the type [CuL2Cl2], where L = 4-methylpyridine, 4-carbinylpyridine, pyridine, 4-acetylpyridine, 4-pyridinecarboxamide, 4-carbomethoxypyridine, and 4-cyanopyridine have been measured. The substituent effect upon the copper–nitrogen (ligand) and copper–chlorine stretching frequencies has also been examined. It was found that the substituents on the pyridine ring not only affected the nature of copper–nitrogen bond, but also the copper–chlorine bond. It appears that an entirely delocalized system exists, involving the chlorine atoms and the substituents in the complexes. Force constants associated with the coordination bond between copper and the nitrogen of the ligands have been calculated by means of an IBM 1620 computer. By comparison of the copper–nitrogen stretching frequencies with the corresponding force constants, and the heats of coordination, it may be concluded that the magnitude of the metal–ligand stretching frequency is directly related to the metal–ligand coordination bond strength for the systems under study.


2018 ◽  
Vol 47 (43) ◽  
pp. 15596-15612 ◽  
Author(s):  
Massinisa Ayad ◽  
Robertus J. M. Klein Gebbink ◽  
Yves Le Mest ◽  
Philippe Schollhammer ◽  
Nicolas Le Poul ◽  
...  

The macrocyclic design of a TPA-based ligand enhances the catalytic properties of the resulting Fe(ii) complexes for cyclohexane oxidation.


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