Copper Coordination Compounds of Polyimidazole-Thioether Ligands. X-ray Structures and Characterization of {Bis[4-((methylthio)ethyl)imidazol-2-yl]methane}bis(tetrafluoroborato)copper(II), Dichloro{(imidazol-2-yl)[4-((methylthio)ethyl)imidazol-2-yl]methane}copper(II), and {[4-(imidazol-2-ylmethyl)imidazol-2-yl][4-((methylthio)ethyl)imidazol-2-yl]methane}bis(perchlorato)copper(II)

1994 ◽  
Vol 33 (13) ◽  
pp. 2808-2814 ◽  
Author(s):  
K. C. Tran ◽  
J. P. Battioni ◽  
J. L. Zimmermann ◽  
C. Bois ◽  
G. J. A. A. Koolhaas ◽  
...  
2020 ◽  
pp. 1-9
Author(s):  
Dickron R. Nahhas ◽  
John F. Corrigan

This work describes the synthesis of group 11 metal trimethylsilylchalcogenolate complexes [(ITr)M-ESiMe3] stabilized by the large NHC ligand bis-1,3-tritylimidazole-2-ylidene (ITr). The thiolates and selenolates of Cu, Ag, and Au are accessed from either [(ITr)MOAc] (M = Cu, Ag) and E(SiMe3)2 or [(ITr)AuCl] and Li[ESiMe3] (E = S, Se). All complexes were characterized spectroscopically and, for the copper coordination compounds, via single crystal X-ray diffraction analysis.


2020 ◽  
Vol 67 (4) ◽  
pp. 1148-1154
Author(s):  
Andrii Fedorchuk ◽  
Evgeny Goreshnik ◽  
Yurii Slyvka ◽  
Marian Mys’kiv

The present work is directed toward preparation and structural characterization of two novel Cu(I) arylsulfonate π-complexes with 3-allyl-2-thiohydantoin, namely [Cu2(Hath)4](C6H5SO3)2 (1) and [Cu2(Hath)4](p-CH3C6H4SO3)2 · 2H2O (2) (Hath = 3-allyl-2-thiohydantoin), obtained by the means of alternating current electrochemical synthesis and studied with X-ray diffraction method. In both structures, the inner coordination sphere is represented by the cationic dimer [Cu2(Hath)4]2+ with one crystallographically independent copper(I) atom which has a trigonal pyramidal coordination environment formed by three Hath thiogroup S atoms and double C=C bond of its allyl group. [Cu2(Hath)4]2+ fragments in both coordination compounds are very similar, despite some divergences such as a big difference in Cu−S distance to the apical S atom (3.0374(8) Å in 1 and 2.7205(9) Å in 2). This difference was explained by the impact of the system of weak interactions, which are quite different.


2016 ◽  
Vol 45 (26) ◽  
pp. 10696-10707 ◽  
Author(s):  
Manuel I. Velasco ◽  
Claudio R. Krapacher ◽  
Rita H. de Rossi ◽  
Laura I. Rossi

The characterization of non-crystalline complexes is very difficult when techniques like X-ray diffraction or NMR are not available. We propose a simple procedure to characterize the physicochemical properties of amorphous new coordination compounds between cyclodextrins (CD) and Cu2+ salts, by several techniques as TGA, FT-IR, EPR.


2009 ◽  
Vol 103 (9) ◽  
pp. 1204-1213 ◽  
Author(s):  
Obdulia Sánchez-Guadarrama ◽  
Horacio López-Sandoval ◽  
Francisco Sánchez-Bartéz ◽  
Isabel Gracia-Mora ◽  
Herbert Höpfl ◽  
...  

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 528
Author(s):  
Chao Liu ◽  
Weiwei Zhang ◽  
Gaigai Cai

Two copper coordination compounds bearing an N,N’-dibenzylethylenediamine ligand, namely [Cu3L(CH3COO)6]n (1) and [(CuCl4)∙(C6H5CH2NH2CH2)2] (2) (L = N,N’-dibenzylethylenediamine) were synthesized by the ethanol refluxing method. Powder X-ray diffraction (PXRD), infrared spectra (IR), elemental analyses, and single crystal X-ray diffraction were used to characterize and verify their structures. Structural analyses showed that the asymmetric unit of compound (1), composed of two Cu(II) cations, three acetate anions, and half of the ligand, was bridged by one acetate to obtain an infinite 1D chain structure. The analyses further showed that the asymmetric unit of compound (2), composed of two crystallographically independent [C6H5CH2NH2CH2]+ units, four chloride anions, and one central Cu(II) cation is connected into an infinite 2D network structure by the hydrogen bonding interactions. The copper compounds were used to catalyze the decomposition of H2O2, and the results showed that both of the compounds exhibited excellent catalytic activities under optimized conditions.


Sign in / Sign up

Export Citation Format

Share Document