Coordination Compounds of Cu(II), Ni(II) Based on Ethyl 4-Benzoate Thiosemicarbazons Derivatives of Salicyl Aldehyde. Antimicrobial and Antifungal Properties

Author(s):  
Anna Rusnac ◽  
G. Balan ◽  
A. Gulea
1966 ◽  
Vol 19 (4) ◽  
pp. 539 ◽  
Author(s):  
GE Coates ◽  
C Kowala ◽  
JM Swan

Various triethylphosphine coordinated gold(1) mercaptides of formula Et3PAuSR (R = Me, Et, Pr, Bu, Bu1, Ph, CH2Ph, β-C10H7, and CH2CH(NH2)C02H), and related sulphur derivatives of formula Et3PAuY (Y = SCN, SC(S)Net2, SC(S)OEt, and SC(NH2)NH2+Br-) have been prepared. Under appropriate conditions, displacement of the sulphur group from the gold atom is observed, either by another sulphur nucleophile, e.g. Et3PAuSR + Et2NCSS- → Et3PAuSC(S)Net2 + RS-, or by a. nucleophile such as Cl-, Br-, I-, NO3-, or CN-.


1990 ◽  
Vol 54 (9) ◽  
pp. 2441-2442
Author(s):  
Hiroshi Kayahara ◽  
Norihisa Shibata ◽  
Koji Tadasa ◽  
Hideo Maeda ◽  
Takashi Kotani ◽  
...  

1994 ◽  
Vol 49 (1) ◽  
pp. 100-110 ◽  
Author(s):  
Hans-Jürgen Plinta ◽  
Ion Neda ◽  
Reinhard Schmutzler

Abstract 1,3-Dimethyl-1,3-diaza-2-fluoro-5,6-benzo-1,3,2-phosphorinane-4-one (1) reacted with (COD)PtCl2 (COD = 1,5-cyclooctadiene) or K2PtCl4 to give the cis-dichloro-platinum(II) complex (2). The reactions of 1 with the tetracarbonyl norbornadiene derivatives of Cr, Mo and W furnished the complexes 3 - 6 . In the case of the chromium and tungsten complexes the trans-isomers 3 and 6 were formed, due to a cis-trans-isomerization. Room temperature and low temperature 31P NMR spectra of a mixture of 5 and 6 show no significant temperature dependence of the cis-trans equilibrium. The reaction of 1 with the pentacarbonyl tetrahydrofuran derivative of W led to the product 7. The spirophosphoranes 8 and 9 were obtained in low yields. The analogous reactions of 10, 15 and 20 with (COD)PtCl2 and the tetracarbonyl norbornadiene derivatives of Cr and Mo furnished the coordination compounds 11-14, 16-18, 21 and 23. In the case of all chromium complexes only the trans-isomers 11,16 and 21 were formed, whereas in the case of molybdenum cis-trans-isomer mixtures 12 and 13, as well as 17 and 18 were obtained. An attempt to obtain the cis-isomer of the molybdenum complex 22 failed. In the case of platinum the expected cis-complexes 14 and 23 were formed, while the attempted synthesis of 19 was unsuccessful. All these results are interpreted in terms of both steric and electronic factors. The ligands 1, 10, 15 and 20 coordinate via phosphorus. The validity of the concept of hard and soft acids and bases (HSAB) was confirmed. The characterization of 2 - 7 , 11-14, 16-18, 21 and 23 rests, especially, on their 1H, 13C and 31P NMR spectra, and their mass and infrared spectra. 31P - 31P coupling constants 2J(PP) for the cis-coordinated complexes 4, 5 and 14 involving two equivalent phosphorus ligands are also reported.


1988 ◽  
Vol 66 (11) ◽  
pp. 2935-2940 ◽  
Author(s):  
Theodore A. Annan ◽  
Dennis G. Tuck

The reaction of indium(I) halides (InX; X = Cl, Br, I) with tetrahalogeno-ortho-quinones (Y4C6O2; Y = Cl, Br) gives the oxidative addition product Y4C6O2InX, These compounds have been isolated as adducts with neutral bidentate donor ligands (N,N,N′,N′-tetramethylethanediamine (tmen), 1,10-phenanthroline) or as salts of the anionic complexes [Y4C6O2InCl2]− or [Y4C6O2In(Cl)Br]−. The number of coordinated tmen molecules, and hence the structure, depends on the method of preparation. Infrared, 1H NMR, and 13C NMR spectroscopy all confirm that these products are all substituted-catecholato derivatives of indium(III), and the structure of these various neutral or anionic derivatives is discussed. The temperature dependence of the 13C NMR spectra shows that the dynamic behaviour of these compounds (in d6-dmso) is similar to that observed in previous studies of indium(III) chelate complexes.


2018 ◽  
Vol 6 (29) ◽  
pp. 13999-14024 ◽  
Author(s):  
Hao Tang ◽  
Mingbo Zheng ◽  
Qin Hu ◽  
Yao Chi ◽  
Bingyan Xu ◽  
...  

Research progress on coordination compound derivatives as electrode materials of rechargeable batteries is summarized and evaluated.


2019 ◽  
Vol 72 (19-21) ◽  
pp. 3222-3236
Author(s):  
Andrii A. Fedorchuk ◽  
Yurii Slyvka ◽  
Vasyl Kinzhybalo ◽  
Iwan Kityk ◽  
Jarosław Jędryka ◽  
...  

1969 ◽  
Vol 47 (4) ◽  
pp. 673-679 ◽  
Author(s):  
A. Storr ◽  
V. G. Wiebe

Although the organo hydride derivatives of boron and aluminium are well characterized, little work has been reported on the corresponding gallium systems. The present study was initiated to determine the relative stabilities of organo gallium hydride derivatives as compared to the stabilities of the corresponding compounds of boron and aluminium. Various preparative routes in this new class of gallium compounds have been investigated. These include the use of organo mercury and organo lithium reagents in reactions with gallium hydride compounds and their halogen substituted derivatives, and also equlibration reactions between gallium hydride and organo gallium compounds. Both infrared and proton magnetic resonance spectroscopy techniques have been used extensively in following the progress of these reactions and in the characterization of the products.


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