The General Theory of Radiative and Non Radiative Transitions in Centrosymmetric Coordination Compounds of the Transition Metal Ions

Author(s):  
Roberto Acevedo
2011 ◽  
Vol 1 (4) ◽  
pp. 309-343 ◽  
Author(s):  
E. K. Beloglazkina ◽  
A. G. Majouga ◽  
E. A. Manzhelii ◽  
N. V. Zyk ◽  
N. S. Zefirov

1996 ◽  
Vol 3 (2) ◽  
pp. 79-83 ◽  
Author(s):  
Claudiu T. Supuran

Complexes of the diuretic benzothiadiazine derivative chlorothiazide (6-chloro-7-sulfamoyl- 1,2,4-benzothiadiazine-1,1-dioxide) with V(IV); Fe(II); Co(II); Ni(II); Cu(II), Ag(I) and U(VI) were prepared and characterized by elemental analysis, spectroscopic, thermogravimetric, magnetic and conductimetric measurements. The complexes behave as effective inhibitors for two isozymes (I and II) of carbonic anhydrase (CA).


Polyhedron ◽  
2006 ◽  
Vol 25 (12) ◽  
pp. 2363-2374 ◽  
Author(s):  
Fabiola Téllez ◽  
Adrian Peña-Hueso ◽  
Noráh Barba-Behrens ◽  
Rosalinda Contreras ◽  
Angelina Flores-Parra

1972 ◽  
Vol 25 (2) ◽  
pp. 289 ◽  
Author(s):  
JF Alcock ◽  
RJ Baker ◽  
AA Diamantis

Ligands containing the N-acylhydrazine grouping, RCONHKH2, act as bidentate chelating agents with transition metal ions. Cationic complexes of coba1t(11), nickel(11), and copper(11) containing the ligands coordinated in the keto form were isolated, but the ligands also reacted in the enol form producing neutral complexes with cobalt(111) and copper(11). Complex formation in the enol form was facilitated by condensation of the ligands with acetone to produce the N'-iso-propylidene derivatives, from which keto complexes were also isolated. Under certain conditions N-acylhydrazines can act as reducing agents, leading to the formation of complexes containing copper in both oxidation states (I) and (11). Using N-benzoylhydrazine, this reaction can be utilized as a benzoylating medium for amines.


2017 ◽  
Vol 57 (3) ◽  
Author(s):  
Daniela Olea-Román ◽  
Juan Carlos Villeda-García ◽  
Raúl Colorado-Peralta ◽  
Alejandro Solano-Peralta ◽  
Mario Sanchez ◽  
...  

The coordination behavior of the antiulcer drug cimetidine (cime) towards transition metal ions was investigated. The synthesis and characterization of [Cr(cime)<sub>2</sub>Cl<sub>2</sub>]Cl·3H<sub>2</sub>O, [Co(cime)Cl<sub>2</sub>]·5H<sub>2</sub>O, [Co(cime)<sub>3</sub>Cl]Cl·3H<sub>2</sub>O, [Ni(cime)Cl<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>]·H<sub>2</sub>O, [Cu(cime)Cl<sub>2</sub>]·2H<sub>2</sub>O, [Cu(cime)<sub>2</sub>Cl(H<sub>2</sub>O)]Cl·H<sub>2</sub>O, [Cu(cime)<sub>3</sub>Cl<sub>2</sub>]·3H<sub>2</sub>O, [Cu<sub>2</sub>(cime)Cl<sub>4</sub>], and [Zn(cime)Cl<sub>2</sub>]·1.5H<sub>2</sub>O are discussed, where cime acts as monodentate (imidazole N3) or bidentate ligand (N3 and S8). IR, UV-vis, EPR and NMR spectroscopies, mass spectrometry (FAB+), were employed for the characterization. In order to identify the most reactive areas of cimetidine, the electrostatic potential map of the ligand was calculated; also the structures of minimum energy of the coordination compounds were modeled using DFT (B3LYP/def2-TZVP) calculations.


2002 ◽  
Vol 339 ◽  
pp. 532-542 ◽  
Author(s):  
Jean Michel Grevy ◽  
Fabiola Tellez ◽  
Sylvain Bernés ◽  
Heinrich Nöth ◽  
Rosalinda Contreras ◽  
...  

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