Characterization and electrochemical studies of molybdenum(VI) dioxodialkylbipyridyl complexes. X-ray crystal structure of MoO2(o-MeC6H4CH2)2(bipy)

1995 ◽  
Vol 20 (5) ◽  
pp. 426-429 ◽  
Author(s):  
Helena Teruel ◽  
Nilia Romero ◽  
Irene Henriquez
2005 ◽  
Vol 8 (1) ◽  
pp. 61-64 ◽  
Author(s):  
Sujoy RoyChowdhury ◽  
Subhajit Dinda ◽  
Santu Chakraborty ◽  
Corine Simonnet ◽  
Alok K. Mukherjee ◽  
...  

2013 ◽  
Vol 34 (10) ◽  
pp. 3093-3097 ◽  
Author(s):  
Khaled Ghasemi ◽  
Ali Reza Rezvani ◽  
Ibrahim Abdul Razak ◽  
Abolghasem Moghimi ◽  
Fatemeh Ghasemi ◽  
...  

1998 ◽  
Vol 37 (21) ◽  
pp. 5602-5610 ◽  
Author(s):  
Gabriele Albertin ◽  
Stefano Antoniutti ◽  
Alessia Bacchi ◽  
Davide Barbera ◽  
Emilio Bordignon ◽  
...  

1996 ◽  
Vol 35 (21) ◽  
pp. 6245-6253 ◽  
Author(s):  
Gabriele Albertin ◽  
Stefano Antoniutti ◽  
Alessia Bacchi ◽  
Emilio Bordignon ◽  
Giancarlo Pelizzi ◽  
...  

2006 ◽  
Vol 84 (2) ◽  
pp. 187-195 ◽  
Author(s):  
B CM Chak ◽  
A McAuley

The synthesis and characterization of the mixed donor ligand N,N′-bis(2′-pyridylmethyl)-1,7-dithia-4,11-diazacyclotetradecane (L4) containing two pendant pyridine arms is described. The macrocycle formation involves reaction of N-tosylbis(2-bromoethyl)amine with N-tosylbis(3-mercaptopropyl)amine at high dilution followed by detosylation at the nitrogen atoms using LiAlH4 in view of the presence of the thioether groups. An X-ray study of the ligand shows the sulphur atoms lie exo to the macrocyclic ring. The nickel(II) and copper(II) complexes of L4 have been characterized and the X-ray structure of the Cu(II) ion exhibits a five-coordinate copper ion despite the presence of six available donor atoms. In the case of ligand N-(2-pyridylmethyl)-1,4,7-trithia-11-azacyclotetradecane (L2), with a single pendant N donor, the Ni(II) complex is distorted octahedral with a molecule of acetonitrile in the sixth site. Details of UV–vis, ESR spectra, and electrochemical studies on the complexes are presented.Key words: synthesis, pendant-armed, mixed donor S,N macrocycles, copper, nickel.


2007 ◽  
Vol 62 (4) ◽  
pp. 495-500 ◽  
Author(s):  
Brajagopal Samanta ◽  
Joy Chakraborty ◽  
Shyamapada Shit ◽  
Stuart R. Batten ◽  
Paul Jensen ◽  
...  

The new complex Cu[L1]Cr2O7has been synthesised with the N,N′-bis(2-pyridylmethylene) butane-1,4-diamine Schiff base L1, [NC5H4CH=N(CH2)4N=CHC5H4N], and characterised with elemental analyses and different spectroscopic and electrochemical studies. The structure of the new complex has been established by single crystal X-ray diffraction. The complex crystallises in the monoclinic system with space group P21/c having cell parameters a = 14.7(5), b = 9.22(2), c = 16.2(5) Å , β = 116.9(1)°, and Z = 4. The Cr2O72− unit is bonded through one terminal oxygen donor end to the central Cu(II) chelated by the Schiff base ligand.


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