Kinetic exchange studies of metal ion substitution in EDTA chelates Fe(III)- UO2 EDTA exchange

1995 ◽  
Vol 199 (4) ◽  
pp. 317-324
Author(s):  
Ecaterina Princz ◽  
Ana Nimara ◽  
Livia Martony
Keyword(s):  
The Analyst ◽  
2010 ◽  
Vol 135 (1) ◽  
pp. 140-148 ◽  
Author(s):  
Wei Zhang ◽  
Jian-Feng Chen ◽  
Liu-Yin Fan ◽  
Cheng-Xi Cao ◽  
Ji-Cun Ren ◽  
...  

2012 ◽  
Vol 48 (47) ◽  
pp. 5826 ◽  
Author(s):  
David A. Leigh ◽  
Paul J. Lusby ◽  
Alexandra M. Z. Slawin ◽  
D. Barney Walker

1988 ◽  
Vol 110 (20) ◽  
pp. 6716-6720 ◽  
Author(s):  
Ruth. Jones ◽  
Peter P. Edwards ◽  
Martin R. Harrison ◽  
Thitinant. Thanyasiri ◽  
Ekkehard. Sinn

1988 ◽  
Vol 41 (6) ◽  
pp. 957 ◽  
Author(s):  
NF Curtis

Reaction of nickel(II) with 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene diperchlorate in the presence of ammonia yields a lilac- coloured complex of nickel(II) with 13-imino-4,4,6,11,11-pentamethyl-3,7,10-triazatetradec-6-en-1-amine, a pentadentate ligand with one primary and two secondary amino, plus one primary and one secondary imino , donor groups. The copper(II) complex of the ligand was formed from the nickel(II) compound by metal-ion substitution. The cations have d-d spectra indicative of five-coordination. The complex cations undergo a reversible protonation reaction with a change from five-coordinate to square planar, with a colour change for nickel(II) from lilac (triplet ground state) to yellow (singlet ground state), and for copper(II) from blue to violet. The compounds of the homologous ligand 4,6,11-triethyl-13-imino-4,11- dimethyl-3,7,10-triazapentadec-6-en-1-amine were similarly prepared, and have similar properties.


2008 ◽  
Vol 47 (23) ◽  
pp. 9240-9247 ◽  
Author(s):  
Sounak Roy ◽  
A. Marimuthu ◽  
Parag A. Deshpande ◽  
M. S. Hegde ◽  
Giridhar Madras

Biochemistry ◽  
2006 ◽  
Vol 45 (10) ◽  
pp. 3226-3234 ◽  
Author(s):  
Mario Cappiello ◽  
Vincenzo Alterio ◽  
Pietro Amodeo ◽  
Antonella Del Corso ◽  
Andrea Scaloni ◽  
...  

1989 ◽  
Vol 156 ◽  
Author(s):  
B. Dabrowski ◽  
D. G. Hinks ◽  
J. D. Jorgensen ◽  
D. R. Richards

ABSTRACTWe have studied mixed-phase samples of bulk LazCuO4 using neutron powder diffraction, thermogravimetric analysis and resistivity measurements. Samples fired at 950°C and slowly cooled form in the K2NiF4 structure with CuO impurities for z<2 and La2O3 impurities for z>2. Neither La-vacancies nor stacking defects were found. The bulk resistivity of the samples show semiconducting behavior which is shorted at 38K by small amounts of superconducting material. The superconductivity is due to the presence of an oxygen-rich phase with stoichiometry La2CuO4.08. The occurrence of superconductivity in pure La2CuO4.08 with the same Tc as observed in the doped La1.85 Sr0.15CuO4 indicates that the excess oxygen provides the same level of doping as metal-ion substitution.


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