ChemInform Abstract: FORMATION CONSTANTS OF BIVALENT METAL ION COMPLEXES WITH DIPHENYL VIOLURIC ACID AND ITS HIGHER ANALOGS

1978 ◽  
Vol 9 (47) ◽  
Author(s):  
P. MATHUR ◽  
D. P. GOEL ◽  
R. P. SINGH
1971 ◽  
Vol 26 (9) ◽  
pp. 867-869 ◽  
Author(s):  
R. K. Mehta ◽  
V. C. Singhi ◽  
R. K. Gupta

Protonation constants (log K1H and log K2H) of the Schiff base derived from 2-hydroxy-1-naphthaldehyde and anthranilic acid and, the formation constants of certain bivalent metal ion chelates have been determined potentiometrically in 50 per cent (vol./vol.) dioxan solutions (μ= 0.1 м NaClO4). The stabilities of these metal chelates are in the order, UO2 > Cu > Ni > Co > Zn > Cd, in which the sequence of those of first transitional metal ion chelates are in agreement with Irving and Williams order.


1976 ◽  
Vol 31 (8) ◽  
pp. 1096-1098 ◽  
Author(s):  
Pavan Mathur ◽  
D. P. Goel ◽  
R. P. Singh

The consecutive formation constants of 1:1, 2:1, 3:1 chelate species formed by the interaction of di-p-tolyl-thiovioluric acid (D-p-TOTVA) with the tripositive lanthanons and yttrium cations were determined potentiometrically at 0.1 µ (NaClO4) at 30± 1°C, in 75% aqueous dioxan.The 1:1 formation constants (log K1) for the complexes increase with the increase in the atomic number of the lanthanon (3), with a break at gadolinium.The results indicate that the ligand bonds bidentately to heavier lanthanons (smaller ionic radii). However, definite dentate character of bonding to lighter (larger ionic radii) lanthanons could not be established.


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