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limiting molar conductivity of the aggregate.
limiting molar conductivity of the monomer.
The molar conductivity of the complexes in DMF at 10−3 M concentration shows that they are non-electrolytes.
The molar conductivity of the electrolytes displayed first a minimum and then a maximum upon increasing salt concentration.
The contribution of this process to the molar conductivity of the solution is calculated from the experimental results by using the Onsager equation and the Walden rule.
The values of limiting molar conductivity of tris alkylenediamine cobalt III) ions decrease with the increase in size of ligand in both the solvents.
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Similar deviations were also observed for the molar conductivities of the polymer in the same solvent systems.
The single ion limiting molar conductivities of quaternary ammonium ions decreased in the order: Me4N+, 14.7 ⪢ Me3EtN+, 14.5 ⪢ Me2Et2N+, 14.2 ⪢ MeEt3N+, 14.0 ⪢ Et4N+, 14.4 S cm2 mol−1.
The limiting molar conductivities of [M DMA 6]2+ (M MN, Co, Ni, Cu, Zn) and BF−4, as well as association constants for Co(BF4 2 in DMA solutions have been calculated.
Molar conductivities of the 1 1 electrolytes LiClO4, LiAsF6, n-Bu4NClO4 and n-Bu4NBPh4 were measured in mixtures of propylene carbonate and dimethoxymethane over the concentration range 0.01−1 × 10−4 mol dm−3.
Therefore, in this work, the molar conductivities of the ILs [RMIm]X (R= propyl, pentyl, and hexyl; X= Br− and Cl−) in different concentrations of N,N′-bis 2-pyridylmethylidene -1,2-diiminoethane (BPIE) Schiff base + acetoN,N′-bis 2-pyridylmethylidene -1,2-diiminoethane
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