Atmaram K. Mapari* Department of Chemistry, Ramnarain Ruia College, Matunga (E), Mumbai: , Maharashtra, India.

Size: px

Start display at page:

Download "Atmaram K. Mapari* Department of Chemistry, Ramnarain Ruia College, Matunga (E), Mumbai: , Maharashtra, India."

Myrtle Thompson
5 years ago
Views:

International Journal of ChemTech Research CDE (USA): IJCRGG, ISS: 0974-490, ISS(nline):455-9555 Vol.0 o.

Atmaram K. apari* Department of Chemistry, Ramnarain Ruia College, atunga (E), umbai: - 40009, aharashtra, India.

1 International Journal of ChemTech Research CDE (USA): IJCRGG, ISS: , ISS(nline): Vol.0 o.5, pp 73-77, 07 Stability Constants of ixed Ligand Complexes of Transition etal(ii) ions with-[(e)--(-chloro-6- methylphenyl)ethanimidoyl]naphthalen--ol and -{(E)-[(- bromophenyl)imino]methyl}phenol. Atmaram K. apari* Department of Chemistry, Ramnarain Ruia College, atunga (E), umbai: , aharashtra, India. Abstract : Binary and ternary complexes of the type -Y and -X-Y [ = Co(II), i(ii), Cu(II) and Zn(II); X = -{(E)-[(-bromophenyl)imino]methyl}phenol and Y = -{(E)-[(- chloro-4-fluorophenyl)imino]methyl}naphthalen--ol] have been examined p-metrically at 7 ± 0.5 o C and at constant ionic strength, μ = 0. (K) in 75 : 5 (v/v),4-dioxne-water medium. The stability constants for Binary (-Y) and ternary (-X-Y) systems were calculated. Keywords : Binary complexes, Ternary complexes, ixed ligand, Stability constant. Introduction Schiff bases play important roles in coordination chemistry as they easily form stable complexes with most transition metal ions [, ]. any attempts have been made to evaluate different factors affecting the stability of the metal chelates along with their stability constants [3-5]. In the present study the stability constants of the mixed ligand complexes of Co(II), i(ii), Cu(II) and Zn(II) with -{(E)-[(- bromophenyl)imino]methyl}phenol (X) as primary ligand (Figure ) and -[(E)--(-chloro-6- methylphenyl)ethanimidoyl]naphthalen--ol (Y) as secondary ligand (Figure ) in 75: 5 (v/v),4-dioxanewater medium at 7 ± 0.5 o C have been reported by employing p-metric titration technique [6-0]. Under identical conditions the stability constants of binary metal complexes of -[(E)--(-chloro-6- methylphenyl)ethanimidoyl]naphthalen--ol(y) have also been investigated. Br Figure. Primary ligand -{(E)-[(-bromophenyl)imino]methyl}phenol

2 Atmaram K. apari /International Journal of ChemTech Research, 07,0(5): C 3 3 C Figure. Secondary ligand -[(E)--(-chloro-6-methylphenyl)ethanimidoyl]naphthalen--ol Experimental The p-meter model no. EQ-64 supplied by Equiptronics, a precision research p-meter with wide range of glass electrode and calomel reference electrode was used for p measurements. The p-meter was standardized with potassium hydrogen phthalate and phosphate buffers before performing the titrations. The solutions of ligands were prepared in,4-dioxane. All the metal ion solutions were prepared in double distilled water and standardized by using conventional procedures []. A solution of K (0. ) was prepared in double distilled water and standardized with standard solution of succinic acid. The titrations were carried out in an inert atmosphere of nitrogen. All the measurements were carried out at temperature 7 ± 0.5 o C. The method of Bjerrum and Calvin as modified by Irving and Rossotti [6,7] was used to determine ñ A (average number of protons associated with secondary ligand ); ñ (average number of secondary ligand molecules attached per metal ion; ñ mix (average number of secondary ligand molecules attached per (.X) - ion); pl (free ligand exponent for binary (-Y) system) and pl mix (free ligand exponent for ternary (-X-Y) system) values. All the solvents and chemicals used were of A R grade. For the determination of proton-ligand stability constant of secondary ligand (Y) and metal-ligand stability constants of binary (-Y) and ternary (-X-Y) complexes, the following sets of solutions were prepared keeping the total volume V o = 40 ml. All titrations were carried out at the ionic strength of 0. using K as an electrolyte in 75:5 (v/v),4-dioxane-water medium against standard carbonate free K (0. ) solution. i. 4.0 ml (0.6 ) ml K (.0 ) +.64 ml distilled water ml,4-dioxane. ii. 4.0 ml (0.6 ) ml K (.0 ) +.64 ml distilled water ml secondary ligand (0.04 ) ml,4-dioxane. iii. 4.0 ml (0.6 ) ml K (.0 ) + requisite volume of metal(ii) chloride solution to give 0.00 metal(ii) chloride concentration in the final solution + requisite amount of distilled water ml secondary ligand (0.04 ) ml,4-dioxane. iv. 4.0 ml (0.6 ) ml K (.0 ) +.64 ml distilled water ml secondary ligand (0.0 ) ml,4-dioxane. v. 4.0 ml (0.6 ) ml K (.0 ) + requisite volume of metal(ii) chloride solution to give 0.00 metal(ii) chloride concentration in the final solution + requisite amount of distilled water ml primary ligand (0.0 ) ml secondary ligand (0.0 ) +.0 ml,4-dioxane. The ratio of metal (): secondary ligand (Y) was maintained at :4 in the binary system. In the ternary system the ratio of metal (): primary ligand (X): secondary ligand (Y) was maintained at ::. The p-meter readings were plotted against the volume of alkali (K) used for each titrations. Result and Discussion Proton-ligand stability constants of secondary ligand (Y) From the titration curves of solutions (i) and (ii), ñ A values at various p were calculated. The proton ligand formation curve was obtained by plotting the values of ñ A vs. p-meter readings. From the graph the

3 Atmaram K. apari /International Journal of ChemTech Research, 07,0(5): values of were evaluated by half integral method (A). The values of were also evaluated using graphical method (B) by plotting the graph of log [ñ A / (-ñ A )] against p and log [(- ñ A ) / (ñ A -)] against p, respectively. The values obtained by method A and B are in agreement with each other, the average values of has been found to be 8.65 and.7 respectively. etal-ligand stability constants of the Binary (-Y) complexes The metal ligand stability constants of binary complexes were evaluated assuming the polynuclear complexes and hydrolyzed products were not formed. The metal-ligand binary binding proposed structure is shown in figure 3. An examination of titration curves indicate that complex formation takes place in the solution on the following grounds: (I) The metal titration curve of solution (iii) shows displacement with respect ligand (Y) titration curve of solution (ii) along the volume axis. This indicates the affinity of the ligand to metal ions which release proton and produce volume difference. (II) The color change of ligand appeared in the presence of metal ion shows the formation of new species due to coordination. (III) The hydrolysis of the metal ion was suppressed due to the complex formation and precipitation did not appear during the titrations. From the titration curves of solutions (ii) and (iii), ñ and pl values were calculated. The formation curves were obtained by plotting the values of ñ vs. pl. From the graph the values of and log Y were evaluated by half integral method (A) and in the similar way the values of Y and Y were evaluated using graphical method (B) by plotting the graph of log [ñ / (-ñ)] against pl and log [(-ñ) / (ñ-)] against pl respectively. The values obtained by method A and B are in agreement with each other, the average Y values of Y and Y, along with metal-ligand stability constants the log β values of the binary complexes are given in Table. Y Y KY The variations of ñ was found to be between for the binary (-Y) complexes of Co(II), i(ii), Cu(II) and Zn(II) metal ions, which indicate that the composition of the complexes were : in solution. The values for the binary complexes of the metal ions are in the following order: Cu(II) > i(ii) > Co(II) > Zn(II). Y C 3 C 3 3 C C3 = Co(II), i(ii), Cu(II) and Zn(II). Figure 3. The metal-ligand binary binding proposed structure. etal-ligand stability constants of the ternary (-X-Y) complexes The metal-ligand stability constants of ternary complexes were evaluated assuming that the formation of polynuclear complexes and hydrolyzed products were not formed. The metal-ligand ternary binding proposed structure is shown in figure 4. An examination of the titration curves indicate that the ternary complexes formation has taken place in the solution on the following grounds: (I) the horizontal distance was measured between ternary titration curves of solution (v) and secondary ligand titration curve of solution (iv), the positive difference shows the earlier release of protons in the formation of ternary complexes. (II) The hydrolysis of the metal ion was suppressed and precipitation did not appear during the titrations. From the titration curves of solutions (iv) and (v), ñ mix and pl mix values were calculated. The values of have been evaluated from the formation curves (ñ mix vs. pl mix ). At ñ mix = 0.5, in the formation curve, X XY pl mix = (method A). The values of were also evaluated by the graphical method (B), by X XY X XY

4 Atmaram K. apari /International Journal of ChemTech Research, 07,0(5): plotting the graph of log [ñ mix / (-ñ mix )] against pl mix. The values of ñ mix vary from , thus confirm the formation of :: mixed ligand complexes. The values obtained by method A and B are in agreement with each other, the average values of are included in Table. X XY X Y The values of XY are slightly lower than Y and higher than Y, which is due to the fact that the tendency of the secondary ligand (Y) to get bound with aquated metal ion [(aq)] + is more than to combine with the metal ion already bound with primary ligand (X) []. The relative stability of the ternary complexes compared with corresponding binary complexes can be qualitatively expressed in many different ways. We have expressed the relative stabilities in terms of Δ T X (Δ T = XY Y ). The Δ T values for all the metal(ii) ions in the present study (Table ) is negative. This indicates that ternary :: (-X-Y) complexes are less stable than binary : (-Y) complexes [3,4]. In the ternary system studied, the order of stability constants of mixed ligand complexes with respect to the metal ions was found to be Cu(II) > I(II) > Co(II) > Zn(II); which is same as in the corresponding binary (-Y) systems. This is in accordance with the Irving-Williams series of stability constant [5,6]. 3 C C 3 Br = Co(II), i(ii), Cu(II) and Zn(II). Figure 4. The metal-ligand ternary binding proposed structure. Table. etal-ligand stability constants of binary (-Y), ternary (-X-Y) systems and Δ T values in 75: 5 (v/v),4-dioxne-water medium at 7 ± 0.5 o C and μ = 0. (K). System Binary (-Y) Ternary (-X-Y) etal-ligand stability constants / Δ T etal(ii) ions () Co(II) i(ii) Cu(II) Zn(II) Y Y Y log β X XY (-Y) and (-X-Y) Δ T Conclusion X Y The value of XY are slightly lower than Y and higher than Y, which is due to the fact that the tendency of the secondary ligand (Y) to get bound with aquated metal ion [(aq)] + is more than to combine with the metal ion already bound with primary ligand (X). The relative stability (Δ T ) values of the ternary complexes with corresponding binary complexes for all the metal(ii) ions in the present study is negative indicating that ternary :: (-X-Y) complexes are less stable than binary : (-Y) complexes. In the ternary system studied, the order of stability constants of mixed ligand complexes with respect to the metal

5 Atmaram K. apari /International Journal of ChemTech Research, 07,0(5): ions was found to be Cu(II) > I(II) > Co(II) > Zn(II); which is same as in the corresponding binary (-Y) systems. References. Spinu C., Pleniceanu. and Tigae C., Biologically Active Transition etal Chelates with a - Thiophenecarboxaldehyde-Derived Schiff Base: Synthesis, Characterization, and Antibacterial Properties, Turk. J. Chem., 008, 3, arke B., arke., Cunningham D., iggins T., cardle P., Cholchu.. and Gara., Transition-metal Schiff-base complexes as ligands in tin chemistry. Part 7. Reactions of organotin(iv) Lewis acids with [(L)] [-i, Cu and Zn; L-,-bis(3-methoxysalicylidene)benzene-,3- diamine and its -,4-diamine analog], J. rganometallic Chem., 998, 55, ukherjee C.. and Ghosh T., ixed ligand complex formation of Cobalt(II), ickel(ii) and Zinc(II) with -Benzenesulphonyl-l-cysteine as primary Ligand and Bipyridine, Ethylenediamine and Glycinate as Secondary Ligands, J. Indian Chem. Soc., 977, 74, Kiramany K., Prashanthi Y., Subhashini.J.P. and Shivraj, Synthesis, characterization and biological activity of metal complexes of 3-amino-5-methyl isoxazole Schiff bases, J. Chem. Pharm. Res. 00, (), Khade B.C., Deore P.. and Arbad B.R., ixed-ligand complex formation of copper (II) with some amino acids and Drug Dapsone, Int. J. Chem. Tech. Res., 00, (), Irving.. and Rossotti.S., ethods for Computing Successive Stability Constants from Experimental Formation Curves, J. Chem. Soc. 953, 74, Irving.. and Rossotti.S., The Calculations of Formations Curves of etal Complexes from p Titration Curves in ixed Solvents, J. Chem. Soc., 954, 76, apari A.K., Stability Constants of ixed Ligand Complexes of Transition etal (II) ions with -{(E)- [(,6-dichloro-3-methylphenyl)imino]methyl}phenol and -{(E)-[(,3-dimethylphenyl) imino]methyl} naphthalen--ol, Int. J. Chem. Tech. Res., 04, 6(), apari A.K., Stability Constants of ixed Ligand Complexes of Transition etal(ii) ions with -{(E)- [(,3-dimethylphenyl) imino]methyl} phenol and -{(E)- [(4-bromo-,6-difluorophenyl)imino] methyl}naphthalen--ol, Int. J. Chem. Tech. Res., 04, 6 (), Ghasemi, lahanbakhsh and Shokrollahi, Potentiometric Study of Binary and ixed Complexes of Imidazole, istamine, istidine and Diacetyl monooxime with Some Transition etal Ions in Aqueous Solution, Iran. J. Chem. & Chem. Eng., 00, 0 (), -8.. Vogel A.I., Text Book of Quantitative Practical Inorganic Chemistry, ELBS, Patel A.K. and Joshi J.D., Potentiometric Studies on ixed Ligand Complexes in Aqueous Solution: (II) + eutral or Charged Primary Ligand + Amino Acid Systems, J. Indian Chem. Soc. 997, 74, Satyanarayana S. and Reddy K.V., Stability Constants of the Binary Complexes of Co(II), i(ii), Cu(II) and Zn(II) with Thiamine and Ternary Complexes with Thiamine as Primary Ligand and Thymine or Uracil as Secondary Ligand, Indian J. Chem. 989, 8(A), eelakantan.a. and air.s., Studies on ickel(ii)-pyridoxamine-imidazole Containing ixed Ligand Complex Systems Iran. J. Chem and Chem. Eng. 004, 3 (), Irving. and William R. J. P., J. Chem. Soc. 953,, Irving. and William R. J. P., ature. 948, 6, *****

Atmaram K. Mapari *Department of Chemistry, Ramnarain Ruia College, Matunga (E), Mumbai: , Maharashtra, India. Abstract

Atmaram K. Mapari *Department of Chemistry, Ramnarain Ruia College, Matunga (E), Mumbai: , Maharashtra, India. Abstract International Journal of Applied Chemistry. ISS 0973-79 Volume 3, umber (07) pp. -8 Research India Publications http://www.ripublication.com Stability Constants of ixed Ligand Complexes of Transition etal(ii)