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Bioinorganic Chemistry and Applications
Volume 2012 (2012), Article ID 984291, 10 pages
http://dx.doi.org/10.1155/2012/984291
Research Article

Thermodynamic Investigation and Mixed Ligand Complex Formation of 1,4-Bis-(3-aminopropyl)-piperazine and Biorelevant Ligands

Department of Chemistry, Faculty of Science, Cairo University, Giza 12613, Egypt

Received 3 July 2012; Revised 7 October 2012; Accepted 8 October 2012

Academic Editor: Anastasios Keramidas

Copyright © 2012 Ahmed A. El-Sherif et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Thermodynamic parameters for protonation of 1,4-bis(3-aminopropyl)-piperazine (BAPP) and its metal complexation with some divalent metal ions were determined in aqueous solution at constant ionic strength (0.1 M NaNO3) using a potentiometric technique. The order of –ΔG0 and –ΔH0 was found to obey , in accordance with the Irving-Williams order. The formation equilibria of zinc (II) complexes and the ternary complexes Zn(BAPP)L, where L = amino acid, amides, or DNA constituents), have been investigated. Ternary complexes are formed by a simultaneous mechanism. The concentration distribution of the complexes in solution was evaluated as a function of pH. Stoichiometry and stability constants for the complexes formed are reported and discussed. The stability of ternary complexes was quantitatively compared with their corresponding binary complexes in terms of the parameter Δlog K.

1. Introduction

Metal complexes of biologically important ligands are sometimes more effective than free ligands [1]. It is not surprising, therefore, that many authors have studied the coordination compounds of several central atoms. Mixed ligand complexes have a key role in biological chemistry [2] because the mixed chelation occurs commonly in biological fluids as millions of potential ligands are likely to compete for metal ions in vivo [3]. These create specific structures [4] and have been implicated in the storage and transport of active substances through membranes. Among these ligands are piperazine and its derivatives. Some piperazine derivatives were found to inhibit acute human immune deficiency HIV virus from chronically and latently infected cells containing proviral DNA [5]. Also the antimalarial activities of piperazine derivatives are also known [6]. The investigation of metal complexes of piperazine compounds will support their biological activity. The study of ternary complexes of transition metal ions with amino acids, peptides, or DNA units has been the focus of increasing research effort [710], which has revealed the role of metal ions at the molecular level. These types of complexes are implicated in the storage and transport of metal ions and of active substances through membranes. So, it is worthwhile to assemble information on their formation, stability, and structure and on the mutual influence of two ligands bound to the same metal ion. Zinc(II), among other transition metal ions, plays a vital role in biological processes. Zinc deficiency can cause unusual disorders in the development of the body, disorders in the metabolic system and prostate gland, and can result in mental retardation. Studies on model complexes of zinc(II) ions have focused to improve the understanding of the structure-reactivity relationship of the active site in zinc-enzymes [1114]. In some of the model complexes the chelating ligands (e.g., polyamines) have been selected to bind to three or four coordination sites of via N-donor atoms, with the next sites being occupied by other ligands [1518].

In view of the above facts and in continuation of our published work on the formation equilibria of amino acids [19, 20], amides [21, 22], and DNA units [23, 24], we report herein the protonation constants of the free ligand (BAPP) and the stepwise stability constants for its complexes with a number of 3d divalent metal ions (Zn2+, Co2+, Ni2+, and Cu2+) and the thermodynamics of these systems. This was done through calculation of stability constants for their complexes at different temperatures. This work is also extended to present some correlations between the thermodynamic functions and some of well-known properties of the metal ions. Ternary complexes involving Zn(II) ion, BAPP and amino acid, peptide, or DNA constituents are investigated.

2. Experimental

2.1. Materials and Reagents

1,4-Bis(3-aminopropyl)-piperazine (BAPP), Ni(NO3)26H2O, and Co(NO3)26H2O were provided from Aldrich Chem. Co. Cu(NO3)23H2O was provided from Fluka. Zn(NO3)26H2O was provided from FSA supplies. The metal ion solutions were prepared by dissolving A.R. grade metal salts in deionized water. Amino acids, peptides, and DNA constituents investigated are: alanine, threonine, serine, ornithine, glutamic acid, histamine2HCl, glycinamide, glutamine, inosine, thymidine, and thymine. These materials were provided by Sigma Chem. Company and used without further purification. All solutions of the above reagents were freshly prepared in deionized water. All other chemicals used were of A.R. grade quality. Carbonate-free NaOH (titrant) was prepared and standardized against potassium hydrogen phthalate solution. The structural formula of BAPP and some selected biorelevant ligands are given in Scheme 1.

984291.sch.001
Scheme 1: Structural formulae of some important investigated ligands.
2.2. Apparatus and Procedures

Potentiometric measurements were made using a Metrohm 686 titroprocessor equipped with a 665 Dosimat (Switzerland—Herisau). A thermostatted glass-cell was used and equipped with a magnetic stirring system, a Metrohm glass electrode, a thermometric probe, a microburettel delivery tube, and a salt bridge connected with the reference cell filled with 0.1 moldm−3 KCl solution in which saturated calomel electrode was dipped. The titroprocessor and electrode were calibrated daily with standard buffer solutions prepared according to NBS specifications at .1°C [25] and I = 0.1 moldm−3, potassium hydrogen phthalate (pH 4.008), and a mixture of KH2PO4 and Na2HPO4 (pH 6.865). The BAPP solution was prepared in the protonated form by dissolving in HNO3 solution. The protonation constant of the ligand was determined potentiometrically by titrating the ligand (40 cm3) solution ( moldm−3) of constant ionic strength 0.1 moldm−3, (adjusted with NaNO3). The stability constants of the binary complexes were determined by titrating 40 cm3 of a solution mixture of , , , or ( moldm−3), the ligand ( moldm−3), and NaNO3 (0.1 moldm−3). The stability constants of the ternary complexes were determined by titrating 40 cm3 of a solution mixture of ( moldm−3), the BAPP ( moldm−3), the ligand ( moldm−3), and NaNO3 (0.1 moldm−3). All titrations were performed in a purified nitrogen atmosphere, using aqueous 0.05 M NaOH as titrant. The pH meter readings were converted into hydrogen ion concentration by titrating HCl solution (0.05 moldm−3) with NaOH solution (0.05 moldm−3) at 25°C and I = 0.1 moldm−3 NaNO3. The pH is plotted against p[H]. The relationship pH−p[H] = 0.05 was observed. [OH-] value was calculated using a pKw value of 13.921 [26]. For the variable temperature studies the following values of pKw were employed at 20°C (pKw = 14.126) at 30°C (pKw = 13.753), at 35°C (pKw = 13.660).

2.3. Data Processing

The calculations were obtained from ca. 100 data points in each titration using the computer program MINIQUAD-75 [27]. The stoichiometry and stability constants of the complexes formed were determined by trying various possible composition models. The model selected gave the best statistical fit and was chemically consistent with the titration data without giving any systematic drifts in the magnitudes of various residuals, as described elsewhere [27]. The fitted model was tested by comparing the experimental titration data points and the theoretical curve calculated from the values of the acid dissociation constant of the ligand and the formation constants of the corresponding complexes. The species distribution diagrams were obtained using the program SPECIES [28] under the experimental condition employed. All measurements were carried out in our laboratory in Cairo University.

3. Results and Discussion

3.1. Protonation Constants of BAPP Ligand

The stoichiometric protonation constants of the investigated BAPP ligand were determined in aqueous solution at 25°C and these constants are tabulated in Table 1. The BAPP ligand studied here have four protonation constants. This is also illustrated in the species distribution of the BAPP ligand in Figure 1. In acidic solution (), BAPP initially exists in the fully protonated form as H4L+4. On rising the pH, the species (H4L+4) lose its protons forming (H3L+3), which is the predominant species in pH range 3.0–7.0. As pH increases, the second and third protons are deprotonated forming the species (H2L+2) and (HL+) with maximum concentration percentage of 93% and 43% at pH 8.5 and 10, respectively. With further increase of pH, the fourth proton begins deprotonation to give the full deprotonated species (L) which is the predominant species at .

tab1
Table 1: Protonation constants of (BAPP) in aqueous solution at different temperatures (at 0.01 M ionic strength).
984291.fig.001
Figure 1: Concentration distribution of various species as a function of pH in the BAPP system (1.25 mM of BAPP).
3.2. Binary Complexes of 1,4-Bis(3-aminopropyl)piperazine (BAPP)

The formation constants of -BAPP complexes were determined. The potentiometric titration curves for Cu2+, Co2+, Ni2+, and Zn2+ with BAPP are significantly lower than the BAPP titration curve, corresponding to formation of a complex through release of a proton. The potentiometric data of -BAPP solution mixture were fitted assuming the formation 1 : 1 species but not 1 : 2 species. The formation of the 1 : 2 complex seems to be hindered because BAPP ligand is a tetradentate ligand. The stability constants of their complexes are given in Table 2.

tab2
Table 2: Stepwise stability constants for the complexation of (BAPP) with 3d divalent metal ions in aqueous solution at 0.1 M NaNO3 at different temperatures.

3.3. Correlation of the Properties of Metal Ions with the Formation Constants of Mixed Ligand Complexes

In an attempt to explain why a given ligand prefers binding to one metal rather than another, it is necessary to correlate the stability constants with the characteristic properties of the metal ions, such as the ionic radius, ionization energy, electronegativity, and the atomic number, investigated. The formation constants of -complexes of bivalent 3d transition metal ions with BAPP as given in Table 2 are in the order: Co2+ (log β110 = 5.59) < Ni2+ (log β110 = 5.88) < Cu2+ (log β110 = 14.26) > Zn2+ (log β110 = 4.74) in accordance with Irving and Williams order [29]. Here we have discussed relationships between the properties of central metal ions reported in Table 3 [30] and the stability constants of complexes. The correlation between the and the reciprocal ionic radii (1/) of the studied bivalent transition metal ions was found to be almost linear (Figure 2). Also, a good linear correlation has been obtained between and the electronegativities of the metal ions under study (Figure 2). This in accordance with the fact that increasing electronegativity of the metal ions (Zn2+ (1.65) < Co2+ (1.88) < Ni2+ (1.91) < Cu2+ (2.0)) will decrease the electronegativity difference between the metal atom and the donor atom of the ligand. Thus, the metal-ligand bond would have more covalent character, which may lead to greater stability of the metal chelates. A good linear relationship has been obtained between and the second ionization potential of the bivalent metal ions under study. In general, it is noted that the stability constant of the Cu2+ complex is quite large compared to the other metals. The ligand field will give Cu2+ some extra stabilization due to tetragonal distortion of the octahedral symmetry [31, 32]. The Cu (II) complex will be further stabilized due to the Jahn-Teller effect [31]. Thus, log value for the Cu2+-complex deviates significantly when log values of metal chelates are plotted against properties of the metal ions.

tab3
Table 3: Atomic number, ionic radius, electronegativity, and ionization potential of the investigated bivalent metal iona.
fig2
Figure 2: Effect of metal ion properties on the stability constants of metal complexes.

3.4. Species Distribution Curves

Estimation of equilibrium concentrations of metal (II) complexes as a function of pH provides a useful picture of metal ion binding in solutions. The concentrations of metal-ligand complexes increase with increasing of pH. The species distribution pattern for Zn(BAPP)2+ complex, taken as a representative of metal ligand complexes, is given in Figure 3. Zn(BAPP)2+ complex starts to form at pH ~ 5 and reaches its maximum concentration of 98% at pH ~ 8.

984291.fig.003
Figure 3: Concentration distribution of various species as a function of pH in the -BAPP system (1.25 mM of Zn2+ and BAPP).
3.5. Effect of Temperature

The values obtained for the thermodynamic parameters , , and , associated with the protonation of BAPP and its complex formation with M(II) species, were calculated from the temperature dependence of the data. and were obtained by linear least square fit of ln versus (ln = + ) leading to an intercept and a slope , where is the equilibrium constant, (Figures 4 and 5), The main conclusions from the data can be summarized as follows. (I)The protonation reactions of the -site of BAPP is exothermicand of comparable and with a net negative (Table 4). Three factors affect the protonation reactions. (i)The neutralization reaction, which is an exothermic reaction process.(ii)Desolvation of ions, which is an endothermic process.(iii)The change of the configuration and the arrangements of the hydrogen bonds around the free and the protonated ligands.The negative indicates that the total number of solvent molecules bound with the dissociated ligand is greater than that originally accompanying the undissociated form. (II)The stability constants of the complexes formed at different temperatures decreased with increasing temperature, confirming that the complexation process is more favorable at lower temperatures. The thermodynamic parameters of metal complexes were calculated by a procedure similar to that used for the protonation of BAPP and the values are recorded in Table 5. It is known that the divalent metal ions exist in solution as octahedrally hydrated species [29] and the obtained values of and can then be considered as sum of two contributions: (a) release of H2O molecules and (b) metal-ligand bond formation. From these results the following conclusions can be reached.(1)All values of for complexation are negative, indicating the spontaneity of the chelation process.(2)The negative values of , show that the chelation process is exothermic, indicating that the complexation reactions are favored at low temperatures.

tab4
Table 4: Thermodynamic parameters for the stepwise protonation of (BAPP) in aqueous solution (at 0.01 M ionic strength)a.
tab5
Table 5: Thermodynamic parameters for ML complexes of (BAPP) with 3d divalent metal ions in aqueous solution at 0.1 M NaNO3 at different temperaturesa.
984291.fig.004
Figure 4: Effect of temperature on stepwise protonation constant of H4BAPP+4. Curves: log corresponds to the 011 species; log corresponds to 012 species; log corresponds to 013 species; log corresponds to 014 species.
984291.fig.005
Figure 5: Effect of temperature on ln of M2+ complexes with BAPP.

3.6. Ternary Complexes Involving Zn2+, BAPP and Amino Acids, Peptides, or DNA Constituents
3.6.1. Ternary Complex Formation Equilibria Involving Amino Acids

Ternary complex formation may proceed either through a stepwise or simultaneous mechanism depending on the chelating potential of BAPP and the other ligand (L). The formation constant of 1 : 1 -BAPP complex is of the same order of magnitude like -ligand (L) complex, (Table 6). It is reasonable to propose that in presence of both ligands, the reaction proceeds by simultaneous mechanism. This assumpation was supported by comparing the experimental potentiometric data with the theoretically calculated (simulated) curve, (Figure 6). Thus, the formation of ternary complex can be described by the following equilibrium (charges are omitted for simplicity): Figure 5 represents such a comparison for threonine system, from which it follows that the experimental data coincide with the theoretical curve. This supports the validity of the ternary complex formation model. The potentiometric data of the ternary complexes involving simple amino acids best fits assuming a complex of stoichiometric coefficient 1110 species for amino acids except for glutamic acid, ornithine, and histamine, where both 1110 and 1111 species are formed. Estimation of the concentration distribution of the various species in solution provides a useful picture of metal ion binding. The speciation diagram for threonine complex, taken as a representative amino acid, is given in Figure 7. The deprotonated species 1110 attains a maximum concentration of 99% at pH 8.8, therefore the ternary complexes of amino acids predominates in the physiological pH range. The pKa values for the histamine complex is 9.24, being higher than that of the protonated imidazole (pKa = 6.12), but closer to that of the protonated amino group () in histamine ligand (pKa = 9.85). This reveals that the proton in the protonated complex would be located mainly on the amino group.

tab6
Table 6: Stability constants of the ternary species in the ZnII-BAPP-amino acid, amide, or DNA constituent systems and proton-association constants and their binary stability constants.
984291.fig.006
Figure 6: Experimental and calculated potentiometric titration curves of the -BAPP-Threonine system.
984291.fig.007
Figure 7: Concentration distribution of various species as a function of pH in the [Zn(BAPP)(threonine)] system (1.25 mM of Zn2+, BAPP, and threonine).

The pKa of the protonated species of Zn(BAPP)-glutamic acid is (7.58), being higher than that of the carboxylate group (pKa = 4.15), but near to that of the protonated amino group (pKa = 9.58), suggesting that the proton in the protonated complex would be located mainly on the amino group, considering the increase in acidity due to complex formation. The species distribution for glutamic acid complex, taken as a representative, is given in Figure 8. The protonated species 1111 complex predominates with formation percentage of (55% at pH ~7.0); the deprotonated species 1110 complex reaches the maximum concentration of 97% at pH ~9.8. Therefore the species 1111 complex predominates in the physiological pH range.

984291.fig.008
Figure 8: Concentration distribution of various species as a function of pH in the [Zn(BAPP)(glutamic acid)] system (1.25 mM of Zn2+, BAPP, and glutamic acid).

Ornithine is α-amino acid having an extra amino group. Ornithine forms protonated complex 1111 species and the pKa value amounts to 7.10. This is fairly comparable with the acid protonation constant of the -amino group, considering the increase in acidity due to complex formation.

3.6.2. Ternary Complex Formation Equilibria Involving Amides

Ternary complex formation of amides proceeds also through simultaneous mechanism (Table 7). The potentiometric data reported for the peptides, serine, and threonine complexes reveals the formation of Zn(BAPP)(L) species rather than the Zn(BAPP)LH−1 species which supports the view that induced ionization of peptide hydrogen would be unfavoured. This finding is in agreement with previous investigation carried out on the Zn(II)-diethylenetriamine-peptide and Zn(II)-nitrilo-tris(methyl phosphonic acid)-peptide systems [33].

tab7
Table 7: .

The glutamine complex is more stable than the glycinamide complex, presumably due to the fact that glutamine carries a negative charge, whereas glycinamide is neutral. The electrostatic interaction between the glutaminate and the positively charged Zn(II) complex would result in a lowering of the free energy of formation.

The speciation diagram of glycinamide complex as a representative of amides is given in Figure 9. The mixed ligand species [Zn(BAPP)L] (1110) starts to form at pH~6.8 and with increasing pH, its concentration increases reaching the maximum of 76% at pH ~ 9. The species with concentration percentage less than 5% were neglected in the concentration distribution plot for clarity.

984291.fig.009
Figure 9: Concentration distribution of various species as a function of pH in the [Zn(BAPP)(glycinamide)] system (1.25 mM of Zn2+, BAPP, and glycinamide).
3.6.3. Ternary Complex Formation Equilibria Involving DNA Units

Inosine is slightly more acidic than the pyrimidinic species (thymine and thymidine). This can be related to the existence of the anion form of purinic derivatives in a higher number of resonance forms due to the presence of two condensed rings in this ligand (inosine). Based on the existing data, thymine and thymidine ligate in the deprotonated form as monoanions, through N3, and they do not form protonated complexes. As a result of the high pKa values of pyrimidines (pKa 9) and the fact that they are monodentates, the complexes are formed only above pH 6, supporting the view that the negatively charged nitrogen donors of pyrimidine bases are important binding sites in the neutral and slightly basic pH ranges. The purines like inosine have two metal ion binding centres N1 and N7 nitrogens. Inosine may become protonated at N(7) with formation of [N(1)H–N(7)H] monocations. In the present study, the pKa of N(1)H was only determined since the pKa of N(7)H is too low to be detected by the potentiometric technique. In the acidic pH-range, N1 remains protonated, while the metal ion is attached to N7. The gradual change from N7-binding to N1-binding with increasing pH has been rather extensively documented by nuclear magnetic resonance (NMR) [34] and electron paramagnetic resonance (EPR) [35] spectroscopic measurements. Consequently, it is proposed that N(1) serves as a coordination site in the mixed ligand complexes of inosine at higher pH values. The speciation of inosine complex is presented in Figure 10, where the species distribution of the complexes is plotted as a function of pH. The complex [Zn(BAPP)L] (1110) reaching a maximum concentration of 94% at pH 9.

984291.fig.0010
Figure 10: Concentration distribution of various species as a function of pH in the [Zn(BAPP)(inosine)] system (1.25 mM of Zn2+, BAPP, and inosine).
3.7. Comparison of the Stability Constant of the Ternary Complexes with Those of the Binary Complexes

One of the most important parameters generally used for indicating the stabilization of the mixed complexes with respect to the binary ones namely is log . It has been widely accepted and used for many years [36] and the advantages in using log K in comparing stabilities of ternary and binary complexes have been reviewed. log10 , the difference between the stabilities of the binary and mixed complexes, expresses the effect of the bounded primary ligand towards an incoming secondary ligand (L). One expects to obtain negative values for log (Table 7), since more coordination positions are available for the bonding of ligand (L) in the binary than in the ternary complexes. This indicates that the secondary ligand (L) amino acid, peptide, or DNA form more stable complexes with zinc (II) ion alone than with -BAPP complex. The log value for deprotonated ternary complexes is given by All values of log for the ternary complexes studied in this paper are listed in Table 7. It is of interest to note that for all the systems listed in Table 7, the values for log are positive; that is, equilibrium 6 is on its right side. According to Sigel [36, 37], the relative stability of a ternary complex Zn(BAPP)L(1110) compared to its binary complex Zn(BAPP) (1100) or Zn(L) (1010) can be expressed quantitatively by (2) and (3). Zn-BAPP (1 : 1) has fewer coordination sites than the aquatic Zn2+ ion complex. Consequently, the secondary ligands (L) are expected to bind to the Zn-BAPP complex with a smaller stability constant than with an aquatic metal ion. Therefore, log10  should be negative and generally have a value between −0.5 and −2.0 [36, 38] depending on the geometry of the complex. For Zn2+ ions, positive values of log10  may be considered as evidence for the occurrence of enhanced stabilities. This may be explained on the premise that: a sort of hydrophobic intramolecular interaction possibly occurred between the hydrophobic moiety of BAPP and the noncoordinating hydrophobic side chain of amino acids in aqueous solutions. Such a hydrophobic interaction has been reported in literature [36, 3941].

4. Conclusions

The present investigation describes the formation equilibria of Zn(II) complexes involving BAPP and some ligands of biological significance. In combination of stability constants data of such complexes with amino acids, peptides, or DNA constituents, it would be possible to calculate the equilibrium distribution of the metal species in biological fluids where all types of ligands are present simultaneously. This would form a clear basis for understanding the mode of action of such metal species under physiological conditions. From the above results, it may be concluded that ternary complex formation of amino acids and peptides proceeds through simultaneous mechanism. The mixed ligand complexes are formed in the physiological pH range, indicating this interaction. The positive value of log is attributed to the extra stability of the ternary complexes.

References

  1. E. Jóna, M. Kubranová, P. Šimon, and J. Mroziński, “Thermochemical investigation: Ni(II)-3-pyridylcarbinol (ronicol) interactions in solid halogeno and thiocyanato complexes,” Journal of Thermal Analysis, vol. 46, no. 5, pp. 1325–1337, 1996. View at Scopus
  2. A. S. Mildvan and M. Cohn, “Kinetic and magnetic resonance studies of the pyruvate kinase reaction. II. Complexes of enzyme, metal, and substrates,” Journal of Biological Chemistry, vol. 241, no. 5, pp. 1178–1193, 1966. View at Scopus
  3. G. M. R. Tombo and D. Bellus, “Chiralität und pflanzenschutz,” Angewandte Chemie, vol. 103, no. 10, pp. 1219–1241, 1991. View at Publisher · View at Google Scholar
  4. E. Bouwman, W. L. Driessen, and J. Reedijk, “Model systems for type I copper proteins: structures of copper coordination compounds with thioether and azole-containing ligands,” Coordination Chemistry Reviews, vol. 104, no. 1, pp. 143–172, 1990. View at Scopus
  5. J. A. Turpin, R. W. Buckheit, D. Derse et al., “Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription,” Antimicrobial Agents and Chemotherapy, vol. 42, no. 3, pp. 487–494, 1998. View at Scopus
  6. M. Medou, G. Priem, L. Rocheblave et al., “Synthesis and anti-HIV activity of α-thiophenoxy-hydroxyethylamide derivatives,” European Journal of Medicinal Chemistry, vol. 34, no. 7-8, pp. 625–638, 1999. View at Scopus
  7. B. Onoa and V. Moreno, “Nickel(II) and copper(II)—L-cysteine, L-methionine, L-tryptophan-nucleotide ternary complexes,” Transition Metal Chemistry, vol. 23, no. 4, pp. 485–490, 1998. View at Scopus
  8. K. Burger, Biocoordination Chemistry: Coordination Equilibria in Biologically Active Systems, E. Horwood, New York, NY, USA, 1990.
  9. R. P. Bonomo, B. Di Blasio, G. Maccarrone et al., “Crystal and molecular structure of the [6-deoxy-6-[(2-(4-imidazolyl)ethyl)amino]cyclomaltoheptaose]copper(II) ternary complex with L-tryptophanate. Role of weak forces in the chiral recognition process assisted by a metallocyclodextrin,” Inorganic Chemistry, vol. 35, no. 15, pp. 4497–4504, 1996. View at Scopus
  10. M. Sabat, B. Lippert, A. Sigel, and H. Sigel, Metal Ions in Biological Systems, vol. 33, Marcel Dekker, New York, NY, USA, 1996.
  11. E. Kimura, T. Koike, and M. Shionoya, “Lewis acids and vanadium,” in Metal Sites in Proteins and Models. Phosphatases, H. A. O. Hill, P. J. Sadler, and A. J. Thomson, Eds., vol. 89, no. 1, Springer, Berlin, Germany, 1997.
  12. T. Koike, M. Inoue, E. Kimura, and M. Shiro, “Novel properties of cooperative dinuclear zinc(II) ions: The selective recognition of phosphomonoesters and their P-O ester bond cleavage by a new dinuclear zinc(II) cryptate,” Journal of the American Chemical Society, vol. 118, no. 13, pp. 3091–3099, 1996. View at Publisher · View at Google Scholar · View at Scopus
  13. T. Koike, S. Kajitani, I. Nakamura, E. Kimura, and M. Shiro, “The catalytic carboxyester hydrolysis by a new zinc(II) complex with an alcohol-pendant cyclen (1-(2-hydroxyethyl)-1,4,7,10-tetraazacyclododecane): a novel model for indirect activation of the serine nucleophile by zinc(II) in zinc enzymes,” Journal of the American Chemical Society, vol. 117, no. 4, pp. 1210–1219, 1995. View at Scopus
  14. E. Kimura, T. Koike, T. Shiota, and Y. Iitaka, “Acid properties of zinc(II) and cadmium(II) in complexation with macrocyclic oxo polyamine ligands,” Inorganic Chemistry, vol. 29, no. 23, pp. 4621–4629, 1990. View at Scopus
  15. X. Zhang and R. Van Eldik, “A functional model for carbonic anhydrase: thermodynamic and kinetic study of a tetraazacyclododecane complex of zinc(II),” Inorganic Chemistry, vol. 34, no. 22, pp. 5606–5614, 1995. View at Scopus
  16. E. Kimura and K. K. Karlin, Progress in Inorganic Chemistry, vol. 41, Wiley, 1994.
  17. E. Kimura, I. Nakamura, T. Koike et al., “Carboxyester hydrolysis promoted by a new zinc(II) macrocyclic triamine complex with an alkoxide pendant: a model study for the serine alkoxide nucleophile in zinc enzymes,” Journal of the American Chemical Society, vol. 116, no. 11, pp. 4764–4771, 1994. View at Scopus
  18. E. Kimura, M. Shionoya, A. Hoshino, T. Ikeda, and Y. Yamada, “A model for catalytically active zinc(II) ion in liver alcohol dehydrogenase: a novel “hydride transfer” reaction catalyzed by zinc(II)-macrocyclic polyamine complexes,” Journal of the American Chemical Society, vol. 114, no. 26, pp. 10134–10137, 1992. View at Scopus
  19. A. A. El-Sherif and M. M. Shoukry, “Ternary copper(II) complexes involving 2-(aminomethyl)-benzimidazole and some bio-relevant ligands. Equilibrium studies and kinetics of hydrolysis for glycine methyl ester under complex formation,” Inorganica Chimica Acta, vol. 360, no. 2, pp. 473–487, 2007. View at Publisher · View at Google Scholar · View at Scopus
  20. A. A. El-Sherif and M. M. Shoukry, “Copper(II) complexes of imino-bis(methyl phosphonic acid) with some bio-relevant ligands. Equilibrium studies and hydrolysis of glycine methyl ester through complex formation,” Journal of Coordination Chemistry, vol. 58, no. 16, pp. 1401–1415, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. A. A. El-Sherif and M. M. Shoukry, “Coordination properties of tridentate (N,O,O) heterocyclic alcohol (PDC) with Cu(II). Mixed ligand complex formation reactions of Cu(II) with PDC and some bio-relevant ligands,” Spectrochimica Acta A, vol. 66, no. 3, pp. 691–700, 2007. View at Publisher · View at Google Scholar · View at Scopus
  22. A. A. El-Sherif, “Mixed-ligand complexes of 2-(aminomethyl)benzimidazole palladium(II) with various biologically relevant ligands,” Journal of Solution Chemistry, vol. 35, no. 9, pp. 1287–1301, 2006. View at Publisher · View at Google Scholar · View at Scopus
  23. A. A. El-Sherif, M. M. Shoukry, and R. Van Eldik, “Complex-formation reactions and stability constants for mixed-ligand complexes of diaqua(2-picolylamine)palladium(II) with some bio-relevant ligands,” Dalton Transactions, no. 7, pp. 1425–1432, 2003. View at Publisher · View at Google Scholar · View at Scopus
  24. M. M. Shoukry, E. M. Khairy, and A. A. El-Sherif, “Ternary complexes involving copper(II) and amino acids, peptides and DNA constituents. The kinetics of hydrolysis of α-amino acid esters,” Transition Metal Chemistry, vol. 27, no. 6, pp. 656–664, 2002. View at Publisher · View at Google Scholar · View at Scopus
  25. R. G. Bates, Determination of pH-Theory and Practice, Wiley-Interscience, New York, NY, USA, 2nd edition, 1975.
  26. A. A. El-Sherif, “Coordination properties of bidentate (N, O) and tridentate (N, O, O) heterocyclic alcohols with dimethyltin (IV) ion,” Journal of Coordination Chemistry, vol. 64, no. 7, pp. 1240–1253, 2011.
  27. P. Gans, A. Sabatini, and A. Vacca, “An improved computer program for the computation of formation constants from potentiometric data,” Inorganica Chimica Acta, vol. 18, pp. 237–239, 1976. View at Scopus
  28. L. Pettit, University of Leeds, Personal Communication.
  29. H. M. N. H. Irving and R. J. P. Williams, “The stability of transition-metal complexes,” Journal of the Chemical Society, pp. 3192–3210, 1952. View at Publisher · View at Google Scholar · View at Scopus
  30. J. E. Huheey, Inorganic Chemistry-Principles of Structure and Reactivity, Harper, New York, NY, USA, 1983.
  31. F. A. Cotton and G. Wilkinson, Advaned Inorganic Chemistry, Wiley, London, UK, 1962.
  32. C. S. G. Phillips and R. J. P. Williams, Inorganic Chemistry: Metals, vol. 2, Oxford University Press, New York, NY, USA, 1966.
  33. M. M. A. Mohamed and A. A. El-Sherif, “Complex formation equilibria between zinc(II), nitrilo-tris(methyl phosphonic acid) and some bio-relevant ligands. The kinetics and mechanism for zinc(II) ion promoted hydrolysis of glycine methyl ester,” Journal of Solution Chemistry, vol. 39, no. 5, pp. 639–653, 2010. View at Publisher · View at Google Scholar · View at Scopus
  34. K. Maskos, “The interaction of metal ions with nucleic acids. A nuclear magnetic resonance relaxation time study of the copper(II)-inosine 5-monophosphate system in solution,” Acta Biochimica Polonica, vol. 28, no. 2, pp. 183–200, 1981. View at Scopus
  35. D. J. Hodgson, “The stereochemistry of metal complexes of nucleic acid constituents,” in Progress in Inorganic Chemistry, S. J. Lippard, Ed., vol. 23, pp. 211–254, John Wiley, New York, NY, USA, 1977. View at Publisher · View at Google Scholar
  36. H. Sigel, Coordination Chemistry, vol. 20, Pergamon Press, Oxford, UK, 1980.
  37. H. Sigel, Metal Ions in Biological Systems, vol. 2, Dekker, New York, NY, USA, 1973.
  38. K. Maskos, “The interaction of metal ions with nucleic acids. A nuclear magnetic resonance relaxation time study of the copper(II)-inosine 5-monophosphate system in solution,” Acta Biochimica Polonica, vol. 28, no. 2, pp. 183–200, 1981. View at Scopus
  39. O. Yamauchi and A. Odani, “Structure-stability relationship in ternary copper(II) complexes involving aromatic amines and tyrosine or related amino acids. Intramolecular aromatic ring stacking and its regulation through tyrosine phosphorylation,” Journal of the American Chemical Society, vol. 107, no. 21, pp. 5938–5945, 1985. View at Scopus
  40. B. E. Fischer and H. Sigel, “Ternary complexes in solution. 35. Intramolecular hydrophobic ligand-ligand interactions in mixed ligand complexes containing an aliphatic amino acid,” Journal of the American Chemical Society, vol. 102, no. 9, pp. 2998–3008, 1980. View at Scopus
  41. A. A. El-Sherif, “Equilibrium studies of binary and mixed-ligand complexes of zinc(II) involving 2-(aminomethyl)-benzimidazole and some bio-relevant,” Journal of Solution Chemistry. In press. View at Publisher · View at Google Scholar