straighter helix than alamethicin, a tightly-packed hexameric model structure has been ... has molecular dimensions and surface electrostatic potential compatible with the observed ... members of SF2 and SF3, respectively, whose crystal.
G. S H A R M A and J. P. T A N D O N. Chemical Laboratories, University of Rajasthan, Jaipur (India). (Z. Naturforsch. 25 b, 22â 26  ; eingegangen am 20.
mately 50 set for partially purified lactate dehydrogenase-1. Changes in coenzyme concentration from 0.10 rnrd to 0.75 mu failed to alter the rates of abortive ...
âEstudios en la formaciÃ³n de coacervados complejos entre quitosana y alginato durante la prepara- ciÃ³n de micropartÃculasâ. La formaciÃ³n de coacervados complejos entre quitosana y alginato fue evaluada duran- te la formaciÃ³n de micropartÃcu
the work day or in the work tasks of the metalworking, building and woodworking industries. The significance of the subjects' health habits, use of ... alone contains products of complete air and carbon combustion (nitrogen, water, and carbon ......
Feb 1, 2008 - decreasing one-by-one culminating in an one-atom wide and four-atom long linear chain of. Au atoms [3,4]. Furthermore, the simultaneously ...
o Elsevier Scientific Publishing Company, Amsterdam - Printed in The ..... a Sargent-Welch 600-rpm synchronous-speed magnetic stirrer (model 576492).
structure of depsipeptides changes depending on the solvent polarity. The solvent polarity ... tunity to elucidate the complexation basis of valinomycin. Considerable work .... ber of intramolecular hydrogen-bonds from 1 to 6 and the number of ...
Conductance measurements of aqueous solutions of succinic acid and of di-sodium succinate were performed from ... Dissociation constants of succinic acid at room .... Table 1. Experimental equivalent conductances of di-sodium succinate and molar cond
photographs for the rubredoxin-FTR system. Fig. 5A is FTR alone, Fig. 5B is rubredoxin alone, and Fig. 5C is a mixture of the two. The light areas on the plates ...
in a stable association without formation of covalent bonds,. 0928-0987/$ ... plex or not and cannot provide a clear answer about the type of complex formed ...
J. 2017, 23, 2133 – 2143 ... 50 GΩ (i.e., G=0.2–0.02 nS; 20–2 10А6 G0) was estimated at ..... However, as manual data selection can never be fully objective,.
molarity was varied between 5 â¢ 10-5 and 1 â¢ 10~2. ... Limiting equivalent conductances xÂ°, association constants KA and standard deviations o obtained for the ...
Feb 2, 2016 - engineering and green chemistry, which promotes sustainable extraction processes as a result of using non petroleum-based solvents and renewable plant material . A holistic, 5-stages recovery process for the extraction of valuable co
Mar 24, 1997 - t Present address: Mitotix, Inc., 1 Kendall Square, Cambridge, MA .... (Pharmacia Biotech, Piscataway, NJ) was added, and the incubation.
tween palmitoyl-CoA and polysaccharide (R. Bergeron and P. Flick, unpublished). From the observed chemical shift of the methylene protons of palmityl-CoA ...
stereochemistry on the interactions between sulfonated polystyrene (PSS) and myoglobin. We have sulfonated polystyrene with a unique stereochemical structure or tacticity, i.e (a) atactic polystyrene (aPS), and (b) isotactic polystyrene (iPS). aPS is
Abbreviations: coprogen, coproporphyrinogen III; CPO, coproporphyrin- ogen III oxidase; FC, ferrochelatase; PPO, protoporphyrinogen IX oxidase; proto ...
oxygen atoms, we have isotopically labeled distinct atoms in carbon monoxide ..... case of ground state oxygen atoms, an initial addition barrier of 0.26 eV has to ...
buffer, pH7.5) and containing Xa (1000 units/ml.). A standard curve was ... MSE Superspeed 40 centrifuge at 4Â° in an 8 x lOml. angle-head rotorat 85000g for ...
BY JOHN M. McKENNA,:~ PE.D., A~rD KINGSLEY M. STEVENS,Â§ M.D.. (From the Merck Institute for Therapeutic Research, West Point, Pennsylvania). PLATv.
Induction of Chimerism with a Chemical Carcinogen1. Yuko Kikuchi2 and Mildred E. Phillips3. Department of Pathology, New York University Medical Center, ...
Products by the Binding of Derivatives of 7-Methylbenz[a]anthracene to DN A in Aqueous ..... pyrene and Its Methylated Derivatives in Relation to the Molecular.
supernatant factors (peptide bond synthesis) and amino acid polymerization into long ... tensively to study the mechanism of protein biosynthesis. With the use of ...
Molecules 2013, 18, 12041-12050; doi:10.3390/molecules181012041 OPEN ACCESS
Conductance Studies on Complex Formation between c-Methylcalixresorcinarene and Titanium (III) in Acetonitrile-H2O Binary Solutions Majid Rezayi 1,2, Yatimah Alias 2,*, Mahnaz M. Abdi 3,*, Kasra Saeedfar 4,5 and Naghmeh Saadati 4 1
Food Quality and Safety Research Department, Food Science and Technology Research Institute, ACECR Mashhad Branch, 91775-1376 Mashhad, Iran Chemistry Department, Faculty of Science, University Malaya, 50603 Kuala Lumpur, Malaysia Department of Chemistry, Faculty of Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor D.E., Malaysia School of Chemical Sciences and Food Technology, Faculty of Science and Technology, University Kebangsaan Malaysia, 43600 Bangi, Selangor D.E., Malaysia Chemistry Department, Faculty of Science, K. N., Toosi University of Technology, 15418-49611 Tehran, Iran
* Authors to whom correspondence should be addressed; E-Mails: [email protected] (Y.A.); [email protected] (M.M.A.); Tel.: +60-389466930 (M.M.A.); Fax: +60-38946 6997 (M.M.A.). Received: 25 April 2013; in revised form: 8 May 2013 / Accepted: 10 May 2013 / Published: 27 September 2013
Abstract: Calixresorcinarenes have proved to be unique molecules for molecular recognition via hydrogen bonding, hydrophobic and ionic interactions with suitable substrates such as cations. The study of the interactions involved in the complexation of different cations with calixresorcinarenes in solvent mixtures is important for a better understanding of the mechanism of biological transport, molecular recognition, and other analytical applications. This article summarizes different aspects of the complexes of the Ti3+ metal cation with c-methylcalixresorcinarene (CMCR) as studied by conductometry in acetonitrile (AN)–water (H2O) binary mixtures at different temperatures. Conductance data show that the metal cation/ligand (ML) stoichiometry of the complexes in solution is 1:1 in all cases. Non-linear behaviour was observed for the variation of logKf of the complexes vs. the composition of the binary solvent mixtures. Selectivity of CMCR for the Ti3+ cation is sensitive to solvent composition; in some cases and at certain compositions of the mixed
Molecules 2013, 18
solvent systems, the selectivity order is changed. Values of thermodynamic parameters ( ΔH cο , ΔS cο ) for formation of the CMCR–Ti3+ complexes in AN–H2O binary systems were obtained from the temperature dependence of stability constants, and the results show that the thermodynamics of complexation reactions are affected by the nature and composition of the mixed solvents. Keywords: conductance data; calixresorcinarenes; titanium(III); c-methylcalixresorcinarene; acetonitrile (AN)-water (H2O); binary mixtures
1. Introduction Investigations with calixarenes and calixresorcinarenes have demonstrated the versatility of these molecules in supermolecular host–guest chemistry . c-Methylcalixresorcinarene (CMCR, Figure 1) is an excellent building block for the construction of a variety of hydrogen-bonded networks, thanks to the large number of hydroxyl groups along its rim, allowing it to act as a hydrogen bond donor in producing extended structures or binding ligands to give an extended cavity capable of taking up large guests, such as ferrocene . Coppens et al. showed that 4,4′-bipyridine is capable of forming a variety of inclusion compounds with CMCR, with the CMCR molecules in any of four conformations: crown, boat, chair and scoop . However, in all reported open boat conformation CMCR molecules, the CMCR either forms a discrete complex with an inorganic ion, or each CMCR molecule hydrogen bonds directly to at least one adjacent CMCR, resulting in ‘brick wall’ motifs, while the bipyridine serves to link these ‘walls’ together. Shivanyuk et al. have reported the ability of CMCR to adopt the boat conformation without forming the brick walls described by Coppens in his investigations of bipyridyl-type ligands . In this instance, chloride ions served to extend the boat-shaped cavity to allow accommodation of the triethylammonium ion. Use of such inorganic ions presents an interesting alternative route to produce extended resorcinarene structures. Recently, calixarenes, which are macrocyclic products of phenol–formaldehyde condensations, have been shown to be amenable to chemical modifications at the upper or lower rim to yield new macromolecules and act as effective ionophores that can selectively bind a range of metals . In addition to calixarenes, structurally related resorcinarenes, which are the macrocyclic products of resorcinol with aldehydes (except formaldehyde), form complexes with both cations and polar organic molecules. Until now, only a few reports on the use of these resorcin[n]arenes for extraction of metals have appeared. Several groups have studied the novel resorcinarenes, and their complexation with alkali metal ions, especially with potassium ions [6,7]. Due to this fact, many researchers have examined a wide range of applications for these macrocyclic compounds in different areas, such as the construction of ion selective electrodes (ISEs) , separation of metal cations , as stationary phases in chromatography columns , in the design of chemical sensors , recognition of isomers , and chemical analysis . In recent years, this branch of chemistry has seen a lot of advances. Many new novel compounds with high selectivities for ion or molecule separation, transport and catalytic purposes have been developed by scientists active in different areas of chemistry. Diverse methods, such as
Molecules 2013, 18
UV–Vis spectroscopy, polarography, potentiometry, and conductometery have been applied to investigation of the complexometric reactions [14,15]. Conductivity measurements are useful tools for investigating complexation, due to their precision, simplicity, and low cost . In this work, complexations between CMCR and titanium (Ti3+) cation in water (H2O), acetonitrile (AN), and their binary mixture solutions at different temperatures have been studied using the conductometric method. The goal of the present investigation was to study the effect of solvent properties and the composition of the binary mixed solvents on the stoichiometry and the selectivity of complexes formed between ligands and cations in various solvent systems. Figure 1. Molecular structure of C-methylcalixresorcinarene (CMCR).
2. Results and Discussion The conductometric method was used in the thermodynamic study of complexation reactions between the CMCR ligand with the Ti(OH)(OH2)52+ cation in acetonitrile–water (AN–H2O) binary mixtures at different temperatures. It was also used to evaluate the effect of the composition of acetonitrile–water binary solutions on the nature of titanium cations. The results could be useful for applications such as the fabrication of ISEs based on macrocyclic ionophores for determining titanium ions in real samples [17–19]. Changes in molar conductivity (Λm) vs. the molar ligand-to-ion ratio of CMCR to the Ti(OH)(OH2)52+ cation ([L]t/[M]t, where [L]t is the total concentration of the ligand and [M]t is the total concentration of the titanium (III) ion) for the complexation reactions were measured in pure AN and in AN–H2O binary systems at three different temperatures. A result in pure H2O was not obtained, due to the low solubility of CMCR. Five typical series of the resulting molar conductance vs. CMCR/Ti(OH)(OH2)52+ molar ratio plots in pure AN and the AN–H2O binary mixtures (mol% H2O = 42.05, 65.91, 81.32 and 92.07) are shown in Figures 2 and 3. As can be seen, the addition of the CMCR ligand to titanium cation solution in pure AN and in AN–H2O binary mixtures at different temperatures increased the molar conductivity (Λm) values as the CMCR/Ti(OH)(OH2)52+ molar ratio increased, which indicates that CMCR–Ti(OH)(OH2)52+ complexes in these systems have higher mobility than the free solvated Ti(OH)(OH2)52+ cation. The slope of the corresponding mole ratio plots changes at the point where the ligand to cation mole ratio corresponds to about a 1:1 complex between the CMCR ligand and the Ti(OH)(OH2)52+ cation. The main goal of the conductometric study was to obtain stability constant complexes between ligands and ions. Formation constants of all the CMCR-Ti(OH)(OH2)52+ complexes in different solvent mixtures at various temperatures, obtained by computer fitting of the molar conductance–mole ratio data, are listed in Table 1.
Molecules 2013, 18
Figure 2. Molar conductance (S cm2.mol−1) vs. [CMCR]/[Ti(OH)(OH2)52+] mole ratio plots in pure AN at various temperatures.
Figure 3. Molar conductance (S cm2.mol−1) vs. [CMCR]/[Ti(OH)(OH2)52+] mole ratio plots in AN–H2O binary mixture (mol% H2O = (a):42.05, (b):65.91, (c):81.32, (d):92.07) at various temperatures.
Molecules 2013, 18
Table 1. Formation constants for different CMCR-Ti(OH)(OH2)52+ complexes in AN–H2O binary mixtures at various temperatures. Medium Pure AN 57.95% AN-42.05% H2O 34.09% AN-65.91% H2O 18.68% AN-81.32% H2O 7.93% AN-92.07% H2O Pure H2O
15 °C 3.59 ± 0.06 3.29 ± 0.03 2.86 ± 0.05 2.97 ± 0.13 2.62 ± 0.16 c
Log Kf ± SD a 25 °C 3.62 ± 0.08 3.30 ± 0.04 3.04 ± 0.07 2.86 ± 0.30 2.83 ± 0.17 c
35 °C 3.65 ± 0.20 3.37 ± 0.18 3.06 ± 0.07 3.02 ± 0.10 2.87 ± 0.21 c
SD = Standard deviation; b the composition of each solvent system is expressed in mole% of each solvent; c ion or ligand salt is insoluble.
From Table 1, it is obvious that the nature of the solvent has a fundamental effect on the stability of the resulting complexes. In most cases, the stability constant of the complexes increases with the temperature in most solvent systems, which is evidence for an endothermic complexation reaction between ligands and ions in the solutions. There are many reasons for discussing the effectiveness of solvents on the stability constant of complexes, owing to the fact that this factor changes from one solvent system to another. As shown in Table 1, the stability of the complex increases with the decreasing solvating power of the solvent mixtures (H2O), as expressed by the Gutman donor number. Water is a solvent with a high solvating ability (DN = 18) and hence solvates the ion more strongly than acetonitrile (DN = 14.1). As a result, replacement of the solvent molecules around the cation by the calixarenes would be energetically expensive. This effect is observed for all different mol% of the AN–H2O mixtures. For instance, the logKf values for (CMCR–Ti(OH)(OH2)5)2+ in 100% AN, 57.95% AN–H2O, 34.09% AN–H2O, 18.68% AN–H2O and 7.93% AN–H2O are 3.62, 3.30, 3.04, 2.86, and 2.83 in 25 °C, respectively. As shown in Figure 4, changes in the stability constant (logKf) of the (CMCR–Ti(OH)(OH2)5)2+ complex vs. the composition of the AN–H2O binary system at various temperatures are not linear. This behaviour is probably due to solvent–solvent interactions that change the structure of the solvent mixtures and therefore change the solvation properties of the titanium cation, the CMCR, and the resulting complex. In addition, preferential solvation of the cation and ligand, as well as the characteristics of its changes with the composition of the mixed solvents and temperature, may be other reasons for this kind of behaviour. The interactions between some binary mixed solvents have been studied. For example, mixing dimethylformamide with acetonitrile induces the mutual destruction of the dipolar structures of these dipolar aprotic liquids and releases the free dipoles. As a result, strong dipolar interaction between acetonitrile and water molecules is expected. Similar behaviour was observed in other cases.
Molecules 2013, 18
Figure 4. Variation of the stability constant (log Kf) of (CMCR-Ti(OH)(OH2)5) 2+ complex with the composition of AN–H2O binary systems at different temperatures: (♦15 °C, ■ 25 °C, ▲ 35 °C).
The two fundamental equations: ∆G = −RT ln Kf and ∆G = ∆H − T∆S were used to compare the contributions of enthalpy and entropy towards the stability of the CMCR–Ti(OH)(OH2)52+ complexes. The enthalpy contribution can be obtained experimentally by using van’t Hoff plots . In order to have a better understanding of the thermodynamics of complexation reactions of Ti(OH)(OH2)5)2+ cations with CMCR, it is useful to investigate the enthalpic and entropic contributions to these reactions. The ΔH cο and ΔS cο of the complexation reactions in different AN–H2O mixtures were evaluated from the temperature dependence of the formation constants by applying a linear leastsquares analysis according to the Van’t Hoff equation. The Van’t Hoff plots of ln Kf vs. 1/T are shown in Figure 5. The enthalpies and entropies of complexation were determined in the usual manner from the slopes and intercepts of the plots, respectively, and the results are listed in Table 2. Figure 5. Van’t Hoff plots for the 1:1 complexation of Ti(OH)(OH2)5)2+ cation with CMCR in AN–H2O binary systems: (mol% AN: ♦ 100, □ 57.95, ▲ 34.09, ∆ 18.68, ■ 7.93).
Molecules 2013, 18
Table 2. Thermodynamic parameters for different CMCR-Ti(OH)(OH2)52+ complexes in various AN–H2O binary mixtures. Medium Pure AN 57.95% AN-42.05% H2O 34.09% AN-65.91% H2O 18.68% AN-81.32% H2O 7.93% AN-92.07% H2O a
SD = Standard deviation; b The composition of each solvent system is expressed in mole% of each solvent.
The calculated thermodynamic parameters ( ΔH cο , ΔGcο , ΔS cο ) at 25 °C for CMCR-Ti(OH)(OH2)52+ complexes in pure AN and AN–H2O binary systems are listed in Table 2. The given experimental values of standard enthalpy ( ΔH cο ) and standard entropy ( ΔS cο ) show that, in most cases, the complexes are enthalpy destabilized, but entropy stabilized. Therefore, the entropy of the complexation reactions is the principal driving force for the formation of these complexes in most solvent systems. The experimental results show that, in most cases, the change in standard enthalpy for the complexation reaction between ligand and ion is negligible; therefore, it seems that the complexation processes in most of the solvent systems are probably athermic. 3. Experimental
3.1. Materials The host CMCR was used as purchased from Fluka (Seelze, Germany). Reagent grade 15% titanium (III) chloride, and dried acetonitrile (max. 0.005%H2O) (all from Merck, Darmstadt, Germany) were of the highest purity available and were used as received. All the AN–H2O mixtures used were prepared by weight. Deionized bi-distilled water was used throughout the experiment. Conductance measurements were carried out with a digital HI 255 conductivity meter (Hanna Instruments, Ann Arbor, MI, USA). A dip-type conductivity cell made of platinum black was used. The cell constant at the different temperatures used was determined by conductivity measurements of a 0.1000 M solution of analytical-grade KCl (Merck) in deionized water. In all measurements, the cell was thermostatted at the desired temperature ±0.01 °C using a 630D thermostat-circulator water bath (Protech, San Antonio, Texas, USA). 3.2. Methodology In a typical experiment, 25 mL of the desired metal ion (5.0 × 10−5 M) were placed in the titration cell, thermostatted to the desired temperature, and the conductance of solution was measured. Then, a known amount of a concentrated CMCR solution (2.5 × 10−3 M) was added in a stepwise manner using a calibrated micropipette. The conductance of the solution was measured after each addition. The ligand solution was added continually until the desired ligand to cation mole ratio was achieved. The formation constants, Kf, and the molar conductances, Λm, of the resulting 1:1 complexes between CMCR and the titanium (III) cation used, in different AN–H2O mixtures and at various temperatures,
Molecules 2013, 18
were calculated by fitting the observed molar conductance, Λobs, at varying [CMCR]/[Ti3+] mole ratios to a previously derived equation that expresses the Λobs as a function of the free and complexed titanium (III) ions. A nonlinear least squares curve fitting using the GENPLOT computer program was applied to evaluate the formation constant and the limiting molar conductance of the resulting 1:1 complexes . In the present work, all of the measured solutions were adjusted in pH range 1–3, and the dominant titanium species were in the form of Ti(OH)(OH2)52+ [17,18,22]. 4. Conclusions
The stability constants of the complex formation between the CMCR and the titanium (III) cations were measured based on the conductometric method in various mole percentages of AN–H2O media systems at different temperatures. The results obtained showed that, in the case of the CMCR– Ti(OH)(OH2)52+ complex, the stability constant of the complex decreased with an increasing percentage of water. The negative quantities of standard Gibbs free energy and the positive values of entropy indicate spontaneous complexation reactions between the CMCR ligand and the titanium (III) cations. CMCR forms a 1:1 complex with the Ti(OH)(OH2)52+ cation at all compositions of the AN–H2O binary solution. The average value of the stability constant (ln Kf) for the CMCR–Ti(OH)(OH2)52+ complexes at 25 °C was 3.13. In conclusion, based on the results obtained, the CMCR ligand can be used as a desired ionophore to detect the titanium (III) cation in the field of the chemical sensor. Acknowledgments
This work was supported by department of chemistry, Unversiti Putra Malaysia, Serdang, Selangor, Malaysia and University of Malaya, Kuala Lumpur, Malaysia by using the High Impact Research Grant UM-MOHE UM.C/625/1/HIR/MOHE/F00004-21001 from the Ministry of Higher Education Malaysia and PV 124-2012A. The authors wish to thank from Aishah Salleh, Seyedeh Belin Tavakoly Sany, Leila Narimani and Chakavak Esmaeili for their valuable assistance. Conflicts of Interest
The authors declare no conflict of interest. References
Brown, P.O.; Enright, G.D.; Ripmeester, J.A. Cationic guests in extended anionic c-methylcalix  resorcinarene-inorganic frameworks: Exercising conformational control over c-methylcalix  resorcinarene. J. Supramol. Chem. 2002, 2, 497–500. Lepakshaiah, M.; Guru Row, T.N. Solid state stacked trimers of 1, 10-phenanthroline in a supramolecular tubular motif of C-methylcalix  resorcinarene. J. Mol. Struct. 2009, 918, 10–13. Ma, B.Q.; Zhang, Y.; Coppens, P. Multiple structures in supramolecular solids: Benzophenone embedded in three different C-Methylcalix  resorcinarene/bipyridine frameworks. Cryst. Growth Des. 2001, 1, 271–275.
Molecules 2013, 18 4.
8. 9. 10.
11. 12. 13. 14.
Shivanyuk, A.; Saadioui, M.; Broda, F.; Thondorf, I.; Vysotsky, M.O.; Rissanen, K.; Kolehmainen, E.; Böhmer, V. Sterically and Guestâ Controlled Self Assembly of Calix  arene Derivatives. Chem.-Eur. J. 2004, 10, 2138–2148. Memon, S.; Akceylan, E.; Sap, B.; Tabakci, M.; Roundhill, D.M.; Yilmaz, M. Polymer supported calix  arene derivatives for the extraction of metals and dichromate anions. J. Polym. Environ. 2003, 11, 67–74. Zhang, Y.; Kim, C.D.; Coppens, P. Does C-methylcalix  resorcinarene always adopt the crown shape conformation? A resorcinarene/bipyridine/decamethylruthenocene supramolecular clathrate with a novel framework structure. Chem. Commun. 2000, 23, 2299–2300. Pashirova, T.N.; Lukashenko, S.S.; Kosacheva, E.M.; Rizvanova, L.Z.; Gainanova, G.A.; Knyazeva, I.R.; Burilov, A.R.; Kudryavtseva, L.A.; Konovalov, A.I. Supramolecular systems based on poly (ethyleneimines) and calix  resorcinarenes with alkylphosphonate fragments. Aggregation and catalytic activity. Russ. Chem. Bull. 2007, 56, 959–966. Mahajan, R.K.; Kaur, R.; Kaur, I.; Sharma, V.; Kumar, M. Mercury (II) ion-selective electrodes based on p-tert-butyl calix  crowns with imine units. Anal. Sci. 2004, 20, 811–814. Dai, S.; Ju, Y.H.; Barnes, C.E. Solvent extraction of strontium nitrate by a crown ether using room-temperature ionic liquids. J. Chem. Soc. Dalton Trans. 1999, 8, 1201–1202. Ding, X.; Nomura, M.; Suzuki, T.; Sugiyama, Y.; Kaneshiki, T.; Fujii, Y. Chromatographic zinc isotope separation by phenol formaldehyde benzo crown resin. J. Chromatogr. A 2006, 1113, 182–185. Gupta, V.K.; Jain, S.; Chandra, S. Chemical sensor for lanthanum (III) determination using azacrown as ionophore in poly (vinyl chloride) matrix. Anal. Chim. Acta 2003, 486, 199–207. Kuhn, R.; Riester, D.; Fleckenstein, B.; Wiesmüller, K.H. Evaluation of an optically active crown ether for the chiral separation of di-and tripeptides. J. Chromatogr. A 1995, 716, 371–379. Yoshio, M.; Noguchi, H. Crown ethers for chemical analysis: A Review. Anal. Lett. 1982, 15, 1197–1276. Rezayi, M.; Ahmadzadeh, S.; Kassim, A.; Lee, Y.H. Thermodynamic studies of complex formation between Co (Salen) ionophore with chromate (II) ions in AN-H2O binary solutions by the conductometric method. Int. J. Electrochem. Sci. 2011, 6, 6350–6359. Ahmadzadeh, S.; Kassim, A.; Rezayi, M.; Rounaghi, G.H. Thermodynamic Study of the Complexation of p-Isopropylcalix  arene with Cs+ Cation in Dimethylsulfoxide-Acetonitrile Binary Media. Molecules 2011, 16, 8130–8142. Ahmadzadeh, S.; Kassim, A.; Rezayi, M.; Abdollahi, Y.; Hossein, G. A conductometric study of complexation reaction between meso-octamethylcalix  pyrrole with titanium cation in acetonitrile-ethanol binary mixtures. Int. J. Electrochem. Sci. 2011, 6, 4749–4759. Rezayi, M.; Heng, L.Y.; Kassim, A.; Ahmadzadeh, S.; Abdollahi, Y.; Jahangirian, H. Immobilization of Ionophore and Surface Characterization Studies of the Titanium (III) Ion in a PVC-Membrane Sensor. Sensors 2012, 12, 8806–8814. Rezayi, M.; Heng, L.Y.; Kassim, A.; Ahmadzadeh, S.; Abdollahi, Y.; Jahangirian, H. Immobilization of tris (2 pyridyl) methylamine in a PVC-Membrane Sensor and Characterization of the Membrane Properties. Chem. Central J. 2012, 6, 40.