ANALYSIS OF SOLVATION NUMBER,ADIABATIC COMPRESSIBILITY AND SPECIFIC ACOUSTIC IMPEDANCE OF GLYCYL AND AMIDE SALTS Padmavathy.R1,JasmineVasanthaRani.E1,Santhakumari.S2,Sujatha.S2 1 Department of Physics,Seethalakshmi Ramaswamy College,Tiruchirappalli,Tamilnadu 2 Department of Physics,Srimathi Indira Gandhi College,Tiruchirappalli,Tamilnadu ABSTRACT Ultrasound is novel and challenging method that is being developed for biomolecules where non-invasive technique is of great interest. Ultrasonic Velocity measurements are highly sensitive to molecular interactions and used to provide qualitative information about the physical nature and strength of the moleculer/ inter-ionic interactions.The aminoacids belong to an important family of biomolecules which serve primarily as the basic building block of all proteins.The Sample glycyl L-leucine is used in the study of protein structure and fuctions .Another Sample sulphanilamide is the potent antibiotic which is important in the control of urinary tract infections and mening gococcal meningitis profilaxes. Solvation is the association of solvent molecules with the solute ions in a solutions .Adiabatic compressibility of a solution varies due to the effect of hydrogen bonding or induced dipoledipole interactions. Specific acoustic impedance is the characteristic impedance of the medium.In the present investigation ,the solutions of different molalities were prepared with the samples in non-aqueous medium and experiments were carried out from a low concentration to high concentration,at different temperature.The measured values of density,viscosity and ultrasonicvelocity were used to compute solvation number,adiabatic compressibility and Specific acoustic impedance.An attempt is made to identify the entry solvate into the Samples and the entry of biological molecules into the Solvate Which supports to identify the molecular structure. KEYWORDS- ion-solvent and solute-solvent interactios. 1 INTRODUCTION Amino acids belong to an important family of biomolecules which serve primarily as the basic building block of all proteins[1].. Ultrasonic studies of solutions yield valuableinformation about the molecular interactions, the nature and strength of the interactions.Sulphanilamide is the parent compound of all the sulpha-durgs which is important in urinarytract infections and meningococcal meningitis profilaxes. In the present work, non-aqueoussolutions of Sulphanilamide and glycyl-L-Leucine have been prepared with differentconcentrations and the experiments were carried out from a low temperature of 50c to a hightemperature of 550c. The ultrasonic velocity data combined with density and viscosityprovides the standard means for determining the Solvation number and acoustical parameters.(adiabaticcompressibility,specific acoustic impedance). EXPERIMENTAL TECHNIQUE Density of the solutions is measured using 25ml specific gravity bottle with accuracy of 0.0001gm/cc. Cannon Fenske viscometer is used for the viscosity measurements, with an accuracy of ± 0.5%. Mittal’s interferometer of frequency 2 MHZ with an accuracy ±0.5m/s is used for the measurement of ultrasonic velocity. COMPUTATION The Solvation number and acoustic parameters are computed by using the formulae. (i)Solvation number (Sn) = n1/n2 [1-β/βo] (ii) Adiabatic compressibility (β) = [1/u2ρ] cm2/dyne (iii)Specific acoustic impedance Z =(ρu)Rayl. 2 TABLES AND FIGURES TABLE-(1)a Solvation number- Glycyl-L-Leucine Molality(m) 50c 150c 250c 350c 450c 550c 0.001 58.82 314.75 343.16 557.71 962.71 1333.57 0.005 43.45 84.78 91.44 145.46 231.97 306.52 0.01 35.69 57.41 75.15 110.24 156.50 193.58 0.015 40.41 53.62 55.44 82.78 115.69 135.45 0.02 38.17 51.79 54.09 68.86 96.37 112.05 SULPHANILAMIDE-TABLE-(1)b Molality(m) 5°c 15°c 25°c 35°c 45°c 55°c 0.001 124.50 357.99 15.97 285.67 492.64 778.43 0.005 186.96 220.10 270.72 327.37 344.78 480.80 0.01 56.74 59.19 72.86 103.49 93.32 120.57 0.015 49.59 52.41 57.42 79.72 77.21 94.55 0.02 40.21 45.50 51.85 68.64 76.46 80.88 3 FIG(1)a Glycyl-L-Leucine Solvation number Vs Molality 1400 1200 5°c Solvation number 1000 15°c 800 25°c 35°c 600 45°c 400 55°c 200 0 .001 .005 .01 0.015 0.02 Molality(m) SULPHANILAMIDE –FIG(1)b Solvation number Vs Molality 800 Solvation number 700 5°c 600 15°c 500 25°c 400 35°c 45°c 300 55°c 200 100 0 .001 .005 .01 .015 .02 Molality(m) 4 Adiabatic compressibility(cm2/dynes)x10-11 Glycyl-L-Leucin- TABLE(2)a Molality(m) Temperature in centigrade 5 15 25 35 45 55 0.001 3.239 3.292 3.359 3.470 3.542 3.590 0.005 3.215 3.275 3.341 3.442 3.507 3.554 0.01 3.194 3.251 3.294 3.379 3.437 3.482 0.015 3.156 3.215 3.281 3.356 3.407 3.465 0.02 3.132 3.179 3.241 3.333 3.374 3.427 SULPHANILAMIDE-TABLE(2)b Molality(m) 5°c 15°c 25°c 35°c 45°c 55°c 0.001 3.23 3.28 3.41 3.52 3.62 3.69 0.005 3.19 3.27 3.35 3.45 3.59 3.66 0.01 3.16 3.24 3.32 3.39 3.55 3.61 0.015 3.14 3.22 3.28 3.36 3.51 3.58 0.02 3.13 3.20 3.28 3.33 3.44 3.54 5 Glycyl-L-LeucineFIG(2)a Adiabatic compressibility(cm2/dynes)x10-11 Adiabatic compressibility vs Molality 3.60 3.55 3.50 3.45 3.40 3.35 3.30 3.25 3.20 3.15 3.10 5°c 15°c 25°c 35°c 45°c 55°c .001 .005 .01 .015 Molality(m) .02 SULFANILAMIDE-FIG(2)b Adiabatic compressibility(cm2/dynes) 10-11 Adiabatic compressibility Vs Molality 3.8 3.7 3.6 5°c 15°c 25°c 35°c 45°c 55°c 3.5 3.4 3.3 3.2 3.1 3.0 .001 .005 .01 .015 .02 Molality(m) SULFAN ILAMID E 6 Specific acoustic impedance (Rayl) Glycyl-L-LeucineMolality(m) TABLE(3)a Temperature in centigrade 5 15 25 35 45 55 0.001 18.83 18.65 18.38 18.00 17.77 17.59 0.005 18.91 18.67 18.43 18.07 17.86 17.67 0.01 18.97 18.73 18.57 18.25 18.04 17.87 0.015 19.08 18.86 18.60 18.31 18.12 17.90 0.02 19.14 18.95 18.71 18.38 18.21 18.01 SULPHANILAMIDE-TABLE(3)b Molality(m) 5°c 15°c 25°c * 35°c 45°c 55°c 0.001 18.85 18.65 18.22 17.87 17.55 17.34 0.005 18.96 18.66 18.45 18.02 17.63 17.40 0.01 19.05 18.74 18.54 18.21 17.74 17.53 0.015 19.13 18.85 18.60 18.27 17.84 17.61 0.02 19.15 18.90 18.68 18.36 18.01 17.71 7 Glycyl-L-LeucineFIG(3)a SPecific accoustic impedance(Rayl) Specific accoustic impedance Vs Molality 5°c 15°c 25°c 35°c 45°c 55°c 19.25 18.75 18.25 17.75 17.25 .001 .005 .01 .015 .02 Molality(m) SULPHANILAMIDE-FIG(3)b Specific accoustic impedance(rayl) Specific accoustic impedance Vs Molality 19.5 5°c 19.0 15°c 18.5 25°c 35°c 18.0 45°c 17.5 55°c 17.0 0.001 0.005 0.01 0.015 Molality(m) 0.02 8 Results and Discussion SOLVATION NUMBER The solvation numbers reflect the dynamic situation of the ion as its moves round the solution[2] comparing the two salts as shown in the table(1)a&b)and fig(1)a&b), the solvation number is a positive.It indicates that the compressibility of the solution is less than the solvent.The salvation approach is used to interpret ion-solvent interaction[3]. The ionsolvent interaction may be due to equal to intermolecular interaction[4]. ADIABATIC COMPRESSIBILITY -The structural changes of molecules in the solution takes place due to the existence of electrostatic field between the interacting molecules[5]..The arrangement of the molecules results in the effect of adiabatic compressibility.compare the both salts, the adiabatic compressibility increases with decrease in molality and rise in temperature [6] shown in table(2)a&b and fig (2)a&b. When the salt is added to the solvent ,the compressibility is lowered. This lowering is attributed to the influence of the electrostatic field of the ions on the surrounding solvent molecules. such a decrease may be due to (i) an increase in the number of incompressible molecule[7,8,9]. (ii) structural changes occurring in the solution .This may be due to the association taking place between the molecules. When the temperature increases, the associated groups of molecules breakdown increasingly and the forces of attraction between the molecules decrease. This leads to an increase in the adiabatic compressibility of the system[10]. SPECIFIC ACOUSTIC IMPEDANCE-The specific acoustic impedance is governed by the internal and elastic properties of the medium. In the present investigation, Z increases with increasing concentration and decreases with increasing temperature, which indicates the absence of complex formation and the existence of solute-solvent interaction. The results are tabulated in the table(3)a&b and shown in the fig (3)a&b for both the salts. This linear increase due to the effect of strong solute-solvent interaction{11] existing in the solutions. The specific acoustic impedance is available as 18.39Rayl at 250c*of formamide from the literature[12]. In the present investigation ,the inter-molecular free length of solutions is found to decrease with respect to the various molality and increases with temperature. These changes reveal the fact that there is a strong interaction exist between the solute and solvent[13]. The comparision of this three parameters gave the good agreement results for molecular interactions. 9 CONCLUSION The field of protein folding and stability has been a critically important area of research for years and remains today as one of the greatest unsolved mysteries. In the present work, a detailed analysis of acoustic and thermodynamic properties was made. The study reveals the fact that the addition solute in the solvent enhances the solute-solvent interaction.This behavior of glycy1-L-Leucine in formamide emphasizes that it act as a structure maker due to its structural stability and Zwitterionic nature. Sulphanilamide compounds identified as chemotherapeutic agents, possess broad spectrum of biological properties[14]. Sulfanilamide is a potent antibiotic because this drug undergoes metabolic alterations in tissues[15] .The detailed study of acoustic parameters suggests that there is a molecular association existing between the molecules of the solution. The addition of solute into the solvent brings about a strong solute-solvent interaction in the solution REFERENCES [1]G.Ravichandran, S.Arumugam and T.K.Nambi Narayanan,J.Pure and Appl. Ultrasonics.34(2012)PP,17-21. [2] Padmavathy,R.,JasmineVasanthaRani.E., and Seethalakshmi,k.,Journal of Acoustic society of India,Vol.38,No.3,2011(140-143) [3] Padova,J.,IsrA.Energycomm.,(1963)1A-823(16PP),A-830(23PP). [4] Modern Electrochemistry,John o.m.,Bockris and Amulya K.NrEEDY,a.plenum/rosetta Edition Vol.1(1977). [5] Beistein.J.ORG.CHEM,2012,8,1393-1399. [6]. Syal V.K.etal.,J.Acous.soc.Ind.,vol 30(2002)84-87 [7]. 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