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  • 1
    ISSN: 1572-8927
    Keywords: Zwitterions ; ampholyte ; dissociation constant ; glycine ; solute-solvent interactions ; ionization ; activity coefficient ; methanol-water ; aqueous mixture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The two thermodynamic dissociation constants of glycine at 11 temperatures from 5 to 55°C in 50 mass % methanol-water mixed solvent have been determined from precise emf measurements with hydrogen-silver bromide electrodes in cells without liquid junction. The first acidic dissociation constant (K 1)for the process HG+⇌H++G± is expressed as a function ofT(oK) by the equation pK 1 = 2043.5/T − 9.6504 + 0.019308T. At 25°C, pK 1is 2.961 in the mixed solvent, as compared with 2.350 in water, with ΔH°=1497 cal-mole−1, ΔG°=4038 cal-mole−1, ΔS°=−8.52 cal-°K−1-mole−1, and ΔC p o =−53 cal-°K−1-mole−1. The second acidic dissociation constant (K 2)for the process G±⇌H++G− over the temperature range studied is given by the equation pK 2 = 3627.1/T − 7.2371 + 0.015587T. At 25°C, pK 2is 9.578 in MeOH−H2O as compared with 9.780 in water, whereas ΔH° is 10,257 cal-mole−1, ΔG° is 13,063 cal-mole−1, ΔS° is −9.41 cal-°K−1-mole−1, and ΔC p o is −43 cal-°K−1-mole−1. The protonated glycine becomes weaker in 50 mass % methanol-water, whereas the second dissociation process becomes stronger despite the lower dielectric constant of the mixed solvent (ω=56.3 at 25°C).
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 6 (1977), S. 475-485 
    ISSN: 1572-8927
    Keywords: Zwitterions ; ampholyte ; dissociation constants ; glycine ; solute-solvent interactions ; ionization ; activity coefficient ; monoglyme-water ; aqueous mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Electromotive-force measurements on cells without liquid junction have been used to determine the pK 1 and pK 2 values of glycine in 50 mass % aqueous monoglyme at 11 temperatures from 5 to 55°C. The change in the first dissociation constant is given as a function of the thermodynamic temperatureT by the equation pK 1=−2058.6/T+15.421−0.019169T, whereas that for the second dissociation constant is given by the equation pK 2=1200.5/T+6.7211−0.0042897T. At 25°C, the pK 1 is 2.806 in the mixed solvent, as compared with 2.350 in water; hence, protonated glycine becomes a weaker acid in the mixed solvent. The pK 2 is 9.453 in the mixed solvent, whereas that in water is 9.780, suggesting that the second dissociation process becomes stronger in terms of acidity. The thermodynamic quantities ΔG o, ΔH o, ΔS o, and ΔC p o have been calculated, and the results have been discussed with respect to preferential solvation and also compared with similar data for the same two processes in 50 mass % methanol.
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  • 3
    ISSN: 1572-8927
    Keywords: MES ; TES ; emf ; standard potential ; zwitterion ; buffer solution ; activity coefficients ; dissociation constants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The equilibrium constants for the dissociation steps of (4-morpholineethanesulfonic acid) (MES) and (2-{[tris(hydroxymethyl)methyl]-1-ethanesulfonic acid (TES) have been determined at 12 and 7 different temperatures, respectively, from 5 to 55°C. The emf measurements were carried out by using a cell without liquid junction of the type: Pt; H2 (g, 1 atm) | buffer(m1), Na salt of buffer(m2), NaCl(m3) | AgCl, Ag. The pK 2 values of MES and TES at 25°C are 6.269 and 7.550. The thermodynamic quantities for the dissociation process have been calculated. These zwitterionic compounds are useful for pH control as standard buffers in the physiological region of pH 5.50 to 6.50 for MES, 6.5 to 7.5 for TES, respectively. Reliable measurements of the pH at isotonic saline solution (I = 0.16m) such as blood and plasma are important for clinical diagnosis.
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  • 4
    ISSN: 1572-8927
    Keywords: Acidic dissociation ; ampholyte dissociation ; dissociation constants ; ionization ; methanol-water solvents ; solute-solvent effects ; N-Tris(hydroxymethyl)methylglycine (“tricine”) ; zwitterions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pK values for the two acidic dissociation steps of the ampholyte N-tris-(hydroxymethyl)methylglycine (“tricine”) in 50 mass % methanol-water solvent have been determined by emf measurements of cells of the type Pt|H2(g, 1 atm), tricine buffer, Br−, AgBr|Ag over the range 5 to 50°C (pK 1)and 5 to 60°C (pK 2).The standard thermodynamic quantities ΔHo, ΔSo, and ΔC p o for the two dissociation processes have been derived and are compared with the corresponding values for tricine and the parent glycine in water and with those for other acids in 50 mass % methanol-water solvent. Both tricine and protonated tricine become weaker acids when methanol is added to the aqueous solvent. It appears that a strong stabilization of the zwitterion in water is responsible for this behavior. This conclusion is supported by comparing the changes in entropy and heat capacity for the dissociation of tricine with the values of these quantities for the dissociation of “model” acids of simple structure, such as ammonium ion and acetic acid.
    Type of Medium: Electronic Resource
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