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Dissociation constants of the ampholyte glycine in 50 mass % methanol-water from 5 to 55°C,with related thermodynamic quantities
Authors:Rabindra N Roy  James J Gibbons  Guilio LaCross Jr  Charles W Krueger
Institution:(1) Department of Chemistry, Drury College, 65802 Springfield, Missouri
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+rlharH++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 DeltaH°=1497 cal-mole–1, DeltaG°=4038 cal-mole–1, DeltaS°=–8.52 cal-°K–1-mole–1, and DeltaC p o =–53 cal-°K–1-mole–1. The second acidic dissociation constant (K 2)for the process G±rlharH++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 DeltaH° is 10,257 cal-mole–1, DeltaG° is 13,063 cal-mole–1, DeltaS° is –9.41 cal-°K–1-mole–1, and DeltaC 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 (ohgr=56.3 at 25°C).
Keywords:Zwitterions  ampholyte  dissociation constant  glycine  solute-solvent interactions  ionization  activity coefficient  methanol-water  aqueous mixture
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