Godec Andrej, Skerjanc Joze
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Askerceva 5, 1000 Ljubljana, Slovenia.
J Phys Chem B. 2005 Jul 14;109(27):13363-7. doi: 10.1021/jp050234a.
The enthalpy changes accompanying the dilution and ionization of poly(L-glutamic acid) in water have been measured at 25 degrees C for two degrees of polymerization (DP = 115 and DP = 480) at various degrees of ionization, alpha, for a concentration range from about 0.2 to 0.002 monomol/L. The heat of dilution displays an unusual dependence on the degree of ionization, which is in sharp contrast to the behavior of other weak carboxylic polyelectrolytes, such as poly(acrylic acid). The exothermic heat effects observed at low values of alpha become endothermic for the region where the helix-coil transition is most pronounced, and for high degrees of ionization, they are exothermic again. Evidently, an endothermic heat effect, produced by an additional conformational transition in the dilution process, is superimposed on the exothermic enthalpy of dilution, and it overweighs the latter in the region of alpha where the conformational transition is prevailing. The calorimetric titration curve, which gives the dependence of the heat of ionization, deltaH(i), on alpha, has a maximum and is typical for poly(carboxylic acids) which undergo pH-induced conformational transition, such as poly(methacrylic acid). The values of deltaH(i) obtained at two polymer concentrations indicate that the enthalpy of ionization depends on the polypeptide concentration.
在25摄氏度下,针对两种聚合度(DP = 115和DP = 480)的聚(L-谷氨酸),在约0.2至0.002单摩尔/升的浓度范围内、不同电离度α的情况下,测量了其在水中稀释和电离时的焓变。稀释热对电离度呈现出异常的依赖性,这与其他弱羧酸类聚电解质(如聚丙烯酸)的行为形成鲜明对比。在低α值时观察到的放热效应,在螺旋-线圈转变最为明显的区域变为吸热,而在高电离度时又再次变为放热。显然,在稀释过程中由额外的构象转变产生的吸热效应叠加在稀释的放热焓之上,并且在构象转变占主导的α区域中,前者超过了后者。给出电离热ΔH(i)对α依赖性的量热滴定曲线有一个最大值,这对于经历pH诱导构象转变的聚(羧酸)(如聚甲基丙烯酸)来说是典型的。在两种聚合物浓度下获得的ΔH(i)值表明,电离焓取决于多肽浓度。