Tellinghuisen Joel
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.
J Phys Chem B. 2007 Oct 4;111(39):11531-7. doi: 10.1021/jp074515p. Epub 2007 Sep 13.
In the study of 1:1 binding, M + X right <==> MX, isothermal titration calorimetry is generally thought to be limited to reactions in which the key parameter, c = K[M]0, can be set in the range 1-1000. In fact, the range of applicability can be extended by a factor of 10-100 at the upper end and as much as 10(5) at the lower, with certain provisos. The present work emphasizes the low-c regime, with the key heat parameter, h identical with DeltaH degrees [M]0, low, as well. Successful determination of K and DeltaH degrees in this region requires that the titration be extended to large excesses of titrant X over titrate M, and then the reaction heat is distributed strongly in favor of the early injections. With decreasing c, DeltaH degrees and the stoichiometry parameter n (often called site number) also become highly correlated and individually indeterminate. However, the product DeltaH degrees x n ( identical with Hn) is well-determined, so if n is known from other information, both K and DeltaH degrees can be determined to quite low c. By varying the titrant volume from injection to injection, one can significantly reduce the uncertainties in the estimated K and Hn values, permitting determination of K to better than 10% and Hn within 3% down to c = 10(-4), even for the low h value of 0.1 cal/L. The titrant volume optimization algorithm yields best results for the minimal number of injections - three when n is fitted, two when it is fixed. At low c, the resulting volume distributions depend nearly exponentially on injection number. This observation facilitates the derivation of similar, near-optimal volume distributions for five- and four-injection procedures that offer two statistical degrees of freedom for analysis. The volume optimization results are tested on the Ba2+/18-crown-6 ether complexation reaction at c = 0.1 and h = 0.16 cal/L, illustrating some practical complications but confirming the utility of the variable-volume protocol.
在1:1结合反应M + X ⇌ MX的研究中,等温滴定量热法通常被认为仅限于关键参数c = K[M]₀可设定在1 - 1000范围内的反应。实际上,在某些条件下,其适用范围在上限可扩展10 - 100倍,在下限可扩展多达10⁵倍。当前工作着重于低c区域,关键热参数h = ΔH°[M]₀也较低。要在该区域成功测定K和ΔH°,需要将滴定扩展至滴定剂X大大过量于被滴定物M,然后反应热强烈地偏向于早期注入分布。随着c减小,ΔH°和化学计量参数n(常称为位点数)也变得高度相关且各自无法确定。然而,乘积ΔH°×n(= Hn)能很好地确定,所以如果从其他信息得知n,那么对于相当低的c,K和ΔH°都能被确定。通过逐次改变滴定剂体积,可以显著降低K和Hn估计值中的不确定性,即使对于低至0.1 cal/L的h值,也能将K测定至优于10%,将Hn测定在3%以内,直至c = 10⁻⁴。滴定剂体积优化算法在最少注入次数时产生最佳结果——拟合n时为三次,固定n时为两次。在低c时,所得体积分布几乎指数地依赖于注入次数。这一观察结果有助于推导用于五注入和四注入程序的类似的、接近最优的体积分布,这些程序为分析提供两个统计自由度。在c = 0.1和h = 0.16 cal/L的Ba²⁺/18 - 冠 - 6醚络合反应上测试了体积优化结果,说明了一些实际的复杂性,但证实了可变体积方案的实用性。