Sit Izaac, Fashina Bidemi T, Baldo Anthony P, Leung Kevin, Grassian Vicki H, Ilgen Anastasia G
Department of Nanoengineering, University of California San Diego La Jolla CA 92093 USA.
Geochemistry Department, Sandia National Laboratories Albuquerque NM 87123 USA
RSC Adv. 2023 Aug 1;13(33):23147-23157. doi: 10.1039/d2ra07944e. eCollection 2023 Jul 26.
Organic acids are prevalent in the environment and their acidity and the corresponding dissociation constants can change under varying environmental conditions. The impact of nanoconfinement (when acids are confined within nanometer-scale domains) on physicochemical properties of chemical species is poorly understood and is an emerging field of study. By combining infrared and Raman spectroscopies with molecular dynamics (MD) simulations, we quantified the effect of nanoconfinement in silica nanopores on one of the fundamental chemical reactions-the dissociation of organic acids. The p of formic and acetic acids confined within cylindrical silica nanopores with 4 nm diameters were measured. MD models were constructed to calculate the shifts in the p values of acetic acid nanoconfined within 1, 2, 3, and 4 nm silica slit pores. Both experiments and MD models indicate a decrease in the apparent acid dissociation constants (, increase in the p values) when organic acids are nanoconfined. Therefore, nanoconfinement stabilizes the protonated species. We attribute this observation to (1) a decrease in the average dielectric response of nanoconfined aqueous solutions where charge screening may be decreased; or (2) an increase in proton concentration inside nanopores, which would shift the equilibrium towards the protonated form. Overall, the results of this study provide the first quantification of the p values for nanoconfined formic and acetic acids and pave the way for a unifying theory predicting the impact of nanoconfinement on acid-base chemistry.
有机酸在环境中普遍存在,其酸度和相应的解离常数会随环境条件的变化而改变。纳米限域(当酸被限制在纳米尺度范围内时)对化学物质物理化学性质的影响目前了解甚少,是一个新兴的研究领域。通过将红外光谱和拉曼光谱与分子动力学(MD)模拟相结合,我们量化了二氧化硅纳米孔中的纳米限域对一种基本化学反应——有机酸解离的影响。测量了直径为4纳米的圆柱形二氧化硅纳米孔中甲酸和乙酸的p值。构建了MD模型来计算乙酸在1、2、3和4纳米二氧化硅狭缝孔中纳米限域时p值的变化。实验和MD模型均表明,当有机酸被纳米限域时,表观酸解离常数降低(p值升高)。因此,纳米限域使质子化物种更加稳定。我们将这一现象归因于:(1)纳米限域水溶液的平均介电响应降低,电荷屏蔽可能减弱;或(2)纳米孔内质子浓度增加,这会使平衡向质子化形式移动。总体而言,本研究结果首次对纳米限域的甲酸和乙酸的p值进行了量化,为预测纳米限域对酸碱化学影响的统一理论铺平了道路。