Related Experiment Video
Updated: Feb 16, 2026

Total Internal Reflection Absorption Spectroscopy TIRAS for the Detection of Solvated Electrons at a Plasma-liquid Interface
Published on: January 24, 2018
Matrix Isolation Spectroscopy: Aqueous p-Toluenesulfonic Acid Solvation
Thien Khuu1, David Anick1, Mary Jane Shultz1
1Laboratory for Aqueous and Surface Studies, Tufts University , Pearson Building, Medford, Massachusetts 02155, United States.
The interaction between p-toluenesulfonic acid (pTSA) and water in a CCl4 matrix reveals water monomers forming clusters. Specific resonances indicate OH-π interactions and pTSA-dihydrate formation.
Area of Science:
- Physical Chemistry
- Spectroscopy
- Chemical Physics
Background:
- Carbon tetrachloride (CCl4) serves as an effective matrix isolation medium due to its transparency in the hydrogen-bonded region.
- Water molecules in CCl4 exhibit restricted rotational motion, existing primarily as monomers.
Purpose of the Study:
- To investigate the interactions between p-toluenesulfonic acid (pTSA) and water at low temperatures (-20 °C) using matrix isolation spectroscopy.
- To elucidate the structural and bonding characteristics of pTSA-water complexes in a CCl4 environment.
Main Methods:
- Matrix isolation infrared (IR) spectroscopy was employed using a CCl4 matrix at -20 °C.
- The study analyzed spectral features, including narrow resonances and broad absorption bands, to identify molecular species and interactions.
Main Results:
- The introduction of pTSA-nH2O resulted in distinct IR absorptions at 3642 cm⁻¹ and 2835 cm⁻¹, alongside a broad band from 3000-3550 cm⁻¹.
- Negative peaks for water monomer stretches indicated a decrease in free monomers, suggesting their incorporation into clusters.
- The 3642 cm⁻¹ resonance was attributed to OH-π interactions within water-rich clusters, while the 2835 cm⁻¹ resonance was assigned to the S-O-H stretch of pTSA-dihydrate.
Conclusions:
- Water monomers in the CCl4 matrix are incorporated into clusters upon interaction with pTSA.
- The study identified specific interactions, including OH-π interactions and the formation of pTSA-dihydrate, providing insights into the acid-water system.
Related Concept Videos
Leveling Effect and Non-Aqueous Acid-Base Solutions
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
Entropy and Solvation
Chemical Reactions in Aqueous Solutions
Solvating Effects
Spectroscopy of Carboxylic Acid Derivatives
IR and UV–Vis Spectroscopy of Carboxylic Acids
However, the stretching absorptions for the C=O bond vary depending on the structure of carboxylic acids. The C=O bond of the free carboxylic acids shows a higher stretching frequency, 1760 cm−1, while H-bonded carboxylic acids (dimers) exhibit stretching absorptions at a lower frequency,...

