Related Experiment Video
Updated: Jul 12, 2026

12:27
Assembly, Tuning and Use of an Apertureless Near Field Infrared Microscope for Protein Imaging
Published on: November 25, 2009
Formic acid aggregation in 2D supersonic expansions probed by FTIR imaging.
Katharina A E Meyer1, Martin A Suhm1
1Institut für Physikalische Chemie, Universität Göttingen, Tammannstr. 6, 37077 Göttingen, Germany.
The Journal of Chemical Physics
|October 17, 2017
Summary
Formic acid trimers' C=O stretching vibrations were identified using FTIR and Raman jet spectroscopy. Shock waves
Area of Science:
- Molecular spectroscopy
- Physical chemistry
- Supersonic jet expansions
Background:
- Formic acid is a fundamental molecule in atmospheric and biological systems.
- Understanding molecular clusters and their behavior is crucial for various scientific fields.
- Supersonic jet expansions are key for studying weakly bound molecular systems under controlled conditions.
Purpose of the Study:
- To assign C=O stretching vibrations of formic acid trimers.
- To investigate the influence of shock waves on molecular cluster formation and decomposition.
- To develop and utilize advanced spectroscopic techniques for cluster analysis.
Main Methods:
- Fourier Transform Infrared (FTIR) and Raman jet spectroscopy were employed.
- FTIR imaging was used to validate spectral assignments based on aggregation.
- A double slit nozzle was developed to merge supersonic jets for localized shock wave studies.
Main Results:
- Specific C=O stretching vibrations for formic acid trimers were successfully assigned.
- The impact of shock waves on the formation and dissociation of formic acid clusters was observed.
- The double slit nozzle enabled a more focused examination of shock wave phenomena.
Conclusions:
- The study provides detailed vibrational assignments for formic acid trimers.
- Shock waves significantly influence the dynamics of molecular clusters in supersonic expansions.
- The developed methodology allows for precise investigation of shock wave effects on molecular systems.
Related Concept Videos
IR and UV–Vis Spectroscopy of Carboxylic Acids
In IR spectroscopy of carboxylic acids, the C=O bond shows a characteristic band between 1710 and 1760 cm⁻¹, and the O–H bond exhibits a broad band between 2500 and 3300 cm⁻¹.
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, 1710 cm−1. The C=O bond of the...
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, 1710 cm−1. The C=O bond of the...
Spectroscopy of Carboxylic Acid Derivatives
Infrared spectroscopy is primarily used to determine the types of bonds and functional groups. In carboxylic acid derivatives, a typical carbonyl bond absorption is observed around 1650–1850 cm−1. For esters, the absorption is recorded at around 1740 cm−1, while acid halides show the absorption at about 1800 cm−1. Another acid derivative, the acid anhydrides, exhibit two carbonyl absorption around 1760 cm−1 and 1820 cm−1, arising from the symmetrical and unsymmetrical carbonyl vibration.
In the...
In the...
IR Spectroscopy: Molecular Vibration Overview
When Infrared (IR) radiation passes through a covalently bonded molecule, the bonds transition from lower to higher vibrational levels. The fundamental vibrational motions that result in infrared absorption can be classified as stretching or bending vibrations.
Stretching vibrations are vibrational motions that occur along the bond line, changing the bond length or distance between two bonded atoms. They are further distinguished as symmetric or asymmetric. In symmetric stretching, the...
Stretching vibrations are vibrational motions that occur along the bond line, changing the bond length or distance between two bonded atoms. They are further distinguished as symmetric or asymmetric. In symmetric stretching, the...
IR Spectroscopy: Hooke's Law Approximation of Molecular Vibration
A covalently bonded heteronuclear diatomic molecule can be modeled as two vibrating masses connected by a spring. The vibrational frequency of the bond can be expressed using an equation derived from Hooke's law, which describes how the force applied to stretch or compress a spring is proportional to the displacement of the spring. In this case, the atoms behave like masses, and the bond acts like a spring.
According to Hooke's law, the vibrational frequency is directly proportional to the...
According to Hooke's law, the vibrational frequency is directly proportional to the...
IR Frequency Region: Fingerprint Region
IR spectra are divided into two main regions: the diagnostic region and the fingerprint region. The diagnostic region of the spectrum lies above 1500 cm−1. The absorptions resulting from single-bond vibrations of the N–H, C–H, and O–H stretch at higher wavenumbers and appear on the left side of the spectrum. The stretching absorptions of the C≡C and C≡N occur between 2100–2300 cm−1. In contrast, those arising from stretching absorptions of the C=O, C=N, and C=C occur between 1600–1850 cm−1.
The...
The...
Atomic Force Microscopy
Atomic force microscopy (AFM) is a type of scanning probe microscopy that can analyze topographic details of various specimens like ceramics, glass, polymers, and biological samples. AFM offers over 1000 times more resolution than the optical imaging system. Images generated from AFM are three-dimensional surface profiles, offering an advantage over the flat, two-dimensional images from other imaging techniques.
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...

