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Related Concept Videos

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview01:02

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview

Ultraviolet–visible (UV–visible or UV–Vis) spectroscopy is an analytical technique that investigates the interaction between matter and UV–Vis light within the electromagnetic spectrum. This method is widely used for its versatility, simplicity, and relatively quick data acquisition, making it valuable for both qualitative and quantitative analysis. When UV–Vis radiation passes through a material,  molecules absorb light depending on the energy required for electronic transitions. As a result...
Infrared (IR) Spectroscopy: Overview01:09

Infrared (IR) Spectroscopy: Overview

When electromagnetic radiation passes through a material, atoms or molecules transition from a lower to a higher energy state by absorbing radiation corresponding to the energy difference between the two states. The absorption of infrared (IR) radiation causes transitions between vibrational energy levels in a molecule. Therefore, IR spectroscopy is a useful analytical tool for determining the molecular structure of molecules.
Different compounds display unique properties due to their...
UV–Vis Spectroscopy of Conjugated Systems01:32

UV–Vis Spectroscopy of Conjugated Systems

Organic compounds with conjugated double bonds show strong absorption features in the UV–visible region of the electromagnetic spectrum attributed to π → π* electronic excitations. Generally, a UV–vis absorption spectrum is recorded as a plot of absorbance vs wavelength. The wavelength of maximum absorbance, which manifests as a peak in the absorption spectrum, is denoted as λmax.
One of the factors influencing λmax is the extent of conjugation in the...
UV–Vis Spectroscopy: Molecular Electronic Transitions01:16

UV–Vis Spectroscopy: Molecular Electronic Transitions

In Ultraviolet–Visible (UV–Vis) spectroscopy, the absorption of electromagnetic radiation is used to probe the electronic structure of molecules. This technique provides insights into molecular electronic transitions, particularly the movement of electrons between different molecular orbitals. Radiation is absorbed if the energy of the electromagnetic radiation passing through the molecule is precisely equal to the energy difference between the excited and ground states. During this process,...
IR Absorption Frequency: Hybridization01:21

IR Absorption Frequency: Hybridization

Hydrocarbons such as alkanes, alkenes, and alkynes show characteristic C–H stretching absorption bands. These IR stretching frequencies depend on the hybridization of the involved carbon atom and can be explained in terms of the s character of each hybridized atomic orbital.
Among the sp, sp2, and sp3 hybridized orbitals, sp orbitals have the maximum s character (50%). Consequently, the electrons are held more closely to the nucleus, resulting in stronger and shorter C–H bonds that stretch at a...
IR Frequency Region: Fingerprint Region01:03

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...

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Related Experiment Video

Updated: Jul 19, 2026

Measurement and Analysis of Atomic Hydrogen and Diatomic Molecular AlO, C2, CN, and TiO Spectra Following Laser-induced Optical Breakdown
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CH5+: the infrared spectrum observed

White1, Tang, Oka

  • 1Department of Chemistry, Department of Astronomy and Astrophysics, and the Enrico Fermi Institute, University of Chicago, Chicago, IL 60637, USA.

Science (New York, N.Y.)
|April 2, 1999
PubMed
Summary

Protonated methane (CH5+) exhibits unique behavior due to its unstable structure and mobile protons. This study reports its complex infrared spectrum, providing crucial spectral data for understanding this ion.

Area of Science:

  • Physical Chemistry
  • Spectroscopy
  • Quantum Mechanics

Background:

  • Protonated methane (CH5+) displays anomalous vibrational and rotational characteristics.
  • Its unique properties stem from nearly degenerate equilibrium structures and rapid proton scrambling.
  • Existing theoretical studies highlight the need for experimental spectral data.

Purpose of the Study:

  • To obtain high-resolution infrared spectral data for protonated methane (CH5+).
  • To investigate the C-H stretching band in the 3.4-micrometer region.
  • To provide experimental evidence for the spectral signature of CH5+.

Main Methods:

  • Acquisition of a complex, high-resolution infrared spectrum.
  • Focus on the spectral region associated with C-H stretching vibrations.

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  • Comparative analysis with spectra of other carbocations.
  • Main Results:

    • A detailed infrared spectrum of CH5+ was successfully recorded.
    • The spectrum covers the characteristic 3.4-micrometer C-H stretching absorption band.
    • Observed spectral features are consistent with the presence of CH5+.

    Conclusions:

    • The reported infrared spectrum provides essential experimental data for protonated methane.
    • While individual line assignments were not made, the overall spectrum strongly suggests CH5+.
    • This spectral data will aid in a deeper understanding of CH5+ quantum mechanics and behavior.