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IR Absorption Frequency: Hybridization01:21

IR Absorption Frequency: Hybridization

887
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...
887
IR Spectroscopy: Molecular Vibration Overview01:24

IR Spectroscopy: Molecular Vibration Overview

3.5K
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...
3.5K
IR Spectroscopy: Hooke's Law Approximation of Molecular Vibration01:16

IR Spectroscopy: Hooke's Law Approximation of Molecular Vibration

2.1K
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...
2.1K
IR Absorption Frequency: Delocalization01:04

IR Absorption Frequency: Delocalization

1.0K
Electron delocalization refers to the distribution of electrons across multiple atoms within a molecule rather than being confined to a single atom or bond. This phenomenon is common in systems with conjugated bonds—structures where alternating single and double bonds allow π-electrons to move freely across the network. The movement of electrons stabilizes the molecule and can affect various chemical properties, including vibrational frequencies observed in IR spectroscopy.
In IR...
1.0K
Infrared (IR) Spectroscopy: Overview01:09

Infrared (IR) Spectroscopy: Overview

3.4K
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...
3.4K
IR Spectrum Peak Broadening: Hydrogen Bonding01:23

IR Spectrum Peak Broadening: Hydrogen Bonding

1.3K
The vibrational frequency of a bond is directly proportional to its bond strength. As a result, stronger bonds vibrate at higher frequencies, while weaker bonds vibrate at lower frequencies. The stretching vibration of the strong O–H bond in alcohols and phenols (very dilute solution or gas phase) appears as a sharp peak at 3600–3650 cm−1.
However, the extent of hydrogen bonding influences the observed stretching frequency and band broadening. Intermolecular or intramolecular...
1.3K

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Updated: Oct 27, 2025

Infrared Degenerate Four-wave Mixing with Upconversion Detection for Quantitative Gas Sensing
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Infrared Degenerate Four-wave Mixing with Upconversion Detection for Quantitative Gas Sensing

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Infrared Open Cavities for Strong Vibrational Coupling.

Bar Cohn1, Kamalika Das1, Arghyadeep Basu1

  • 1Schulich Faculty of Chemistry and Solid State Institute, Technion - Israel Institute of Technology, Haifa 3200003, Israel.

The Journal of Physical Chemistry Letters
|July 22, 2021
PubMed
Summary
This summary is machine-generated.

We achieved strong coupling between mid-infrared antenna-lattice resonances and molecular vibrations. This breakthrough enables enhanced light-matter interactions for vibrational polaritons research.

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Area of Science:

  • Plasmonics
  • Mid-infrared spectroscopy
  • Light-matter interactions

Background:

  • Subwavelength plasmonic nanoparticle arrays act as open cavities for strong light-matter coupling.
  • Realizing such strong coupling in the mid-infrared (mid-IR) spectral region has been challenging.

Purpose of the Study:

  • To demonstrate narrow bandwidth lattice resonances in the mid-IR.
  • To achieve strong coupling between antenna-lattice resonances (ALR) and molecular vibrational modes.

Main Methods:

  • Fabrication of large-area arrays of half-wavelength mid-IR antennas.
  • Tuning ALR to match molecular vibrational transition frequencies.
  • Characterization of polaritonic transitions and dispersion.

Main Results:

  • Achieved resonance quality factors above 200, significantly reducing bandwidth.
  • Demonstrated strong coupling between ALR and carbonyl stretching in PMMA.
  • Observed polaritonic transition splitting and bandwidth reduction below bare molecular transitions.

Conclusions:

  • The study successfully demonstrates strong coupling in the mid-IR using antenna-lattice resonances.
  • This work opens new avenues for exploring vibrational polaritons and their dynamics.
  • The findings are crucial for advancing mid-IR plasmonic applications.