Related Experiment Video

Updated: Jun 19, 2026

Ultrafast Time-resolved Near-IR Stimulated Raman Measurements of Functional π-conjugate Systems
09:57

Ultrafast Time-resolved Near-IR Stimulated Raman Measurements of Functional π-conjugate Systems

Published on: February 10, 2020

Generation of vibrational and rotational emissions by four-wave Raman mixing using an ultraviolet femtosecond pump

Y Irie, T Imasaka

    Optics Letters
    |October 29, 2009
    PubMed

    More Related Videos

    Direct Imaging of Laser-driven Ultrafast Molecular Rotation10:52

    Direct Imaging of Laser-driven Ultrafast Molecular Rotation

    Published on: February 4, 2017

    Rejection of Fluorescence Background in Resonance and Spontaneous Raman Microspectroscopy15:04

    Rejection of Fluorescence Background in Resonance and Spontaneous Raman Microspectroscopy

    Published on: May 18, 2011

    Related Concept Videos

    Raman Spectroscopy Instrumentation: Overview01:26

    Raman Spectroscopy Instrumentation: Overview

    A conventional Raman spectrophotometer includes a laser source, a sample holding system, a wavelength selector, and a detector.
    The monochromatic laser source, typically using visible or near-infrared radiation, generates a highly focused beam of light. This light interacts with the molecules of the sample, scattering some of the light. Liquid and gaseous samples are usually tested in ordinary glass capillaries, while solids can be analyzed as powders packed in capillaries or as potassium...
    Raman Spectroscopy: Overview01:20

    Raman Spectroscopy: Overview

    The underlying principle of Raman spectroscopy is based on the interaction between light and matter, specifically molecules' inelastic scattering of photons. When a monochromatic beam of light, typically from a laser source, interacts with a sample, most scattered light has the same frequency as the incident light. This is known as Rayleigh scattering.
    However, a small fraction of the scattered light exhibits a frequency shift due to the exchange of energy between the incident photons and the...
    IR Spectroscopy: Molecular Vibration Overview01:24

    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...
    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 Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations01:08

    IR Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations

    Identical bonds within a polyatomic group can stretch symmetrically (in-phase) or asymmetrically (out-of-phase). Similar to hydrogen bonding, these vibrations also influence the shape of the IR peak. Generally, asymmetric stretching frequencies are higher than symmetric stretching frequencies. For example, primary amines exhibit two distinct IR peaks between 3300–3500 cm−1 corresponding to the symmetric and asymmetric N-H stretching, while secondary amines exhibit a single stretching vibration...