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Related Concept Videos

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...
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...
Applications of IR Spectroscopy: Overview01:11

Applications of IR Spectroscopy: Overview

The non-destructive nature and ability to provide valuable chemical information make IR spectroscopy a versatile technique with broad applications in various scientific and industrial fields. IR spectroscopy is commonly used to identify and characterize organic and inorganic compounds. It provides information about the functional groups present in a molecule and the bonding between atoms. This helps in the structural elucidation of compounds during organic synthesis, pharmaceutical research,...
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...
IR Spectrometers01:25

IR Spectrometers

There are two main infrared (IR) spectrophotometers: dispersive IR spectrometers and Fourier transform infrared (FTIR) spectrometers. In a dispersive IR spectrometer, a beam of infrared radiation produced by a hot wire is divided into two parallel equal-intensity beams using mirrors. One beam passes through the sample, while another is a reference beam. The beams then move through the monochromator, which separates the radiations into a continuous spectrum of different frequencies. The...
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...

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Conducting Hyperscanning Experiments with Functional Near-Infrared Spectroscopy
06:42

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Published on: January 19, 2019

Spectral domain detection in low-coherence spectroscopy.

Nienke Bosschaart1, Maurice C G Aalders, Ton G van Leeuwen

  • 1Biomedical Engineering and Physics, Academic Medical Center, University of Amsterdam, P.O. Box 22700, NL-1100 DE Amsterdam, The Netherlands.

Biomedical Optics Express
|October 2, 2012
PubMed
Summary

Spectral domain detection in low-coherence spectroscopy (sdLCS) offers improved speed and sensitivity for measuring tissue optical properties. This new method was validated computationally and experimentally, showing accurate results for attenuation, absorption, and scattering coefficients.

Keywords:
(030.1640) Coherence(160.4760) Optical properties(170.6510) Spectroscopy, tissue diagnostics(300.6190) Spectrometers

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Published on: October 11, 2016

Area of Science:

  • Biomedical Optics
  • Spectroscopy
  • Tissue Optics

Background:

  • Low-coherence spectroscopy (LCS) enables quantitative, wavelength-resolved optical property measurements within defined tissue volumes.
  • Current LCS methods primarily use time-domain detection (tdLCS).
  • Spectral domain detection (sdLCS) offers theoretical advantages in speed and sensitivity over tdLCS.

Purpose of the Study:

  • Introduce and validate a novel spectral domain detection method for LCS (sdLCS).
  • Optimize sdLCS sensitivity as a function of measurement depth.
  • Compare sdLCS performance against established tdLCS methods.

Main Methods:

  • Developed a spectral domain detection system for low-coherence spectroscopy.
  • Validated the sdLCS method using computational simulations.
  • Experimentally verified the sdLCS method on a phantom with known optical properties.

Main Results:

  • The sdLCS method achieved optimal sensitivity dependent on measurement depth.
  • Computational simulations confirmed the method's validity.
  • Experimental results on a phantom showed good agreement between sdLCS measurements and expected optical properties.
  • sdLCS measurements correlated well with those obtained using tdLCS.

Conclusions:

  • The developed sdLCS method provides accurate quantitative measurement of tissue optical properties.
  • sdLCS demonstrates a viable and advantageous alternative to tdLCS for optical property characterization.
  • This technique holds potential for advancing non-invasive tissue diagnostics and research.