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CHHATRAPATI SHAHU JI MAHARAJ UNIVERSITY KANPUR
STUDY OF RAMAN SPECTROSCOPY
DIWAKAR KUMAR MISHRA
M PHARM 1ST YEAR
PHARMACEUTICAL CHEMISTRY
SCHOOL OF PHARMACEUTICAL SCIENCES
PRESENTED BY-
Raman Spectroscopy
Sir C. V. Raman, who won the 1930
Nobel Prize in Physics “for his work on
the scattering of light and for the
discovery of the effect named after
him"
Introductio
n
• Raman Spectroscopy is a non-destructive chemical analysis
technique which provides detailed information about chemical
structure, phase and polymorphy, crystallinity and molecular
interactions.
• It is based upon the interaction of light with the chemical bonds
within a material.
• Raman spectroscopy was discovered by C. V. Raman in 1928.
• Raman spectroscopy deals with the scattering of light.
• It is a spectroscopic technique used to observe vibration,
rotational and other low-frequency modes in a system.
• Raman spectroscopy is commonly used in chemistry to provide a
fingerprint by which molecules can be identified.
PRINCIPLE
• When radiation from a source is passed through a sample, some of the
radiation is scattered by the molecules present. The beam of radiation
is merely dispersed in space.
• Three types of scattering occur. They are called Rayleigh scattering,
Stokes scattering, and anti-Stokes scattering.
• Rayleigh scattering occurs as a result of elastic collisions between
the photons and the molecules in the sample; no energy is lost on
collision.
• Some of the photons are scattered with less energy after their
interaction with molecules and some photons are scattered with more
energy. These spectral lines are called Raman lines.
• The Raman-Stokes lines are from those photons scattered with less
energy than the incident radiation; the Raman-anti-Stokes lines are
from the photons scattered with more energy.
• The differences in the energies of the scattered photons from the
incident photons have been found to correspond to vibrational
transitions.
Energy level
diagram
INSTRUMENTATION
1 Source:
• The sources used in modern Raman spectrometry are nearly always lasers
because their high intensity is necessary to produce Raman scattering of
sufficient intensity to be measured with a reasonable signal-to-noise
ratio.
• Because the intensity of Raman scattering varies as the fourth power
of the frequency, argon and krypton ion sources that emit in
the blue and green region of the spectrum have and advantage over the
other sources.
2. Sample Illumination System
Liquid Samples: A major advantage of sample handling in Raman
spectroscopy compared with infrared arises because water is a weak
Raman scattered but a strong absorber of infrared radiation. Thus,
aqueous solutions can be studied by Raman spectroscopy but not by
infrared. This advantage is particularly important for biological and
inorganic systems and in studies dealing with water pollution
problems.
Solid Samples: Raman spectra of solid samples are often
acquired by filling a small cavity with the sample after it has been
ground to a fine powder. Polymers can usually be examined directly
with no sample pretreatment.
Gas samples: Gas are normally contain in glass tubes, 1-2 cm in
diameter and about imm thick. Gases can also be sealed in small
capillary tubes
3. Raman Spectrometers
• Raman spectrometers were similar in design and used the same type
of components as the classical ultraviolet/visible dispersing
instruments.
• Most employed double grating systems to minimize the spurious
radiation reaching the transducer. Photomultipliers served as
transducers.
• Now Raman spectrometers being marketed are either Fourier transform
instruments equipped with cooled germanium transducers or
multichannel instruments based upon charge- coupled devices
APPLICATION
Raman Spectra of Organic Species
Raman spectra are similar to infrared spectra in that they have regions
that are useful for functional group detection and fingerprint regions that
permit the identification of specific compounds.
Raman spectra yield more information about certain types of organic
compounds than do their infrared counterparts.
Quantitative applications
Raman spectra tend to be less cluttered with peaks than infrared spectra.
As a consequence, peak overlap in mixtures is less likely, and quantitative
measurements are simpler. In addition, Raman sampling devices are not
subject to attack by moisture, and small amounts of water in a sample do
not interfere.
Biological Applications of Raman Spectroscopy
Raman spectroscopy has been applied widely for the study of biological
systems.
The advantages of his technique include the small sample requirement, the
minimal sensitivity toward interference by water, the spectral detail, and
the conformational and environmental sensitivity
Thank
you

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Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis

  • 1. CHHATRAPATI SHAHU JI MAHARAJ UNIVERSITY KANPUR STUDY OF RAMAN SPECTROSCOPY DIWAKAR KUMAR MISHRA M PHARM 1ST YEAR PHARMACEUTICAL CHEMISTRY SCHOOL OF PHARMACEUTICAL SCIENCES PRESENTED BY-
  • 2. Raman Spectroscopy Sir C. V. Raman, who won the 1930 Nobel Prize in Physics “for his work on the scattering of light and for the discovery of the effect named after him"
  • 3. Introductio n • Raman Spectroscopy is a non-destructive chemical analysis technique which provides detailed information about chemical structure, phase and polymorphy, crystallinity and molecular interactions. • It is based upon the interaction of light with the chemical bonds within a material. • Raman spectroscopy was discovered by C. V. Raman in 1928. • Raman spectroscopy deals with the scattering of light. • It is a spectroscopic technique used to observe vibration, rotational and other low-frequency modes in a system. • Raman spectroscopy is commonly used in chemistry to provide a fingerprint by which molecules can be identified.
  • 4. PRINCIPLE • When radiation from a source is passed through a sample, some of the radiation is scattered by the molecules present. The beam of radiation is merely dispersed in space. • Three types of scattering occur. They are called Rayleigh scattering, Stokes scattering, and anti-Stokes scattering. • Rayleigh scattering occurs as a result of elastic collisions between the photons and the molecules in the sample; no energy is lost on collision. • Some of the photons are scattered with less energy after their interaction with molecules and some photons are scattered with more energy. These spectral lines are called Raman lines. • The Raman-Stokes lines are from those photons scattered with less energy than the incident radiation; the Raman-anti-Stokes lines are from the photons scattered with more energy. • The differences in the energies of the scattered photons from the incident photons have been found to correspond to vibrational transitions.
  • 6.
  • 8. 1 Source: • The sources used in modern Raman spectrometry are nearly always lasers because their high intensity is necessary to produce Raman scattering of sufficient intensity to be measured with a reasonable signal-to-noise ratio. • Because the intensity of Raman scattering varies as the fourth power of the frequency, argon and krypton ion sources that emit in the blue and green region of the spectrum have and advantage over the other sources.
  • 9. 2. Sample Illumination System Liquid Samples: A major advantage of sample handling in Raman spectroscopy compared with infrared arises because water is a weak Raman scattered but a strong absorber of infrared radiation. Thus, aqueous solutions can be studied by Raman spectroscopy but not by infrared. This advantage is particularly important for biological and inorganic systems and in studies dealing with water pollution problems. Solid Samples: Raman spectra of solid samples are often acquired by filling a small cavity with the sample after it has been ground to a fine powder. Polymers can usually be examined directly with no sample pretreatment. Gas samples: Gas are normally contain in glass tubes, 1-2 cm in diameter and about imm thick. Gases can also be sealed in small capillary tubes
  • 10. 3. Raman Spectrometers • Raman spectrometers were similar in design and used the same type of components as the classical ultraviolet/visible dispersing instruments. • Most employed double grating systems to minimize the spurious radiation reaching the transducer. Photomultipliers served as transducers. • Now Raman spectrometers being marketed are either Fourier transform instruments equipped with cooled germanium transducers or multichannel instruments based upon charge- coupled devices
  • 11. APPLICATION Raman Spectra of Organic Species Raman spectra are similar to infrared spectra in that they have regions that are useful for functional group detection and fingerprint regions that permit the identification of specific compounds. Raman spectra yield more information about certain types of organic compounds than do their infrared counterparts. Quantitative applications Raman spectra tend to be less cluttered with peaks than infrared spectra. As a consequence, peak overlap in mixtures is less likely, and quantitative measurements are simpler. In addition, Raman sampling devices are not subject to attack by moisture, and small amounts of water in a sample do not interfere. Biological Applications of Raman Spectroscopy Raman spectroscopy has been applied widely for the study of biological systems. The advantages of his technique include the small sample requirement, the minimal sensitivity toward interference by water, the spectral detail, and the conformational and environmental sensitivity