MOHAMED NIJAS V
S5
I.S.P
CONTENT
 SPECTROSCOPY.
 IR SPECTROSCOPY.
 MOLECULAR VIBRATIONS.
 EXPERIMENTAL SETUP.
 FUTURE DIRECTIONS.
SPECTROSCOPY???
 Method of “Seeing the unseeable”
 Using electromagnetic radiation to obtain
information about atoms and molecules that are
too small to see.
Atoms
Molecules
E
M
R
Spectroscopy is an instrumentally aided study of
the interactions between matter (sample being
analyzed) and energy (any portion of the
electromagnetic spectrum)
EMR ANALYTE SPECTROPHOTOGRAPH
1.UV-Visible radiations--------excitation of electrons---------UV-visible spectrum
2.IR-radiations------------------vibration changes in electrons--------IR spectrum
3.Radio frequency---------------spin rotational changes-------------N.M.R spectrum
Conc. should be lower
IR SPECTROPHOTOMETRY
Energy of molecule = Electronic energy+
Vibrational energy + Rotational energy
 Concerned with the study of absorption of infrared
radiation, which causes vibrational transition in the
molecule.
 Thus known as Vibrational spectroscopy.
 Mainly used in structure elucidation to determine
the functional groups.
Most of the analytical applications are confined to the
middle IR region because absorption of organic
molecules are high in this region.
IR region: 0.8
µm (800nm) to
1000 µm (1mm)
Near IR: 0.8-2
µm
Middle IR: 2-15
µm
Far IR: 15-1000
µm
PRINCIPLE OF IR SPECTROSCOPY
 Molecules are made up of atoms linked by chemical bonds.
The movement of atoms and the chemical bonds look like
spring and balls (vibration).
 This characteristic vibration are called
Natural frequency of vibration.
 Applied infrared frequency = Natural frequency of vibration
 Change in dipole moment is required
MOLECULAR VIBRATIONS
Bending vibrationsStretching vibrations
 Vibration or oscillation
along the line of bond
 Change in bond length
 Occurs at higher energy:
4000-1250 cm-1
a) Symmetrical stretching
b) Asymmetrical stretching
•Vibration not along the
line of bond
•Bond angle is altered
•Occurs at low energy:
1400-666 cm-1
a) In plane bending
b) Out plane bending
a) Symmetrical stretching:
2 bonds increase or decrease in length simultaneously.
H
H
C
STRECHING VIBRATIONS
b) Asymmetrical stretching
 in this, one bond length is increased and other is decreased.
H
H
C
a) In plane bending
i. Scissoring:
 2 atoms approach each other
 Bond angles are decrease
H
H
CC
ii. Rocking:
 Movement of atoms take place in the same direction.
H
H
CC
b) Out plane bending
i. Wagging:
 2 atoms move to one side of the plane. They move up and down
the plane.
ii. Twisting:
 One atom moves above the plane and another atom moves
below the plane.
H
H
CC
H
H
CC
EXPERIMENTAL SETUP
COMPONENTS
1. Source
2. Fore optics
3. Monochromator
4. Detector
5. Recorder
SOURCE
•Ideal => black body radiator
•COMMONLY USED =>globar FILAMENT &NERNST GLOWER
•Globar- resistance rod of silicon carbide
•Nernst glower-a spindle of rare earth
oxide(thorium,zirconium,etc)
•Globar-for longer wavelengths
•Nernst glower-for shorter wavelengths
FORE OPTICS
•CONSISTS OF SOURCE,MIRRORS
M1,M2 AND A ROTATING MIRROR M
•M1,M2 DIVIDES THE BEAM
•M ALTERNATELY ALLOWS
THESAMPLE BEAM AND
REFERENCE BEAM TO PASS
THROUGH
MONOCHROMATOR
 Splits the polychromatic readiation to component
wavelengths.
 Make use of prisms or grating or both.
 Resolution depends on slit width and quality of mirrors.
 Rock salt prism is generally use d in the range of 650-
4000cm-1
DETECTOR
•Measure the radiant energy by its heating effect.
•Thermopiles bolometer and golay cells are generally used
•Photoconductivity is also used.
•Radiation is allowed to fall on photo conducting material and the
conductivity of the material is measured continuously by a bridge network.
•Once the sample absorbs radiation, there will be inequality between the
two radiations and signal will be produced.
THE RECORDER
•The amplified signal is used to move an attenuator which cuts
down the radiation coming out of the reference beam until
energy balance is restored.
•This is achieved by a motor which drives the comb into the
reference beam when an absorbing band is encountered and
out of the beam when the band is passed over.
•The recorder pen is also coupled to this motor so that the
comb movement is followed exactly y the pen
Basics of infrared spectroscopy
Basics of infrared spectroscopy

Basics of infrared spectroscopy

  • 1.
  • 2.
    CONTENT  SPECTROSCOPY.  IRSPECTROSCOPY.  MOLECULAR VIBRATIONS.  EXPERIMENTAL SETUP.  FUTURE DIRECTIONS.
  • 3.
    SPECTROSCOPY???  Method of“Seeing the unseeable”  Using electromagnetic radiation to obtain information about atoms and molecules that are too small to see. Atoms Molecules E M R
  • 4.
    Spectroscopy is aninstrumentally aided study of the interactions between matter (sample being analyzed) and energy (any portion of the electromagnetic spectrum) EMR ANALYTE SPECTROPHOTOGRAPH 1.UV-Visible radiations--------excitation of electrons---------UV-visible spectrum 2.IR-radiations------------------vibration changes in electrons--------IR spectrum 3.Radio frequency---------------spin rotational changes-------------N.M.R spectrum Conc. should be lower
  • 5.
    IR SPECTROPHOTOMETRY Energy ofmolecule = Electronic energy+ Vibrational energy + Rotational energy  Concerned with the study of absorption of infrared radiation, which causes vibrational transition in the molecule.  Thus known as Vibrational spectroscopy.  Mainly used in structure elucidation to determine the functional groups.
  • 6.
    Most of theanalytical applications are confined to the middle IR region because absorption of organic molecules are high in this region. IR region: 0.8 µm (800nm) to 1000 µm (1mm) Near IR: 0.8-2 µm Middle IR: 2-15 µm Far IR: 15-1000 µm
  • 7.
    PRINCIPLE OF IRSPECTROSCOPY  Molecules are made up of atoms linked by chemical bonds. The movement of atoms and the chemical bonds look like spring and balls (vibration).  This characteristic vibration are called Natural frequency of vibration.  Applied infrared frequency = Natural frequency of vibration  Change in dipole moment is required
  • 8.
    MOLECULAR VIBRATIONS Bending vibrationsStretchingvibrations  Vibration or oscillation along the line of bond  Change in bond length  Occurs at higher energy: 4000-1250 cm-1 a) Symmetrical stretching b) Asymmetrical stretching •Vibration not along the line of bond •Bond angle is altered •Occurs at low energy: 1400-666 cm-1 a) In plane bending b) Out plane bending
  • 9.
    a) Symmetrical stretching: 2bonds increase or decrease in length simultaneously. H H C STRECHING VIBRATIONS
  • 10.
    b) Asymmetrical stretching in this, one bond length is increased and other is decreased. H H C
  • 11.
    a) In planebending i. Scissoring:  2 atoms approach each other  Bond angles are decrease H H CC
  • 12.
    ii. Rocking:  Movementof atoms take place in the same direction. H H CC
  • 13.
    b) Out planebending i. Wagging:  2 atoms move to one side of the plane. They move up and down the plane. ii. Twisting:  One atom moves above the plane and another atom moves below the plane. H H CC H H CC
  • 14.
  • 15.
    COMPONENTS 1. Source 2. Foreoptics 3. Monochromator 4. Detector 5. Recorder
  • 16.
    SOURCE •Ideal => blackbody radiator •COMMONLY USED =>globar FILAMENT &NERNST GLOWER •Globar- resistance rod of silicon carbide •Nernst glower-a spindle of rare earth oxide(thorium,zirconium,etc) •Globar-for longer wavelengths •Nernst glower-for shorter wavelengths
  • 17.
    FORE OPTICS •CONSISTS OFSOURCE,MIRRORS M1,M2 AND A ROTATING MIRROR M •M1,M2 DIVIDES THE BEAM •M ALTERNATELY ALLOWS THESAMPLE BEAM AND REFERENCE BEAM TO PASS THROUGH
  • 18.
    MONOCHROMATOR  Splits thepolychromatic readiation to component wavelengths.  Make use of prisms or grating or both.  Resolution depends on slit width and quality of mirrors.  Rock salt prism is generally use d in the range of 650- 4000cm-1
  • 19.
    DETECTOR •Measure the radiantenergy by its heating effect. •Thermopiles bolometer and golay cells are generally used •Photoconductivity is also used. •Radiation is allowed to fall on photo conducting material and the conductivity of the material is measured continuously by a bridge network. •Once the sample absorbs radiation, there will be inequality between the two radiations and signal will be produced.
  • 20.
    THE RECORDER •The amplifiedsignal is used to move an attenuator which cuts down the radiation coming out of the reference beam until energy balance is restored. •This is achieved by a motor which drives the comb into the reference beam when an absorbing band is encountered and out of the beam when the band is passed over. •The recorder pen is also coupled to this motor so that the comb movement is followed exactly y the pen