BRIEF REVIEW OF EMR,
UV-VISIBLE SPECTROSCOPY
AND CHROMOPHORE
CONCEPT
INTRODUCTION
What is Spectroscopy?
- Spectroscopic techniques involve the study of
interaction of matter with electromagnetic
radiations.
- Electromagnetic radiation, which is made up of
photons, have both wave as well as particle
characteristics.
- Matter/atoms/molecules shows unique
characters by releasing or absorbing the
radiation.
 When electromagnetic radiation travels
through a medium containing atoms, there are
three possibilities-
1. There is no absorption of light
2. There maybe reflection, refraction, or
scattering of light
3. There maybe absorption of energy.
In case of absorption,
The atoms are excited to their excited
state, and then they return to the
ground state, which is a more
stable state, with emission of
energy.
UV-Visible Spectroscopic techniques
utilize the measurement of this
emitted energy, for analytical
purposes.
ELECTRO MAGNETIC RADIATION
EMR is a form of energy that
is transmitted through space
at an enormous velocity.
 EMR is made up of discrete
particles called photons.
 EMR have both wave characteristic
and particle characteristics.
Waves or Particles
• Electromagnetic radiation has properties of
waves but also can be thought of as stream of
particles.
Example: Light
• Light as a wave: Light behaves as a
transverse wave which we can filter using
polarized lenses.
• Light as particles (photons).
A photon is a tiny
particle that comprises
waves of electromagnetic
radiation.
As shown by
Maxwell, photons are just
electric fields traveling
through
space. Photons have no
charge, no resting mass,
and travel at the speed of
light.
A photon
Representation of an Electromagnetic wave
FREQUENCY point in unit time.
Units- Hz (Hertz)
Number of complete wavelength units passing through
a given) or cps (cycles per second).
WAVE LENGTH
Distance between the two peaks.
Units- metres, centimetres, millimetres, nanometers
WAVE NUMBER
Number of waves per cm.
Expressed in cm-1
Type of Electro Magnetic Radiation
• Cosmic rays
• Gama rays
• X- rays
• UV radiation
• Visible radiation
• IR radiation
• Microwaves
• Radio waves
The energy of EMR can be given
by the equation
E = h‫ט‬
Where E = Energy of radiation
h= Plank’s constant ( 6.624 X 10 -34
JSec)
‫ט‬ = Frequency of radiation
velocity of light in vacuum/
wavelength
Or
3 X 108 msec-1 / wavelength
Hence E = h‫ט‬ = hc/ λ = hc‫ט‬
UV – VISIBLE SPECTROSCOPY
 The wavelength of UV- Visible ranges from 200nm – 800nm
 Wavelength for UV ranges from 200nm-400nm
 Wavelength for visible ranges from 400nm-800nm.
Types of spectroscopy:
Absorption
Emission
Scattering
THE ELECTROMAGNETIC SPECTRUM
Ultraviolet region : 180-400 nm ( 200 – 380 nm used for analytical purposes,
also called as the near ultraviolet region.)
Vacuum ultraviolet region : 1 – 180 nm
Visible region : 400 – 750 nm
Infrared region : 780 nm – 300 
VISIBLE SPECTRUM
Used for quantitative analysis and serve as an
useful auxiliary tool for structural elucidation.
UNITS USE IN UV-VISIBLE SPECTOSCOPY
For the measurement of wavelength in UV-Visible
spectroscopy following units are used,
nm (nanometer)
Ǻ (angstrom)
cm-1(centimeter inverse)
1 nm=10 Ǻ=10-7cm
ELECTRONIC TRANSITIONS
 Absorption of ultraviolet and visible
radiation in organic molecules is restricted to
certain functional groups (chromophores) that
contain valence electrons of low excitation
energy.
This is because the superposition of
rotational and vibrational transitions on the
electronic transitions gives a combination of
overlapping lines.
CHROMOPHORE
The functional group gives colour
to a compound. Example nitro
group.
Exhibits absorption of
electromagnetic radiations in the
visible or ultraviolet region.
Chromophores -one of two forms:
Conjugated pi systems
Common examples include retinal, various food
colourings, lycopene, β-carotene and
anthocyanins, fabric dyes (azo compounds), etc.
METAL COMPLEXES
 Chlorophyll
 Haemoglobin
Their interaction with EMR
 Straightens in response to a photon γ (light), of the
correct wavelength
AUXOCHROMES
Group of atoms attached to a chromophore
which modifies their ability to absorb light
Example: -OH , - NH2 , Aldehydes
A functional group of atoms with non-bonded
electrons which is attached to a chromophore
This occurs due to the presence of at least one
lone pair of electrons
Benzene no colour (chromophore
absent)
Nitrobenzene (pale yellow colour)
nitro group.
Para-hydroxynitrobenzene exhibits a deep
yellow color. Here an auxochrome (-OH) is
conjugated with the chromophore -NO2.
There are mainly two types of
auxochromes-
1. Acidic -COOH, -OH, -SO3H
2. Basic -NHR, -NR2, -NH2
 Lambert’s Law Vs Beer’s Law
DEVIATION FROM BEER’S LAW
 In presence of impurities.
 If monochromatic light is not used.
 If the width of slit is not proper.
 If undesirable radiations fall on the detector.
 If solution species under goes polymerization.
 Beer’s law can’t be applied to suspension.
Instrumentation
1. Colorimeters ( for the Visible
region )
2. Spectrophotometers ( for the
Ultraviolet region)
Colorimeters
 These are instruments used to measure the
absorbance of light in the visible region.
 Measurement of the wavelength and the intensity
of electromagnetic radiation in the visible
region of the spectrum.
 It is used extensively for identification and
determination of concentrations of substances
that absorb light.
 They are comparatively inexpensive and less
accurate.
 The range of wavelength used is small.
E.g. 400-700nm
Spectrophotometer
 Spectrophotometers are instruments used
for the quantitative measurement of
reflection or transmission properties of a
material as a function of wavelength.
 They can be used over a wider
wavelength range e.g.. 300-900 nm or
sometimes up to 1000nm and are very
accurate.
Instrumentation
Colorimeters
 Source of light
 Filters
 Sample Cells
 Detectors
Spectrophotometers
 Source of light
 Monochromator
s
 Sample Cells
 Detectors
 Recorders
Source of light
Colorimeters
 The visible
spectrum ranges
from 400-800 nm.
 Common sources
of light-
 Tungsten Filament
Lamp
 Carbon Arc Lamp
Spectrophotometers
 The Ultraviolet region
ranges from 180-
400nm.
 Sources of light -
 Hydrogen discharge
Lamp
 Deuterium Lamp
 Xenon Discharge
Lamp
 Mercury Arc Lamp
Filters and Monochromators
 Filters and Monochromators act as
wavelength selectors.
 Colorimeters commonly use filters while
monochromators are seen in
spectrophotometers.
 Filters are comparatively less accurate as
wavelength selectors than
monochromators.
Filters
 There are two types of filters-
Absorption Filters
Interference filters
Absorption Filters
 Chiefly made of glass which are coated
with pigments
 Or they contain colored gelatin sheets
sandwiched between two glass sheets.
 These filters absorb the unwanted
radiation and transmit only the required
radiation.
 They are less accurate since their band
pass is more than 30nm.
Monochromators
 They are better and more efficient in
converting polychromatic light into
monochromatic light.
 Parts of a monochromator-
 Entrance slit
 Collimator
 Grating or Prism
 Exit slit
Sample cells
 These are cells or cuvettes used to hold the
sample solutions.
 A cuvette (French: cuvette = "little
vessel").
 The material of these cells do not absorb at
the wavelength being observed.
 Glass is used for the visible region, while for
the UV region cells made of quartz are used.
 Cells are mostly cylindrical or rectangular in
shape and of 1cm (short) to 10cm (long)
wavelength.
 Quartz exists in two forms, the normal α-
quartz and the high-temperature β-quartz,
both of which are chiral. The transformation
from α-quartz to β-quartz takes place
abruptly at 573 °C (846 K; 1,063 °F).
Detectors
 Detectors used in UV-Visible
Spectrophotometers can be called as
Photometric detectors.
 Principle –
 When a particular wavelength of radiation
passes through a sample solution, a part
of it is absorbed and some part of it is
transmitted. The amount of transmitted
radiation is measured by a detector.
Different types of detectors
1. Barrier Layer cell or Photo Voltaic Cell
2. Photo tubes or Photo emissive cells
3. Photo multiplier tubes
Applications
1. Quality control and purity – Colorimeters can
be used to detect impurities.
2. Quantitative analysis
3. Determination of Ligand-metal ratio
4. Structure ellucidation of organic compunds
5. Determination of pka values of indicators
6. Determination of molecular weight of amines
7. Determination of elements, ions or functional
groups.
8. Determination of organic substances and
pharmaceuticals.
9. Chemical Kinetics.
10. Proteins estimation
11. Enzymes Assay
12. DNA/RNA estimation
REFERENCES
 Anjaneyulu Y, Chandrasekhar K, Manickam Valli, A Textbook of Analytical Chemistry,
Pharma Book Syndicate, Hyderabad, 2006 edition, Page No 351.
 Willard Hobart H, Marritt Lynne L, Dean John A, Settle Frank A, Instrumental
methods of analysis, CBS Publishers and Distributors, New Delhi, seventh edition, Page
No 97,100.
Khopkar S.M. ,Basic concept of analytical chemistry, New Age International (P)
Limited, Publishers, New Delhi, third edition 2008Page No 245.
Instrumental methods of analysis ,seventh edition by Hobart H.
Willard,Lynne L. Merritt,John A. Dean,Frank A. Settle,pp-118
Instrumental methods of chemical analysis fifth edition by Gurdeep R.
Chatwal,Sham K. Anand pp-2.149
A textbook Analytical Chemistry by Y.Anjaneyulu,K.Chandrasekhar,Valli
Manickan,pp-362.
Introduction of instrumental analysis,third edition by Robert D. Braun,pp-
261-263.
Uv visiblr spectroscopy

Uv visiblr spectroscopy

  • 1.
    BRIEF REVIEW OFEMR, UV-VISIBLE SPECTROSCOPY AND CHROMOPHORE CONCEPT
  • 2.
    INTRODUCTION What is Spectroscopy? -Spectroscopic techniques involve the study of interaction of matter with electromagnetic radiations. - Electromagnetic radiation, which is made up of photons, have both wave as well as particle characteristics. - Matter/atoms/molecules shows unique characters by releasing or absorbing the radiation.  When electromagnetic radiation travels through a medium containing atoms, there are three possibilities- 1. There is no absorption of light 2. There maybe reflection, refraction, or scattering of light 3. There maybe absorption of energy.
  • 3.
    In case ofabsorption, The atoms are excited to their excited state, and then they return to the ground state, which is a more stable state, with emission of energy. UV-Visible Spectroscopic techniques utilize the measurement of this emitted energy, for analytical purposes.
  • 4.
    ELECTRO MAGNETIC RADIATION EMRis a form of energy that is transmitted through space at an enormous velocity.  EMR is made up of discrete particles called photons.
  • 5.
     EMR haveboth wave characteristic and particle characteristics. Waves or Particles • Electromagnetic radiation has properties of waves but also can be thought of as stream of particles. Example: Light • Light as a wave: Light behaves as a transverse wave which we can filter using polarized lenses. • Light as particles (photons).
  • 6.
    A photon isa tiny particle that comprises waves of electromagnetic radiation. As shown by Maxwell, photons are just electric fields traveling through space. Photons have no charge, no resting mass, and travel at the speed of light. A photon
  • 7.
    Representation of anElectromagnetic wave
  • 8.
    FREQUENCY point inunit time. Units- Hz (Hertz) Number of complete wavelength units passing through a given) or cps (cycles per second). WAVE LENGTH Distance between the two peaks. Units- metres, centimetres, millimetres, nanometers WAVE NUMBER Number of waves per cm. Expressed in cm-1
  • 12.
    Type of ElectroMagnetic Radiation • Cosmic rays • Gama rays • X- rays • UV radiation • Visible radiation • IR radiation • Microwaves • Radio waves
  • 15.
    The energy ofEMR can be given by the equation E = h‫ט‬ Where E = Energy of radiation h= Plank’s constant ( 6.624 X 10 -34 JSec) ‫ט‬ = Frequency of radiation
  • 16.
    velocity of lightin vacuum/ wavelength Or 3 X 108 msec-1 / wavelength Hence E = h‫ט‬ = hc/ λ = hc‫ט‬
  • 17.
    UV – VISIBLESPECTROSCOPY  The wavelength of UV- Visible ranges from 200nm – 800nm  Wavelength for UV ranges from 200nm-400nm  Wavelength for visible ranges from 400nm-800nm. Types of spectroscopy: Absorption Emission Scattering
  • 18.
    THE ELECTROMAGNETIC SPECTRUM Ultravioletregion : 180-400 nm ( 200 – 380 nm used for analytical purposes, also called as the near ultraviolet region.) Vacuum ultraviolet region : 1 – 180 nm Visible region : 400 – 750 nm Infrared region : 780 nm – 300 
  • 19.
  • 20.
    Used for quantitativeanalysis and serve as an useful auxiliary tool for structural elucidation. UNITS USE IN UV-VISIBLE SPECTOSCOPY For the measurement of wavelength in UV-Visible spectroscopy following units are used, nm (nanometer) Ǻ (angstrom) cm-1(centimeter inverse) 1 nm=10 Ǻ=10-7cm
  • 21.
    ELECTRONIC TRANSITIONS  Absorptionof ultraviolet and visible radiation in organic molecules is restricted to certain functional groups (chromophores) that contain valence electrons of low excitation energy. This is because the superposition of rotational and vibrational transitions on the electronic transitions gives a combination of overlapping lines.
  • 24.
    CHROMOPHORE The functional groupgives colour to a compound. Example nitro group. Exhibits absorption of electromagnetic radiations in the visible or ultraviolet region.
  • 25.
    Chromophores -one oftwo forms: Conjugated pi systems Common examples include retinal, various food colourings, lycopene, β-carotene and anthocyanins, fabric dyes (azo compounds), etc.
  • 26.
  • 27.
    Their interaction withEMR  Straightens in response to a photon γ (light), of the correct wavelength
  • 28.
    AUXOCHROMES Group of atomsattached to a chromophore which modifies their ability to absorb light Example: -OH , - NH2 , Aldehydes A functional group of atoms with non-bonded electrons which is attached to a chromophore This occurs due to the presence of at least one lone pair of electrons
  • 29.
    Benzene no colour(chromophore absent) Nitrobenzene (pale yellow colour) nitro group. Para-hydroxynitrobenzene exhibits a deep yellow color. Here an auxochrome (-OH) is conjugated with the chromophore -NO2.
  • 30.
    There are mainlytwo types of auxochromes- 1. Acidic -COOH, -OH, -SO3H 2. Basic -NHR, -NR2, -NH2
  • 32.
     Lambert’s LawVs Beer’s Law
  • 33.
    DEVIATION FROM BEER’SLAW  In presence of impurities.  If monochromatic light is not used.  If the width of slit is not proper.  If undesirable radiations fall on the detector.  If solution species under goes polymerization.  Beer’s law can’t be applied to suspension.
  • 34.
    Instrumentation 1. Colorimeters (for the Visible region ) 2. Spectrophotometers ( for the Ultraviolet region)
  • 35.
    Colorimeters  These areinstruments used to measure the absorbance of light in the visible region.  Measurement of the wavelength and the intensity of electromagnetic radiation in the visible region of the spectrum.  It is used extensively for identification and determination of concentrations of substances that absorb light.  They are comparatively inexpensive and less accurate.  The range of wavelength used is small. E.g. 400-700nm
  • 37.
    Spectrophotometer  Spectrophotometers areinstruments used for the quantitative measurement of reflection or transmission properties of a material as a function of wavelength.  They can be used over a wider wavelength range e.g.. 300-900 nm or sometimes up to 1000nm and are very accurate.
  • 39.
    Instrumentation Colorimeters  Source oflight  Filters  Sample Cells  Detectors Spectrophotometers  Source of light  Monochromator s  Sample Cells  Detectors  Recorders
  • 40.
    Source of light Colorimeters The visible spectrum ranges from 400-800 nm.  Common sources of light-  Tungsten Filament Lamp  Carbon Arc Lamp Spectrophotometers  The Ultraviolet region ranges from 180- 400nm.  Sources of light -  Hydrogen discharge Lamp  Deuterium Lamp  Xenon Discharge Lamp  Mercury Arc Lamp
  • 41.
    Filters and Monochromators Filters and Monochromators act as wavelength selectors.  Colorimeters commonly use filters while monochromators are seen in spectrophotometers.  Filters are comparatively less accurate as wavelength selectors than monochromators.
  • 42.
    Filters  There aretwo types of filters- Absorption Filters Interference filters
  • 43.
    Absorption Filters  Chieflymade of glass which are coated with pigments  Or they contain colored gelatin sheets sandwiched between two glass sheets.  These filters absorb the unwanted radiation and transmit only the required radiation.  They are less accurate since their band pass is more than 30nm.
  • 44.
    Monochromators  They arebetter and more efficient in converting polychromatic light into monochromatic light.  Parts of a monochromator-  Entrance slit  Collimator  Grating or Prism  Exit slit
  • 45.
    Sample cells  Theseare cells or cuvettes used to hold the sample solutions.  A cuvette (French: cuvette = "little vessel").  The material of these cells do not absorb at the wavelength being observed.  Glass is used for the visible region, while for the UV region cells made of quartz are used.  Cells are mostly cylindrical or rectangular in shape and of 1cm (short) to 10cm (long) wavelength.  Quartz exists in two forms, the normal α- quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F).
  • 47.
    Detectors  Detectors usedin UV-Visible Spectrophotometers can be called as Photometric detectors.  Principle –  When a particular wavelength of radiation passes through a sample solution, a part of it is absorbed and some part of it is transmitted. The amount of transmitted radiation is measured by a detector.
  • 48.
    Different types ofdetectors 1. Barrier Layer cell or Photo Voltaic Cell 2. Photo tubes or Photo emissive cells 3. Photo multiplier tubes
  • 49.
    Applications 1. Quality controland purity – Colorimeters can be used to detect impurities. 2. Quantitative analysis 3. Determination of Ligand-metal ratio 4. Structure ellucidation of organic compunds 5. Determination of pka values of indicators 6. Determination of molecular weight of amines 7. Determination of elements, ions or functional groups. 8. Determination of organic substances and pharmaceuticals. 9. Chemical Kinetics. 10. Proteins estimation 11. Enzymes Assay 12. DNA/RNA estimation
  • 50.
    REFERENCES  Anjaneyulu Y,Chandrasekhar K, Manickam Valli, A Textbook of Analytical Chemistry, Pharma Book Syndicate, Hyderabad, 2006 edition, Page No 351.  Willard Hobart H, Marritt Lynne L, Dean John A, Settle Frank A, Instrumental methods of analysis, CBS Publishers and Distributors, New Delhi, seventh edition, Page No 97,100. Khopkar S.M. ,Basic concept of analytical chemistry, New Age International (P) Limited, Publishers, New Delhi, third edition 2008Page No 245. Instrumental methods of analysis ,seventh edition by Hobart H. Willard,Lynne L. Merritt,John A. Dean,Frank A. Settle,pp-118 Instrumental methods of chemical analysis fifth edition by Gurdeep R. Chatwal,Sham K. Anand pp-2.149 A textbook Analytical Chemistry by Y.Anjaneyulu,K.Chandrasekhar,Valli Manickan,pp-362. Introduction of instrumental analysis,third edition by Robert D. Braun,pp- 261-263.