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Dr. Satish S. Kola
(Assistant professor )
PHOTOCHEMISTRY
Department of chemistry
M.G. Arts, Science and Late N.P. Commerce College
Armori
Dr. SATISH KOLA 11
What is
Photochemistry?
Its reaction of matte
r with light!
Mr
. Photo
12
Dr. SATISH KOLA
CHARACTERISTICS OF LIGHT
 Light = band of waves of different wavelengths
Increase in wavelengths (nm)
Increase in frequency (energy)
13
Dr. SATISH KOLA
(Light) Electromagnetic spectrum important for photochemistry:
14
Dr. SATISH KOLA
• Wavelength (): Distance between successive crests or troughs
• Frequency (): Number of crests or troughs that pass a point per second
• Speed of light (c) c =  
• Solar energy (Es): (Es = h) It’s the energy come from the sun or other
radiant source.
 The dual nature of light: It means that, in some experiments, light behaves
as a wave, In other experiments, light behaves as a particle.
11
15
Dr. SATISH KOLA
PARTICLE CHARACTERISTICS OF LIGHT:
 Light = flux of discrete units (i.e quanta) called photons.
Fireworks:
12
Dr. SATISH KOLA
SiO2 (glass, quartz);
ABSORBANCE, COLOUR AND TRANSPARENCY OF MATERIALS:
Transparent materials absorb no light in the visible wavelength range, and
hence have no energy states separated by between 1.65 and 3.10eV.
Examples:
Water soluble polymers like:
Poly(acrylic acid) (PAA)
C(Diamond);
13
Dr. SATISH KOLA
ABSORBANCE, COLOUR AND TRANSPARENCY OF MATERIALS:
Opaque materials: are absorb light in all the visible wavelength range,
and hence have many energy states separated by between 1.65 and
3.10eV.
Examples:
• C(graphite) also absorbs light at all wavelengths, but is black and not
reflective like a metal.
• Some metals (Cu, Fe…)
are coloured as well as reflective.
18
Dr. SATISH KOLA
 Dyes and many other materials may
be coloured because they absorb
some of the wavelengths in the
visible range.
UV Absorbance – Sunscreens:
 Absorbance in the ultraviolet (UV) range in
important for transparent materials. UV is
higher energy light, and UV absorbance
can lead to photochemical reactions and
the formation of highly reactive free
radicals. As with ionizing radiation these
can lead to cell damage and (skin) cancer.
19
Dr. SATISH KOLA
o Ordinary reaction (thermal or dark reaction):
o Its occurs by absorption of heat energy from outside in absence of light.
1. The reacting molecules are energised
20
2. Molecular collision is occurred
3. Product is formed
Steps of Ordinary reactions
11
0
Dr. SATISH KOLA
o Photochemical reaction:
o Its a reaction which takes place by absorption of the visible and ultraviolet
radiations (200-800 nm)
o Photochemical reaction
leads to the heating of
the atmosphere during
the daytime by
absorption of ultraviolet
radiation.
 Mechanism of photochemical reactions occurring during atmospheric:
Photochemical change occurs only by absorption of photons.
21
Dr. SATISH KOLA
o Photochemical reaction includes the absorption of visible radiation
during photosynthesis.
 Without photochemical processes, the Earth would be simply a warm,
sterile, rock.
Schematic of photosynthesis in plants.
The carbohydrates produced are stored
in or used by the plant.
Overall equation for the type of
photosynthesis that occurs in plants
22
Dr. SATISH KOLA
o Photochemistry:
o Its the branch of chemistry which deals with the study of photochemical
reactions.
o Demonstration of a Photochemical reaction
23
Dr. SATISH KOLA
o Difference between photochemical and thermochemical reactions
24
Dr. SATISH KOLA
ENERGY TRANSITIONS:
• Molecules absorb radiation by increasing internal energy:
Internal energy  electronic, vibrational, & rotational states
• Energy requirements:
(1). Electronic transitions
 UV-vis ( 400-700 nm)
(2). Vibrational transitions
 Near-IR (700-2000 nm)
(3). Rotational transitions
 Far-IR-Mic (> 2000 nm)
26
Dr. SATISH KOLA
Typical electronic transitions: Typical Molecular vibrations
Typical Molecular rotations
27
Dr. SATISH KOLA
What Happens When Radiation Hits a Molecule?
28
Dr. SATISH KOLA
Absorption and Emission:
• An electronic transition occurs when an electron changes from state to
another.
• The orbital it is leaving must be partly filled (it contains at least one
electron), and the orbital it is entering must be partly unfilled
(it contains less than two electrons).
29
Dr. SATISH KOLA
Absorption or Absorbance: An electron absorbs the energy of a
photon, and jumps from a lower into a higher energy orbital.
Emission: An electron jumps from a higher into a lower orbital, and
releases (emits) a photon of energy equal to the difference.
30
o Light absorption
o When light is passed through a medium, a part of it is absorbed. This
absorbed portion of light which causes photochemical reactions.
oLet a beam of monochromatic light pass through a thickness dx of the
medium. The intensity of radiation reduces from I to I-dI.
o The intensity of radiation can be defined as the
number of photons that pass across a unit area
in unit time.
o Let us denote the number of incident photons
by N and the number absorbed in thickness dx
by dN.
o The fraction of photons absorbed is then dN/N
which is proportional to thickness dx. That is,
31
Dr. SATISH KOLA
o where b is proportionality constant called absorption coefficient.
o Let us set I = I0 at x = 0 and integrate. This gives
o Lambert first derived equation (1) and it is known as Lambert Law. Beer
extended this relation to solutions of compounds in transparent solvents.
The equation (1) then takes the form (2).
Lambert-Beer Law. This law forms the basis
of spectrophotometric methods of chemical
analysis.
o where C = molar concentration; ∈ is a constant characteristic of the solute called the
molar absorption coefficient.
32
Dr. SATISH KOLA
b = x
Beer-Lambert Law :
The attenuation of a
beam by absorbance
is typically
represented in two
ways:
1. Fraction or Percent
Transmission (%T)
2. Absorbance (A)
33
Dr. SATISH KOLA
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Dr. SATISH KOLA
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Dr. SATISH KOLA
36
Dr. SATISH KOLA
ABSORBANCE SPECTROMETRY
 Determines concentration of a substance in solution
 Measures light absorbed by solution at a specific wavelength
 Visible region: low energy electronic transition due to:
a. Compounds containing transition metals
b. Large aromatic structures & conjugated double bond systems
 UV region (200-400 nm):
c. Small conjugated ring systems
d. Carbonyl compounds
37
Dr. SATISH KOLA
o Determination of absorbed intensity
o A photochemical reaction occurs by the absorption of photons of light by the
molecules.
o Therefore, it is essential to determine the absorbed intensity of light for a
study of the rate of reaction.
Schematic diagram of the spectrophotometer used for measurement of light intensity
A sample UV-Vis spectrum.
38
Dr. SATISH KOLA
o Steps of absorbance measurements
1. Light beam from a suitable source (tungsten filament or mercury
vapour lamp) is rendered parallel by the lens.
2.The beam then passes through a ‘filter’ or monochrometer which yields
light of one wavelength only. The monochromatic light enters the reaction
cell made of quartz.
3.The part of light that is not absorbed strikes the detector. Thus the
intensity of light is measured first with the empty cell and then the cell
filled with the reaction sample.
4.The first reading gives the incident intensity, I0, and the second gives
the transmitted intensity, I. The difference, I0 – I = Ia, is the absorbed
intensity.
39
Dr. SATISH KOLA
o The detector generally used for the measurement of intensity of
transmitted light is :
(a) a thermopile (b) photoelectric cell (c) a chemical actinometer.
40
Dr. SATISH KOLA 12
9
o LAWSOF PHOTOCHEMISTRY
1) Grothus–Draper Law (qualitative aspect)
It is only the absorbed light radiations that are effective in producing a
chemical reaction.
2) Stark-Einstein Law of Photochemical Equivalence
Stark and Einstein (1905) studied the quantitative aspect of photochemical
reactions by application of Quantum theory of light.
Illustration of Law of Photochemical
equivalence; absorption of one
photon decomposes one molecule.
41
Dr. SATISH KOLA
o In a photochemical reaction, each molecule of the reacting
substance absorbs a single photon of radiation causing the
reaction and is activated to form the products.
o In practice, we use molar quantities. That is, one mole of A absorbs one
mole of photons or one einstein of energy, E. The value of E can be
calculated by using the expression given below:
42
Dr. SATISH KOLA
o Primary and Secondary reactions:
The overall photochemical reaction may consist of :
(a) a primary reaction: proceeds by absorption of radiation.
(b)secondary reaction: is a thermal reaction which occurs subsequent to
the primary reaction.
For example, the decomposition of HBr occurs as follows :
o Evidently, the primary reaction only obeys the law of photochemical equivalence strictly. The
secondary reactions have no concern with the law.
43
Dr. SATISH KOLA
o Quantum yield (or Quantum efficiency) (ᶲ)
o For a reaction that obeys strictly the Einstein law, one molecule
decomposes per photon, the quantum yield φ = 1.
o When two or more molecules are decomposed per photon, φ > 1 and the
reaction has a high quantum yield.
o If the number of molecules decomposed is less than one per photon, φ <
1 the reaction has a low quantum yield.
44
Dr. SATISH KOLA
o Causes of high quantum yield
The chief reasons for high quantum yield are :
(1) Reactions subsequent to the Primary reaction:
(2) A reaction chain forms many molecules per photon:
 A reaction chain steps:
1) Initiation……………….>
2) Self-propagating……>
45
3) Termination………….>
The number of HCl molecules formed
for a photon of light is very high. The
quantum yield of the
reaction varies from 104 to 106
Dr. SATISH KOLA
o Causes of low quantum yield
(1) Deactivation of reacting molecules:
46
Dr. SATISH KOLA
(2) Occurrence of reverse of primary reaction:
Dimerization ofAnthracene:
o The quantum yield should be 2 but it is actually found to be 0.5.
The low quantum yield is explained as the reaction is
accompanied by fluorescence which deactivates the excited
anthracene molecules. Furthermore, the above reaction is
reversible.
47
Dr. SATISH KOLA
(3) Recombination of dissociated fragments:
Combination of H2 and Br2.
2
48
o The reaction (2) is extremely slow. The reactions (3), (4) and (5), depend directly or
indirectly on (2) and so are very slow. Therefore most of the Br atoms produced in the
primary process recombine to give back Br2 molecules.
o Thus the HBr molecules obtained per quantum is extremely small. The quantum yield of
the reaction is found to be 0.01 at ordinary temperature.
Dr. SATISH KOLA
CALCULATION OF QUANTUM YIELD
By definition, the quantum yield, , of a photochemical reaction is expressed as :
Thus we can calculate quantum yield from :
(a) The amount of the reactant decomposed in a given time and
(b) The amount of radiation energy absorbed in the same time
o The radiation energy is absorbed by a chemical system as photons.
Therefore we should know the energy associated with a photon or a mole
of photons.
49
Dr. SATISH KOLA
The energyof photons; einstein
o We know that the energy of a photon (or quantum), ∈ , is given by the
equation:
h = Planck’s constant (6.624 × 10– 27 erg-sec)
v = frequency of radiation
λ = wavelength of radiation
c = velocity of light (3 × 1010 cm sec– 1) o If λ is given in cm, the energy is expressed in ergs.
The energy, E, of an Avogadro number (N) of photons is referred to as one einstein:
Substituting the values of N (= 6.02 × 1023), h and c, in (2), we have:
50
13
9
Dr. SATISH KOLA
If λ is expressed in Å units (1Å = 10– 8 cm),
Since 1 cal = 4.184 × 107 erg, energy in calories would be:
51
o It is evident from (3) that the numerical value of einstein varies inversely as the
wavelength of radiation.
o The higher the wavelength, the smaller will be the energy per einstein.
Electron-volt (eV) is another
commonly used energy unit,
1 eV = 1.6 x 10-19 J.
Dr. SATISH KOLA
SOLVED PROBLEM 1. Calculate the energy associated with (a) one photon;
(b) one einstein of radiation of wavelength 8000 Å. h = 6.62 × 10–27 erg-sec; c =
3 × 1010 cm sec–1.
SOLUTION
(a) Energy of a photon
(b) Energy per einstein
52
Dr. SATISH KOLA
SOLVED PROBLEM 2. When a substance Awas exposed to light, 0.002 mole of it
reacted in 20 minutes and 4 seconds. In the same time Aabsorbed 2.0 × 106 photons
of light per second. Calculate the quantum yield of the reaction. (Avogadro number
N = 6.02 × 1023)
SOLUTION
Number of molecules of Areacting = 0.002 × N = 0.002 × 6.02 × 1023
Number of photons absorbed per second = 2.0 × 106
Number of photons absorbed in 20 minutes and 4 seconds = 2.0 × 106 × 1204
Quantum yield
53
Dr. SATISH KOLA
SOLVED PROBLEM 3. When irradiated with light of 5000 Å wavelength, 1 × 10–
4 mole of a substance is decomposed. How many photons are absorbed during the
reaction if its quantum efficiency is 10.00. (Avogadro number N = 6.02 × 1023)
SOLUTION
Quantum efficiency of the reaction = 10.00
No. of moles decomposed = 1 × 10–4
No. of molecules decomposed = 1 × 10–4 × 6.02 × 1023 = 6.02 x 1019
we know that,
54
Dr. SATISH KOLA
SOLVED PROBLEM 4. When propionaldehyde is irradiated with light of λ =
3020 Å, it is decomposed to form carbon monoxide.
CH3CH2CHO + hv ⎯⎯→ CH3CH3 + CO
The quantum yield for the reaction is 0.54. The light energy absorbed is 15000 erg
mol in a given time. Find the amount of carbon monoxide formed in moles in the
same time.
SOLUTION
55
Dr. SATISH KOLA
PHOTOSENSITIZED REACTIONS
o In many photochemical reactions the reactant molecule does not absorb the
radiation required for the reaction. Hence the reaction is not possible.
o In such cases the reaction may still occur if a foreign species such as mercury
vapour is present.
o Aspecies which can both absorb and transfer radiant energy for activation of the
reactant molecule, is called a photosensitizer. The reaction so caused is called a
photosensitized reaction.
Hg + hv ⎯⎯→ Hg*
Hg* +A⎯⎯→ A* + Hg
Reaction between H2 and CO:
Hg + hv ⎯⎯→ Hg* Primary absorption
Hg* + H2 ⎯⎯→ 2H * + Hg Energy transfer
H + CO ⎯⎯→ HCO
56
Some glyoxal, CHO-CHO, is also formed by dimerization of formyl radicals, HCO.
Dr. SATISH KOLA
EMISSION:
•An electron jumps from a
higher into a lower orbital,
and releases (emits) a photon
of energy equal to the
difference (∆E = hv).
•Luminescence (emission of
light) works on the basis that
if a molecule is excited above
its ground state, then it must
de-excite
release
either non-radiative
somehow and
excess energy as
or
radiative energy.
57
Dr. SATISH KOLA
 A good starting point for a discussion of
luminescence (fluorescence or
phosphorescence) principle is a simplified
Jablonski diagram.
•The Jablonski diagram is employed to
represent the energy levels of a molecule. As
depicted in JD, S0, S1 and S2 represent ground,
first and second singlet electronic states,
respectively, whereas T1 and T2 describe first
and second triplet electronic states,
respectively.
•Each electronic energy level of a molecule also
has numerous vibrational (v) and rotational (n)
energy sublevels.
Jablonski diagram (JD)
58
Dr. SATISH KOLA
(JD)
10-15 s
10-11 s
10-9 to 10-7 s
10-5 to 10-s
Absorbance
energy
59
Dr. SATISH KOLA
PHOTOPHYSICAL PROCESSES:
o If the absorbed radiation is not used to cause a chemical change, it is re-emitted
as light of longer wavelength. The three such photophysical processes which can
occur are :
(1) Fluorescence (2) Phosphorescence (3) Chemiluminescence
o Fluorescence
 Process at which certain molecules (or atoms) when exposed to light radiation of
short wavelength (high frequency), emit light of longer wavelength.
 Substance that exhibits fluorescence is called fluorophore.
 Florescence stops as soon as the incident radiation is cut off.
Examples:
exhibits blue
(a)a solution of quinine sulphate on exposure to visible light,
fluorescence.
(b) a solution of chlorophyll in ether shows blood red fluorescence.
Dr. SATISH KOLA 14
9
Molecular formulas of common dyes of fluorescent probes (fluorophores)
64
Dr. SATISH KOLA
o Fluorescence depends on:
1. pH
2. Solvent
3. Temperature
4. Salts
5. Concentration
65
Dr. SATISH KOLA
Demonstration of a Solvent Sensitive Fluorophore
Corrected fluorescence emission spectra of DOS in
cyclohexane(CH), toluene (T), ethylacetate(EA) and
butanol(Bu). The dashed line shows the emission of
DOS from DPPC vesicles
66
Solvent Polarity
Dr. SATISH KOLA
Fluorescent minerals, shown under ultraviolet light:
67
Dr. SATISH KOLA
 The colour of fluorescence depends on the wavelength of light emitted.
68
Dr. SATISH KOLA
Phosphorescence
69
 When a substance absorbs radiation of high frequency and emits light even after the
incident radiation is cut off, the process is called phosphorescence.
 The substance which shows phosphorescence is called phosphorescent substance.
 Phosphorescence is chiefly caused by ultraviolet and visible light. It is generally shown
by solids.
Examples:
(a) Sulphates of calcium, barium and strontium exhibit phosphorescence.
(b)Fluorescein in boric acid shows phosphorescence in the blue region at 570nm
wavelength.
o Phosphorescence could be designated as delayed fluorescence.
A+ hv ⎯⎯→ A* ⎯slow⎯→ hv′
Dr. SATISH KOLA
Phosphorescent powder under:
70
visible light, ultraviolet light, darkness
Dr. SATISH KOLA
71
Dr. SATISH KOLA
The observed fluorescence lifetime can be measured by
using a pulsed laser technique:
77
Dr. SATISH KOLA
Chemiluminescence:
o The emission of light as a result of chemical action is called chemiluminescence. The
reaction is referred to as a chemiluminescent reaction.
o Chemiluminescent reaction is the reverse of a photochemical reaction which proceeds
by absorption of light.
o The light emitted in a chemiluminescent reaction is also called ‘cold light’because it is
produced at ordinary temperature.
o In a chemiluminescent reaction, the energy released in the reaction makes the product
molecule electronically excited. The excited molecule then gives up its excess energy
as visible light while reverting to ground state.
Dr. SATISH KOLA
Chemiluminescence of fireflies and luminol
Examples:
(a)The glow of fireflies due to the aerial oxidation of luciferin (a protein) in the presence of
enzyme luciferase.
(b) The oxidation of 5-aminophthalic cyclic hydrazide (luminol) by hydrogen peroxide in
alkaline solution, producing bright green light.
Dr. SATISH KOLA

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Photochemistry PPT.pptx

  • 1. Dr. Satish S. Kola (Assistant professor ) PHOTOCHEMISTRY Department of chemistry M.G. Arts, Science and Late N.P. Commerce College Armori Dr. SATISH KOLA 11
  • 2. What is Photochemistry? Its reaction of matte r with light! Mr . Photo 12 Dr. SATISH KOLA
  • 3. CHARACTERISTICS OF LIGHT  Light = band of waves of different wavelengths Increase in wavelengths (nm) Increase in frequency (energy) 13 Dr. SATISH KOLA
  • 4. (Light) Electromagnetic spectrum important for photochemistry: 14 Dr. SATISH KOLA
  • 5. • Wavelength (): Distance between successive crests or troughs • Frequency (): Number of crests or troughs that pass a point per second • Speed of light (c) c =   • Solar energy (Es): (Es = h) It’s the energy come from the sun or other radiant source.  The dual nature of light: It means that, in some experiments, light behaves as a wave, In other experiments, light behaves as a particle. 11 15 Dr. SATISH KOLA
  • 6. PARTICLE CHARACTERISTICS OF LIGHT:  Light = flux of discrete units (i.e quanta) called photons. Fireworks: 12 Dr. SATISH KOLA
  • 7. SiO2 (glass, quartz); ABSORBANCE, COLOUR AND TRANSPARENCY OF MATERIALS: Transparent materials absorb no light in the visible wavelength range, and hence have no energy states separated by between 1.65 and 3.10eV. Examples: Water soluble polymers like: Poly(acrylic acid) (PAA) C(Diamond); 13 Dr. SATISH KOLA
  • 8. ABSORBANCE, COLOUR AND TRANSPARENCY OF MATERIALS: Opaque materials: are absorb light in all the visible wavelength range, and hence have many energy states separated by between 1.65 and 3.10eV. Examples: • C(graphite) also absorbs light at all wavelengths, but is black and not reflective like a metal. • Some metals (Cu, Fe…) are coloured as well as reflective. 18 Dr. SATISH KOLA
  • 9.  Dyes and many other materials may be coloured because they absorb some of the wavelengths in the visible range. UV Absorbance – Sunscreens:  Absorbance in the ultraviolet (UV) range in important for transparent materials. UV is higher energy light, and UV absorbance can lead to photochemical reactions and the formation of highly reactive free radicals. As with ionizing radiation these can lead to cell damage and (skin) cancer. 19 Dr. SATISH KOLA
  • 10. o Ordinary reaction (thermal or dark reaction): o Its occurs by absorption of heat energy from outside in absence of light. 1. The reacting molecules are energised 20 2. Molecular collision is occurred 3. Product is formed Steps of Ordinary reactions 11 0 Dr. SATISH KOLA
  • 11. o Photochemical reaction: o Its a reaction which takes place by absorption of the visible and ultraviolet radiations (200-800 nm) o Photochemical reaction leads to the heating of the atmosphere during the daytime by absorption of ultraviolet radiation.  Mechanism of photochemical reactions occurring during atmospheric: Photochemical change occurs only by absorption of photons. 21 Dr. SATISH KOLA
  • 12. o Photochemical reaction includes the absorption of visible radiation during photosynthesis.  Without photochemical processes, the Earth would be simply a warm, sterile, rock. Schematic of photosynthesis in plants. The carbohydrates produced are stored in or used by the plant. Overall equation for the type of photosynthesis that occurs in plants 22 Dr. SATISH KOLA
  • 13. o Photochemistry: o Its the branch of chemistry which deals with the study of photochemical reactions. o Demonstration of a Photochemical reaction 23 Dr. SATISH KOLA
  • 14. o Difference between photochemical and thermochemical reactions 24 Dr. SATISH KOLA
  • 15. ENERGY TRANSITIONS: • Molecules absorb radiation by increasing internal energy: Internal energy  electronic, vibrational, & rotational states • Energy requirements: (1). Electronic transitions  UV-vis ( 400-700 nm) (2). Vibrational transitions  Near-IR (700-2000 nm) (3). Rotational transitions  Far-IR-Mic (> 2000 nm) 26 Dr. SATISH KOLA
  • 16. Typical electronic transitions: Typical Molecular vibrations Typical Molecular rotations 27 Dr. SATISH KOLA
  • 17. What Happens When Radiation Hits a Molecule? 28 Dr. SATISH KOLA
  • 18. Absorption and Emission: • An electronic transition occurs when an electron changes from state to another. • The orbital it is leaving must be partly filled (it contains at least one electron), and the orbital it is entering must be partly unfilled (it contains less than two electrons). 29 Dr. SATISH KOLA
  • 19. Absorption or Absorbance: An electron absorbs the energy of a photon, and jumps from a lower into a higher energy orbital. Emission: An electron jumps from a higher into a lower orbital, and releases (emits) a photon of energy equal to the difference. 30
  • 20. o Light absorption o When light is passed through a medium, a part of it is absorbed. This absorbed portion of light which causes photochemical reactions. oLet a beam of monochromatic light pass through a thickness dx of the medium. The intensity of radiation reduces from I to I-dI. o The intensity of radiation can be defined as the number of photons that pass across a unit area in unit time. o Let us denote the number of incident photons by N and the number absorbed in thickness dx by dN. o The fraction of photons absorbed is then dN/N which is proportional to thickness dx. That is, 31 Dr. SATISH KOLA
  • 21. o where b is proportionality constant called absorption coefficient. o Let us set I = I0 at x = 0 and integrate. This gives o Lambert first derived equation (1) and it is known as Lambert Law. Beer extended this relation to solutions of compounds in transparent solvents. The equation (1) then takes the form (2). Lambert-Beer Law. This law forms the basis of spectrophotometric methods of chemical analysis. o where C = molar concentration; ∈ is a constant characteristic of the solute called the molar absorption coefficient. 32 Dr. SATISH KOLA
  • 22. b = x Beer-Lambert Law : The attenuation of a beam by absorbance is typically represented in two ways: 1. Fraction or Percent Transmission (%T) 2. Absorbance (A) 33 Dr. SATISH KOLA
  • 26. ABSORBANCE SPECTROMETRY  Determines concentration of a substance in solution  Measures light absorbed by solution at a specific wavelength  Visible region: low energy electronic transition due to: a. Compounds containing transition metals b. Large aromatic structures & conjugated double bond systems  UV region (200-400 nm): c. Small conjugated ring systems d. Carbonyl compounds 37 Dr. SATISH KOLA
  • 27. o Determination of absorbed intensity o A photochemical reaction occurs by the absorption of photons of light by the molecules. o Therefore, it is essential to determine the absorbed intensity of light for a study of the rate of reaction. Schematic diagram of the spectrophotometer used for measurement of light intensity A sample UV-Vis spectrum. 38 Dr. SATISH KOLA
  • 28. o Steps of absorbance measurements 1. Light beam from a suitable source (tungsten filament or mercury vapour lamp) is rendered parallel by the lens. 2.The beam then passes through a ‘filter’ or monochrometer which yields light of one wavelength only. The monochromatic light enters the reaction cell made of quartz. 3.The part of light that is not absorbed strikes the detector. Thus the intensity of light is measured first with the empty cell and then the cell filled with the reaction sample. 4.The first reading gives the incident intensity, I0, and the second gives the transmitted intensity, I. The difference, I0 – I = Ia, is the absorbed intensity. 39 Dr. SATISH KOLA
  • 29. o The detector generally used for the measurement of intensity of transmitted light is : (a) a thermopile (b) photoelectric cell (c) a chemical actinometer. 40 Dr. SATISH KOLA 12 9
  • 30. o LAWSOF PHOTOCHEMISTRY 1) Grothus–Draper Law (qualitative aspect) It is only the absorbed light radiations that are effective in producing a chemical reaction. 2) Stark-Einstein Law of Photochemical Equivalence Stark and Einstein (1905) studied the quantitative aspect of photochemical reactions by application of Quantum theory of light. Illustration of Law of Photochemical equivalence; absorption of one photon decomposes one molecule. 41 Dr. SATISH KOLA
  • 31. o In a photochemical reaction, each molecule of the reacting substance absorbs a single photon of radiation causing the reaction and is activated to form the products. o In practice, we use molar quantities. That is, one mole of A absorbs one mole of photons or one einstein of energy, E. The value of E can be calculated by using the expression given below: 42 Dr. SATISH KOLA
  • 32. o Primary and Secondary reactions: The overall photochemical reaction may consist of : (a) a primary reaction: proceeds by absorption of radiation. (b)secondary reaction: is a thermal reaction which occurs subsequent to the primary reaction. For example, the decomposition of HBr occurs as follows : o Evidently, the primary reaction only obeys the law of photochemical equivalence strictly. The secondary reactions have no concern with the law. 43 Dr. SATISH KOLA
  • 33. o Quantum yield (or Quantum efficiency) (ᶲ) o For a reaction that obeys strictly the Einstein law, one molecule decomposes per photon, the quantum yield φ = 1. o When two or more molecules are decomposed per photon, φ > 1 and the reaction has a high quantum yield. o If the number of molecules decomposed is less than one per photon, φ < 1 the reaction has a low quantum yield. 44 Dr. SATISH KOLA
  • 34. o Causes of high quantum yield The chief reasons for high quantum yield are : (1) Reactions subsequent to the Primary reaction: (2) A reaction chain forms many molecules per photon:  A reaction chain steps: 1) Initiation……………….> 2) Self-propagating……> 45 3) Termination………….> The number of HCl molecules formed for a photon of light is very high. The quantum yield of the reaction varies from 104 to 106 Dr. SATISH KOLA
  • 35. o Causes of low quantum yield (1) Deactivation of reacting molecules: 46 Dr. SATISH KOLA
  • 36. (2) Occurrence of reverse of primary reaction: Dimerization ofAnthracene: o The quantum yield should be 2 but it is actually found to be 0.5. The low quantum yield is explained as the reaction is accompanied by fluorescence which deactivates the excited anthracene molecules. Furthermore, the above reaction is reversible. 47 Dr. SATISH KOLA
  • 37. (3) Recombination of dissociated fragments: Combination of H2 and Br2. 2 48 o The reaction (2) is extremely slow. The reactions (3), (4) and (5), depend directly or indirectly on (2) and so are very slow. Therefore most of the Br atoms produced in the primary process recombine to give back Br2 molecules. o Thus the HBr molecules obtained per quantum is extremely small. The quantum yield of the reaction is found to be 0.01 at ordinary temperature. Dr. SATISH KOLA
  • 38. CALCULATION OF QUANTUM YIELD By definition, the quantum yield, , of a photochemical reaction is expressed as : Thus we can calculate quantum yield from : (a) The amount of the reactant decomposed in a given time and (b) The amount of radiation energy absorbed in the same time o The radiation energy is absorbed by a chemical system as photons. Therefore we should know the energy associated with a photon or a mole of photons. 49 Dr. SATISH KOLA
  • 39. The energyof photons; einstein o We know that the energy of a photon (or quantum), ∈ , is given by the equation: h = Planck’s constant (6.624 × 10– 27 erg-sec) v = frequency of radiation λ = wavelength of radiation c = velocity of light (3 × 1010 cm sec– 1) o If λ is given in cm, the energy is expressed in ergs. The energy, E, of an Avogadro number (N) of photons is referred to as one einstein: Substituting the values of N (= 6.02 × 1023), h and c, in (2), we have: 50 13 9 Dr. SATISH KOLA
  • 40. If λ is expressed in Å units (1Å = 10– 8 cm), Since 1 cal = 4.184 × 107 erg, energy in calories would be: 51 o It is evident from (3) that the numerical value of einstein varies inversely as the wavelength of radiation. o The higher the wavelength, the smaller will be the energy per einstein. Electron-volt (eV) is another commonly used energy unit, 1 eV = 1.6 x 10-19 J. Dr. SATISH KOLA
  • 41. SOLVED PROBLEM 1. Calculate the energy associated with (a) one photon; (b) one einstein of radiation of wavelength 8000 Å. h = 6.62 × 10–27 erg-sec; c = 3 × 1010 cm sec–1. SOLUTION (a) Energy of a photon (b) Energy per einstein 52 Dr. SATISH KOLA
  • 42. SOLVED PROBLEM 2. When a substance Awas exposed to light, 0.002 mole of it reacted in 20 minutes and 4 seconds. In the same time Aabsorbed 2.0 × 106 photons of light per second. Calculate the quantum yield of the reaction. (Avogadro number N = 6.02 × 1023) SOLUTION Number of molecules of Areacting = 0.002 × N = 0.002 × 6.02 × 1023 Number of photons absorbed per second = 2.0 × 106 Number of photons absorbed in 20 minutes and 4 seconds = 2.0 × 106 × 1204 Quantum yield 53 Dr. SATISH KOLA
  • 43. SOLVED PROBLEM 3. When irradiated with light of 5000 Å wavelength, 1 × 10– 4 mole of a substance is decomposed. How many photons are absorbed during the reaction if its quantum efficiency is 10.00. (Avogadro number N = 6.02 × 1023) SOLUTION Quantum efficiency of the reaction = 10.00 No. of moles decomposed = 1 × 10–4 No. of molecules decomposed = 1 × 10–4 × 6.02 × 1023 = 6.02 x 1019 we know that, 54 Dr. SATISH KOLA
  • 44. SOLVED PROBLEM 4. When propionaldehyde is irradiated with light of λ = 3020 Å, it is decomposed to form carbon monoxide. CH3CH2CHO + hv ⎯⎯→ CH3CH3 + CO The quantum yield for the reaction is 0.54. The light energy absorbed is 15000 erg mol in a given time. Find the amount of carbon monoxide formed in moles in the same time. SOLUTION 55 Dr. SATISH KOLA
  • 45. PHOTOSENSITIZED REACTIONS o In many photochemical reactions the reactant molecule does not absorb the radiation required for the reaction. Hence the reaction is not possible. o In such cases the reaction may still occur if a foreign species such as mercury vapour is present. o Aspecies which can both absorb and transfer radiant energy for activation of the reactant molecule, is called a photosensitizer. The reaction so caused is called a photosensitized reaction. Hg + hv ⎯⎯→ Hg* Hg* +A⎯⎯→ A* + Hg Reaction between H2 and CO: Hg + hv ⎯⎯→ Hg* Primary absorption Hg* + H2 ⎯⎯→ 2H * + Hg Energy transfer H + CO ⎯⎯→ HCO 56 Some glyoxal, CHO-CHO, is also formed by dimerization of formyl radicals, HCO. Dr. SATISH KOLA
  • 46. EMISSION: •An electron jumps from a higher into a lower orbital, and releases (emits) a photon of energy equal to the difference (∆E = hv). •Luminescence (emission of light) works on the basis that if a molecule is excited above its ground state, then it must de-excite release either non-radiative somehow and excess energy as or radiative energy. 57 Dr. SATISH KOLA
  • 47.  A good starting point for a discussion of luminescence (fluorescence or phosphorescence) principle is a simplified Jablonski diagram. •The Jablonski diagram is employed to represent the energy levels of a molecule. As depicted in JD, S0, S1 and S2 represent ground, first and second singlet electronic states, respectively, whereas T1 and T2 describe first and second triplet electronic states, respectively. •Each electronic energy level of a molecule also has numerous vibrational (v) and rotational (n) energy sublevels. Jablonski diagram (JD) 58 Dr. SATISH KOLA
  • 48. (JD) 10-15 s 10-11 s 10-9 to 10-7 s 10-5 to 10-s Absorbance energy 59 Dr. SATISH KOLA
  • 49. PHOTOPHYSICAL PROCESSES: o If the absorbed radiation is not used to cause a chemical change, it is re-emitted as light of longer wavelength. The three such photophysical processes which can occur are : (1) Fluorescence (2) Phosphorescence (3) Chemiluminescence o Fluorescence  Process at which certain molecules (or atoms) when exposed to light radiation of short wavelength (high frequency), emit light of longer wavelength.  Substance that exhibits fluorescence is called fluorophore.  Florescence stops as soon as the incident radiation is cut off. Examples: exhibits blue (a)a solution of quinine sulphate on exposure to visible light, fluorescence. (b) a solution of chlorophyll in ether shows blood red fluorescence. Dr. SATISH KOLA 14 9
  • 50. Molecular formulas of common dyes of fluorescent probes (fluorophores) 64 Dr. SATISH KOLA
  • 51. o Fluorescence depends on: 1. pH 2. Solvent 3. Temperature 4. Salts 5. Concentration 65 Dr. SATISH KOLA
  • 52. Demonstration of a Solvent Sensitive Fluorophore Corrected fluorescence emission spectra of DOS in cyclohexane(CH), toluene (T), ethylacetate(EA) and butanol(Bu). The dashed line shows the emission of DOS from DPPC vesicles 66 Solvent Polarity Dr. SATISH KOLA
  • 53. Fluorescent minerals, shown under ultraviolet light: 67 Dr. SATISH KOLA
  • 54.  The colour of fluorescence depends on the wavelength of light emitted. 68 Dr. SATISH KOLA
  • 55. Phosphorescence 69  When a substance absorbs radiation of high frequency and emits light even after the incident radiation is cut off, the process is called phosphorescence.  The substance which shows phosphorescence is called phosphorescent substance.  Phosphorescence is chiefly caused by ultraviolet and visible light. It is generally shown by solids. Examples: (a) Sulphates of calcium, barium and strontium exhibit phosphorescence. (b)Fluorescein in boric acid shows phosphorescence in the blue region at 570nm wavelength. o Phosphorescence could be designated as delayed fluorescence. A+ hv ⎯⎯→ A* ⎯slow⎯→ hv′ Dr. SATISH KOLA
  • 56. Phosphorescent powder under: 70 visible light, ultraviolet light, darkness Dr. SATISH KOLA
  • 58. The observed fluorescence lifetime can be measured by using a pulsed laser technique: 77 Dr. SATISH KOLA
  • 59. Chemiluminescence: o The emission of light as a result of chemical action is called chemiluminescence. The reaction is referred to as a chemiluminescent reaction. o Chemiluminescent reaction is the reverse of a photochemical reaction which proceeds by absorption of light. o The light emitted in a chemiluminescent reaction is also called ‘cold light’because it is produced at ordinary temperature. o In a chemiluminescent reaction, the energy released in the reaction makes the product molecule electronically excited. The excited molecule then gives up its excess energy as visible light while reverting to ground state. Dr. SATISH KOLA
  • 60. Chemiluminescence of fireflies and luminol Examples: (a)The glow of fireflies due to the aerial oxidation of luciferin (a protein) in the presence of enzyme luciferase. (b) The oxidation of 5-aminophthalic cyclic hydrazide (luminol) by hydrogen peroxide in alkaline solution, producing bright green light. Dr. SATISH KOLA