UV-VISIBLE SPECTROSCOPY

PRESENTED BY:
GABRIEL ENGONGA
FLORA DIKE NGOZI 1
 Electromagnetic radiation
Energy of an EMR
Electromagnetic spectrum & it’s regions
 Spectroscopy & it’s types
 Colorimetry
UV-spectroscopy
 Electronic transitions
Terms used in UV-Visible spectroscopy
Absorption band & it’s types
Beer lambert’s law & it’s
deviations
⓫ Reference 2
  Electromagnetic radiation is a type of energy that is
transmitted through space at enormous velocities.

 Radiant energy has wave nature and being associated

with electric as well as magnetic field,these radiations
are called electromagnetic radiation.

 Electromagnetic radiation has it’s origin in atomic and

molecular processes.

3
 The field may be represented as electric and magnetic
vectors oscillating in mutually perpendicular planes.

Electromagnei Radiatio
tc n
Ele<:trl Fleki
e oseuosen

4
 The energy of an EMR can be given by the following
equation:
E=hµ

Where E= Energy of radiation

h=Planck’s constant
µ=Frequency of
radiation

5
Frequency(µ)= c/λ
Where c=velocity of light in vacuum
λ= wavelength

:-Hence, E=hµ

E=hc/λ

Therefore,energy of a radiation depends upon frequency

and wavelength of radiation.

6
·, J , J "' f f ( l ', l ' J J J _,
',r '1 _ , ·,' J J f
,
The arrangement obtained by arranging various types
of electromagnetic waves or radiations in order of their
increasing wavelegth or decreasing frequencies is
called electromagnetic spectrum.

The electromagnetic spectrum is divided into a

number of regions; these are artificial divisions in the
sense that they have been defined solely as a result of
differences in the instrumentation required for
producing and detecting radiation of a given frequency
range.
7
 ---------- Wavelength(m)-------------
10- 10-5 10-3 10-1 101 103
7
1 1 1
Gamma' 1 1
1 X-rays 1 Microwavest Radio frequency
rays 1 1
1

102 101 1012 10 10 104

0 4 8 6
-- Frequency (s-1)

Visiblregion

400 50 60 700 750nm

0 0
8
 Higher
Visible Spectrum
Lower
Frequenc Frequenc
y y

uv IR

400 500 600 700 800

Wavelen th in nanometers

 Ultraviolet: 190~400nm
 Violet: 400 - 420 nm
 420 - 440 nm
Indigo:
 Blue: 440 - 490 nm
 490 - 570 nm
Green:
 Yellow: 570 - 585 nm
 585 - 620 nm
Orange:
 Red: 620 - 780 nm
9
spectroscopy

10
SPECTROSCOPY

Spectroscopy is the measurement and

interpretation of electromagnetic radiation
absorbed or emitted when the molecules or
atoms or ions of a sample moves from one
energy state to another energy state

11
' J/ 1 •
/1 ~
r: ÍJ .
...
r f
I J
J ...
J f, J 1 f) ': (
J -
ÍJ
..
) I

J J ..
J .

1) Atomic spectroscopy :
H takes
e
r
e
,t
h
2)Molecular spectroscopy :
e
cHere,the changes in takes
henergy
place at molecular level. a
Eg: UV spectroscopy,colorimetry,infra
n
red spectroscopy g 12

e
 Absorption spectrophotometry can be
defined as the measurement of absorption of radiant
energy by various substances.It involves the
measurement of absorptive capacity for radiant energy
in the visible,UV and IR regions of the spectrum.

13
o λ- 400-800nm
o Coloured substance absorbs light of different λ in
different manner and hence get an absorption
curve
o The λ at which maximum absorption takes place is
called as λmax
o λmax is characteristic for every coloured
o substance
On plotting a graph of concentration v/s
in determining the
absorbance,we getconcentration
a calibrationorcurve
amount of ais
that
drug substance in the given sample solution.
useful 14
15
 UV spectroscopy is concerned with the study of absorption
of uv radiation which ranges from 200-400nm.
 Valence electrons absorb the energy thereby
molecules undergoes transition from ground state to
excited
state.
 This absorption is characteristic and depends on
the nature of electrons present.
 Types of electrons
σ electrons: in saturated compounds
π electrons: in unsaturated compounds
n electrons: in non bonded electrons

16
 Antibondin CT"
n CT* CT"--- (J" * g *
" 7 Antibondin
TT--- TT * rr *
---7 g
e 7 Non-
bonding n
e Bondin rr
g
e Bondin CT
g "

17
 1) σ-σ*
 σ electron from orbital is excited to corresponding
anti-bonding orbital σ*.

 The energy required is large for this transition.

 The organic compounds in which all the valence shell

electrons are involved in the formation of σ bond do
not show absorption in normal uv region (200-400nm)

 This transition is observed with saturated compounds.

18
 Eg: Methane(CH₄) has C-H bond only and can undergo σ-
σ* transition and shows absorption maxima at 122nm.

 The usual spectroscopic technique cannot be used below

200 nm.

 To study this high energy transition,the entire region

should be evacuated (Vacuum uv region)

 Here,the excitation ocuurs with net retention of electronic

spin

 This region is less informative

19
 2) π-π*
 π electron in a bonding orbital is excited to
corresponding anti-bonding orbital π*.

 Energy required is less when compared to n-σ*

 Compounds containing multiple bonds like

alkenes,alkynes,carbonyls,nitriles,aromatic
compounds etc undergo π-π* transition.

Eg:Alkenes generally absorb in the region 170-205nm.

20
 Absorption usually occurs in the ordinary uv
spectrophotometer

 Absorption bands in unconjugated alkenes (170-

190nm)

 Absorption bands in carbonyls (180 nm)

 Introduction of alkyl group in olefinic linkage

produces bathochromic shift

21
 3) n-σ*
 Saturated compounds containing one hetero atom
with unshared pair of electrons(n) like O,N,S and
halogens are capable of n-σ* transition.

 These transition require less energy than σ-σ*

transition.

 In saturated alkyl halides, the energy required for

transition decrease with increase in the size of halogen
atom (or decrease in electronegativity)

22
 Eg:Methyl chloride has a λmax of 173nm.

Methyl iodide has a λmax of 258nm.

 This type of transition is very sensitive to hydrogen

bonding
Eg: Alcohol & amines

 Hydrogen bonding shift the uv absorptions to

shorter wavelength.

23
 4) n-π*

 An electron from non-bonding orbital is promoted to

anti-bonding π* orbital.

 Compounds containing double bonds involving

hetero atoms(C=O,N=O) undergo such type of
transitions.

 This transition require minimum energy out of all

transitions and shows absorption band at longer
wavelength around 300nm.
24
 Eg:Saturated aldehydes shows both type of transitions
(n-π*, π-π*) at {low energy and high energy}
around 290 and 180 nm.

25
TERMS USED IN UV-
VISIBLE SPECTROSCOPY

26
 Chromophore is defined as the nucleus or any
isolated covalently bonded group responsible for the
absorption of light radiation.

 Any group which exhibits absorption of

electromagnetic radiations in the visible or ultraviolet
region.
C=C , C=O ,NO2 etc

 Some of the important chromophores are

carbonyls,acids,esters,nitrile,ethylenic groups.
27
Chromophores: examples

Chromophore Example Excitation }\max• nm E Solvent

C=C Ethene n-> n- 17 15,000 hexane

1

c:c 1-Hexyne rt.;,» n- 180 10,000 hexane

n-> n* 290 15 hexane

C=O Ethanal n-> n- 180 10,0 hexane
00

n-> n* 275 17 ethanol

N=O Nitromethane n-> n- 200 5,00 ethanol
0

C-X· X=Br Methyl bromide n->cr* 205 200 hexane

'
X=I Methyl lodide n-> o" 255 360 hexane

5928
 These are co-ordinatively saturated or un-saturated
groups which themselves do not absorb radiations,but
when present alongwith a chromophore enhances the
absorbing properties of chromophore.

 Also known as colour enhancing group.

 All auxochromes have one or more non-bonding pair

of electrons.
-NH2 ,-OH ,-OR,-COOH etc
 It extend the conjugation of a chromophore by
sharing the non-bonding electrons. 29
AUXOCHRO E
e.g Benzene A.m - 255
.. ax nm
OH
Pheno Amax 270 nm
J ~

Anilin A.na - 280 nm

e ) N 2
I

30
 ABSORPTION &
INTENSITY SHIFTS

31
 1) Bathochromic shift(red shift)

 When the absorption maxima(λmax)of a compound

shifts to longer wavelength,it is known as
bathochromic shift or red shift.

 The effect is due to the presence of auxochrome or by

change of solvent.

 Eg: The n-π* transition for carbonyl compounds

experiences bathochromic shift when the polarity of
solvent is decreased.
32
 2) Hypsochromic shift(blue shift)

 When the absorption maxima (λmax) of a compound

shifts to a shorter wavelength,it is known as
hypsochromic shift or blue shift.

 The effect is due to the presence of a group causes

removal of conjugation or by change of solvent.

33
Eg:

+ HCl + cr

Aniline shows blue shift in acidic medium since it loses

conjugation. Aniline(280nm) & Anilinium ion (-
203nm).

34
3) Hyperchromic effect

Pytidine 2-methyl pyridine

Ama,. = Ama~= 260 nm
257 nm e ~ 3560
35
E= 2750
4) Hypochromic effect

CH3

Naphthalene 2- naphthalen
E= methyl e
19000 E= 10250
36
SHIFTS & EFFECTS

-- Blu
e
~ shift
!::
~
<
.
;..
t::J
o
.
<o
C I
Hypochrornic shíft
J

A,n.tl(
Wavelcngth 37
(A)
ABSORPTION
BANDS

38
 r
l ) J

~
I
 The spectrum consist of sharp peaks and each peak will
correspond to the promotion of electron from one
electronic level to another.

 During promotion,the electron moves from a given

vibrational and rotational level within one electronic mode
to the other within the next electronic mode.

 Thus,there will be a large no of possible transitions

 Hence,not just one but a large no. of wavelengths which

are close enough will be absorbed resulting in the
formation of bands 39
1) K – Band
 K-Bands originate due to π-π* transition from a
compound containing a conjugated system

 Such type of bands arise in compounds like

dienes,polyenes and enones etc.

Compound Transition λmax(nm) εmax

Acetophenone π-π* 240 13,000

1,3-butadiene π-π* 217 21,000

40
 (
-
 R-Band transition originate due to n-π* transition of a
single chromophoric group and having atleast one
lone pair of electrons on the hetero atom

 These are less intense with εmax value below 100

Compound Transition λmax(nm) εmax

Acetone n-π* 270 15

Acetaldehyde n-π* 293 12

41
 Such type of bands arise due to π-π* transition in
aromatic or hetero-aromatic molecules.

 Benzene shows absorption peaks between 230-

270nm.when a chromophoric group is attached to the
benzene ring ,the B-Bands are observed at longer
wavelengths than the more intense K-Bands.

Compound Transition λmax(nm) εmax

Benzene π-π* 255 215

Phenol π- π* 270 1450

42
/J . J ·,.-- ) r-
r- r:
 E-Band originate due to the electronic transitions in
the benzenoid systems of three ethylenic bonds which
are in closed cyclic conjugation.
 These are further characterized as E1 and E2 bands
 E1 band which appear at shorter wavelength is
usually
compound
more intensewhich appears
than the E2 bandatfor
longer wavelength.
the same
Compound E1 Band E1 Band E2 Band E2 Band

λmax(nm) εmax λmax(nm) εmax

Benzene 184 50,000 204 79,000

Napthalene 221 133,000 286 9,300

43
La
w

44
BEER’S LAW
According to this law,when a beam of monochromatic
radiation is passed through a solution of absorbing species,the
intensity of beam of monochromatic light decreases exponentially
with increase in concentration of absorbing species

-dI/dc α I
LAMBERT’S LAW
Lambert’s law states that the rate of decrease of
intensity of monochromatic light with the thickness of the
medium is directly proportional to the intensity of incident
light.
-dI/dt α I

45
 .1 1 ~ l j 'J l /'-,l J J ', J .) rr- /; J '
'
) r(
r J
l J
f¡
'.

fj j j
'. ,/ )
!
According to beer’s law,
-dI α I
dc
The decrease in the intensity of light (I) with
concentration(c) is proportional to intensity of
incident light(I)
-dI = K.I { removing & introducing the
dc constant of proportionality
“K”}
-dI = K.dc { rearranging terms}
I
46
On Integrating the equation,

- ∫dI = K. ∫dc
I
-ln I = K.c + b {b constant of integration}
When concentration =0, there is no absorbance,Hence I=I₀
Substituting in equation 
-ln I₀ = K*0+b
-ln I₀ = b
Substituting the value of b in equation
-ln I = K.c-ln I₀
ln I₀ - ln I = Kc { since log A-logB = log A }
B
ln I₀ = Kc
I
47
 I₀ = ekc { removing natural log }
I
I = e-kc {making inverse on both sides}

I₀

I = I₀e-kc  [equation for beer’s law]

According to lambert’s law,

-dI α I
dt
This eqn be simplified by replacing ‘c’ with ‘t’ in
can
I = I₀e-kt 

Eqn  &  can be combined to get I = I₀e-kct 48

Converting natural log to base 10 & K= k x 0.4343

I = ₁₀-kct { rearranging terms }

I₀

I₀ = ₁₀kct { inverse on both sides}

I
T on both sides ,
aking log = Kct 
l
og I₀
Here, Transmittance T = I₀ , Absorbance,A = log 1
I
I T

49
 A = log 1
T
A = log 1 { Since T = I₀ }
I/I₀ I
A =log I₀ 
I
Using eqn & , since A =log I₀ and log I₀ = Kct ,
I I
A= Kct
Instead of K, we can ε
use
A = εct { Mathematical eqn for beer lambert’s
law}

50
 F an partlcu lar wavelength,
or y
Concentrat on

•
&bC
•
Mol/l

Ab or anc
P th 1 cm
ngth'
olar ab orptlv ty ~ U(mol cm)

51
 Positiv Ideal
e
deviano
n

Concentration
52
There are 3 types of deviations usually observed

A)The real limitation of the law is that the beer’s law is

successful in describing the absorption behaviour of
dilute solutions only.

B)CHEMICAL DEVIATIONS:

Association of molecules
This can be explained by taking the examples of
methylene blue at small concentration(10‾⁵ molar) and
at concentration above 10‾⁵molar.

53
 Dissociation of molecules
This can be explained by the fact that dichromate
ions posses their maximum absorbance at 450nm
which is orange in colour .But upon dilution,it will be
dissociated to chromate ions having maximum
absorbance at 410nm which is yellow in colour.

 This law is not valid in case if the absorbing material

is coagulated into a small number of large units.

This law shows deviation if the absorbing material at

the required wavelength contains presence of
impurities.

54
 This law is not applicable in case of suspension.

C)INSTRUMENTAL DEVIATIONS:

 Strict adherence of an absorbing system to this law is

observed only when the radiation used is monochromatic.

 Stray radiation,slit width also causes deviation.

Hence,the reasons for the deviation depends on

environment such as temperature,pressure,solvent,
refractive index of the sample

55
 Absorbance
0.800
λ=430nm
0.600 λ=570nm

0.400

0.200

0.00
0.00 4.00 8.00 12.00 16.00 concentration
56
 /Í J
I

 Absorbance
0.800 ε=1000 ε=1500

0.600
ε=1750
0.400

0.200

0.00 2.0 4.0 6.0 8.0 10.0 concentration

57
 j ) ! /, (

Absorbance 0.0%
 2.0 0.2%

 1%

 1.0 5%

 0
 2.5 5.0 7.5 10 concentration

58
1)Elementary organic spectroscopy,principles & chemical
applications,Y.R Sharma,Revised edition,pg n.o
18,26,27
2) Pharmaceutical chemistry,Instrumental
techniques,vol 2,Leslie.G.chatten,pg n.o 21-24
3)Principles and practice of analytical chemistry,F.W
Fifield & D.kealey, 5th edition ,pg n.o 270-274
4)Pharmaceutical analysis,P.Parimoo, pg n.o
147,151,152,165
5)Industrial methods of chemical
analysis,B.K Sharma,pg n.o 46-65,91-113
59



THANKYOU…
61