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CHROMOPHORE CONCEPT
PRESENTED BY;
AISWARYA.A.T
I MPharm.,
DEPARTMENT OF PHARMACY PRACTICE
GRACE COLLEGE OF PHARMACY
CHROMOPHORE
 Defined as any isolated covalently bonded group
that shows a characteristic absorption of
Electromagnetic radiation in the UV or visible
region.
It is a Greek word.
Chroma = “color” & phoros = “bearer”
Compound containing chromophore is CHROMOGEN
Eg: C=C, C=O, NO2
TYPES OF CHROMOPHORES
1. INDEPENDENT CHROMOPHORES
If one chromophore is required to impart colour
Eg: Azo group –N=N-, Nitroso group –NO-
2. DEPENDENT CHROMOPHORES
If more than one chromophore is required to impart colour
Eg: Acetone having one ketone group is colorless whereas
diacetyl having two ketone groups is yellow.
Groups λmax
C – C 1350
C = C 1900
C = O 1900
2800
O – H 1850
NO2 2800
C6H5( PHENYL) 1950
2500
SIMPLE CHROMOPHORIC GROUPS
Auxochrome
A saturated/ unsaturated group with non bonding
electrons when attached to chromophore altering both
wavelength as well as intensity of absorption.
Eg: OH, NH2, NHR, COOH, CN, Cl etc..
Two types:
1) Basic/positive auxochromic groups
Effective in acid solutions
Eg: OH, OR, NHR etc.
2) Acidic/negative auxochromic groups
Effective in alkaline solutions
Eg: NO, CO, CN etc.
CHANGESIN POSITION& INTENSITYOF ABSORPTION
For isolated chromophore groups such as –C=C- absorption
takes place at far UV which cannot be easily studied but the
position & intensity can be modified:
bathochromic
hypsochromic hyperchromic
hypochromic
200 wavelength 800
absorbance
λ max
BATHOCHROMIC SHIFT/ RED SHIFT
•Shift of absorption maximum towards longer
wavelength
•Due to presence of groups like OH, NH2 etc.
(auxochromes)
Eg: ethylene shows absorption at 170nm whereas
1,3-butadiene shows at 217nm.
HYPSOCHROMIC SHIFT / BLUE SHIFT
•Shift of absorption maximum towards shorter
wavelength
•May be caused by removal of conjugation
Eg: In Aniline, absorption takes place at 280nm.
In acidic solutions, absorption takes place at
200nm
HYPERCHROMIC SHIFT
Increase in intensity of absorption
By introduction of ‘auxochrome’
Eg: introduction of methyl group in position 2 of
pyridine increases intensity of absorpion from
2750 to 3560
HYPOCHROMIC SHIFT
Decrease in intensity of absorption
Eg: introduction of methyl group in position 2 of
biphenyl group causes hypochromic effect because
of distortion
THANK YOU!!!

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Chromophore concept

  • 1. CHROMOPHORE CONCEPT PRESENTED BY; AISWARYA.A.T I MPharm., DEPARTMENT OF PHARMACY PRACTICE GRACE COLLEGE OF PHARMACY
  • 2. CHROMOPHORE  Defined as any isolated covalently bonded group that shows a characteristic absorption of Electromagnetic radiation in the UV or visible region. It is a Greek word. Chroma = “color” & phoros = “bearer” Compound containing chromophore is CHROMOGEN Eg: C=C, C=O, NO2
  • 3. TYPES OF CHROMOPHORES 1. INDEPENDENT CHROMOPHORES If one chromophore is required to impart colour Eg: Azo group –N=N-, Nitroso group –NO- 2. DEPENDENT CHROMOPHORES If more than one chromophore is required to impart colour Eg: Acetone having one ketone group is colorless whereas diacetyl having two ketone groups is yellow.
  • 4. Groups λmax C – C 1350 C = C 1900 C = O 1900 2800 O – H 1850 NO2 2800 C6H5( PHENYL) 1950 2500 SIMPLE CHROMOPHORIC GROUPS
  • 5. Auxochrome A saturated/ unsaturated group with non bonding electrons when attached to chromophore altering both wavelength as well as intensity of absorption. Eg: OH, NH2, NHR, COOH, CN, Cl etc..
  • 6. Two types: 1) Basic/positive auxochromic groups Effective in acid solutions Eg: OH, OR, NHR etc. 2) Acidic/negative auxochromic groups Effective in alkaline solutions Eg: NO, CO, CN etc.
  • 7. CHANGESIN POSITION& INTENSITYOF ABSORPTION For isolated chromophore groups such as –C=C- absorption takes place at far UV which cannot be easily studied but the position & intensity can be modified: bathochromic hypsochromic hyperchromic hypochromic 200 wavelength 800 absorbance λ max
  • 8. BATHOCHROMIC SHIFT/ RED SHIFT •Shift of absorption maximum towards longer wavelength •Due to presence of groups like OH, NH2 etc. (auxochromes) Eg: ethylene shows absorption at 170nm whereas 1,3-butadiene shows at 217nm.
  • 9. HYPSOCHROMIC SHIFT / BLUE SHIFT •Shift of absorption maximum towards shorter wavelength •May be caused by removal of conjugation Eg: In Aniline, absorption takes place at 280nm. In acidic solutions, absorption takes place at 200nm
  • 10. HYPERCHROMIC SHIFT Increase in intensity of absorption By introduction of ‘auxochrome’ Eg: introduction of methyl group in position 2 of pyridine increases intensity of absorpion from 2750 to 3560 HYPOCHROMIC SHIFT Decrease in intensity of absorption Eg: introduction of methyl group in position 2 of biphenyl group causes hypochromic effect because of distortion