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PRESENTATION ON
ABSORPTION AND
INTENSITY SHIFT
Chromophore: A covalently unsaturated group
responsible for electronic absorption. or Any group of
atoms that absorbs light whether or not a color is
thereby produced
eg: NO2, N=O, C=O, C=N, C=C, C=S etc
Auxochrome: A saturated group with non-bonding
electron when attached to chromophore alters both
wave lengths as well as intensity of absorption
e.g. OH, NH2, NHR etc
Concept of chromophore & auxochrome
1
• BATHOCHROMIC SHIFT
2
• HYPSOCHROMIC SHIFT
3
• HYPERCHROMIC SHIFT
• HYPOCHROMIC SHIFT
4
Auxochromic substituents may have any of 4 effects on
chromophore
-Absorption shifted toward longer
wave length.
-Due to the change of solvent and
auxochrome.
Example:
BATHOCHROMIC SHIFT ( RED SHIFT1
2: an auxochrome group like –OH , OCH3 , -CH3 show
bathochromic shift
1:n-∏* transition for carbonyl compound experiences
the bathochromic shift when the polarity of the
solvent decreased.
3: bathochromic shift also result s from the increase of
conjugated system.
-Shift toward shorter wave length .
-Due to the change of solvent towards higher
polarity or removal of conjugation or due to
the effect of auxochrome.
-eg:
Hypsochromic shift ( blue shift)2
 Substitution on carbonyl group by an auxochrome
with a lone pair of electrons, such as- NR2 ,- NHR,
OH ,-OR, -X as in amide ,acid ,acid chlorides, esters
gives a pronounced hypsochromic effect on n-∏*
transition.
-Shift due to increase in intensity .
-Due to introduction of auxochrome.
-Alkyl substitution produces hyperchromic effect
-Example: pyridine -257nm and Emax is 2750;
- 2-methy pyridine – 262 nm and Emax – 3560
HYPERCHROMIC SHIFT3
Inverse of hyperchromic shift
-I.e. decrease of intensity
--introduction of any group to the compound s which
going to alter the molecular pattern of the compound
results in hypochromic shift.
-- ex: biphinyl absorption is 250 nm and Emax -19000
--where 2- methyl biphinyl has an absorption of
257nm and E max is 1o250
HYPOCHROMIC SHIFT)4
THAT’S ALL AND
THANKS TO ALL

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Absorption and intensity shift

  • 2.
  • 3.
  • 4. Chromophore: A covalently unsaturated group responsible for electronic absorption. or Any group of atoms that absorbs light whether or not a color is thereby produced eg: NO2, N=O, C=O, C=N, C=C, C=S etc Auxochrome: A saturated group with non-bonding electron when attached to chromophore alters both wave lengths as well as intensity of absorption e.g. OH, NH2, NHR etc Concept of chromophore & auxochrome
  • 5. 1 • BATHOCHROMIC SHIFT 2 • HYPSOCHROMIC SHIFT 3 • HYPERCHROMIC SHIFT • HYPOCHROMIC SHIFT 4 Auxochromic substituents may have any of 4 effects on chromophore
  • 6.
  • 7. -Absorption shifted toward longer wave length. -Due to the change of solvent and auxochrome. Example: BATHOCHROMIC SHIFT ( RED SHIFT1
  • 8. 2: an auxochrome group like –OH , OCH3 , -CH3 show bathochromic shift 1:n-∏* transition for carbonyl compound experiences the bathochromic shift when the polarity of the solvent decreased.
  • 9. 3: bathochromic shift also result s from the increase of conjugated system.
  • 10. -Shift toward shorter wave length . -Due to the change of solvent towards higher polarity or removal of conjugation or due to the effect of auxochrome. -eg: Hypsochromic shift ( blue shift)2
  • 11.
  • 12.  Substitution on carbonyl group by an auxochrome with a lone pair of electrons, such as- NR2 ,- NHR, OH ,-OR, -X as in amide ,acid ,acid chlorides, esters gives a pronounced hypsochromic effect on n-∏* transition.
  • 13. -Shift due to increase in intensity . -Due to introduction of auxochrome. -Alkyl substitution produces hyperchromic effect -Example: pyridine -257nm and Emax is 2750; - 2-methy pyridine – 262 nm and Emax – 3560 HYPERCHROMIC SHIFT3
  • 14. Inverse of hyperchromic shift -I.e. decrease of intensity --introduction of any group to the compound s which going to alter the molecular pattern of the compound results in hypochromic shift. -- ex: biphinyl absorption is 250 nm and Emax -19000 --where 2- methyl biphinyl has an absorption of 257nm and E max is 1o250 HYPOCHROMIC SHIFT)4