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Spectrofluorimetry
        Jobin Kunjumon Vilapurathu
        MPharm (Pharmacy Practice)
Introduction
• Absorption of uv/visible radiation causes
  transition of electrons from ground state (low
  energy) to excited state (high energy).
• As excited state is not stable, excess energy is
  lost by
  ▫ Collisional deactivation
  ▫ Emission of radiation (Photo Luminescence)
• Emission Spectroscopy : emission of radiation is
  studied.
Understanding the terms……..
• Singlet ground state : state in which electrons in a
  molecule are paired. [ ]
• Singlet excited state: state in which electrons are
  unpaid but of opposite spins. [ ]
• Triplet state: state in which unpaired electrons of
  same spin are present. [ ]
• Excitation process: absorption of energy or light
  followed by conversion from ground state to excite
  state.
• Relaxation process: process by which atom or
  molecule losses energy & returns to ground state.
Photo Luminescence
• Light without heat or cold light
• Basically of 2 types
  ▫ Fluorescence: part of energy is lost due to
    vibrational transitions and remaining energy is
    emitted as uv/visible radiation of longer
    wavelength than incident light.
  ▫ Phosphorescence: under favorable
    conditions, excited singlet state undergo transition
    to triplet state. Emission of radiation when e-
    undergo transition from triplet state to ground
    state.
Classification
• Based on the wavelength of emitted radiation
  when compared to absorbed radiation
 ▫ Stokes fluorescence: wavelength of emitted
   radiation is longer than absorbed radiation
 ▫ Anti-stokes’s fluorescence: wavelength of emitted
   radiation is shorter than absorbed radiation.
 ▫ Resonance fluorescence: wavelength of emitted
   radiation is equal to that of absorbed radiation.
Actors affecting fluorescence intensity
• Conjugation: molecule must have conjugation ( π electron)
  so that uv/vis radiation can be absorbed
• Nature of substituent groups:
  ▫ e- donating groups like NH2, OH groups enhance fluorescence.
  ▫ e- withdrawing groups like NO2, COOH reduce fluorescence.
• Fluorescent intensity is directly proportional to
  concentration.
• Increase in viscosity leads to decreased collisions of
  molecules there by increasing fluorescent intensity.
• More rigid the structure of molecule, more the intensity of
  fluorescence.
• Increase in temp leads to increased collisions b/w
  molecules decreasing fluorescent intensity.
• Presence of O2 decreases the fluorescence and so de-
  aerated solutions must be used and compare result
  obtained from that of O2 containing solution.
Instrumentation
                    I0             It
                         Sample
 Lamp                    Cell



          Primary
                              Ie
          filter

                                   Secondary
                                   Filter




                                   Photo
                                   Multiplier
                                   tube
• Source of light
  ▫ Mercury vapour lamp : Hg vapour in high
    pressure (8 atm) gives intense lines on continuous
    background above 350nm.
  ▫ Xenon arc lamp: gives more intense radiation.
  ▫ Tungsten lamp: used if excitation has to be done
    in vis region.
• Filters and monochromators
  ▫ In fluorimeter 10 filter ( absorb vis radiation and
    transmit uv radiation) and 20 filter (absorb uv
    radiation and transmit vis radiation) are present.
  ▫ In spectrofluorimeters, excitation
    monochromators and emission monochromator
    are present.
• Sample cells
 ▫ Sample cells are cylindrical or polyhedral made up
   of colour corrected fused glass & path length
   normally 10mm to 1cm.
• Detectors
 ▫ Photo voltaic cell, photo tubes or photo multiplier
   tubes can be used.
Advantages
• More sensitive when compared to other
  absorption techniques. Concentrations as low as
  μg/ml or ng/ml can be determined.
• Precision upto 1% can be achieved easily
• As both excitation & emission wave lengths are
  characteristic it is more specific than absorption
  methods.
Applications of Spectrofluorimetry
• Determination of Organic substances
  ▫ Plant pigments, steroids, proteins, naphthols etc can
    be determined at low concentrations.
  ▫ Generally used to carry out qualitative as well as
    quantitative analysis for a great aromatic compounds
    present in cigarette smoking, air pollutant
    concentrates & automobile exhausts.
• Determination of inorganic substances
• Extensively used in the field of nuclear research for
  the determination of uranium salts.
• Determination of vitamin B1 (thiamine) in food
  samples like meat cereals etc.
• Determination of Vitamin B2 (riboflavin). This
  method is generally used to measure the amount of
  impurities present in the sample.
• Most important applications are found in the
  analyses of food products, pharmaceuticals,
  clinical samples and natural products.
• Fluorescent indicators:
 ▫ Intensity and colour of the fluorescence of many
   substances depend upon the pH of solutions.
   These are called as fluorescent indicators and are
   generally used in acid base titrations.
 ▫ Eg: Eosin – pH 3.0-4.0 – colourless to green
 ▫ Fluorescien – pH 4.0-6.0 – colourless to green
Spectrofluorimetry

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Spectrofluorimetry

  • 1. Spectrofluorimetry Jobin Kunjumon Vilapurathu MPharm (Pharmacy Practice)
  • 2. Introduction • Absorption of uv/visible radiation causes transition of electrons from ground state (low energy) to excited state (high energy). • As excited state is not stable, excess energy is lost by ▫ Collisional deactivation ▫ Emission of radiation (Photo Luminescence) • Emission Spectroscopy : emission of radiation is studied.
  • 3.
  • 4. Understanding the terms…….. • Singlet ground state : state in which electrons in a molecule are paired. [ ] • Singlet excited state: state in which electrons are unpaid but of opposite spins. [ ] • Triplet state: state in which unpaired electrons of same spin are present. [ ] • Excitation process: absorption of energy or light followed by conversion from ground state to excite state. • Relaxation process: process by which atom or molecule losses energy & returns to ground state.
  • 5. Photo Luminescence • Light without heat or cold light • Basically of 2 types ▫ Fluorescence: part of energy is lost due to vibrational transitions and remaining energy is emitted as uv/visible radiation of longer wavelength than incident light. ▫ Phosphorescence: under favorable conditions, excited singlet state undergo transition to triplet state. Emission of radiation when e- undergo transition from triplet state to ground state.
  • 6.
  • 7. Classification • Based on the wavelength of emitted radiation when compared to absorbed radiation ▫ Stokes fluorescence: wavelength of emitted radiation is longer than absorbed radiation ▫ Anti-stokes’s fluorescence: wavelength of emitted radiation is shorter than absorbed radiation. ▫ Resonance fluorescence: wavelength of emitted radiation is equal to that of absorbed radiation.
  • 8. Actors affecting fluorescence intensity • Conjugation: molecule must have conjugation ( π electron) so that uv/vis radiation can be absorbed • Nature of substituent groups: ▫ e- donating groups like NH2, OH groups enhance fluorescence. ▫ e- withdrawing groups like NO2, COOH reduce fluorescence. • Fluorescent intensity is directly proportional to concentration. • Increase in viscosity leads to decreased collisions of molecules there by increasing fluorescent intensity. • More rigid the structure of molecule, more the intensity of fluorescence. • Increase in temp leads to increased collisions b/w molecules decreasing fluorescent intensity. • Presence of O2 decreases the fluorescence and so de- aerated solutions must be used and compare result obtained from that of O2 containing solution.
  • 9. Instrumentation I0 It Sample Lamp Cell Primary Ie filter Secondary Filter Photo Multiplier tube
  • 10. • Source of light ▫ Mercury vapour lamp : Hg vapour in high pressure (8 atm) gives intense lines on continuous background above 350nm. ▫ Xenon arc lamp: gives more intense radiation. ▫ Tungsten lamp: used if excitation has to be done in vis region. • Filters and monochromators ▫ In fluorimeter 10 filter ( absorb vis radiation and transmit uv radiation) and 20 filter (absorb uv radiation and transmit vis radiation) are present. ▫ In spectrofluorimeters, excitation monochromators and emission monochromator are present.
  • 11. • Sample cells ▫ Sample cells are cylindrical or polyhedral made up of colour corrected fused glass & path length normally 10mm to 1cm. • Detectors ▫ Photo voltaic cell, photo tubes or photo multiplier tubes can be used.
  • 12. Advantages • More sensitive when compared to other absorption techniques. Concentrations as low as μg/ml or ng/ml can be determined. • Precision upto 1% can be achieved easily • As both excitation & emission wave lengths are characteristic it is more specific than absorption methods.
  • 13. Applications of Spectrofluorimetry • Determination of Organic substances ▫ Plant pigments, steroids, proteins, naphthols etc can be determined at low concentrations. ▫ Generally used to carry out qualitative as well as quantitative analysis for a great aromatic compounds present in cigarette smoking, air pollutant concentrates & automobile exhausts. • Determination of inorganic substances • Extensively used in the field of nuclear research for the determination of uranium salts. • Determination of vitamin B1 (thiamine) in food samples like meat cereals etc. • Determination of Vitamin B2 (riboflavin). This method is generally used to measure the amount of impurities present in the sample.
  • 14. • Most important applications are found in the analyses of food products, pharmaceuticals, clinical samples and natural products. • Fluorescent indicators: ▫ Intensity and colour of the fluorescence of many substances depend upon the pH of solutions. These are called as fluorescent indicators and are generally used in acid base titrations. ▫ Eg: Eosin – pH 3.0-4.0 – colourless to green ▫ Fluorescien – pH 4.0-6.0 – colourless to green