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RESONANCE RAMAN SPECTROSCOPY

Resonance Raman Spectroscopy

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Page 1: Resonance Raman Spectroscopy

RESONANCE RAMAN SPECTROSCOPY

Page 2: Resonance Raman Spectroscopy

OverviewBrief introduction on Resonance Raman

Scattering.Advantages of RRS.Why intensity of the scattered radiation is

enhanced? Quantum Mechanical Theory of normal

Resonance Raman Scattering.Theory of Resonance Raman Scattering.A-term Resonance Raman Scattering.B- term resonance Raman Scattering.

Page 3: Resonance Raman Spectroscopy

What is Resonance Raman Scattering?

The wave number of the exciting radiation is close or same with that of an electronic transition.

Page 4: Resonance Raman Spectroscopy

Advantages of Resonance Raman Spectroscopy.Enhancement of intensities of partticular

bands.High sensitivity….Analytical tool for the study of chromophores.Detailed information about those excited

states which raman active.

Page 5: Resonance Raman Spectroscopy

Why intensity is enhanced?

Irradiance.

Transition Polarisibillity tensor.

Wave number of incident radiation.

i- is the initial state.f – is the final state.

The above expression is the intensity of scattered radiation at 90• angle.

What is transition polarizability tensor?What is irradiance?What is damping factor?

Page 6: Resonance Raman Spectroscopy

Theory of normal Raman Scattering

Adiabatic Born Oppenheimer approximation……??

Formed by product of the pure vibrationaland the pure electronic state.

Electronic state parametrically dependent on the normal co-ordinate of the molecule.Electronic transition moment also dependent on normal co-ordinate.

The electronic and vibrational part of the integrals can be seperated.

Page 7: Resonance Raman Spectroscopy

When excitation far from any region of electronic absorption…..normal Raman.The denominators in the transition polarizability

are large.

With all these approximation………..

What is the significance of each term?Rayleigh Scattering , Raman Scattering,

overtone and combination band.

Page 8: Resonance Raman Spectroscopy

Theory of Resonance Raman Scattering(1)Adiabatic Born Oppenheimer approximation is

assumed to valid.

H T perturbation description to vibronic coupling……..

Variation of transition moment Is related with the vatriation of Hamiltonian with normal co-ordinate can mix the state e with Other state s.

Page 9: Resonance Raman Spectroscopy

Four contribution to the transition polarizability……

What is vibronic coupling ? Is Born Oppenheimer Approx. applicable under

strong vibronic coupling?

Brief discussion on each term

Page 10: Resonance Raman Spectroscopy

A-term Resonance Raman Scattering

What are the conditions for A-term contribution to RRS?

What is Frank Condon factor?The technique requires the excitation within the

contour of intense absorption band.Excitation with in the contour of weak band

(like spin forbidden transition ) would not be expected to give significant A term.

Page 11: Resonance Raman Spectroscopy

Non-zero Vibrational overlap integralWhen Vibrational wave functions are non orthogonal.This condition arises when….there is either…

1) A difference in vibrational wave number i.e. change in shape of the potential surface.

2) A displacement of the potential energy minimum along normal co-ordinate.

3) This occurs only in totally symmetric modes of vibration…….why?

Page 12: Resonance Raman Spectroscopy

Orthogonality condition is not removed

Produces non zero overlap integral For both totally symmetric and not Totally sym.mode.

These two only applicable to the totallySymmetric mode .

Page 13: Resonance Raman Spectroscopy

B-term Resonance Raman Scattering

Conditions : 1)vibronic coupling . 2) both resonant transition and transitions are electric dipole

allowed. B-term is very much smaller than A –term when A term is more important than B-term?When B term is more important than A-term?

Page 14: Resonance Raman Spectroscopy

THANK YOU