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What is a Virtual state?

Short Answer

Expert verified

Part a: The virtual state is the term used to describe the intermediate state produced in the Raman process

Part b: A virtual state is an intermediate state sometimes described as imaginary in a multi step process that mediates otherwise forbidden transitions.

Step by step solution

01

Background

In most Raman experiments, the incident radiation is not near( or at) an absorbing wavelength , and so you will never access a real, honest to god excited state ( stationary state). ( If it was close to an absorbing wavelength, we would be talking about a resonance Raman experiment.)

02

Explanation

Now obviously something is going on between the molecule and the incident light. what you are really doing ia preparing a superposition of real excited states, or stationary states, of your hamiltonian, so its energy is undefined. ( you are free to compute an expectation value though.)

03

Step:3  Conclusion

The virtual state doesn't last forever, and when it decays, scatters radiation in some direction ( it doesn't matter where, unless you are doing an angle resolved Raman experiment.)

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Most popular questions from this chapter

The following questions all deal with the similarities and differences between IR spectrometry and Raman spectrometry.

(a) What are the requirements for a vibrational mode in a molecule to show IR absorption? What are the requirements for a vibrational mode to be Raman active? Why do these requirements differ? Under what circumstances will vibrational modes by both Raman and IR be active? Under what circumstances will vibrational modes be Raman active but not IR active and vice versa?

(b) Consider the molecule chloroacetonitrile (ClCH2CN). How many vibrational modes should this molecule have? Why might one observe fewer Raman bands than expected?

(c) Chloroacetonitrile shows a strong Raman band at 2200cm-1due to the C-N stretching mode. The corresponding IR absorption is very weak or absent. By comparing spectra in the 2200cm-1region, what can you conclude about the C-N stretching mode in chloroacetonitrile?

(d) Compare and contrast IR and Raman spectrometry with respect to optics, cell materials, sample handling, solvent compatibility, and applicability to various sample types.

(e) Compare and contrast the sources and transducers used in Raman spectrometers to those used in FTIR instruments. Consider both FT-Raman and dispersive Raman spectrometers in your comparison.

(f) Compare and contrast IR and Raman spectrometry with respect to qualitative usefulness, detection limits, quantitative analysis, and instrumental complexity.

Assume the excitation sources in Problem 18-3 have the same power. (a) Compare the relative intensities of the Raman lines of the antihistamine for each of the two excitation sources. (b) If the intensities were recorded with a typical monochromator photomultiplier system, why would the measured intensity ratios differ from the ratio calculated in part (a)?

What is a virtual state?

The following Raman data were obtained for CHCl3with the polarizer of the spectrometer set (1) parallel to the plane of polarization of the laser and (2) at 90ยฐto the plane of the source.

Calculate the depolarization ratio and indicate which Raman lines are polarized.

An antihistamine shows sharp peaks at Raman shifts of v=488,725,875,925,and 1350cm-1. At what wavelengths in nanometers would the Stokes and anti-Stokes lines for the antihistamine appear if the source were

(a) a helium-neon laser (632.8 nm)?

(b) an argon-ion laser (488.0 nm)?

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